Next Article in Journal
Calprotectin and Imbalances between Acute-Phase Mediators Are Associated with Critical Illness in COVID-19
Next Article in Special Issue
Activation and Function of NLRP3 Inflammasome in Bone and Joint-Related Diseases
Previous Article in Journal
A Novel High Content Angiogenesis Assay Reveals That Lacidipine, L-Type Calcium Channel Blocker, Induces In Vitro Vascular Lumen Expansion
Previous Article in Special Issue
Osteoarthritis Pain
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
IJMS
Volume 23
Issue 9
10.3390/ijms23094895
ijms-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Positive and Negative Regulators of Sclerostin Expression

by
Rina Iwamoto
1,
Masanori Koide
1,
Nobuyuki Udagawa
2 and
Yasuhiro Kobayashi
1,*
1
Division of Hard Tissue Research, Institute for Oral Science, Matsumoto Dental University, 1780 Gobara Hiro-oka, Shiojiri 399-0781, Nagano, Japan
2
Department of Biochemistry, Matsumoto Dental University, 1780 Gobara Hiro-oka, Shiojiri 399-0781, Nagano, Japan
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2022, 23(9), 4895; https://doi.org/10.3390/ijms23094895
Submission received: 11 April 2022 / Revised: 27 April 2022 / Accepted: 27 April 2022 / Published: 28 April 2022
(This article belongs to the Special Issue Bone and Cartilage Biology)
Browse Figures
Versions Notes

Abstract

:
Sclerostin is secreted from osteocytes, binds to the Wnt co-receptor Lrp5/6, and affects the interaction between Wnt ligands and Lrp5/6, which inhibits Wnt/β-catenin signals and suppresses bone formation. Sclerostin plays an important role in the preservation of bone mass by functioning as a negative regulator of bone formation. A sclerostin deficiency causes sclerosteosis, which is characterized by an excess bone mass with enhanced bone formation in humans and mice. The expression of sclerostin is positively and negatively regulated by many factors, which also govern bone metabolism. Positive and negative regulators of sclerostin expression and their effects are introduced and discussed herein based on recent and previous findings, including our research.

1. Introduction

Bone tissues repeat a cycle of bone resorption and formation throughout their life after reaching their peak bone mass [1,2,3,4]. This process, called bone remodeling, is performed to preserve bone mass and maintain calcium homeostasis. Osteoclasts, multinucleated bone-resorbing cells, differentiate from monocyte/macrophage progenitor cells [5]. Their differentiation is tightly regulated by osteoblast-lineage cells, such as osteoblasts and osteocytes [6,7]. Osteoblasts constitutively express macrophage colony-stimulating factors (M-CSF; encoded by the Csf1 gene), an essential cytokine for the differentiation and survival of macrophage-lineage cells, including osteoclasts, and osteoblasts and osteocytes inducibly express a receptor activator of the NF-κB ligand (RANKL; encoded by the Tnfsf11 gene), an essential cytokine for osteoclastogenesis, when stimulated with bone-resorbing factors [8,9]. Osteoprotegerin (OPG; encoded by the Tnfrsf11b gene) is also expressed by osteoblast-lineage cells to inhibit osteoclastogenesis [10]. When M-CSF binds to its receptor Csf1r, and RANKL binds to receptor activator of NF-κB (RANK; encoded by the Tnfrsf11a gene) in osteoclast precursors, the differentiation of osteoclasts is initiated. Mature osteoclasts adhere to the bone surface and then secrete hydrogen chloride and several proteases, including cathepsin K, into bone resorption lacunae for the resorption of mineralized matrices and matrix proteins, such as type I collagens [11].
After the completion of osteoclastic bone resorption, osteoblasts secrete and add new bone matrices to resorption lacunae. Some osteoblasts are embedded in the newly formed matrix and differentiate into osteocytes [12]. Osteocytes communicate with each other or with osteoblasts and osteoclasts through their dendrites to sense mechanical stimuli transmitted in bone and then regulate bone remodeling. Recent studies revealed that osteocytes function as an endocrine organ to actively regulate bone mineral metabolism by secreting the phosphate-metabolic hormone Fibroblast growth factor 23 as well as RANKL and OPG [13,14]. Osteocytes also secrete Wnt1 and the Wnt inhibitor sclerostin to tightly regulate bone mass [15,16].
Cytokine Wnt ligands are involved in the development of organs and the maintenance of stem cells in various tissues [17]. In 2001, low-density lipoprotein receptor-related protein 5 (LRP5) was identified as a causative gene for osteoporosis pseudoglioma syndrome (OMIM: 258770) and functions as a Wnt co-receptor to promote bone accrual by enhancing Wnt/β-catenin signals [18]. Sost was also identified as a causative gene for sclerosteosis (OMIM: 269500) and Van Buchem disease (OMIM: 239100) [19,20,21]. Since then, a large number of studies have reported the roles of Wnt ligands and Wnt inhibitors in bone metabolism in addition to the successful application of sclerostin antibodies to the treatment of osteoporosis. In this review, we focus on positive and negative regulators of sclerostin expression and discuss previous and recent findings, including our research, the mechanisms by which sclerostin is expressed in osteocytes, and how these factors regulate its expression.

2. The Canonical Wnt Signaling and Its Role in Bone Formation

Wnt signals induce various biological events through β-catenin-dependent canonical and -independent non-canonical pathways [17]. In the absence of Wnt ligands, β-catenin is phosphorylated by the β-catenin destruction complex of Axin2, adenomatous polyposis polyps, and glycogen synthase kinase-3β, and phosphorylated β-catenin is then ubiquitinated and degraded by proteasomes. Once Wnt ligands bind to their receptor complex of Frizzled and the co-receptor LRP5/6, the activity of the β-catenin destruction complex is suppressed and β-catenin accumulates in the cytosol. Accumulated β-catenin is translocated into the nucleus and promotes the expression of its target genes together with T-cell factor (TCF)/lymphocyte enhancer factor 1.
Limb bud mesenchymal cell-selective (Prrx1-Cre; Wnt1fl/fl) and osteoblast-lineage cell-selective (Osterix-Cre; Wnt1fl/fl or Dmp1-Cre; Wnt1fl/fl) Wnt1-deficient mice exhibited a low bone mass phenotype [22,23,24]. Furthermore, the overexpression of Wnt1 promoted the nuclear translocation of β-catenin in the murine embryo fibroblast cell line C3H10T1/2 [22]. The decreased expression of target genes for the canonical Wnt pathways was detected in bone tissues from Osterix-Cre; Wnt1fl/fl mice [23]. Collectively, these findings indicate that Wnt1 promotes bone formation via the canonical Wnt pathway. Furthermore, the osteoblast-lineage cell-specific expression of Wnt1 increased bone mass. The enhancing effects of Wnt1 on bone mass were not cancelled by the loss of Lrp5, even though Lrp5-deficient mice exhibited a low bone mass [24]. This finding suggests that Wnt1 positively regulated bone mass in a Lrp5-independent manner. Moreover, Cawthorn et al. reported that the overexpression of Wnt6, Wnt10a, and Wnt10b promoted osteoblast differentiation in the bone marrow stromal cell line ST2 and suppressed adipocyte differentiation in cultures of the preadipocyte cell line 3T3-L1 [25]. The knockdown of β-catenin in these cells impaired Wnt6-, Wnt10a-, and Wnt10b-induced osteoblastogenesis and promoted adipogenesis [25]. Therefore, the activation of canonical Wnt pathways in osteoblast-lineage cells drives anabolic effects on bone. Further studies are needed to clarify which Wnt ligands are important for the promotion of bone formation in vivo.

3. Mechanism of Action of Sclerostin

Sclerostin (encoded by the Sost gene) binds to the Wnt co-receptor LRP5/6 and inhibits Wnt/β-catenin signals. A previous study using nuclear magnetic resonance spectroscopy showed the three-dimensional structure of sclerostin [26]. The long N- and C-terminal regions of sclerostin are unstructured and highly flexible. The remaining region forms three loop structures with a cysteine knot. The extracellular domain of LRP5/6 consists of four β-propeller/epidermal growth factor repeats and three low-density lipoprotein (LDL) repeats. Holdsworth et al. demonstrated that the NXI (Asn-X-Ile) motif in the loop2 region of sclerostin was important for binding to the E1 domain of LRP6 [27]. Kim et al. recently showed that the affinity of sclerostin was higher for LRP6 containing the E1-E2 domains than for that containing E1 only [28]. This finding indicates that sclerostin binds to the E2 domain of LRP6 as well as its E1 domain. Furthermore, the C-terminal region of sclerostin was shown for the first time to bind to the E2 domain of LRP6. Therefore, the loop2 and c-terminal regions of sclerostin interact with the E1 and E2 domains of LRP5/6, respectively.
Bourhis et al. investigated the mechanisms by which Wnt ligands bind to LRP5/6 and showed that Wnt3a interacted with the E3 and E4 domains of LRP6 and that Wnt9b interacted with its E1 and E2 domains [29]. Therefore, Wnt ligands bind to their binding domains of LRP5/6, which differ depending on each ligand.
Since sclerostin binds to the E1-E2 domains of LRP6, it may inhibit Wnt signals induced by Wnt1, Wnt2, and Wnt9a, which bind to E1-E2 of LRP6. In contrast, sclerostin cannot inhibit Wnt3a-induced Wnt signals. Furthermore, the loop2, but not c-terminal, region of sclerostin is important for its inhibitory effects on Wnt1. In contrast, the c-terminal region of sclerostin is more important for its inhibitory effects on Wnt2 and Wnt9b. Dkk1 was shown to bind to the E1 and E3 domains of LRP6 and inhibited Wnt1, Wnt2, Wnt9b, and Wnt3a [28,30]. Therefore, structure–functional interactions among Wnt ligands, receptors, and Lrp5/6 have been clarified.
LRP4 is required for the binding of sclerostin to LRP5/6. Patients with mutations (R1170W, W1186S) in the Lrp4 gene exhibited a high bone mass, similar to patients with sclerosteosis [31,32]. These mutations were detected in the central domain of the third propeller of LRP4, which is needed for the interaction with sclerostin. Mice, in which the mutation (R1170W) was introduced into the Lrp4 gene using a CRISPR/Cas9 approach, exhibited a high bone mass [33]. Serum sclerostin levels were higher in osteoblast-lineage cell-selective Lrp4-deficient mice. This finding suggests that Lrp4 retains sclerostin in bone tissues. Therefore, LRP4 appears to facilitate the binding of sclerostin to LRP5/6 in the microenvironment of bone tissues.

