Next Article in Journal
Preparation and Characterisation of Acid–Base-Change-Sensitive Binary Biopolymer Films with Olive Oil and Ozonated Olive Oil Nano/Microcapsules and Added Hibiscus Extract
Next Article in Special Issue
Coregulators Reside within Drosophila Ecdysone-Inducible Loci before and after Ecdysone Treatment
Previous Article in Journal
Transcriptome and Metabolome Analyses Reveal Perfluorooctanoic Acid-Induced Kidney Injury by Interfering with PPAR Signaling Pathway
Previous Article in Special Issue
Polycomb Recruiters Inside and Outside of the Repressed Domains
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
IJMS
Volume 24
Issue 14
10.3390/ijms241411501
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:
Article

Drosophila Phosphatase of Regenerating Liver Is Critical for Photoreceptor Cell Polarity and Survival during Retinal Development

by
Shu-Fen Chen
1,†,
Hsin-Lun Hsien
1,2,†,
Ting-Fang Wang
1,2 and
Ming-Der Lin
1,3,*
1
Department of Molecular Biology and Human Genetics, Tzu Chi University, 701 Zhongyang Rd., Sec. 3, Hualien 97004, Taiwan
2
Department of Life Sciences, Tzu Chi University, 701 Zhongyang Rd., Sec. 3, Hualien 97004, Taiwan
3
Institute of Medical Sciences, Tzu Chi University, 701 Zhongyang Rd., Sec. 3, Hualien 97004, Taiwan
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Int. J. Mol. Sci. 2023, 24(14), 11501; https://doi.org/10.3390/ijms241411501
Submission received: 24 June 2023 / Revised: 11 July 2023 / Accepted: 14 July 2023 / Published: 15 July 2023
(This article belongs to the Special Issue Molecular Genetics of Drosophila Development)
Browse Figures
Versions Notes

Abstract

:
Establishing apicobasal polarity, involving intricate interactions among polarity regulators, is key for epithelial cell function. Though phosphatase of regenerating liver (PRL) proteins are implicated in diverse biological processes, including cancer, their developmental role remains unclear. In this study, we explore the role of Drosophila PRL (dPRL) in photoreceptor cell development. We reveal that dPRL, requiring a C-terminal prenylation motif, is highly enriched in the apical membrane of developing photoreceptor cells. Moreover, dPRL knockdown during retinal development results in adult Drosophila retinal degeneration, caused by hid-induced apoptosis. dPRL depletion also mislocalizes cell adhesion and polarity proteins like Armadillo, Crumbs, and DaPKC and relocates the basolateral protein, alpha subunit of Na+/K+-ATPase, to the presumed apical membrane. Importantly, this polarity disruption is not secondary to apoptosis, as suppressing hid expression does not rescue the polarity defect in dPRL-depleted photoreceptor cells. These findings underscore dPRL’s crucial role in photoreceptor cell polarity and emphasize PRL’s importance in establishing epithelial polarity and maintaining cell survival during retinal development, offering new insights into PRL’s role in normal epithelium.

1. Introduction

Drosophila photoreceptor cells are specialized epithelial neurons with pronounced apicobasal polarity. A single layer of epithelial cells forms the larval eye imaginal disc, which progressively differentiates into the adult compound eye during pupal development. From 37% pupal development (p.d.) onward, the apical membranes of photoreceptor cells shift 90 degrees towards the ommatidial center and start to extend downward to the base of the ommatidium [1]. By 50% p.d., this shift is completed, and the apical membrane of the photoreceptor cells is clearly separated from the basolateral membrane by the adherens junction (AJ). The AJ coalesces to form a homogenous zonula adherens of photoreceptor epithelium. At later stages of retinal development, the apical membrane gradually subdivides into apical and sub-apical domains, which further differentiate into the photosensing rhabdomere and supporting stalk membrane of adult photoreceptor cells, respectively (Figure 1A) [1].
The establishment of apicobasal polarity in an epithelial cell relies on complex interplay among apical polarity regulators, AJ components, and basolateral polarity regulators [2]. Crumbs (Crb), an apical polarity regulator, is exclusively localized to the apical membrane and is necessary for the maintenance of the apical membrane and the formation of AJ [3,4]. Drosophila atypical protein kinase C (DaPKC), another apical component, is negatively regulated by its binding partner Par6 [5]. Through the interaction between Crb and Par6, DaPKC is recruited to the subapical domain of photoreceptor cells [6]. DaPKC then phosphorylates Bazooka (Baz) at serine 980 to exclude Baz from the subapical domain [6], and thus restricts Baz to AJ for assembling AJ components, such as Drosophila E-Cadherin (DE-Cad) and Armadillo (Arm), to form zonula adherens [7,8]. Therefore, a complex interaction among polarity regulators establishes the apicobasal polarity of the photoreceptor epithelium. However, the detailed mechanism for the specification of photoreceptor cell polarity remains to be explored.
Phosphatase of regenerating liver (PRL) proteins are part of the non-classical protein tyrosine phosphatase IVa (PTP4a) family, which functions to remove a phosphate group from its substrate protein. PRL has a shallow active site pocket, suggesting it is a dual-specific phosphatase that can act on either tyrosine or serine/threonine residues [9,10]. The mammalian PRL family consists of three homologous genes (PRL-1, -2, and -3), whereas invertebrates, like Drosophila, have only one PRL ortholog gene in their genome [11]. PRL family phosphatases have a conserved CX5R catalytic signature and a C-terminal CaaX motif for prenylation. Prenylation allows PRL to associate with membranous structures, such as the plasma membrane and endosomes [12,13]. Although PRL was originally identified as an immediate-early growth response gene in regenerating liver [14,15], subsequent studies have shown that the overexpression of PRL phosphatases could result in cancer metastasis by stimulating cell proliferation and migration [16,17,18].
While most PRL-related studies focus on its correlation with cancer progression, the physiological function of PRL in the developmental process remains unclear. Knockout studies in mice have shown that deficiencies of PRL-1 [19] or PRL-3 [20,21] do not present noticeable abnormalities during embryonic development and can survive into adulthood. By contrast, PRL-2-null mice exhibited defective placental development and atrophied testes with low sperm counts after birth [22,23]. In Xenopus laevis, although PRL-1 and PRL-2 have not yet been assayed, PRL-3 is involved in controlling the migration of neural crest cells and the determination of neural crest territory [24,25]. In Drosophila, PRL (dPRL) is highly expressed in the developing mid-guts and central nervous system during embryogenesis [11]. In larval stage, dPRL is ubiquitously expressed in the plasma membrane of imaginal discs [11,23] and has shown apical localization in the wing imaginal disc [26]. Despite these observations, the biological significance of dPRL’s apical localization in normal epithelium has not been fully investigated.
Given the distinct polarity of Drosophila photoreceptor cells within the retinal epithelium, these cells present an ideal model to investigate the potential role of dPRL in the apical membrane. In this study, we demonstrate that Drosophila PRL exhibits an apical localization in the photoreceptor epithelium of the pupal retina at 50% pupal development (p.d.). The depletion of dPRL expression causes disruption of photoreceptor cell polarity, as evidenced by the mislocalization of polarity components. Additionally, we found that dPRL was essential for the survival of the photoreceptor epithelium, as its depletion caused a retinal degeneration phenotype. The functions of dPRL in the establishment of cell polarity and cell survival may be independent because the blockage of apoptosis could not rescue the polarity disruption phenotypes in dPRL-depleted photoreceptor cells. In conclusion, our study uncovered and presented a novel function of PRL in the regulation of apico-basal polarity of photoreceptor cells during Drosophila retinal development.

