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Article
Peer-Review Record

Dental Pulp Stem Cells Modulate Inflammasome Pathway and Collagen Deposition of Dermal Fibroblasts

Cells 2024, 13(10), 836; https://doi.org/10.3390/cells13100836
by Giada Zanini 1,†, Giulia Bertani 2,†, Rosanna Di Tinco 2, Alessandra Pisciotta 2, Laura Bertoni 2, Valentina Selleri 1,3, Luigi Generali 2, Alessandra Marconi 2, Anna Vittoria Mattioli 3,4, Marcello Pinti 1,*, Gianluca Carnevale 2 and Milena Nasi 2
Reviewer 1: Anonymous
Reviewer 2: Anonymous
Cells 2024, 13(10), 836; https://doi.org/10.3390/cells13100836
Submission received: 27 February 2024 / Revised: 8 May 2024 / Accepted: 13 May 2024 / Published: 14 May 2024
(This article belongs to the Special Issue Adult Stem Cells in Human Disease)

Round 1

Reviewer 1 Report

Comments and Suggestions for Authors

In this paper entitled "Dental Pulp Stem Cells Modulate Inflammasome Pathway and Collagen Deposition of Dermal Fibroblasts”, Giada Zanini et al. investigated DPSC and fibroblast interaction on inflammatory mediators expression and collagen protein.

The data are novel and somewhat interesting, however, this reviewer thinks that experimental designs and the conclusion may not be significant to the standard of Cells journal. It`s generally known that stem cells are secretory and affect the behavior of target cells in various ways. There are many studies of stem cell (and interacting cells) phenotype changes under inflammatory stimulation. The authors used a simple two cells culture system and examined the expression of common inflammatory molecules using the PCR and IHC without showing any mechanisms or in vivo study.

 

Stem cell behavior significantly alters depending on the concentration of inflammatory agents. The authors need to provide phenotype changes (or justifications) in different parameters.

 

Rather than just listing expressions of common inflammatory mediators, I would suggest pinpointing a major inflammatory molecule and seeking its mechanism.

 

Need higher-magnification IHC images (e.g. confocal) for Figure 6. Also, provide whether these increased expressions are from the fibroblasts or stem cells with a marker analysis (e.g. stem cell for STRO-1 & fibroblasts for FSP).

 

 

More importantly, for the mechanism, you may apply a key inflammatory agent inhibitor (or siRNA) without DPSC to see if this disrupts collagen protein expressions on fibroblasts. 

Author Response

Please, see the attached file. 

Author Response File: Author Response.pdf

Reviewer 2 Report

Comments and Suggestions for Authors

This study  is an interesting  and valuable to the existing  literature. The  introduction, results and discussion  are well written, however,  some points  need  more explanation.

Comments

 Material and Methods :

2.2. Cell Culture -   “Fibroblasts and DPSCs were seeded on six-well plates at a density of 2,5x105 and 2x105, respectively”.  Why the  cells were seeded in different density?

- in co-culture the ratio between the different cells is important.

Results:

Figure 1 A  legend   is confusing for reader.  Please correct because should be IL-1, IL-6 and IL-8 upper panels.

Figure 6 COLL1A1 staining panels; cc(NS 24h) and cc S 24h is poor quality.

I recommended this manuscript to minor revision for future process.

Author Response

Please see the attachment.

Author Response File: Author Response.pdf

Round 2

Reviewer 1 Report

Comments and Suggestions for Authors

The authors addressed most concerns within limited time and resources, and the manuscript is acceptable to publish in its current form.

Author Response

We thank the reviewer for appreciating our effort to fulfill her/his requests, and for considering our manuscript acceptable for publication.

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