4. Roles of Sclerostin in Bone Development and Bone Formation

Sclerostin was initially considered to be an inhibitor of bone morphogenetic protein (BMP) because of its homology to the differential screening-selected gene in neuroblastoma family members, such as the BMP antagonist noggin. Immunoprecipitation assays showed that sclerostin bound to BMP6 and that this binding was competitively inhibited by the BMP receptor BMPRIA. Sclerostin mildly suppressed the phosphorylation of SMAD by BMP6 and the mineralization of human mesenchymal cells. Sost transgenic mice had a low bone mass with impaired bone formation [34]. Sclerostin was subsequently shown to bind to LRP5/6 and suppress Wnt/β-catenin signaling [35].
Four-month-old Sost-deficient (Sost KO) mice showed a high bone mass phenotype with increased bone formation and unchanged bone resorption [36,37]. Bone mineral density was significantly higher in Sost KO mice at 4 weeks of age, and the difference in bone mineral density between wild-type and Sost KO mice increased with aging. In addition, there were no gross abnormalities in the tibia at E14.5 or in the head and forelimbs on postnatal day 1. We also generated Sost KO mice, examined their bone phenotype [38], and found that bone mass was normal in 6-week-old Sost KO mice (unpublished data). These findings indicate that sclerostin is not involved in bone development. The percentage of sclerostin-positive osteocytes in bone was reported to be lower in 3-day-old mice than in 4-week-old mice [39]. The percentage of sclerostin-positive osteocytes also increased with aging [40]. Collectively, these findings indicate that sclerostin does not play an important role in skeletal development, which may be due to its low expression during the developmental process.

5. Roles of Sclerostin in Bone Resorption

Mice, in which the constitutively active form of β-catenin was expressed in osteoblasts, exhibited an osteopetrotic phenotype with impaired osteoclastogenesis due to the increased expression of OPG [41]. The proximal 3.6 kb OPG promoter assay revealed that TCF proteins, together with β-catenin, induced the expression of OPG in osteoblasts. Furthermore, osteoblast-selective β-catenin conditional knockout mice had a markedly decreased bone mass with an increased number of osteoclasts on the endocortical surfaces due to the decreased expression of OPG in osteoblasts and osteocytes [41]. These findings suggest that the activation of Wnt/β-catenin signals in osteoblasts induces the expression of OPG, which, in turn, suppresses osteoclast differentiation.
Although the activation of Wnt/β-catenin signals suppresses bone resorption, serum levels of bone resorption markers, such as TRAP5b, and histomorphometric markers of osteoclast surface/bone surface were normal in 4-month-old Sost KO mice [36,37]. In contrast, bone resorption was reportedly impaired in Lrp4 cKO mice. Chang et al. reported mild decreases in the number of osteoclasts in 3-month-old male, but not female, osteocalcin (Ocn)-cre; Lrp4fl/fl mice [32]. Furthermore, Xiong et al. showed that the serum level of the bone resorption marker deoxypyridinoline and the number of osteoclasts were markedly lower in 3-month-old Ocn-Cre; Lrp4fl/fl mice [42]. A treatment with sclerostin increased RANKL expression and decreased OPG expression in bone marrow stromal cell cultures prepared from wild-type mice, but not those from Lrp4 KO mice. Sclerostin also up-regulated RANKL expression in human osteoblast-like cells and mouse osteocyte-like MLO-Y4 cells [43]. These findings indicate that the binding of sclerostin to Lrp4 increased the expression of RANKL and decreased the expression of OPG. However, this model does not explain why bone resorption was suppressed in Lrp4 KO mice, but not in Sost KO mice. Therefore, the binding of unidentified ligands to Lrp4 may enhance RANKL expression.

6. The Structure of the Sost Gene

Loss-of-function mutations in the Sost gene cause sclerosteosis (OMIM: 269500) and Van Buchem disease (OMIM: 239100), which are both characterized by a high bone mass. Three mutations have been identified in the Sost gene of patients with sclerosteosis: the C69T mutation in the first exon and two splicing mutations [19]. Baleman et al. reported one splicing mutation and two nonsense mutations in the second exon [20]. In patients with Van Buchem disease, no mutations were found in the coding region of the Sost gene, whereas a 52 kb deletion was identified between the Sost and MEOX1 genes. This deletion started 35 kb downstream of the Sost gene [21].
Mice expressing the wild-type Sost gene exhibited a low bone mass, whereas those expressing the Sost gene lacking the 52 kb region lost in Van Buchem disease did not. Furthermore, ECR5 was important for the bone-specific expression of sclerostin among the seven regions conserved in the 52 kb region of the human and mouse Sost gene. These findings revealed that the ECR5 region is required for the expression of sclerostin in bone [44]. The Mef-binding motif was detected in the ECR5 region based on the inhibitory effects of parathyroid hormone (PTH) on sclerostin expression. Among Mef family members, the expression of Mef2c was the highest in bone, suggesting that it was recruited into ECR5, which, in turn, induced the expression of sclerostin. Osteoblast and osteocyte-specific Mef2c cKO mice or osteoblast and osteocyte-specific deletion of ECR5 mice showed a high bone mass, similar to Sost KO mice [45]. Therefore, Mef2c binds to the bone tissue-specific enhancer ECR5 and induces the expression of sclerostin in osteocytes (Figure 1).

7. Regulation of Sclerostin Expression

7.1. PTH

The anabolic effects of PTH on bone are exerted in part by inhibiting the expression of sclerostin [46]. Since HDAC family members reportedly suppress the transcriptional activity of Mef2, the role of HDAC in the inhibitory effects of PTH on sclerostin expression was investigated [47,48]. The overexpression of HDAC5 suppressed the activity of the Sost enhancer in UMR106 cells, which are known to express sclerostin. Moreover, the knockdown of HDAC5 promoted the transcriptional activity of Mef2c in osteocyte-like cells. The percentage of sclerostin-positive osteocytes increased in Hdac5 KO mice. Wein et al. showed that the knockdown of Class II HDAC HDAC4/5 cancelled the inhibitory effects of PTH on sclerostin expression and also that salt-inducible kinase (SIK) 2 mediated the PTH-induced suppression of HDAC4/5 activity [49]. In the absence of PTH signals, SIK phosphorylates HDACs, which results in their cytosolic retention. PTH signals inhibit SIK2 and then suppress the phosphorylation of HDAC4/5. Dephosphorylated HDACs are retained in the nucleus, suppress the transcriptional activity of Mef2c, and then inhibit the expression of sclerostin (Figure 1). The SIK2 inhibitors YKL-05-093 and -099 have been developed, and the administration of YKL-05-099 increased bone mass with enhanced bone formation in 8-week-old male mice. In addition, sclerostin was more recently reported to be degraded in lysosomes. A stimulation with fluid shear stress and PTH degraded the sclerostin protein in bone, osteocyte-like cells, and UMR106 cells within 30 min [50]. This finding suggests that the rapid degradation of sclerostin in osteocytes is also important for decreasing sclerostin proteins as soon as possible. Further studies are needed to clarify the importance of the rapid lysosomal degradation of sclerostin for the bone anabolic effects of FSS and PTH in vivo.

7.2. PGE2

Prostaglandin E2 (PGE2) binds to EPs1–4 receptors. EP2 and EP4 are coupled to the Gs protein and activate adenylate cyclase-cAMP-PKA signals. EP1 is coupled to Gq-phospholipase C. EP3 is coupled to Gi and inhibits adenylate cyclase [51]. Treatments with PGE2 have been shown to suppress sclerostin expression in UMR106 cells [52,53,54]. The siRNA-mediated knockdown of EP2 and EP4 and treatments with receptor-specific agonists revealed that EP2 mediated the suppressive effects of PGE2 on sclerostin expression in UMR106 cells. A treatment with PGE2 was previously reported to decrease sclerostin expression, even in UMR106 cells, in which the expression of Mef2c was suppressed by siRNA, suggesting that the effects of PGE2 were not mediated by Mef2c [52]. However, PGE2 may inhibit the residual activity of Mef2c to suppress sclerostin expression due to the incomplete knockdown of Mef2c. Therefore, further studies are needed to clarify the roles of PGE2 in sclerostin expression in bone metabolic diseases, including osteoporosis.