2. Results

2.1. dPRL Is Enriched in the Apical Membrane of Photoreceptor Cells at 50% Pupal Development

From 37% to 50% of pupal development (p.d.), the apical membrane of the photoreceptor cell undergoes a 90-degree shift towards the ommatidial center [1]. This membrane is enriched with F-actin and can be easily demarcated by the adherens junctions (AJs) marked by Drosophila β-catenin Armadillo (Arm) or Drosophila E-Cadherin (DE-Cad). The AJs delineate the boundary between the apical and basolateral membranes. Following 50% p.d., the apical membrane of photoreceptor cells further differentiates into the rhabdomere, enriched with F-actin, and the subapical stalk membrane, marked by Crumbs (Crb) or Drosophila atypical protein kinase C (DaPKC) [1] (Figure 1A).
At 50% p.d., endogenous dPRL is predominantly localized in the apical membrane at the ommatidia center, with residual localization in the basolateral membrane (Figure 1B). This localization is adjacent to the adherens junctions, as marked by Arm (Figure 1C,D). To further validate dPRL’s apical localization, we examined the localization of GFP-tagged dPRL in the retina, using the pan-retinal driver GMR-Gal4 [27] to drive the expression of the UAS-GFP-dPRL transgene. Consistent with the localization of endogenous dPRL at 50% p.d., the majority of the GFP-dPRL signal (Figure 1E) was concentrated in the apical membrane, outlined by the presence of the adherens junction component, DE-Cad (Figure 1F,G). Within the apical membrane, GFP-dPRL (Figure 1H,K) partially co-localized with the subapical stalk membrane markers Crb (Figure 1I,J) and DaPKC (Figure 1L,M). Furthermore, GFP-dPRL (Figure 1O,P) was found to co-localize with F-actin in the apical membrane.

2.2. The Prenylation Motif Is Essential for dPRL’s Localization to the Apical Membrane of Photoreceptor Cells

The C-terminal CAAX prenylation motifs in mammalian PRLs are known to be required for their association with membranous structures (Figure 2A) [12,13,28,29]. To investigate whether the C-terminal CSVQ sequence of dPRL is required for its association with the apical membrane in photoreceptor cells, we generated UAS-GFP-dPRLC173S transgenic flies carrying a Cys173 to Ser substitution to disrupt the prenylation motif. In photoreceptor cells of the developing retinas at 50% p.d., GFP-dPRL was primarily localized to the apical membrane, co-localizing with F-actin (Figure 2B–F). In contrast, GFP-dPRLC173S accumulated in the cytosol adjacent to the apical membrane (Figure 2G,J,K) and was even mislocalized to the nucleus (Figure 2G–I). These results indicate that the C-terminal CSVQ sequence is crucial for targeting dPRL to the apical membrane of photoreceptor cells during retinal development.

2.3. Knockdown of dPRL Leads to Retinal Degeneration

To elucidate the potential role of dPRL in retinal development, we employed an in vivo RNA interference (RNAi) strategy to suppress dPRL expression in the retina. The successful knockdown of dPRL was confirmed through immunostaining, as demonstrated in Figure S1E. In these experiments, we utilized GMR-Gal4 to drive the simultaneous expression of UAS-dPRL-IR45518 and UAS-dicer2 transgenes, generating dPRL inverted-repeat (IR) RNA sequences for dPRL knockdown and Dicer 2 for enhancing RNAi efficiency, respectively [30]. For simplicity, this specific genetic combination is referred to as dPRL-RNAi. In the GMR-Gal4; UAS-dicer2 control flies, no discernible abnormalities in the compound eyes were observed (Figure 3A). Conversely, dPRL-RNAi flies exhibited noticeable compound eye aberrations, including eye roughening, thinning, and loss of pigmentation (Figure 3B). These phenotypes were successfully reproduced using a distinct RNAi line, UAS-dPRL-IR107836, which carries an IR sequence of dPRL that differs from that of UAS-dPRL-IR45518.
To gain a deeper understanding of the eye aberration phenotypes observed in dPRL-RNAi flies, we employed transmission electron microscopy for examination. The adult retina of Gal4-driver control flies displayed a regular array of ommatidia (Figure 3C). Contrarily, the adult retina of dPRL-RNAi flies was characterized by the presence of numerous vacuoles (Figure 3D, arrows), indicative of severe degeneration, and deterioration of the cornea and pseudocone was also noted (Figure 3D, arrowheads). In addition to the adult eye, we examined the pupal retina of dPRL-RNAi flies. The pupal retina of GMR-Gal4; UAS-dicer2 control flies at 50% p.d. exhibited a regular hexagonal array of ommatidia (Figure 3E), and the F-actin, which is enriched in the apical membrane of the photoreceptor cell, was readily observable at the center of each ommatidium (Figure 3E, arrows). However, in the pupal retina of dPRL-RNAi flies at 50% p.d., the ommatidia were irregularly positioned (Figure 3F) and the F-actin was mislocalized (Figure 3F, arrows). Collectively, our results demonstrate that the knockdown of dPRL in the developing retina disrupts the regular array of ommatidia in the pupal retina and induces retinal degeneration in adult compound eyes.

2.4. Knockdown of dPRL Triggers Apoptosis Mediated by the Proapoptotic Gene Hid

The retinal degeneration phenotype observed in dPRL-RNAi flies suggests that apoptosis could be the cause. To validate this, we used the baculovirus anti-apoptotic protein p35 to potentially reverse the eye phenotype of dPRL-RNAi flies. We observed that the expression of p35 mitigated the loss-of-pigmentation phenotype in dPRL-RNAi flies (Figure 4A,B), indicating that dPRL-knockdown-induced retinal degeneration primarily results from apoptosis. In Drosophila, apoptosis can be triggered by the expression of proapoptotic genes such as reaper, grim, and hid. To determine whether these proapoptotic genes were activated following dPRL knockdown, we used a microRNA technique [31] to suppress the expression of these genes and assess the impact on the eye degeneration phenotype of dPRL-RNAi flies. The result showed that the concurrent knockdown of reaper, grim, and hid fully reversed the loss-of-pigmentation phenotype of dPRL-RNAi flies (Figure 4C). However, the individual knockdown of either reaper (Figure 4D) or grim (Figure 4E) was insufficient to completely rescue the eye defects of dPRL-RNAi flies. Interestingly, the sole knockdown of hid significantly mitigates the eye phenotype of dPRL-RNAi flies (Figure 4F). Our results suggest that the proapoptotic gene hid is involved in the retinal degeneration observed following dPRL knockdown.

2.5. Polarity of Photoreceptor Cells was Disrupted in the Pupal Retina of dPRL-Knockdowned Flies

Given the predominant localization of dPRL in the apical membrane of developing photoreceptor cells, we hypothesized its potential role in establishing photoreceptor polarity. We first inspected the AJ components in the pupal retina of dPRL-RNAi flies at 50% p.d. Compared to the GMR-Gal4; UAS-dicer2 control retina (Figure 5A–C), we observed significant mislocalization of the AJ component, Arm, in the dPRL-RNAi retina (Figure 5E). In some ommatidia of dPRL-RNAi flies, the AJ between adjacent photoreceptor cells was either fused or could not be identified (Figure 5F). Further, we examined the sub-apical membrane integrity of photoreceptor cells in the ommatidia of dPRL-RNAi flies and found that both DaPKC and Crb lost their sub-apical membrane localization (DaPKC, Figure 5J–L; Crb, Figure 5P–R) compared to the control retinas (DaPKC, Figure 5G–I; Crb, Figure 5M–O). The disruption of AJs, which delineate the boundary between the apical and basolateral membranes, could imply the mislocalization of basolateral membrane proteins to the apical membrane. In the GMR-Gal4; UAS-dicer2 control retina, the alpha subunit of the Na+/K+-ATPase was specifically localized to the basolateral membrane [32] (Figure 5S–U). However, in dPRL-RNAi flies, we observed the mislocalization of the alpha subunit of the Na+/K+-ATPase to the apical membrane, where it colocalized with F-actin in the photoreceptor cells (Figure 5V–X, arrow). These results suggest that dPRL is vital for the apicobasal polarity of photoreceptor cells, and its depletion could disrupt AJs, leading to the mislocalization of polarity-determining proteins.

