Next Article in Journal
Association of Thymidylate Synthase (TS) Gene Polymorphisms with Incidence and Prognosis of Coronary Artery Disease
Next Article in Special Issue
Effect of Cannabidiol on Human Peripheral Blood Mononuclear Cells and CD4+ T Cells
Previous Article in Journal
Anticancer Study of a Novel Pan-HDAC Inhibitor MPT0G236 in Colorectal Cancer Cells
Previous Article in Special Issue
Hyperoside as a UV Photoprotective or Photostimulating Compound—Evaluation of the Effect of UV Radiation with Selected UV-Absorbing Organic Compounds on Skin Cells
 
 
Article
Peer-Review Record

Holothurian Wall Hydrolysate Ameliorates Cyclophosphamide-Induced Immunocompromised Mice via Regulating Immune Response and Improving Gut Microbiota

Int. J. Mol. Sci. 2023, 24(16), 12583; https://doi.org/10.3390/ijms241612583
by Chen Yan, Huiru Qu, Xinli Li * and Bin Feng *
Reviewer 1:
Reviewer 2: Anonymous
Reviewer 3:
Int. J. Mol. Sci. 2023, 24(16), 12583; https://doi.org/10.3390/ijms241612583
Submission received: 11 July 2023 / Revised: 30 July 2023 / Accepted: 7 August 2023 / Published: 9 August 2023

Round 1

Reviewer 1 Report

It is a very well done article from the point of view of research methodology. In my opinion, the article could be improved by taking into account the presence of boron in the hydrolyzate, the latest research shows that boron is an essential element in healthy symbiosis. The dysbiosis improvement effects can also be due to the high boron content in the hydrolyzate, seeing that Sea cucumber has a high boron content over 50 ppm!

Author Response

Please see the attachment.

Author Response File: Author Response.doc

Reviewer 2 Report

This manuscript presented an investigation of the role of holothurian wall hydrolysates in injury repair to intestinal barrier and maintanance of gut microbiota balance. The work shows the value of holothurian wall hydrolysates. However, it was presented with a series of flaws:

1. Figure 1 doesn't show any meaningful data.

2. Table 1 needs explanation on how it was generated. And in what order the data is organized.

3. In line 142-144, it is obvious from Figure 2B that NC (also N240) shows 2-fold increase in spleen index compared to CTX (and N240 may be 1.5-fold). What is the criterion here to define significance?

4. In Section 2.3 and Figure 3, Figure 3A needs to be re-organized into 2-columns by 6-rows (HE/PAS as column title). The HE staining clearly shows PC is very similar to CTX as opposed to the statement in line 161.

5. In Section 2.4 and Figure 4, Figure 4A(panel 2 and 3) shows NC is significantly different than N240 again in contrary to the authors' statement (line 183). And western blots (panel 2 and 3) don't match H&E in Figure 3A. Figure 4 is missing figure title and subtitles.

 

Minor:

6. Figure 6,7,10 need higher resolution.

7. Line 11, "...closely related to the integrity of intestinal barrier and the balance of gut microbiota".

8. "Ameliorates".

Needs more proofreading

Author Response

Please see the attachment.

Author Response File: Author Response.doc

Reviewer 3 Report

The manuscript describes the amelioration of cyclophosphamide-induced immunocompromised mice via regulating immune response and improving gut microbiota by holothurian wall hydrolysates. The topic is relevant to the aim and scope of the Int. J. Mol. Sci.. The manuscript is well written and easy to follow. Some clarifications in the texts are needed. Overall, this manuscript meets the standard for acceptance after addressing the below comments:

 

1)      Since there are a lot of abbreviations used in this manuscript, it would be better to include a separate section for the abbreviation, for example, ZO-1, PC, TRL, MAPK, PI3K, AKT, and so on. Actually these are quite familiar to the biologists, but research papers should be general to all readers.

2)      Figures are little recognizable, especially Figure 6, 7, and, 9. Please modify them.

3)      What is the variable on the vertical axis in Figure 6? The variable looks missing.

4)      In Figure 4, the effect of HWH is presented with the amount of the protein expression. Then, why is the effect presented in Figure 5 with the relative mRNA level rather than the expression?

5)      Why is the relative mRNA level of TNF-α in Figure 5 extraordinary high at N240, although IL-6 and IL-1β is not quite high?

6)      Please elaborate the experimental steps for staining. What is the dye concentration and its volume used to the slide? What is the staining time after the dye solution was added?

Author Response

Please see the attachment.

Author Response File: Author Response.doc

Round 2

Reviewer 3 Report

The response 6 should be included in the manuscript. The other issues have been addressed.

Author Response

Please see the attachment.

Author Response File: Author Response.pdf

Back to TopTop