7.3. Mechanical Loading

Mechanical loading promotes bone formation and increases bone mass. Osteocytes sense mechanical loading transmitted to bone and down-regulate the expression of sclerostin [55,56]. In contrast, the expression of sclerostin was increased in the unloaded tibiae of tail suspension model mice [56]. These findings indicate that mechanical loading decreases the expression of sclerostin, which, in turn, promotes bone formation.
Previous studies proposed a mechanism by which mechanical loading increases bone mass [57,58]. Since the Ca channel piezo is activated by mechanical stimuli in several cells, the bone phenotypes of osteoblast-specific (Osteocalcin-Cre; Piezo1fl/fl) and osteoblast/osteocyte-specific (Dmp1-Cre; Piezo1fl/fl) Piezo1 cKO were investigated [59,60]. These mice exhibited a low bone mass with impaired bone formation and the mild enhancement of bone resorption. The stimulation with mechanical loading increased the expression of osteoblast marker genes, such as Alpl (encoding alkaline phosphatase) and Bglap (encoding osteocalcin), in control osteoblasts, but not in Piezo1 cKO osteoblasts (Osteocalcin-Cre; Piezo1fl/fl) [59]. The expression of Wnt1 mRNA was decreased in 5-week-old Dmp1-Cre; Piezo1fl/fl mice [60]. However, the expression of sclerostin remained unchanged. The treatment of the osteocyte-like cell line MLO-Y4 with the Piezo1 agonist Yoda1 decreased the expression of sclerostin and increased that of Wnt1. Furthermore, mechanical loading decreased sclerostin expression in osteocyte-like IDG-SW3 cells. In contrast, the inhibitory effects of mechanical loading on sclerostin expression were abrogated by the treatment with the Piezo1 inhibitor GsMTx4 and Akt inhibitor IV as well as the knockout of the Piezo1 gene in these cells [61]. These findings suggest that Piezo1 activates Akt signals and then suppresses the expression of sclerostin. The mechanisms by which Akt signals suppress sclerostin expression and the reason why the deletion of Piezo1 had no effect on sclerostin expression in vivo currently remain unclear. PGE2 is reportedly involved in the suppressive effects of mechanical loading on sclerostin expression [52]. Collectively, these findings indicate that Piezo1 signals cooperate with PGE2 signals to suppress sclerostin expression in vivo.

7.4. Gp130 and IL-6 Family Cytokines

Leukemia inhibitory factor (LIF), oncostatin M (OSM), and cardiotrophin-1 (CT-1) were previously shown to inhibit the expression of sclerostin in UMR106 cells [62]. OSM was highly expressed in osteoblasts, suggesting that OSM secreted from osteoblasts functions as a positive regulator of bone mass to suppress sclerostin expression and promote bone formation. CT-1 expression was detected in osteoclasts and enhanced bone formation [63]. Therefore, CT-1 suppresses sclerostin expression and plays an important role in the transition from bone resorption to formation during bone remodeling. However, the importance of LIF in the suppression of sclerostin expression has not yet been elucidated.
OPG KO mice exhibited a low bone mass with enhanced bone resorption and formation [64]. The expression of Axin2, a target gene of Wnt/β-catenin signals, and the number of β-catenin-positive osteoblasts were increased in bone tissues from these mice, suggesting the enhancement of Wnt/β-catenin signals in OPG KO mice [54]. An increase in the expression of any Wnt ligand has not yet been detected in OPG KO mice. In contrast, the expression of sclerostin was markedly decreased in these mice, suggesting that enhanced bone resorption or osteoclasts themselves suppress sclerostin expression. The treatment of UMR106 cells with conditioned medium (CM) prepared from osteoclast cultures inhibited sclerostin expression. Using protein arrays, LIF was proposed as a candidate factor that suppresses sclerostin expression. A real-time PCR analysis and immunohistochemical studies revealed that LIF was highly expressed in osteoclasts. A recent study using RNA sequencing and gene expression analyses also showed that LIF was highly expressed in human osteoclasts in vitro, but not in human osteocyte- and osteoblast-enriched fractions prepared from bone biopsies [65]. This finding also indicates that LIF is highly expressed in human osteoclasts as well as in mouse osteoclasts. The administration of an anti-RANKL antibody completely inhibited osteoclast formation in OPG KO mice, which resulted in the complete disappearance of LIF-positive osteoclasts and increases in sclerostin-positive osteocytes. Anti-LIF neutralizing antibodies, but not anti-OSM or anti-CT-1 neutralizing antibodies, cancelled the inhibitory effects of osteoclast CM on sclerostin expression in UMR106 cell cultures. These findings indicate that LIF secreted from osteoclasts acts in osteocytes and then suppresses sclerostin expression, which, in turn, promotes bone formation. Therefore, LIF secreted from osteoclasts may act in osteocytes as a coupling factor between bone resorption and formation (Figure 2).
To clearly observe cells expressing sclerostin, Sost Green/+ mice, in which a part of exon 1 after the Sost start codon was replaced with ZsGreen cDNA (coding green fluorescent protein), were generated [38]. The number of ZsGreen-positive osteocytes was lower in trabecular bone than in cortical bone. In contrast, the number of osteoclasts was higher in trabecular bone. When anti-RANKL antibodies were injected into wild-type mice, the number of LIF-positive osteoclasts in trabecular bone markedly decreased, whereas the number of sclerostin-positive osteocytes increased. This finding suggests that osteoclast-derived LIF suppresses sclerostin expression, thereby promoting bone remodeling. Gp130 and IL-6 family cytokines are known to activate JAK-Stat signals. Therefore, further studies are needed to clarify how these cytokines suppress sclerostin expression through these signals.

7.5. 1α,25(OH)2D3

Chromatin immunoprecipitation coupled with high-throughput sequencing showed that 1α,25(OH)2D3 suppressed sclerostin expression; however, the binding of vitamin D receptors (VDR) was not observed adjacent to the Sost gene in IDG-SW3 cell cultures [66]. A mini gene assay showed that the deletion of the ECR5 region and mutations in Mef2-binding sites on the Sost gene abrogated the suppressive effects of the PKA activator forskolin on sclerostin expression, but not those of 1α,25(OH)2D3. The deletion of a 1 kb proximal promoter of the Sost gene also did not alter the effects of 1α,25(OH)2D3. These findings suggest that 1α,25(OH)2D3 suppresses sclerostin expression in Mef2c- and proximal promoter-independent manners.
A real-time PCR analysis showed that sclerostin expression levels in bone were higher in osteoblast-lineage cell-selective VDR cKO mice than in control mice [67]. The administration of the vitamin D3 analog eldecalcitol increased sclerostin expression in bone tissues from control mice, but not those from VDR cKO [67]. These findings indicate that endogenous 1α,25(OH)2D3 suppresses sclerostin expression via VDR and that a pharmacological dose of vitamin D3 enhances sclerostin expression. Wijenayaka et al. reported that 1α,25(OH)2D3 increased sclerostin expression in human primary osteoblasts [68]. They also demonstrated that a VDR-responsive element at a position -6216 bp upstream of the transcription start site on the human Sost gene was essential for 1α,25(OH)2D3 responsiveness [68]. Therefore, the effects of 1α,25(OH)2D3 on sclerostin expression may differ between humans and mice. Furthermore, there may be a difference in the mechanisms of action of endogenous and exogenous 1α,25(OH)2D3, including its analogs.

8. Positive Regulators of Sclerostin Expression

A previous study reported that BMP2 increased the expression of the transcriptional factor osterix and sclerostin in primary osteoblasts [69]. An in situ hybridization analysis showed that osterix-positive areas overlapped with sclerostin-positive areas in embryonic calvariae and limb buds, suggesting that BMP2 enhanced sclerostin expression by inducing the expression of osterix [69]. An analysis of osteoblast-lineage cell-selective Bmpr1a cKO mice revealed that BMP signals enhanced the expression of sclerostin and Dkk1 through Smad- and p38 mitogen-activated protein kinase (p38MAPK)-dependent signals, respectively [70]. Osteoblast-lineage cell-selective Bmpr1a cKO mice exhibited a high bone mass with increased bone formation due to the suppression of sclerostin and Dkk1 expression. Since Smad-binding sites have not yet been identified adjacent to the Sost gene, it currently remains unclear whether BMP2-Smad signals directly regulate sclerostin expression.
Dkk1 is a target gene for Wnt/β-catenin signals. The administration of anti-sclerostin antibodies has been shown to enhance Wnt/β-catenin signals, which increased the expression of Dkk1 [71]. In contrast, the administration of anti-Dkk1 antibodies increased the expression of sclerostin [72], suggesting that sclerostin and Dkk1 are target genes for Wnt/β-catenin signals. Therefore, the expression of sclerostin is positively regulated by BMP and Wnt signals.
After bone mass plateaus at approximately 20 years of age, it gradually decreases with aging. Aged humans and animals exhibited a low turnover in bone metabolism, with significant decreases in both bone resorption and formation. Previous studies investigated whether changes in sclerostin expression were associated with a low bone mass with aging. Serum sclerostin levels were significantly higher in men than in women and positively correlated with age in both groups [73]. Other studies demonstrated that serum sclerostin levels were higher in aged men and women [74,75]. Roforth et al. reported that the mRNA expression of Sost did not significantly differ between young (mean age, 30.0 years) and old (mean age, 72.9 years) women [75]. Serum sclerostin levels correlated with total hip bone mineral density; however, higher serum sclerostin levels were associated with a greater risk of hip fractures in older women [76]. In contrast, serum sclerostin levels were associated with a low risk of fractures, low bone mineral density, and low turnover of bone metabolism [77]. The mRNA expression of Sost in bone tissues was higher in 6-week-old mice than in 6- and 18-month-old mice [78]. Furthermore, the depletion of senescent cells reportedly reduced the mRNA expression of Sost in aged mice [79]. Therefore, there is currently no consensus on the mRNA expression of Sost in humans or mice. These findings indicate that aging is not a major factor regulating sclerostin expression in osteocytes. Aging may also affect the positive and negative regulators of sclerostin expression described above, thereby intricately regulating sclerostin expression in aged bone tissues.