2.6. Polarity Disruption of Photoreceptor Cells in dPRL-Depleted Retina was Not a Secondary Effect of Apoptosis

Given that the silencing of dPRL disrupted both photoreceptor cell polarity and induced apoptosis, we questioned whether the polarity disruption could be a secondary effect resulting from cell death. To test this hypothesis, we suppressed apoptosis in dPRL-knockdown flies by inhibiting hid expression, as shown in Figure 4F, then assessed photoreceptor cell polarity in pupal retinas. In control pupal retinas at 50% p.d. from flies carrying the GMR-Gal4 driver with UAS-dicer2 and UAS-hid-miRNA transgenes, the polarity of photoreceptor cells was normal, with both the sub-apical marker Crb (Figure 6A–C) and the basolateral membrane marker, the alpha subunit of Na+/K+-ATPase (Figure 6G–I), localizing properly. However, in photoreceptor cells of dPRL-RNAi flies carrying a UAS-hid-miRNA transgene, we observed a reduction in Crb expression in the sub-apical membrane (Figure 6D–F) and a mislocalization of the alpha subunit of Na+/K+-ATPase (Figure 6J–L) to the apical membrane. These results suggest that the disruption in photoreceptor cell polarity caused by dPRL knockdown operates independently of apoptosis.

3. Discussion

In this study, we demonstrate that dPRL is primarily localized to the apical membrane of developing photoreceptor cells. Regarding dPRL’s role in the development of the retina, we found that its depletion disrupts the apico-basal polarity of photoreceptor cells. PRL’s function in the establishment of apical-basal polarity in the normal epithelium could potentially be universal, as evidenced by the formation of multiple ectopic apical membrane initiation sites enriched with PRL-3 when human PRL-3 is overexpressed in 3D-cultured non-cancerous Madin–Darby canine kidney (MDCK) cells [33]. Given that the disruption of epithelial architecture is a fundamental event in epithelial tumorigenesis, our findings establish a connection between PRL’s normal function in epithelial cells and its role in human cancers.
The establishment of epithelial cell polarity is known to be contingent on a complex interplay between components of cell adhesion and cell polarity complexes. DaPKC, one of these components, plays a pivotal role in forming adherens junctions (AJs) during the remodeling of apico-basal polarity in photoreceptor cells. Specifically, DaPKC phosphorylates Baz, excluding it from the apical membrane, which in turn confines Baz to the future AJ through Crb activity [6]. Following this, Baz recruits components such as Arm and DE-Cad to establish the AJ [7,8]. In pupal eye discs with dPRL depletion, we observed the disruptions of AJs (Figure 4D–F), accompanied by a loss of apical localization of both DaPKC and Crb in photoreceptor cells (Figure 4J–L,P–R). The disruption of photoreceptor cell polarity of dPRL-RNAi flies can be traced back to at least 40% p.d., a time point that immediately follows the onset of the apical membrane shift observed at 37% p.d. (Figure S1). These findings suggest that dPRL acts genetically upstream of DaPKC and Crb in the establishment of photoreceptor cell polarity. The observed disruption of AJs in dPRL-depleted photoreceptor cells could potentially be explained by the absence of DaPKC from the apical membrane. GSK3β, known to directly phosphorylate DaPKC, triggers its ubiquitin-mediated proteasomal degradation. This process is pivotal in the establishment of apical-basal polarity during Drosophila embryogenesis [34,35]. Interestingly, AKT has been found to phosphorylate and inhibit GSK3β [36]. It is conceivable that PRL phosphatases could modulate this pathway. Supporting this notion, studies have found that PRL-2 in mouse placenta [23] and human PRL-3 in HeLa cells [37] can activate AKT kinase through the downregulation of PTEN, a well-established antagonist of the PI3K pathway. Furthermore, human PRL-3 has been reported to interact with and deactivate the SHP2 phosphatase, a negative regulator of EGF-dependent PI3K activation [38,39,40]. Based on these studies, we postulate that dPRL may influence the AKT-GSK3β-DaPKC pathway either directly or indirectly. This, in turn, could alter the localization and stability of DaPKC at the apical membrane, impacting apical-basal polarity. Alternatively, dPRL might influence AJ formation through interactions with Cadherin, a notion supported by studies showing that human PRL-3 has been implicated in the epithelial–mesenchymal transition (EMT) via a Cadherin-related signaling pathway [37,41]. However, the exact mechanisms by which dPRL influences DaPKC localization, and whether they directly interact, remain to be determined.
We also found that dPRL depletion induced cell death in the developing retina (Figure 3B,D). This effect could be mitigated by either overexpressing the caspase inhibitor p35 or by silencing the proapoptotic gene hid via miRNA (Figure 4), suggesting that dPRL depletion triggers hid-mediated apoptosis. Several pathways may be responsible for the induction of apoptosis following dPRL depletion, including the c-Jun N-terminal kinase (JNK) signaling pathway and p53, both of which have previously been reported to induce hid expression. JNK signaling has been shown to promote hid transcription following UV exposure in the developing retina [41], while p53 has been reported to induce hid expression in embryos or larvae after radiation exposure [42,43]. This idea is further supported by a previous study demonstrating that mouse PRL-3 knockdown triggers cell cycle arrest through the upregulation of p53 [44]. Additionally, the apoptosis-mediated retinal degeneration observed in dPRL-depleted retinas could be due to direct or indirect disruptions to photoreceptor cell polarity. This possibility is supported by findings showing that cells with polarity deficiencies trigger apoptosis via JNK signaling activation [45,46,47]. Considering the hypothesis that disruptions in epithelial polarity might trigger apoptosis to remove potential tumor cells, our study offers insights into the developmental functions of PRL in both normal epithelia and cancer progression. Further research is needed to fully elucidate how dPRL regulates cell polarity and the intimate relationship it has with cell survival.

4. Materials and Methods

4.1. Drosophila Stocks

Drosophila stocks were maintained on a standard cornmeal medium. The following transgenic stocks were utilized in this study: P{w+; UAS-GFP::dPRLWT}, P{w+; UAS-GFP::dPRLC173S}, P{w+; GMR-RGH-miRNA} [34], P{w+; GMR-reaper-miRNA} [34], P{w+; GMR-grim-miRNA} [34], P{w+; GMR-hid-miRNA} [34], P{w+; UAS-dPRL-IR45518} (Vienna Drosophila Resource Center (VDRC, Vienna, Austria, stock No. 45518), GMR-Gal4 (Bloomington Drosophila Stock Center (BDSC, Bloomington, IN, USA, stock No. 1104), UAS-dicer2 (BDSC, stock No. 24646), P{w+; UAS-p35} (BDSC, stock No. 5072). To ensure the GAL4 expression and efficiency for RNA interference, flies were raised at 27 °C for pupal dissection. The wild-type coding sequence of dPRL were subcloned into the pUAST vector containing a GFP coding sequence upstream of the cloning site for transgenes. The QuikChange Lightning Site-Directed Mutagenesis kit (Agilent Technologies, Santa Clara, CA, USA) was used to generate the Cys173 to Ser substitution in the dPRL coding sequence. Transgenic flies were generated according to the standard protocol via microinjection.

