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The transcriptional profile of keloidal Schwann cells
Recently, a specific Schwann cell type with profibrotic and tissue regenerative properties that contributes to keloid formation has been identified. In the present study, we reanalyzed published single-cell RNA sequencing (scRNA-seq) studies of keloids, healthy skin, and normal scars to reliably det...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9722693/ https://www.ncbi.nlm.nih.gov/pubmed/36333467 http://dx.doi.org/10.1038/s12276-022-00874-1 |
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author | Direder, Martin Wielscher, Matthias Weiss, Tamara Laggner, Maria Copic, Dragan Klas, Katharina Bormann, Daniel Vorstandlechner, Vera Tschachler, Erwin Jan Ankersmit, Hendrik Mildner, Michael |
author_facet | Direder, Martin Wielscher, Matthias Weiss, Tamara Laggner, Maria Copic, Dragan Klas, Katharina Bormann, Daniel Vorstandlechner, Vera Tschachler, Erwin Jan Ankersmit, Hendrik Mildner, Michael |
author_sort | Direder, Martin |
collection | PubMed |
description | Recently, a specific Schwann cell type with profibrotic and tissue regenerative properties that contributes to keloid formation has been identified. In the present study, we reanalyzed published single-cell RNA sequencing (scRNA-seq) studies of keloids, healthy skin, and normal scars to reliably determine the specific gene expression profile of keloid-specific Schwann cell types in more detail. We were able to confirm the presence of the repair-like, profibrotic Schwann cell type in the datasets of all three studies and identified a specific gene-set for these Schwann cells. In contrast to keloids, in normal scars, the number of Schwann cells was not increased, nor was their gene expression profile distinctly different from that of Schwann cells of normal skin. In addition, our bioinformatics analysis provided evidence for a role of transcription factors of the AP1, STAT, and KLF families, and members of the IER genes in the dedifferentiation process of keloidal Schwann cells. Together, our analysis strengthens the role of the profibrotic Schwann cell type in the formation of keloids. Knowledge of the exact gene expression profile of these Schwann cells will facilitate their identification in other organs and diseases. |
format | Online Article Text |
id | pubmed-9722693 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97226932022-12-22 The transcriptional profile of keloidal Schwann cells Direder, Martin Wielscher, Matthias Weiss, Tamara Laggner, Maria Copic, Dragan Klas, Katharina Bormann, Daniel Vorstandlechner, Vera Tschachler, Erwin Jan Ankersmit, Hendrik Mildner, Michael Exp Mol Med Article Recently, a specific Schwann cell type with profibrotic and tissue regenerative properties that contributes to keloid formation has been identified. In the present study, we reanalyzed published single-cell RNA sequencing (scRNA-seq) studies of keloids, healthy skin, and normal scars to reliably determine the specific gene expression profile of keloid-specific Schwann cell types in more detail. We were able to confirm the presence of the repair-like, profibrotic Schwann cell type in the datasets of all three studies and identified a specific gene-set for these Schwann cells. In contrast to keloids, in normal scars, the number of Schwann cells was not increased, nor was their gene expression profile distinctly different from that of Schwann cells of normal skin. In addition, our bioinformatics analysis provided evidence for a role of transcription factors of the AP1, STAT, and KLF families, and members of the IER genes in the dedifferentiation process of keloidal Schwann cells. Together, our analysis strengthens the role of the profibrotic Schwann cell type in the formation of keloids. Knowledge of the exact gene expression profile of these Schwann cells will facilitate their identification in other organs and diseases. Nature Publishing Group UK 2022-11-04 /pmc/articles/PMC9722693/ /pubmed/36333467 http://dx.doi.org/10.1038/s12276-022-00874-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Direder, Martin Wielscher, Matthias Weiss, Tamara Laggner, Maria Copic, Dragan Klas, Katharina Bormann, Daniel Vorstandlechner, Vera Tschachler, Erwin Jan Ankersmit, Hendrik Mildner, Michael The transcriptional profile of keloidal Schwann cells |
title | The transcriptional profile of keloidal Schwann cells |
title_full | The transcriptional profile of keloidal Schwann cells |
title_fullStr | The transcriptional profile of keloidal Schwann cells |
title_full_unstemmed | The transcriptional profile of keloidal Schwann cells |
title_short | The transcriptional profile of keloidal Schwann cells |
title_sort | transcriptional profile of keloidal schwann cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9722693/ https://www.ncbi.nlm.nih.gov/pubmed/36333467 http://dx.doi.org/10.1038/s12276-022-00874-1 |
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