9. Role of Sclerostin in Rheumatoid Arthritis

Sclerostin is certainly involved in the onset of osteoporosis because the administration of anti-sclerostin antibodies (Romosozumab) increased bone formation and decreased bone resorption, which, in turn, markedly increased bone mass in osteoporosis models and patients as previously reported [80,81,82,83,84]. In addition to this, several studies reported that the effects of sclerostin antibodies on bone loss were associated with inflammatory bone diseases such as rheumatoid arthritis. The administration of sclerostin antibody reportedly prevented the decreased systemic bone mineral density, but not focal inflammations such as joint swelling and synovitis, or the focal bone erosions [85,86]. These findings indicate that the sclerostin inhibition effectively increases systemic bone mass even under inflammatory conditions. Furthermore, Wehmeyer et al. reported that sclerostin was expressed in synovial tissues from rheumatoid arthritis patients, and the paw swelling and joint destruction were exacerbated in human tumor necrosis factor-α (TNF) transgenic arthritis models when the Sost gene was targeted in those mice [87]. Sclerostin inhibited TNF-induced activation of p38MAPK in fibroblast-like synoviocytes. The expressions of Sost and Dkk1 were transiently increased before the onset of arthritis in adjuvant-induced arthritis models, suggesting that sclerostin expression is associated with the onset of arthritis as well as Dkk1 [88,89]. Thus, in addition to the inhibitor of Wnt/β-catenin signals, sclerostin may have a role in the suppression of TNF-induced inflammation in rheumatoid arthritis.

10. Role of Sclerostin in Bone Cancers Including Multiple Myeloma

Sclerostin is involved in bone loss associated with multiple myeloma and bone cancers and possibly involved in their pathogenesis [90]. The application of anti-sclerostin antibodies is expected for the treatments of bone cancers. Clinical studies reported that serum levels of sclerostin positively correlate with the progression of multiple myeloma as well as those of macrophage inflammatory protein-1α which is secreted from multiple myeloma plasma cells and involved in the development of myeloma-related bone diseases [90,91,92]. Eda et al. investigated sources of sclerostin and efficiencies of treatments with anti-sclerostin antibodies with a proteasome inhibitor Carfilzomib approved for the treatment of multiple myeloma using humanized multiple myeloma xenograft model mice [92]. Multiple myeloma cells reportedly stimulated the expression of sclerostin in osteoblasts through Dkk1. An immunohistochemical study showed that myeloma cells were markedly decreased in these mice treated with anti-sclerostin antibodies and Carfilzomib, but not treated with only anti-sclerostin antibodies or Carfilzomib. Sclerostin also secreted from myeloma cells and inhibited the differentiation of human bone marrow stroma cells into osteoblasts in cultures [93]. In contrast, MacDonald et al. showed that the expression of sclerostin was not detected in plasma cells from 630 myeloma patients or 54 myeloma cell lines and that the anti-sclerostin antibody failed to reduce tumor burden [94]. Thus, roles of sclerostin in the development of multiple myeloma have been controversial.
Breast cancer cells in bone metastasis regions reportedly expressed sclerostin, and treatment of breast cancer cells with anti-sclerostin antibodies inhibited the proliferation and migration of these cells in cultures [95]. However, treatment with anti-sclerostin antibodies failed to suppress tumor growth in xenograft model mice, in which breast cancer cells were injected into their bone marrows. Hesse et al. reported that sclerostin secreted from breast cancer cells induced muscle fiber atrophy by enhancing NF-κB and p38MAPK signals as well as enhancements of bone destructions by the inhibition of Wnt/β-catenin signals in osteoblasts [96]. Anti-sclerostin antibodies reduced bone metastasis of breast cancer cells with the suppression of bone destructions. They also decreased muscle fiber atrophy by partially restoring pax7-positive satellite cells. Mechanistically, the cancer-induced muscle fiber atrophy was mediated by bone matrix-derived transforming growth factor-β released by the enhanced bone resorption. These findings suggest that anti-sclerostin antibodies are effective not only the prevention of bone destructions, but also the improvement of muscle functions impaired by breast cancer metastasis. Further studies are needed to clarify the mechanisms by which ectopic expression of sclerostin occurs in multiple myeloma and bone metastasis of breast cancers.

11. Conclusions

In this review, we focused on positive and negative regulators of sclerostin expression in osteocytes and discussed the molecular mechanisms by which they regulate sclerostin expression (see Table 1). Among them, the suppressive effects of PTH on sclerostin expression have been intensively investigated. The findings obtained led to the development of small-molecule SIK2 inhibitors that suppress sclerostin expression, thereby increasing bone mass. These SIK2 inhibitors may replace anti-sclerostin antibodies in the treatment of osteoporosis in the future. However, the regulatory mechanisms underlying sclerostin expression by most of these factors, except for PTH, have not yet been elucidated at the molecular level. These mechanisms will be clarified in the future, and new drugs that suppress sclerostin expression will be developed for the treatment of bone metabolic diseases.

Author Contributions

R.I. and Y.K. wrote the manuscript. R.I. prepared the figures. All authors (R.I., M.K., N.U. and Y.K.) discussed the interpretation of previous findings introduced in the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This study was supported by JSPS KAKENHI Grant numbers JP21K21027 (R.I.), JP22K17008 (R.I.), JP19K22729 (M.K.), JP21H03125 (N.U.), JP20K20394 (Y.K.), and JP20K21689 (N.U.).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