4.2. Transmission Electron Microscopy (TEM) for Adult Retina

Adult flies were fixed in a solution containing 2% paraformaldehyde and 2% glutaraldehyde in 0.1 M cacodylate buffer, pH 7.3, and incubated at 4 °C. Subsequent to hand dissection, the heads were subjected to an additional 2 h incubation in fixative at 4 °C. This was followed by post-fixation with 1% OsO4 in 0.1 M cacodylate buffer at room temperature. The heads were then stained en bloc with 2% aqueous uranyl acetate for 1 h, followed by a series of dehydration steps using alcohol, and finally embedded in Spurr’s resin (Electron Microscopy Sciences, Hatfield, PA, USA, Cat. No. 14300). Eye sections were prepared using a Leica EM UC6 ultramicrotome and visualized using a Hitachi H7500 transmission electron microscope.

4.3. Drosophila Whole-Mount Immunostaining of Pupal Retina

Pupal retinas at the specified developmental stages were hand-dissected and fixed for 20 min in 4% formaldehyde. Upon fixative removal, the fixed retinas were washed multiple times in PBST (PBS containing 0.3% Triton X-100). Retinas were then blocked with 2% bovine serum albumin in PBST for 1 h and incubated overnight at 4 °C with primary antibodies diluted in PBS. After incubation, the retinas were washed three times for 20 min each in PBST and subsequently incubated for 2 h at room temperature with secondary antibodies in PBST. Following three additional 30 min washes in PBST, retinas were mounted using an anti-fade mounting solution. The primary antibodies used were rabbit anti-dPRL (1:100 dilution) [11], mouse anti-Arm (Developmental Studies Hybridoma Bank (DSHB), Iowa, IA, USA, Product ID: N27-A1, 1:50 dilution), mouse anti-alpha subunit of Na+/K+-ATPase (DSHB, Product ID: a5, 1:20 dilution), rat anti-DE-Cad (DSHB, Product ID: DCAD2, 1:20 dilution), mouse anti-Crumbs (Developmental Studies Hybridoma Bank, Product ID: Cq4, 1:20 dilution), and rabbit anti-DaPKC (Santa Cruz, Dallas, TX, USA, Cat. No. SC-216, 1:50 dilution). The fluorescent-labeled secondary antibodies used were goat-anti-rabbit Alexa Fluor 488 (Invitrogen, Waltham, MA, USA, Cat. No. A-11008, 1:400 dilution), goat anti-rat Alexa Fluor 633 (Invitrogen, Cat. No. A-21094, 1:400 dilution), and goat anti-mouse Alexa Fluor 633 (Invitrogen, Cat. No. A-21050, 1:400 dilution). For nuclear stain, DAPI solution (1 mg/mL) was used (Sigma-Aldrich, Burlington, MA, USA, Cat. No. MBD0015, 1:1000 dilution). F-actin was labeled with rhodamine-conjugated phalloidin (Sigma-Aldrich, Cat. No. 77418, 1:200 dilution).

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/ijms241411501/s1.

Author Contributions

Conceptualization, M.-D.L.; formal analysis, S.-F.C., H.-L.H., and T.-F.W.; funding acquisition, M.-D.L.; investigation, S.-F.C., H.-L.H., and T.-F.W.; methodology, S.-F.C. and M.-D.L.; supervision, M.-D.L.; validation, S.-F.C., H.-L.H., and T.-F.W.; visualization, M.-D.L.; writing—original draft, M.-D.L.; writing—review and editing, M.-D.L. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the National Sciences and Technology Council (NSTC) of Taiwan, grant numbers 101-2311-B-320-001-MY3 to M.-D.L. and 102-2811-B-320-001 to S.-F.C.; and Tzu Chi University, grant number TCMRC-P-104010-01 to M.-D.L.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data are contained within the article.

Acknowledgments

We express our gratitude to Chun-Hong Chen at the National Health Research Institutes, Taiwan, for providing P{w+; GMR-RGH-miRNA}, P{w+; GMR-reaper-miRNA}, P{w+; UAS-grim-miRNA} and P{w+; GMR-hid-miRNA} fly stocks. Our thanks also go to the FlyCore in Taiwan for their microinjection services, as well as the Vienna Drosophila RNAi Center, and the Bloomington Stock Center for providing fly stocks. We acknowledge the Genomics Center for Clinical and Biotechnological Applications of the National Core Facility for Biopharmaceuticals, Taiwan (NSTC 111-2740-B-A49-001) for their sequencing services. We also thank the Core Facility Center of Tzu Chi University (TCU) for confocal microscopy and the Electron Microscopy Laboratory of TCU for transmission electron microscopy. M.-D. Lin particularly wishes to express special thanks to Ji-Hshiung Chen and Ingrid Y Liu at TCU for their encouragement and insightful comments on the manuscript.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of the data; in the writing of the manuscript; or in the decision to publish the results.