No new data were created and analyzed in this study. Data sharing is not applicable to this article.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Zaidi, M. Skeletal remodeling in health and disease. Nat. Med. 2007, 13, 791–801. [Google Scholar] [CrossRef] [PubMed]
  2. Sims, N.A.; Gooi, J.H. Bone remodeling: Multiple cellular interactions required for coupling of bone formation and resorption. Semin. Cell. Dev. Biol. 2008, 19, 444–451. [Google Scholar] [CrossRef] [PubMed]
  3. Feng, X.; McDonald, J.M. Disorders of bone remodeling. Annu. Rev. Pathol. 2011, 6, 121–145. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Robling, A.G.; Castillo, A.B.; Turner, C.H. Biomechanical and molecular regulation of bone remodeling. Annu. Rev. Biomed. Eng. 2006, 8, 455–498. [Google Scholar] [CrossRef]
  5. Boyle, W.J.; Simonet, W.S.; Lacey, D.L. Osteoclast differentiation and activation. Nature 2003, 423, 337–342. [Google Scholar] [CrossRef]
  6. Nakashima, T.; Hayashi, M.; Fukunaga, T.; Kurata, K.; Oh-Hora, M.; Feng, J.Q.; Bonewald, L.F.; Kodama, T.; Wutz, A.; Wagner, E.F.; et al. Evidence for osteocyte regulation of bone homeostasis through RANKL expression. Nat. Med. 2011, 17, 1231–1234. [Google Scholar] [CrossRef]
  7. Xiong, J.; Onal, M.; Jilka, R.L.; Weinstein, R.S.; Manolagas, S.C.; O’Brien, C.A. Matrix-embedded cells control osteoclast formation. Nat. Med. 2011, 17, 1235–1241. [Google Scholar] [CrossRef] [Green Version]
  8. Suda, T.; Takahashi, N.; Udagawa, N.; Jimi, E.; Gillespie, M.T.; Martin, T.J. Modulation of osteoclast differentiation and function by the new members of the tumor necrosis factor receptor and ligand families. Endocr. Rev. 1999, 20, 345–357. [Google Scholar] [CrossRef]
  9. Yasuda, H.; Shima, N.; Nakagawa, N.; Yamaguchi, K.; Kinosaki, M.; Mochizuki, S.; Tomoyasu, A.; Yano, K.; Goto, M.; Murakami, A.; et al. Osteoclast differentiation factor is a ligand for osteoprotegerin/osteoclastogenesis-inhibitory factor and is identical to TRANCE/RANKL. Proc. Natl. Acad. Sci. USA 1998, 95, 3597–3602. [Google Scholar] [CrossRef] [Green Version]
  10. Simonet, W.S.; Lacey, D.L.; Dunstan, C.R.; Kelley, M.; Chang, M.S.; Lüthy, R.; Nguyen, H.Q.; Wooden, S.; Bennett, L.; Boone, T.; et al. Osteoprotegerin: A novel secreted protein involved in the regulation of bone density. Cell 1997, 89, 309–319. [Google Scholar] [CrossRef] [Green Version]
  11. Takayanagi, H. The role of NFAT in osteoclast formation. Ann. N. Y. Acad. Sci. 2007, 1116, 227–237. [Google Scholar] [CrossRef] [PubMed]
  12. Franz-Odendaal, T.A.; Hall, B.K.; Witten, P.E. Buried alive: How osteoblasts become osteocytes. Dev. Dyn. 2006, 23, 176–190. [Google Scholar] [CrossRef] [PubMed]
  13. Dallas, S.L.; Prideaux, M.; Bonewald, L.F. The osteocyte: An endocrine cell... and more. Endocr. Rev. 2013, 34, 658–690. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Sapir-Koren, R.; Livshits, G. Osteocyte control of bone remodeling: Is sclerostin a key molecular coordinator of the balanced bone resorption-formation cycles? Osteoporos. Int. 2014, 25, 2685–2700. [Google Scholar] [CrossRef] [PubMed]
  15. Joeng, K.S.; Lee, Y.C.; Lim, J.; Chen, Y.; Jiang, M.M.; Munivez, E.; Ambrose, C.; Lee, B.H. Osteocyte-specific WNT1 regulates osteoblast function during bone homeostasis. J. Clin. Investig. 2017, 127, 2678–2688. [Google Scholar] [CrossRef] [Green Version]
  16. Van Bezooijen, R.L.; Roelen, B.A.; Visser, A.; van der Wee-Pals, L.; de Wilt, E.; Karperien, M.; Hamersma, H.; Papapoulos, S.E.; Ten Dijke, P.; Löwik, C.W. Sclerostin is an osteocyte-expressed negative regulator of bone formation, but not a classical BMP antagonist. J. Exp. Med. 2004, 199, 805–814. [Google Scholar] [CrossRef]
  17. Logan, C.Y.; Nusse, R. The Wnt signaling pathway in development and disease. Annu. Rev. Cell. Dev. Biol. 2004, 20, 781–810. [Google Scholar] [CrossRef] [Green Version]
  18. Gong, Y.; Slee, R.B.; Fukai, N.; Rawadi, G.; Roman-Roman, S.; Reginato, A.M.; Wang, H.; Cundy, T.; Glorieux, F.H.; Lev, D.; et al. Osteoporosis-Pseudoglioma Syndrome Collaborative Group. LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development. Cell 2001, 107, 513–523. [Google Scholar] [CrossRef] [Green Version]
  19. Brunkow, M.E.; Gardner, J.C.; Van Ness, J.; Paeper, B.W.; Kovacevich, B.R.; Proll, S.; Skonier, J.E.; Zhao, L.; Sabo, P.J.; Fu, Y.; et al. Bone dysplasia sclerosteosis results from loss of the SOST gene product, a novel cystine knot-containing protein. Am. J. Hum. Genet. 2001, 68, 577–589. [Google Scholar] [CrossRef] [Green Version]
  20. Balemans, W.; Ebeling, M.; Patel, N.; Van Hul, E.; Olson, P.; Dioszegi, M.; Lacza, C.; Wuyts, W.; Van Den Ende, J.; Willems, P.; et al. Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST). Hum. Mol. Genet. 2001, 10, 537–543. [Google Scholar] [CrossRef] [Green Version]
  21. Balemans, W.; Patel, N.; Ebeling, M.; Van Hul, E.; Wuyts, W.; Lacza, C.; Dioszegi, M.; Dikkers, F.G.; Hildering, P.; Willems, P.J.; et al. Identification of a 52 kb deletion downstream of the SOST gene in patients with van Buchem disease. J. Med. Genet. 2002, 39, 91–97. [Google Scholar] [CrossRef] [PubMed]
  22. Wang, F.; Tarkkonen, K.; Nieminen-Pihala, V.; Nagano, K.; Majidi, R.A.; Puolakkainen, T.; Rummukainen, P.; Lehto, J.; Roivainen, A.; Zhang, F.P.; et al. Mesenchymal Cell-Derived Juxtacrine Wnt1 Signaling Regulates Osteoblast Activity and Osteoclast Differentiation. J. Bone Miner. Res. 2019, 34, 1129–1142. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Wang, F.; Rummukainen, P.; Heino, T.J.; Kiviranta, R. Osteoblastic Wnt1 regulates periosteal bone formation in adult mice. Bone 2021, 143, 115754. [Google Scholar] [CrossRef] [PubMed]
  24. Luther, J.; Yorgan, T.A.; Rolvien, T.; Ulsamer, L.; Koehne, T.; Liao, N.; Keller, D.; Vollersen, N.; Teufel, S.; Neven, M.; et al. Wnt1 is an Lrp5-independent bone-anabolic Wnt ligand. Sci. Transl. Med. 2018, 10, eaau7137. [Google Scholar] [CrossRef] [Green Version]
  25. Cawthorn, W.P.; Bree, A.J.; Yao, Y.; Du, B.; Hemati, N.; Martinez-Santibañez, G.; MacDougald, O.A. Wnt6, Wnt10a and Wnt10b inhibit adipogenesis and stimulate osteoblastogenesis through a β-catenin-dependent mechanism. Bone 2012, 50, 477–489. [Google Scholar] [CrossRef] [Green Version]
  26. Veverka, V.; Henry, A.J.; Slocombe, P.M.; Ventom, A.; Mulloy, B.; Muskett, F.W.; Muzylak, M.; Greenslade, K.; Moore, A.; Zhang, L.; et al. Characterization of the structural features and interactions of sclerostin: Molecular insight into a key regulator of Wnt-mediated bone formation. J. Biol. Chem. 2009, 284, 10890–10900. [Google Scholar] [CrossRef] [Green Version]
  27. Holdsworth, G.; Slocombe, P.; Doyle, C.; Sweeney, B.; Veverka, V.; Le Riche, K.; Franklin, R.J.; Compson, J.; Brookings, D.; Turner, J.; et al. Characterization of the interaction of sclerostin with the low density lipoprotein receptor-related protein (LRP) family of Wnt co-receptors. J. Biol. Chem. 2012, 287, 26464–26477. [Google Scholar] [CrossRef] [Green Version]
  28. Kim, J.; Han, W.; Park, T.; Kim, E.J.; Bang, I.; Lee, H.S.; Jeong, Y.; Roh, K.; Kim, J.; Kim, J.S.; et al. Sclerostin inhibits Wnt signaling through tandem interaction with two LRP6 ectodomains. Nat. Commun. 2020, 11, 5357. [Google Scholar] [CrossRef]
  29. Bourhis, E.; Tam, C.; Franke, Y.; Bazan, J.F.; Ernst, J.; Hwang, J.; Costa, M.; Cochran, A.G.; Hannoush, R.N. Reconstitution of a frizzled8.Wnt3a.LRP6 signaling complex reveals multiple Wnt and Dkk1 binding sites on LRP6. J. Biol. Chem. 2010, 285, 9172–9179. [Google Scholar] [CrossRef] [Green Version]
  30. Matoba, K.; Mihara, E.; Tamura-Kawakami, K.; Miyazaki, N.; Maeda, S.; Hirai, H.; Thompson, S.; Iwasaki, K.; Takagi, J. Conformational Freedom of the LRP6 Ectodomain Is Regulated by N-glycosylation and the Binding of the Wnt Antagonist Dkk1. Cell. Rep. 2017, 18, 32–40. [Google Scholar] [CrossRef] [Green Version]
  31. Leupin, O.; Piters, E.; Halleux, C.; Hu, S.; Kramer, I.; Morvan, F.; Bouwmeester, T.; Schirle, M.; Bueno-Lozano, M.; Fuentes, F.J.; et al. Bone overgrowth-associated mutations in the LRP4 gene impair sclerostin facilitator function. J. Biol. Chem. 2011, 286, 19489–19500. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  32. Chang, M.K.; Kramer, I.; Huber, T.; Kinzel, B.; Guth-Gundel, S.; Leupin, O.; Kneissel, M. Disruption of Lrp4 function by genetic deletion or pharmacological blockade increases bone mass and serum sclerostin levels. Proc. Natl. Acad. Sci. USA 2014, 111, E5187–E5195. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Bullock, W.A.; Hoggatt, A.M.; Horan, D.J.; Elmendorf, A.J.; Sato, A.Y.; Bellido, T.; Loots, G.G.; Pavalko, F.M.; Robling, A.G. Lrp4 Mediates Bone Homeostasis and Mechanotransduction through Interaction with Sclerostin In Vivo. iScience 2019, 20, 205–215. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  34. Winkler, D.G.; Sutherland, M.K.; Geoghegan, J.C.; Yu, C.; Hayes, T.; Skonier, J.E.; Shpektor, D.; Jonas, M.; Kovacevich, B.R.; Staehling-Hampton, K.; et al. Osteocyte control of bone formation via sclerostin, a novel BMP antagonist. EMBO J. 2003, 22, 6267–6276. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  35. Li, X.; Zhang, Y.; Kang, H.; Liu, W.; Liu, P.; Zhang, J.; Harris, S.E.; Wu, D. Sclerostin binds to LRP5/6 and antagonizes canonical Wnt signaling. J. Biol. Chem. 2005, 280, 19883–19887. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  36. Li, X.; Ominsky, M.S.; Niu, Q.T.; Sun, N.; Daugherty, B.; D’Agostin, D.; Kurahara, C.; Gao, Y.; Cao, J.; Gong, J.; et al. Targeted deletion of the sclerostin gene in mice results in increased bone formation and bone strength. J. Bone Miner. Res. 2008, 23, 860–869. [Google Scholar] [CrossRef]
  37. Lin, C.; Jiang, X.; Dai, Z.; Guo, X.; Weng, T.; Wang, J.; Li, Y.; Feng, G.; Gao, X.; He, L. Sclerostin mediates bone response to mechanical unloading through antagonizing Wnt/beta-catenin signaling. J. Bone Miner. Res. 2009, 24, 1651–1661. [Google Scholar] [CrossRef]
  38. Koide, M.; Yamashita, T.; Murakami, K.; Uehara, S.; Nakamura, K.; Nakamura, M.; Matsushita, M.; Ara, T.; Yasuda, H.; Penninger, J.M.; et al. Sclerostin expression in trabecular bone is downregulated by osteoclasts. Sci. Rep. 2020, 10, 13751. [Google Scholar] [CrossRef]
  39. Watanabe, T.; Tamamura, Y.; Hoshino, A.; Makino, Y.; Kamioka, H.; Amagasa, T.; Yamaguchi, A.; Iimura, T. Increasing participation of sclerostin in postnatal bone development, revealed by three-dimensional immunofluorescence morphometry. Bone 2012, 51, 447–458. [Google Scholar] [CrossRef]
  40. Thompson, M.L.; Jimenez-Andrade, J.M.; Mantyh, P.W. Sclerostin Immunoreactivity Increases in Cortical Bone Osteocytes and Decreases in Articular Cartilage Chondrocytes in Aging Mice. J. Histochem. Cytochem. 2016, 64, 179–189. [Google Scholar] [CrossRef] [Green Version]
  41. Glass, D.A., 2nd; Bialek, P.; Ahn, J.D.; Starbuck, M.; Patel, M.S.; Clevers, H.; Taketo, M.M.; Long, F.; McMahon, A.P.; Lang, R.A.; et al. Canonical Wnt signaling in differentiated osteoblasts controls osteoclast differentiation. Dev. Cell 2005, 8, 751–764. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  42. Xiong, L.; Jung, J.U.; Wu, H.; Xia, W.F.; Pan, J.X.; Shen, C.; Mei, L.; Xiong, W.C. Lrp4 in osteoblasts suppresses bone formation and promotes osteoclastogenesis and bone resorption. Proc. Natl. Acad. Sci. USA 2015, 112, 3487–3492. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  43. Wijenayaka, A.R.; Kogawa, M.; Lim, H.P.; Bonewald, L.F.; Findlay, D.M.; Atkins, G.J. Sclerostin stimulates osteocyte support of osteoclast activity by a RANKL-dependent pathway. PLoS ONE 2011, 6, e25900. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  44. Loots, G.G.; Kneissel, M.; Keller, H.; Baptist, M.; Chang, J.; Collette, N.M.; Ovcharenko, D.; Plajzer-Frick, I.; Rubin, E.M. Genomic deletion of a long-range bone enhancer misregulates sclerostin in Van Buchem disease. Genome Res. 2005, 15, 928–935. [Google Scholar] [CrossRef] [Green Version]
  45. Collette, N.M.; Genetos, D.C.; Economides, A.N.; Xie, L.; Shahnazari, M.; Yao, W.; Lane, N.E.; Harland, R.M.; Loots, G.G. Targeted deletion of Sost distal enhancer increases bone formation and bone mass. Proc. Natl. Acad. Sci. USA 2012, 109, 14092–14097. [Google Scholar] [CrossRef] [Green Version]
  46. Keller, H.; Kneissel, M. SOST is a target gene for PTH in bone. Bone 2005, 37, 148–158. [Google Scholar] [CrossRef]
  47. Wein, M.N.; Spatz, J.; Nishimori, S.; Doench, J.; Root, D.; Babij, P.; Nagano, K.; Baron, R.; Brooks, D.; Bouxsein, M.; et al. HDAC5 controls MEF2C-driven sclerostin expression in osteocytes. J. Bone Miner. Res. 2015, 30, 400–411. [Google Scholar] [CrossRef] [Green Version]
  48. Baertschi, S.; Baur, N.; Lueders-Lefevre, V.; Voshol, J.; Keller, H. Class I and IIa histone deacetylases have opposite effects on sclerostin gene regulation. J. Biol. Chem. 2014, 289, 24995–25009. [Google Scholar] [CrossRef] [Green Version]
  49. Wein, M.N.; Liang, Y.; Goransson, O.; Sundberg, T.B.; Wang, J.; Williams, E.A.; O’Meara, M.J.; Govea, N.; Beqo, B.; Nishimori, S.; et al. SIKs control osteocyte responses to parathyroid hormone. Nat. Commun. 2016, 7, 13176. [Google Scholar] [CrossRef]
  50. Gould, N.R.; Williams, K.M.; Joca, H.C.; Torre, O.M.; Lyons, J.S.; Leser, J.M.; Srikanth, M.P.; Hughes, M.; Khairallah, R.J.; Feldman, R.A.; et al. Disparate bone anabolic cues activate bone formation by regulating the rapid lysosomal degradation of sclerostin protein. eLife 2021, 10, e64393. [Google Scholar] [CrossRef]
  51. Narumiya, S.; Sugimoto, Y.; Ushikubi, F. Prostanoid receptors: Structures, properties, and functions. Physiol Rev. 1999, 79, 1193–1226. [Google Scholar] [CrossRef] [PubMed]
  52. Galea, G.L.; Sunters, A.; Meakin, L.B.; Zaman, G.; Sugiyama, T.; Lanyon, L.E.; Price, J.S. Sost down-regulation by mechanical strain in human osteoblastic cells involves PGE2 signaling via EP4. FEBS Lett. 2011, 585, 2450–2454. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  53. Genetos, D.C.; Yellowley, C.E.; Loots, G.G. Prostaglandin E2 signals through PTGER2 to regulate sclerostin expression. PLoS ONE 2011, 6, e17772. [Google Scholar] [CrossRef] [PubMed]
  54. Koide, M.; Kobayashi, Y.; Yamashita, T.; Uehara, S.; Nakamura, M.; Hiraoka, B.Y.; Ozaki, Y.; Iimura, T.; Yasuda, H.; Takahashi, N.; et al. Bone Formation Is Coupled to Resorption Via Suppression of Sclerostin Expression by Osteoclasts. J. Bone Miner. Res. 2017, 32, 2074–2086. [Google Scholar] [CrossRef] [Green Version]
  55. Robling, A.G.; Niziolek, P.J.; Baldridge, L.A.; Condon, K.W.; Allen, M.R.; Alam, I.; Mantila, S.M.; Gluhak-Heinrich, J.; Bellido, T.M.; Harris, S.E.; et al. Mechanical stimulation of bone in vivo reduces osteocyte expression of Sost/sclerostin. J. Biol. Chem. 2008, 283, 5866–5875. [Google Scholar] [CrossRef] [Green Version]
  56. Qin, L.; Liu, W.; Cao, H.; Xiao, G. Molecular mechanosensors in osteocytes. Bone Res. 2020, 8, 23. [Google Scholar] [CrossRef]
  57. Bergmann, P.; Body, J.J.; Boonen, S.; Boutsen, Y.; Devogelaer, J.P.; Goemaere, S.; Kaufman, J.; Reginster, J.Y.; Rozenberg, S. Loading and skeletal development and maintenance. J. Osteoporos. 2010, 2011, 786752. [Google Scholar] [CrossRef] [Green Version]
  58. Klein-Nulend, J.; Bacabac, R.G.; Bakker, A.D. Mechanical loading and how it affects bone cells: The role of the osteocyte cytoskeleton in maintaining our skeleton. Eur. Cell Mater. 2012, 24, 278–291. [Google Scholar] [CrossRef]