References

  1. Longley, R.L., Jr.; Ready, D.F. Integrins and the development of three-dimensional structure in the Drosophila compound eye. Dev. Biol. 1995, 171, 415–433. [Google Scholar] [CrossRef]
  2. Flores-Benitez, D.; Knust, E. Dynamics of epithelial cell polarity in Drosophila: How to regulate the regulators? Curr. Opin. Cell Biol. 2016, 42, 13–21. [Google Scholar] [CrossRef] [PubMed]
  3. Izaddoost, S.; Nam, S.C.; Bhat, M.A.; Bellen, H.J.; Choi, K.W. Drosophila Crumbs is a positional cue in photoreceptor adherens junctions and rhabdomeres. Nature 2002, 416, 178–183. [Google Scholar] [CrossRef] [PubMed]
  4. Pellikka, M.; Tanentzapf, G.; Pinto, M.; Smith, C.; McGlade, C.J.; Ready, D.F.; Tepass, U. Crumbs, the Drosophila homologue of human CRB1/RP12, is essential for photoreceptor morphogenesis. Nature 2002, 416, 143–149. [Google Scholar] [CrossRef] [PubMed]
  5. Atwood, S.X.; Chabu, C.; Penkert, R.R.; Doe, C.Q.; Prehoda, K.E. Cdc42 acts downstream of Bazooka to regulate neuroblast polarity through Par-6 aPKC. J. Cell Sci. 2007, 120 Pt 18, 3200–3206. [Google Scholar] [CrossRef] [Green Version]
  6. Walther, R.F.; Pichaud, F. Crumbs/DaPKC-dependent apical exclusion of Bazooka promotes photoreceptor polarity remodeling. Curr. Biol. 2010, 20, 1065–1074. [Google Scholar] [CrossRef] [Green Version]
  7. Harris, T.J.; Peifer, M. Adherens junction-dependent and -independent steps in the establishment of epithelial cell polarity in Drosophila. J. Cell Biol. 2004, 167, 135–147. [Google Scholar] [CrossRef] [Green Version]
  8. McGill, M.A.; McKinley, R.F.; Harris, T.J. Independent cadherin-catenin and Bazooka clusters interact to assemble adherens junctions. J. Cell Biol. 2009, 185, 787–796. [Google Scholar] [CrossRef] [Green Version]
  9. Kozlov, G.; Cheng, J.; Ziomek, E.; Banville, D.; Gehring, K.; Ekiel, I. Structural insights into molecular function of the metastasis-associated phosphatase PRL-3. J. Biol. Chem. 2004, 279, 11882–11889. [Google Scholar] [CrossRef] [Green Version]
  10. Jeong, D.G.; Kim, S.J.; Kim, J.H.; Son, J.H.; Park, M.R.; Lim, S.M.; Yoon, T.S.; Ryu, S.E. Trimeric structure of PRL-1 phosphatase reveals an active enzyme conformation and regulation mechanisms. J. Mol. Biol. 2005, 345, 401–413. [Google Scholar] [CrossRef]
  11. Lin, M.D.; Lee, H.T.; Wang, S.C.; Li, H.R.; Hsien, H.L.; Cheng, K.W.; Chang, Y.D.; Huang, M.L.; Yu, J.K.; Chen, Y.H. Expression of phosphatase of regenerating liver family genes during embryogenesis: An evolutionary developmental analysis among Drosophila, amphioxus, and zebrafish. BMC Dev. Biol. 2013, 13, 18. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Zeng, Q.; Si, X.; Horstmann, H.; Xu, Y.; Hong, W.; Pallen, C.J. Prenylation-dependent association of protein-tyrosine phosphatases PRL-1, -2, and -3 with the plasma membrane and the early endosome. J. Biol. Chem. 2000, 275, 21444–21452. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Wang, J.; Kirby, C.E.; Herbst, R. The tyrosine phosphatase PRL-1 localizes to the endoplasmic reticulum and the mitotic spindle and is required for normal mitosis. J. Biol. Chem. 2002, 277, 46659–46668. [Google Scholar] [CrossRef] [Green Version]
  14. Diamond, R.H.; Cressman, D.E.; Laz, T.M.; Abrams, C.S.; Taub, R. PRL-1, a unique nuclear protein tyrosine phosphatase, affects cell growth. Mol. Cell. Biol. 1994, 14, 3752–3762. [Google Scholar] [CrossRef] [PubMed]
  15. Mohn, K.L.; Laz, T.M.; Hsu, J.C.; Melby, A.E.; Bravo, R.; Taub, R. The immediate-early growth response in regenerating liver and insulin-stimulated H-35 cells: Comparison with serum-stimulated 3T3 cells and identification of 41 novel immediate-early genes. Mol. Cell. Biol. 1991, 11, 381–390. [Google Scholar] [CrossRef]
  16. Bessette, D.C.; Qiu, D.; Pallen, C.J. PRL PTPs: Mediators and markers of cancer progression. Cancer Metastasis Rev. 2008, 27, 231–252. [Google Scholar] [CrossRef] [PubMed]
  17. Funato, Y.; Hashizume, O.; Miki, H. Phosphatase-independent role of phosphatase of regenerating liver in cancer progression. Cancer Sci. 2023, 114, 25–33. [Google Scholar] [CrossRef]
  18. Rubio, T.; Kohn, M. Regulatory mechanisms of phosphatase of regenerating liver (PRL)-3. Biochem. Soc. Trans. 2016, 44, 1305–1312. [Google Scholar] [CrossRef] [Green Version]
  19. Jiao, Y.; Ye, D.Z.; Li, Z.; Teta-Bissett, M.; Peng, Y.; Taub, R.; Greenbaum, L.E.; Kaestner, K.H. Protein tyrosine phosphatase of liver regeneration-1 is required for normal timing of cell cycle progression during liver regeneration. Am. J. Physiol. Gastrointest Liver Physiol. 2015, 308, G85–G91. [Google Scholar] [CrossRef] [Green Version]
  20. Yan, H.; Kong, D.; Ge, X.; Gao, X.; Han, X. Generation of conditional knockout alleles for PRL-3. J. Biomed. Res. 2011, 25, 438–443. [Google Scholar] [CrossRef]
  21. Zimmerman, M.W.; Homanics, G.E.; Lazo, J.S. Targeted deletion of the metastasis-associated phosphatase Ptp4a3 (PRL-3) suppresses murine colon cancer. PLoS ONE 2013, 8, e58300. [Google Scholar] [CrossRef] [Green Version]
  22. Dong, Y.; Zhang, L.; Bai, Y.; Zhou, H.M.; Campbell, A.M.; Chen, H.; Yong, W.; Zhang, W.; Zeng, Q.; Shou, W.; et al. Phosphatase of regenerating liver 2 (PRL2) deficiency impairs Kit signaling and spermatogenesis. J. Biol. Chem. 2014, 289, 3799–3810. [Google Scholar] [CrossRef] [Green Version]
  23. Dong, Y.; Zhang, L.; Zhang, S.; Bai, Y.; Chen, H.; Sun, X.; Yong, W.; Li, W.; Colvin, S.C.; Rhodes, S.J.; et al. Phosphatase of regenerating liver 2 (PRL2) is essential for placental development by down-regulating PTEN (Phosphatase and Tensin Homologue Deleted on Chromosome 10) and activating Akt protein. J. Biol. Chem. 2012, 287, 32172–32179. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Maacha, S.; Planque, N.; Laurent, C.; Pegoraro, C.; Anezo, O.; Maczkowiak, F.; Monsoro-Burq, A.H.; Saule, S. Protein tyrosine phosphatase 4A3 (PTP4A3) is required for Xenopus laevis cranial neural crest migration in vivo. PLoS ONE 2013, 8, e84717. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Deichmann, C.; Link, M.; Seyfang, M.; Knotz, V.; Gradl, D.; Wedlich, D. Neural crest specification by Prohibitin1 depends on transcriptional regulation of prl3 and vangl1. Genesis 2015, 53, 627–639. [Google Scholar] [CrossRef] [PubMed]
  26. Pagarigan, K.T.; Bunn, B.W.; Goodchild, J.; Rahe, T.K.; Weis, J.F.; Saucedo, L.J. Drosophila PRL-1 is a growth inhibitor that counteracts the function of the Src oncogene. PLoS ONE 2013, 8, e61084. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  27. Phelps, C.B.; Brand, A.H. Ectopic gene expression in Drosophila using GAL4 system. Methods 1998, 14, 367–379. [Google Scholar] [CrossRef] [Green Version]
  28. Cates, C.A.; Michael, R.L.; Stayrook, K.R.; Harvey, K.A.; Burke, Y.D.; Randall, S.K.; Crowell, P.L.; Crowell, D.N. Prenylation of oncogenic human PTP(CAAX) protein tyrosine phosphatases. Cancer Lett. 1996, 110, 49–55. [Google Scholar] [CrossRef]
  29. Sun, J.P.; Luo, Y.; Yu, X.; Wang, W.Q.; Zhou, B.; Liang, F.; Zhang, Z.Y. Phosphatase activity, trimerization, and the C-terminal polybasic region are all required for PRL1-mediated cell growth and migration. J. Biol. Chem. 2007, 282, 29043–29051. [Google Scholar] [CrossRef] [Green Version]
  30. Dietzl, G.; Chen, D.; Schnorrer, F.; Su, K.C.; Barinova, Y.; Fellner, M.; Gasser, B.; Kinsey, K.; Oppel, S.; Scheiblauer, S.; et al. A genome-wide transgenic RNAi library for conditional gene inactivation in Drosophila. Nature 2007, 448, 151–156. [Google Scholar] [CrossRef]
  31. Chen, C.H.; Huang, H.; Ward, C.M.; Su, J.T.; Schaeffer, L.V.; Guo, M.; Hay, B.A. A synthetic maternal-effect selfish genetic element drives population replacement in Drosophila. Science 2007, 316, 597–600. [Google Scholar] [CrossRef] [PubMed]
  32. Yasuhara, J.C.; Baumann, O.; Takeyasu, K. Localization of Na/K-ATPase in developing and adult Drosophila melanogaster photoreceptors. Cell Tissue Res. 2000, 300, 239–249. [Google Scholar] [CrossRef] [PubMed]
  33. Lujan, P.; Varsano, G.; Rubio, T.; Hennrich, M.L.; Sachsenheimer, T.; Galvez-Santisteban, M.; Martin-Belmonte, F.; Gavin, A.C.; Brugger, B.; Kohn, M. PRL-3 disrupts epithelial architecture by altering the post-mitotic midbody position. J. Cell Sci. 2016, 129, 4130–4142. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  34. Colosimo, P.F.; Liu, X.; Kaplan, N.A.; Tolwinski, N.S. GSK3beta affects apical-basal polarity and cell-cell adhesion by regulating aPKC levels. Dev. Dyn. 2010, 239, 115–125. [Google Scholar] [CrossRef] [PubMed]
  35. Kaplan, N.A.; Colosimo, P.F.; Liu, X.; Tolwinski, N.S. Complex interactions between GSK3 and aPKC in Drosophila embryonic epithelial morphogenesis. PLoS ONE 2011, 6, e18616. [Google Scholar] [CrossRef] [Green Version]
  36. Frame, S.; Cohen, P.; Biondi, R.M. A common phosphate binding site explains the unique substrate specificity of GSK3 and its inactivation by phosphorylation. Mol. Cell 2001, 7, 1321–1327. [Google Scholar] [CrossRef]
  37. Wang, H.; Quah, S.Y.; Dong, J.M.; Manser, E.; Tang, J.P.; Zeng, Q. PRL-3 down-regulates PTEN expression and signals through PI3K to promote epithelial-mesenchymal transition. Cancer Res. 2007, 67, 2922–2926. [Google Scholar] [CrossRef] [Green Version]
  38. Chong PS, Y.; Zhou, J.; Lim JS, L.; Hee, Y.T.; Chooi, J.Y.; Chung, T.H.; Tan, Z.T.; Zeng, Q.; Waller, D.D.; Sebag, M.; et al. IL6 Promotes a STAT3-PRL3 Feedforward Loop via SHP2 Repression in Multiple Myeloma. Cancer Res. 2019, 79, 4679–4688. [Google Scholar] [CrossRef]
  39. Lazo, J.S.; Isbell, K.N.; Vasa, S.A.; Llaneza, D.C.; Rastelli, E.J.; Wipf, P.; Sharlow, E.R. Disruption of Ovarian Cancer STAT3 and p38 Signaling with a Small-Molecule Inhibitor of PTP4A3 Phosphatase. J. Pharmacol. Exp. Ther. 2023, 384, 429–438. [Google Scholar] [CrossRef]
  40. Zhang, S.Q.; Tsiaras, W.G.; Araki, T.; Wen, G.; Minichiello, L.; Klein, R.; Neel, B.G. Receptor-specific regulation of phosphatidylinositol 3′-kinase activation by the protein tyrosine phosphatase Shp2. Mol. Cell. Biol. 2002, 22, 4062–4072. [Google Scholar] [CrossRef] [Green Version]
  41. Liu, Y.; Zhou, J.; Chen, J.; Gao, W.; Le, Y.; Ding, Y.; Li, J. PRL-3 promotes epithelial mesenchymal transition by regulating cadherin directly. Cancer Biol. Ther. 2009, 8, 1352–1359. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  42. Brodsky, M.H.; Weinert, B.T.; Tsang, G.; Rong, Y.S.; McGinnis, N.M.; Golic, K.G.; Rio, D.C.; Rubin, G.M. Drosophila melanogaster MNK/Chk2 and p53 regulate multiple DNA repair and apoptotic pathways following DNA damage. Mol. Cell. Biol. 2004, 24, 1219–1231. [Google Scholar] [CrossRef] [Green Version]
  43. Moon, N.S.; Di Stefano, L.; Morris, E.J.; Patel, R.; White, K.; Dyson, N.J. E2F and p53 induce apoptosis independently during Drosophila development but intersect in the context of DNA damage. PLoS Genet. 2008, 4, e1000153. [Google Scholar] [CrossRef] [PubMed]
  44. Basak, S.; Jacobs, S.B.; Krieg, A.J.; Pathak, N.; Zeng, Q.; Kaldis, P.; Giaccia, A.J.; Attardi, L.D. The metastasis-associated gene Prl-3 is a p53 target involved in cell-cycle regulation. Mol. Cell 2008, 30, 303–314. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  45. Brumby, A.M.; Richardson, H.E. scribble mutants cooperate with oncogenic Ras or Notch to cause neoplastic overgrowth in Drosophila. EMBO J. 2003, 22, 5769–5779. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  46. Igaki, T.; Pagliarini, R.A.; Xu, T. Loss of cell polarity drives tumor growth and invasion through JNK activation in Drosophila. Curr. Biol. 2006, 16, 1139–1146. [Google Scholar] [CrossRef] [Green Version]
  47. Uhlirova, M.; Jasper, H.; Bohmann, D. Non-cell-autonomous induction of tissue overgrowth by JNK/Ras cooperation in a Drosophila tumor model. Proc. Natl. Acad. Sci. USA 2005, 102, 13123–13128. [Google Scholar] [CrossRef]
Ijms 24 11501 g001 550
Figure 1. Localization of dPRL to the apical membrane of photoreceptor cells. (A) Schematic illustration of the cross section of a photoreceptor cluster at 50% p.d. The most apical region of the photoreceptor cells, the future rhabdomere, is enriched with F-actin (green). Localization of Crumbs (Crb)/Drosophila atypical protein kinase C (DaPKC) to the sub-apical membrane and that of DE-Cadherin (DE-Cad)/Armadillo (Arm) to the adherens junction (Aj) are marked with red and blue, respectively. (B–P) Analysis of colocalization between dPRL and other polarity proteins in pupal retina at 50% p.d. (B) The localization of endogenous dPRL was visualized by immunostaining using anti-dPRL antibody. dPRL was enriched in the apical membrane with minor localization to the basolateral membrane. Note that dPRL was also localized on the plasma membrane of pigment cells surrounding the photoreceptor cell clusters. (E,H,K,N) Localization of GFP-dPRL. Signals of dPRL came from the expression of UAS-GFP-dPRL driven by GMR-Gal4 driver. (C,F,I,L,O) Localization of Arm, DE-Cad, Crb, and DaPKC were revealed by immunostaining; the F-actin was stained by rhodamine-conjugated phalloidin. (D,G,J,M,P) Merged images. Colocalization was identified in GFP-dPRL/Crb (J, partial colocalization), dPRL/DaPKC (M, partial colocalization), and dPRL/F-actin (P, colocalization).
Figure 1. Localization of dPRL to the apical membrane of photoreceptor cells. (A) Schematic illustration of the cross section of a photoreceptor cluster at 50% p.d. The most apical region of the photoreceptor cells, the future rhabdomere, is enriched with F-actin (green). Localization of Crumbs (Crb)/Drosophila atypical protein kinase C (DaPKC) to the sub-apical membrane and that of DE-Cadherin (DE-Cad)/Armadillo (Arm) to the adherens junction (Aj) are marked with red and blue, respectively. (B–P) Analysis of colocalization between dPRL and other polarity proteins in pupal retina at 50% p.d. (B) The localization of endogenous dPRL was visualized by immunostaining using anti-dPRL antibody. dPRL was enriched in the apical membrane with minor localization to the basolateral membrane. Note that dPRL was also localized on the plasma membrane of pigment cells surrounding the photoreceptor cell clusters. (E,H,K,N) Localization of GFP-dPRL. Signals of dPRL came from the expression of UAS-GFP-dPRL driven by GMR-Gal4 driver. (C,F,I,L,O) Localization of Arm, DE-Cad, Crb, and DaPKC were revealed by immunostaining; the F-actin was stained by rhodamine-conjugated phalloidin. (D,G,J,M,P) Merged images. Colocalization was identified in GFP-dPRL/Crb (J, partial colocalization), dPRL/DaPKC (M, partial colocalization), and dPRL/F-actin (P, colocalization).
Ijms 24 11501 g001
Ijms 24 11501 g002 550
Figure 2. The subcellular localization of GFP-dPRL and GFP-dPRLC173S in photoreceptor cells. (A) Multiple sequence alignment of PRL proteins in humans and Drosophila. The C(X)5R phosphatase catalytic site and the CAAX prenylation motif are highlighted. The position of Cys173 in dPRL is marked with a red asterisk. Green represents identical residues, blue indicates residues with similar properties, and yellow marks consensus residues. (B–K) Immunostaining was performed on the pupal retina at 50% p.d. GFP is depicted in green, DAPI in blue, and F-actin in red. (B–F) Pupal retina expressing GFP-tagged wild-type dPRL, genotype: GMR-Gal4/+; UAS-GFP-dPRL/+. (B) GFP-dPRL was localized to the plasma membrane, with marked enrichment at the apical membrane of photoreceptor cells. (C) Nuclei were stained with DAPI. (D) Merged image of (B,C). (E) F-actin was highly enriched at the apical membrane of photoreceptor cells. (F) Merged image of (B,E), indicating co-localization of dPRL with F-actin at the apical membrane. (G–K) Pupal retina expressing GFP-tagged dPRL carrying a Cys173 to Ser substitution, genotype: GMR-Gal4/+; UAS-GFP-dPRLC173S/+. (G) GFP-dPRLC173S was found to be mislocalized in the photoreceptor cells, notably accumulating in the cytosol near the apical membrane and within the nucleus. (H) Nuclei were stained with DAPI. (I) Merged image of (G,H). (J) F-actin staining. (K) Merged image of (G,J), demonstrating that GFP-dPRLC173S did not co-localize with F-actin. Scale bars represent 5 µm.
Figure 2. The subcellular localization of GFP-dPRL and GFP-dPRLC173S in photoreceptor cells. (A) Multiple sequence alignment of PRL proteins in humans and Drosophila. The C(X)5R phosphatase catalytic site and the CAAX prenylation motif are highlighted. The position of Cys173 in dPRL is marked with a red asterisk. Green represents identical residues, blue indicates residues with similar properties, and yellow marks consensus residues. (B–K) Immunostaining was performed on the pupal retina at 50% p.d. GFP is depicted in green, DAPI in blue, and F-actin in red. (B–F) Pupal retina expressing GFP-tagged wild-type dPRL, genotype: GMR-Gal4/+; UAS-GFP-dPRL/+. (B) GFP-dPRL was localized to the plasma membrane, with marked enrichment at the apical membrane of photoreceptor cells. (C) Nuclei were stained with DAPI. (D) Merged image of (B,C). (E) F-actin was highly enriched at the apical membrane of photoreceptor cells. (F) Merged image of (B,E), indicating co-localization of dPRL with F-actin at the apical membrane. (G–K) Pupal retina expressing GFP-tagged dPRL carrying a Cys173 to Ser substitution, genotype: GMR-Gal4/+; UAS-GFP-dPRLC173S/+. (G) GFP-dPRLC173S was found to be mislocalized in the photoreceptor cells, notably accumulating in the cytosol near the apical membrane and within the nucleus. (H) Nuclei were stained with DAPI. (I) Merged image of (G,H). (J) F-actin staining. (K) Merged image of (G,J), demonstrating that GFP-dPRLC173S did not co-localize with F-actin. Scale bars represent 5 µm.
Ijms 24 11501 g002
Ijms 24 11501 g003 550
Figure 3. Retinal phenotypes of dPRL-RNAi flies. (A,B) Comparison of eye phenotypes between the driver control and dPRL-RNAi flies. (A) Gal4-driver control (UAS-dicer2; GMR-Gal4/+), demonstrating a wild-type phenotype. (B) dPRL-RNAi flies (UAS-dicer2; GMR-Gal4/+; UAS-dPRL-IR45518/+), showing loss of pigmentation, thinning, and roughened eyes. (C,D) Interior structures of adult retinas, as seen in longitudinal sections imaged using a transmission electron microscope. (C) Gal4-driver control (UAS-dicer2; GMR-Gal4/+). (D) Retina of dPRL-RNAi flies, exhibiting vacuoles (indicated by arrows) and a fused cornea (indicated by arrowheads). (E,F) Pupal retinas at 50% p.d (pupal development) with F-actin (red) localization visualized by rhodamine-conjugated phalloidin staining. Dotted lines outline individual ommatidia. (E) Wild-type pupal retina exhibits a hexagonal array of ommatidia with F-actin concentrated at the apical membrane of photoreceptor cells. (F) In the pupal retina of dPRL-RNAi flies, ommatidia are irregularly arranged and F-actin is either mislocalized (asterisk) or absent (arrow).
Figure 3. Retinal phenotypes of dPRL-RNAi flies. (A,B) Comparison of eye phenotypes between the driver control and dPRL-RNAi flies. (A) Gal4-driver control (UAS-dicer2; GMR-Gal4/+), demonstrating a wild-type phenotype. (B) dPRL-RNAi flies (UAS-dicer2; GMR-Gal4/+; UAS-dPRL-IR45518/+), showing loss of pigmentation, thinning, and roughened eyes. (C,D) Interior structures of adult retinas, as seen in longitudinal sections imaged using a transmission electron microscope. (C) Gal4-driver control (UAS-dicer2; GMR-Gal4/+). (D) Retina of dPRL-RNAi flies, exhibiting vacuoles (indicated by arrows) and a fused cornea (indicated by arrowheads). (E,F) Pupal retinas at 50% p.d (pupal development) with F-actin (red) localization visualized by rhodamine-conjugated phalloidin staining. Dotted lines outline individual ommatidia. (E) Wild-type pupal retina exhibits a hexagonal array of ommatidia with F-actin concentrated at the apical membrane of photoreceptor cells. (F) In the pupal retina of dPRL-RNAi flies, ommatidia are irregularly arranged and F-actin is either mislocalized (asterisk) or absent (arrow).
Ijms 24 11501 g003
Ijms 24 11501 g004 550
Figure 4. Knockdown of the proapoptotic gene hid rescued the loss-of-pigmentation phenotype observed in dPRL-RNAi flies. (A) Eye phenotype of dPRL-RNAi flies. (B–F) Effects of expressing the anti-apoptotic protein p35 or knocking down proapoptotic genes using miRNAs in dPRL-RNAi flies. (B) Eye phenotype following ectopic expression of the anti-apoptotic gene p35. (C) Eye phenotype after combined knockdown of proapoptotic genes reaper, grim, and hid using a miRNA construct (RGH-miRNA). (D) Eye phenotype following reaper knockdown using miRNA. (E) Eye phenotype following grim knockdown using miRNA. (F) Eye phenotype after hid knockdown using miRNA. Eye phenotypes were successfully rescued in panels (B,C,F). There is a high degree of phenotypic consistency (>80%) within each genotype. The images displayed herein represent the typical eye morphology for each respective genotype.
Figure 4. Knockdown of the proapoptotic gene hid rescued the loss-of-pigmentation phenotype observed in dPRL-RNAi flies. (A) Eye phenotype of dPRL-RNAi flies. (B–F) Effects of expressing the anti-apoptotic protein p35 or knocking down proapoptotic genes using miRNAs in dPRL-RNAi flies. (B) Eye phenotype following ectopic expression of the anti-apoptotic gene p35. (C) Eye phenotype after combined knockdown of proapoptotic genes reaper, grim, and hid using a miRNA construct (RGH-miRNA). (D) Eye phenotype following reaper knockdown using miRNA. (E) Eye phenotype following grim knockdown using miRNA. (F) Eye phenotype after hid knockdown using miRNA. Eye phenotypes were successfully rescued in panels (B,C,F). There is a high degree of phenotypic consistency (>80%) within each genotype. The images displayed herein represent the typical eye morphology for each respective genotype.
Ijms 24 11501 g004
Ijms 24 11501 g005 550
Figure 5. Mislocalization of apicobasal polarity proteins in the photoreceptor cells of dPRL-RNAi flies. Immunostaining was conducted on pupal retinas from either the Gal4-driver control (UAS-dicer2; GMR-Gal4/+) or dPRL-RNAi flies (UAS-dicer2; GMR-Gal4/+; UAS-dPRL-IR45518/+) to illustrate the localization of polarity proteins in photoreceptor cell clusters at 50% p.d. (A–F) Pupal retinas from Gal4-driver control (A–C) and dPRL-RNAi flies (D–F) were stained with phalloidin for labelling F-actin (A,C,D,F; red) and with an antibody against Arm (B,C,E,F; green). (G–L) Pupal retinas from Gal4-driver control (G-I) and dPRL-RNAi flies (J-L) were stained with phalloidin for labelling F-actin (G,I,J,L; red,) and an antibody against DaPKC (H,I,K,L; green). (M–R) Pupal retinas from Gal4-driver control (M–O) and dPRL-RNAi flies (P–R) were stained with phalloidin for labelling F-actin (M,O,P,R; red) and an antibody against Crb (N,O,Q,R; green). (S–X) Pupal retinas from Gal4-driver control (S–U) and dPRL-RNAi flies (V–X) were stained with phalloidin for labelling F-actin (S,U,V,X; red) and an antibody against the alpha subunit of Na+/K+-ATPase (T,U,W,X; green). Arrows in panels W and X highlight the mislocalization of the Na+/K+-ATPase (green) to the apical membrane, which is marked by F-actin (red). Scale bars represent 5 µm.
Figure 5. Mislocalization of apicobasal polarity proteins in the photoreceptor cells of dPRL-RNAi flies. Immunostaining was conducted on pupal retinas from either the Gal4-driver control (UAS-dicer2; GMR-Gal4/+) or dPRL-RNAi flies (UAS-dicer2; GMR-Gal4/+; UAS-dPRL-IR45518/+) to illustrate the localization of polarity proteins in photoreceptor cell clusters at 50% p.d. (A–F) Pupal retinas from Gal4-driver control (A–C) and dPRL-RNAi flies (D–F) were stained with phalloidin for labelling F-actin (A,C,D,F; red) and with an antibody against Arm (B,C,E,F; green). (G–L) Pupal retinas from Gal4-driver control (G-I) and dPRL-RNAi flies (J-L) were stained with phalloidin for labelling F-actin (G,I,J,L; red,) and an antibody against DaPKC (H,I,K,L; green). (M–R) Pupal retinas from Gal4-driver control (M–O) and dPRL-RNAi flies (P–R) were stained with phalloidin for labelling F-actin (M,O,P,R; red) and an antibody against Crb (N,O,Q,R; green). (S–X) Pupal retinas from Gal4-driver control (S–U) and dPRL-RNAi flies (V–X) were stained with phalloidin for labelling F-actin (S,U,V,X; red) and an antibody against the alpha subunit of Na+/K+-ATPase (T,U,W,X; green). Arrows in panels W and X highlight the mislocalization of the Na+/K+-ATPase (green) to the apical membrane, which is marked by F-actin (red). Scale bars represent 5 µm.
Ijms 24 11501 g005
Ijms 24 11501 g006 550
Figure 6. Suppression of apoptosis could not rescue the photoreceptor cell polarity defect caused by dPRL knockdown. (A–C,G–I) Show representative ommatidia from control flies expressing the Gal4 driver and hid-miRNA (genotype: UAS-dicer2; GMR-Gal4/+; UAS-hid-miRNA/+). (D–F,J–L) Show representative ommatidia from dPRL-RNAi flies expressing hid-miRNA (genotype: UAS-dicer2; GMR-Gal4/+; UAS-hid-miRNA/UAS-dPRL-IR45518). Pupal retinas at 50% p.d. were fixed and stained for F-actin with rhodamine-conjugated phalloidin to mark the apical membrane, along with Crumbs (Crb, green) in (A–F), or the alpha subunit of Na+/K+-ATPase (green) in (G–L). Notably, despite suppression of apoptosis through the expression of hid-miRNA, Crb (E) and Na+/K+-ATPase (K) were still mislocalized in the dPRL-knockdown retina. Scale bars represent 5 µm.
Figure 6. Suppression of apoptosis could not rescue the photoreceptor cell polarity defect caused by dPRL knockdown. (A–C,G–I) Show representative ommatidia from control flies expressing the Gal4 driver and hid-miRNA (genotype: UAS-dicer2; GMR-Gal4/+; UAS-hid-miRNA/+). (D–F,J–L) Show representative ommatidia from dPRL-RNAi flies expressing hid-miRNA (genotype: UAS-dicer2; GMR-Gal4/+; UAS-hid-miRNA/UAS-dPRL-IR45518). Pupal retinas at 50% p.d. were fixed and stained for F-actin with rhodamine-conjugated phalloidin to mark the apical membrane, along with Crumbs (Crb, green) in (A–F), or the alpha subunit of Na+/K+-ATPase (green) in (G–L). Notably, despite suppression of apoptosis through the expression of hid-miRNA, Crb (E) and Na+/K+-ATPase (K) were still mislocalized in the dPRL-knockdown retina. Scale bars represent 5 µm.
Ijms 24 11501 g006
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Chen, S.-F.; Hsien, H.-L.; Wang, T.-F.; Lin, M.-D. Drosophila Phosphatase of Regenerating Liver Is Critical for Photoreceptor Cell Polarity and Survival during Retinal Development. Int. J. Mol. Sci. 2023, 24, 11501. https://doi.org/10.3390/ijms241411501

AMA Style

Chen S-F, Hsien H-L, Wang T-F, Lin M-D. Drosophila Phosphatase of Regenerating Liver Is Critical for Photoreceptor Cell Polarity and Survival during Retinal Development. International Journal of Molecular Sciences. 2023; 24(14):11501. https://doi.org/10.3390/ijms241411501

Chicago/Turabian Style

Chen, Shu-Fen, Hsin-Lun Hsien, Ting-Fang Wang, and Ming-Der Lin. 2023. "Drosophila Phosphatase of Regenerating Liver Is Critical for Photoreceptor Cell Polarity and Survival during Retinal Development" International Journal of Molecular Sciences 24, no. 14: 11501. https://doi.org/10.3390/ijms241411501

APA Style

Chen, S. -F., Hsien, H. -L., Wang, T. -F., & Lin, M. -D. (2023). Drosophila Phosphatase of Regenerating Liver Is Critical for Photoreceptor Cell Polarity and Survival during Retinal Development. International Journal of Molecular Sciences, 24(14), 11501. https://doi.org/10.3390/ijms241411501

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