  59. Sun, W.; Chi, S.; Li, Y.; Ling, S.; Tan, Y.; Xu, Y.; Jiang, F.; Li, J.; Liu, C.; Zhong, G.; et al. The mechanosensitive Piezo1 channel is required for bone formation. eLife 2019, 8, e47454. [Google Scholar] [CrossRef]
  60. Li, X.; Han, L.; Nookaew, I.; Mannen, E.; Silva, M.J.; Almeida, M.; Xiong, J. Stimulation of Piezo1 by mechanical signals promotes bone anabolism. eLife 2019, 8, e49631. [Google Scholar] [CrossRef]
  61. Sasaki, F.; Hayashi, M.; Mouri, Y.; Nakamura, S.; Adachi, T.; Nakashima, T. Mechanotransduction via the Piezo1-Akt pathway underlies Sost suppression in osteocytes. Biochem. Biophys. Res. Commun. 2020, 521, 806–813. [Google Scholar] [CrossRef] [PubMed]
  62. Walker, E.C.; McGregor, N.E.; Poulton, I.J.; Solano, M.; Pompolo, S.; Fernandes, T.J.; Constable, M.J.; Nicholson, G.C.; Zhang, J.G.; Nicola, N.A.; et al. Oncostatin M promotes bone formation independently of resorption when signaling through leukemia inhibitory factor receptor in mice. J. Clin. Investig. 2010, 120, 582–592. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  63. Walker, E.C.; McGregor, N.E.; Poulton, I.J.; Pompolo, S.; Allan, E.H.; Quinn, J.M.; Gillespie, M.T.; Martin, T.J.; Sims, N.A. Cardiotrophin-1 is an osteoclast-derived stimulus of bone formation required for normal bone remodeling. J. Bone Miner. Res. 2008, 23, 2025–2032. [Google Scholar] [CrossRef]
  64. Nakamura, M.; Udagawa, N.; Matsuura, S.; Mogi, M.; Nakamura, H.; Horiuchi, H.; Saito, N.; Hiraoka, B.Y.; Kobayashi, Y.; Takaoka, K.; et al. Osteoprotegerin regulates bone formation through a coupling mechanism with bone resorption. Endocrinology 2003, 144, 5441–5449. [Google Scholar] [CrossRef] [Green Version]
  65. Weivoda, M.M.; Chew, C.K.; Monroe, D.G.; Farr, J.N.; Atkinson, E.J.; Geske, J.R.; Eckhardt, B.; Thicke, B.; Ruan, M.; Tweed, A.J.; et al. Identification of osteoclast-osteoblast coupling factors in humans reveals links between bone and energy metabolism. Nat. Commun. 2020, 11, 87. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  66. St John, H.C.; Bishop, K.A.; Meyer, M.B.; Benkusky, N.A.; Leng, N.; Kendziorski, C.; Bonewald, L.F.; Pike, J.W. The osteoblast to osteocyte transition: Epigenetic changes and response to the vitamin D3 hormone. Mol. Endocrinol. 2014, 28, 1150–1165. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  67. Nakamichi, Y.; Udagawa, N.; Horibe, K.; Mizoguchi, T.; Yamamoto, Y.; Nakamura, T.; Hosoya, A.; Kato, S.; Suda, T.; Takahashi, N. VDR in Osteoblast-Lineage Cells Primarily Mediates Vitamin D Treatment-Induced Increase in Bone Mass by Suppressing Bone Resorption. J. Bone Miner. Res. 2017, 32, 1297–1308. [Google Scholar] [CrossRef] [PubMed]
  68. Wijenayaka, A.R.; Yang, D.; Prideaux, M.; Ito, N.; Kogawa, M.; Anderson, P.H.; Morris, H.A.; Solomon, L.B.; Loots, G.G.; Findlay, D.M.; et al. 1α,25-dihydroxyvitamin D3 stimulates human SOST gene expression and sclerostin secretion. Mol. Cell Endocrinol. 2015, 413, 157–167. [Google Scholar] [CrossRef] [Green Version]
  69. Ohyama, Y.; Nifuji, A.; Maeda, Y.; Amagasa, T.; Noda, M. Spaciotemporal association and bone morphogenetic protein regulation of sclerostin and osterix expression during embryonic osteogenesis. Endocrinology 2004, 145, 4685–4692. [Google Scholar] [CrossRef]
  70. Kamiya, N.; Kobayashi, T.; Mochida, Y.; Yu, P.B.; Yamauchi, M.; Kronenberg, H.M.; Mishina, Y. Wnt inhibitors Dkk1 and Sost are downstream targets of BMP signaling through the type IA receptor (BMPRIA) in osteoblasts. J. Bone Miner. Res. 2010, 25, 200–210. [Google Scholar] [CrossRef] [Green Version]
  71. Florio, M.; Gunasekaran, K.; Stolina, M.; Li, X.; Liu, L.; Tipton, B.; Salimi-Moosavi, H.; Asuncion, F.J.; Li, C.; Sun, B.; et al. A bispecific antibody targeting sclerostin and DKK-1 promotes bone mass accrual and fracture repair. Nat. Commun. 2016, 7, 11505. [Google Scholar] [CrossRef] [PubMed]
  72. Witcher, P.C.; Miner, S.E.; Horan, D.J.; Bullock, W.A.; Lim, K.E.; Kang, K.S.; Adaniya, A.L.; Ross, R.D.; Loots, G.G.; Robling, A.G. Sclerostin neutralization unleashes the osteoanabolic effects of Dkk1 inhibition. JCI Insight 2018, 3, e98673. [Google Scholar] [CrossRef] [PubMed]
  73. Mödder, U.I.; Hoey, K.A.; Amin, S.; McCready, L.K.; Achenbach, S.J.; Riggs, B.L.; Melton, L.J., 3rd; Khosla, S. Relation of age, gender, and bone mass to circulating sclerostin levels in women and men. J. Bone Miner. Res. 2011, 26, 373–379. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  74. Bhattoa, H.P.; Wamwaki, J.; Kalina, E.; Foldesi, R.; Balogh, A.; Antal-Szalmas, P. Serum sclerostin levels in healthy men over 50 years of age. J. Bone Miner. Metab. 2013, 31, 579–584. [Google Scholar] [CrossRef]
  75. Roforth, M.M.; Fujita, K.; McGregor, U.I.; Kirmani, S.; McCready, L.K.; Peterson, J.M.; Drake, M.T.; Monroe, D.G.; Khosla, S. Effects of age on bone mRNA levels of sclerostin and other genes relevant to bone metabolism in humans. Bone 2014, 59, 1–6. [Google Scholar] [CrossRef] [Green Version]
  76. Arasu, A.; Cawthon, P.M.; Lui, L.Y.; Do, T.P.; Arora, P.S.; Cauley, J.A.; Ensrud, K.E.; Cummings, S.R.; Study of Osteoporotic Fractures Research Group. Serum sclerostin and risk of hip fracture in older Caucasian women. J. Clin. Endocrinol. Metab. 2012, 97, 2027–2032. [Google Scholar] [CrossRef] [Green Version]
  77. Szulc, P.; Bertholon, C.; Borel, O.; Marchand, F.; Chapurlat, R. Lower fracture risk in older men with higher sclerostin concentration: A prospective analysis from the MINOS study. J. Bone Miner. Res. 2013, 28, 855–864. [Google Scholar] [CrossRef]
  78. Rauner, M.; Sipos, W.; Pietschmann, P. Age-dependent Wnt gene expression in bone and during the course of osteoblast differentiation. Age 2008, 30, 273–282. [Google Scholar] [CrossRef] [Green Version]
  79. Farr, J.N.; Xu, M.; Weivoda, M.M.; Monroe, D.G.; Fraser, D.G.; Onken, J.L.; Negley, B.A.; Sfeir, J.G.; Ogrodnik, M.B.; Hachfeld, C.M.; et al. Targeting cellular senescence prevents age-related bone loss in mice. Nat. Med. 2017, 23, 1072–1079. [Google Scholar] [CrossRef]
  80. Padhi, D.; Jang, G.; Stouch, B.; Fang, L.; Posvar, E. Single-dose, placebo-controlled, randomized study of AMG 785, a sclerostin monoclonal antibody. J. Bone Miner. Res. 2011, 26, 19–26. [Google Scholar] [CrossRef]
  81. McClung, M.R.; Grauer, A.; Boonen, S.; Bolognese, M.A.; Brown, J.P.; Diez-Perez, A.; Langdahl, B.L.; Reginster, J.-Y.; Zanchetta, J.R.; Wasserman, S.M.; et al. Romosozumab in postmenopausal women with low bone mineral density. N. Engl. J. Med. 2014, 370, 412–420. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  82. Cosman, F.; Crittenden, D.B.; Adachi, J.D.; Binkley, N.; Czerwinski, E.; Ferrari, S.; Hofbauer, L.C.; Edith Lau, E.; Lewiecki, E.M.; Miyauchi, A.; et al. Romosozumab Treatment in Postmenopausal Women with Osteoporosis. N. Engl. J. Med. 2016, 375, 1532–1543. [Google Scholar] [CrossRef] [PubMed]
  83. Singh, S.; Dutta, S.; Khasbage, S.; Kumar, T.; Sachin, J.; Sharma, J.; Varthya, S.B. A systematic review and meta-analysis of efficacy and safety of Romosozumab in postmenopausal osteoporosis. Osteoporos. Int. 2022, 33, 1–12. [Google Scholar] [CrossRef] [PubMed]
  84. Reid, I.R.; Billington, E.O. Drug therapy for osteoporosis in older adults. Lancet 2022, 399, 1080–1092. [Google Scholar] [CrossRef]
  85. Chen, X.X.; Baum, W.; Dwyer, D.; Stock, M.; Schwabe, K.; Ke, H.Z.; Stolina, M.; Schett, G.; Bozec, A. Sclerostin inhibition reverses systemic, periarticular and local bone loss in arthritis. Ann. Rheum. Dis. 2013, 72, 1732–1736. [Google Scholar] [CrossRef] [Green Version]
  86. Marenzana, M.; Vugler, A.; Moore, A.; Robinson, M. Effect of sclerostin-neutralising antibody on periarticular and systemic bone in a murine model of rheumatoid arthritis: A microCT study. Arthritis Res. Ther. 2013, 15, R125. [Google Scholar] [CrossRef] [Green Version]
  87. Wehmeyer, C.; Frank, S.; Beckmann, D.; Böttcher, M.; Cromme, C.; König, U.; Fennen, M.; Held, A.; Paruzel, P.; Hartmann, C.; et al. Sclerostin inhibition promotes TNF-dependent inflammatory joint destruction. Sci. Transl. Med. 2016, 8, 330ra35. [Google Scholar] [CrossRef]
  88. Courbon, G.; Lamarque, R.; Gerbaix, M.; Caire, R.; Linossier, M.T.; Laroche, N.; Thomas, M.; Thomas, T.; Vico, L.; Marotte, H. Early sclerostin expression explains bone formation inhibition before arthritis onset in the rat adjuvant-induced arthritis model. Sci. Rep. 2018, 8, 3492. [Google Scholar] [CrossRef]
  89. Diarra, D.; Stolina, M.; Polzer, K.; Zwerina, J.; Ominsky, M.S.; Dwyer, D.; Korb, A.; Smolen, J.; Hoffmann, M.; Scheinecker, C.; et al. Dickkopf-1 is a master regulator of joint remodeling. Nat. Med. 2007, 13, 156–163. [Google Scholar] [CrossRef]
  90. Gau, Y.C.; Yeh, T.J.; Hsu, C.M.; Hsiao, S.Y.; Hsiao, H.H. Pathogenesis and Treatment of Myeloma-Related Bone Disease. Int. J. Mol. Sci. 2022, 23, 3112. [Google Scholar] [CrossRef]
  91. Terpos, E.; Christoulas, D.; Katodritou, E.; Bratengeier, C.; Gkotzamanidou, M.; Michalis, E.; Delimpasi, S.; Pouli, A.; Meletis, J.; Kastritis, E.; et al. Elevated circulating sclerostin correlates with advanced disease features and abnormal bone remodeling in symptomatic myeloma: Reduction post-bortezomib monotherapy. Int. J. Cancer 2012, 131, 1466–1471. [Google Scholar] [CrossRef] [PubMed]
  92. Eda, H.; Santo, L.; Wein, M.N.; Hu, D.Z.; Cirstea, D.D.; Nemani, N.; Tai, Y.T.; Raines, S.E.; Kuhstoss, S.A.; Munshi, N.C.; et al. Regulation of Sclerostin Expression in Multiple Myeloma by Dkk-1: A Potential Therapeutic Strategy for Myeloma Bone Disease. J. Bone Miner. Res. 2016, 31, 1225–1234. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  93. Colucci, S.; Brunetti, G.; Oranger, A.; Mori, G.; Sardone, F.; Specchia, G.; Rinaldi, E.; Curci, P.; Liso, V.; Passeri, G.; et al. Myeloma cells suppress osteoblasts through sclerostin secretion. Blood Cancer J. 2011, 1, e27. [Google Scholar] [CrossRef] [PubMed]
  94. McDonald, M.M.; Reagan, M.R.; Youlten, S.E.; Mohanty, S.T.; Seckinger, A.; Terry, R.L.; Pettitt, J.A.; Simic, M.K.; Cheng, T.L.; Morse, A.; et al. Inhibiting the osteocyte-specific protein sclerostin increases bone mass and fracture resistance in multiple myeloma. Blood 2017, 129, 3452–3464. [Google Scholar] [CrossRef] [Green Version]
  95. Zhu, M.; Liu, C.; Li, S.; Zhang, S.; Yao, Q.; Song, Q. Sclerostin induced tumor growth, bone metastasis and osteolysis in breast cancer. Sci. Rep. 2017, 7, 11399. [Google Scholar] [CrossRef]
  96. Hesse, E.; Schröder, S.; Brandt, D.; Pamperin, J.; Saito, H.; Taipaleenmäki, H. Sclerostin inhibition alleviates breast cancer-induced bone metastases and muscle weakness. JCI Insight 2019, 5, e125543. [Google Scholar] [CrossRef]
Ijms 23 04895 g001 550
Figure 1. Structure of the Sost gene and effects of PTH on the expression of sclerostin. PTH signals suppress the expression of sclerostin. In the absence of PTH signals, salt-inducible kinase (SIK) 2 phosphorylates HDAC4/5 to promote the cytoplasmic retention of HDAC4/5. MEF2c binds to ECR5 (enhancer region) of the Sost gene to promote the expression of sclerostin. PTH signals inhibit the phosphorylation of HDAC4/5 by SIK2. Dephosphorylated HDAC4/5 remain in the nucleus and inhibit the transcriptional activity of MEF2c. YKL-05-099, a small-molecule SIK inhibitor, mimics the effects of PTH. PTH, parathyroid hormone; SIK, salt-inducible kinase; HDAC, histone deacetylase; MEF, myocyte enhancer factor; ECR, evolutionarily conserved region; MEOX1, mesenchyme homeobox 1.
Figure 1. Structure of the Sost gene and effects of PTH on the expression of sclerostin. PTH signals suppress the expression of sclerostin. In the absence of PTH signals, salt-inducible kinase (SIK) 2 phosphorylates HDAC4/5 to promote the cytoplasmic retention of HDAC4/5. MEF2c binds to ECR5 (enhancer region) of the Sost gene to promote the expression of sclerostin. PTH signals inhibit the phosphorylation of HDAC4/5 by SIK2. Dephosphorylated HDAC4/5 remain in the nucleus and inhibit the transcriptional activity of MEF2c. YKL-05-099, a small-molecule SIK inhibitor, mimics the effects of PTH. PTH, parathyroid hormone; SIK, salt-inducible kinase; HDAC, histone deacetylase; MEF, myocyte enhancer factor; ECR, evolutionarily conserved region; MEOX1, mesenchyme homeobox 1.
Ijms 23 04895 g001
Ijms 23 04895 g002 550
Figure 2. Roles of LIF, CT-1, and OSM in bone remodeling. Osteoclast-derived LIF, CT-1, and osteoblast-derived OSM inhibit the expression of sclerostin in osteocytes. These cytokines bind to gp130 and LIFR/OSMR, and may inhibit Sost expression via the JAK-Stat signal. The inhibition of sclerostin expression enhances Wnt/β-catenin signals in osteoblasts, which, in turn, promote bone formation. LIF, leukemia inhibitory factor; CT-1, cardiotropin-1; OSM, oncostatin M; LIFR, LIF receptor; OSMR, OSM receptor; JAK-Stat, janus kinase-signal transducer and activator of transcription.
Figure 2. Roles of LIF, CT-1, and OSM in bone remodeling. Osteoclast-derived LIF, CT-1, and osteoblast-derived OSM inhibit the expression of sclerostin in osteocytes. These cytokines bind to gp130 and LIFR/OSMR, and may inhibit Sost expression via the JAK-Stat signal. The inhibition of sclerostin expression enhances Wnt/β-catenin signals in osteoblasts, which, in turn, promote bone formation. LIF, leukemia inhibitory factor; CT-1, cardiotropin-1; OSM, oncostatin M; LIFR, LIF receptor; OSMR, OSM receptor; JAK-Stat, janus kinase-signal transducer and activator of transcription.
Ijms 23 04895 g002
Table
Table 1. Regulators of sclerostin expression.
Table 1. Regulators of sclerostin expression.
Negative RegulatorCell Line or Animal ModelsSost Exp/SclerostinRefs
PTHCol1-Cre; Mef2cfl/fl↓[45]
UMR106 cell↓[46,48]
Hdac5 KO↓[47]
Ocy454 cell↓[47,50]
Tibiae from PTH-treated mice↓[49]
Dmp1-Cre; Hdac4fl/fl; Hdac5−/−↓[49]
PGE2UMR106 cell↓[52,53,54]
Mechanical loadingUMR106 cell with fluid shear stress↓[50]
Saos2 cell with mechanical strain↓[52]
IDG-SW3 cell with mechanical strain↓[61]
gp130 and IL-6 family cytokinesUMR106 cell treated with LIF↓[54]
calvarial osteoblasts treated with OSM↓[62]
UMR106 cell treated with LIF, OSM, CT-1↓[62]
1α,25(OH)2D3IDG-SW3 cell↓[66]
Osterix-Cre; VDRfl/fl mice↓[67]
long bones from Eldecalcitol-treated mice↑[67]
human primary osteoblast↑[68]
Positive RegulatorCell Line or Animal ModelsSost Exp/SclerostinRefs
BMPCol1-CreER; Bmpr1afl/fl↑[70]
WntAdministration of anti-DKK1 antibody↑[72]
Aginghuman serum↑[74,75]
human bone samples→[75]
Mouse bone↑[78]
depletion of senescence cells↑[79]
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Iwamoto, R.; Koide, M.; Udagawa, N.; Kobayashi, Y. Positive and Negative Regulators of Sclerostin Expression. Int. J. Mol. Sci. 2022, 23, 4895. https://doi.org/10.3390/ijms23094895

AMA Style

Iwamoto R, Koide M, Udagawa N, Kobayashi Y. Positive and Negative Regulators of Sclerostin Expression. International Journal of Molecular Sciences. 2022; 23(9):4895. https://doi.org/10.3390/ijms23094895

Chicago/Turabian Style

Iwamoto, Rina, Masanori Koide, Nobuyuki Udagawa, and Yasuhiro Kobayashi. 2022. "Positive and Negative Regulators of Sclerostin Expression" International Journal of Molecular Sciences 23, no. 9: 4895. https://doi.org/10.3390/ijms23094895

APA Style

Iwamoto, R., Koide, M., Udagawa, N., & Kobayashi, Y. (2022). Positive and Negative Regulators of Sclerostin Expression. International Journal of Molecular Sciences, 23(9), 4895. https://doi.org/10.3390/ijms23094895

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop