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Y-27632 acts beyond ROCK inhibition to maintain epidermal stem-like cells in culture
Conditional reprogramming is a cell culture technique that effectively immortalizes epithelial cells with normal genotypes by renewing epidermal stem cells. Y-27632, a compound that promotes conditional reprogramming through an unknown mechanism, was developed to inhibit the two Rho-associated kinas...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10508688/ https://www.ncbi.nlm.nih.gov/pubmed/37698512 http://dx.doi.org/10.1242/jcs.260990 |
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author | Witkowski, Travis A. Li, Bin Andersen, Jason G. Kumar, Bhavna Mroz, Edmund A. Rocco, James W. |
author_facet | Witkowski, Travis A. Li, Bin Andersen, Jason G. Kumar, Bhavna Mroz, Edmund A. Rocco, James W. |
author_sort | Witkowski, Travis A. |
collection | PubMed |
description | Conditional reprogramming is a cell culture technique that effectively immortalizes epithelial cells with normal genotypes by renewing epidermal stem cells. Y-27632, a compound that promotes conditional reprogramming through an unknown mechanism, was developed to inhibit the two Rho-associated kinase (ROCK) isoforms. We used human foreskin keratinocytes (HFKs) to study the role of Y-27632 in conditional reprogramming and learn how ROCKs control epidermal stem cell renewal. In conditional reprogramming, Y-27632 increased HFK adherence to culture dishes, progression through S, G2 and M phases of the cell cycle, and epidermal stem cell marker levels. Although this correlated with ROCK inhibition by Y-27632, we generated CRISPR–Cas9-mediated HFK ROCK knockouts to test the direct role of ROCK inhibition. Knockout of single ROCK isoforms was insufficient to disrupt ROCK activity or promote HFK propagation without Y-27632. Although ROCK activity was reduced, HFKs with double knockout of ROCK1 and ROCK2 still required Y-27632 to propagate. Y-27632 was the most effective among the ROCK inhibitors we tested at promoting HFK proliferation and epidermal stem cell marker expression. Thus, the ability of Y-27632 to promote an epidermal stem cell state in conditional reprogramming not only depends upon ROCK inhibition but also acts via as-yet-unidentified mechanisms. Epidermal stem cell renewal might in part be regulated by ROCKs, but also involves additional pathways. |
format | Online Article Text |
id | pubmed-10508688 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-105086882023-09-20 Y-27632 acts beyond ROCK inhibition to maintain epidermal stem-like cells in culture Witkowski, Travis A. Li, Bin Andersen, Jason G. Kumar, Bhavna Mroz, Edmund A. Rocco, James W. J Cell Sci Research Article Conditional reprogramming is a cell culture technique that effectively immortalizes epithelial cells with normal genotypes by renewing epidermal stem cells. Y-27632, a compound that promotes conditional reprogramming through an unknown mechanism, was developed to inhibit the two Rho-associated kinase (ROCK) isoforms. We used human foreskin keratinocytes (HFKs) to study the role of Y-27632 in conditional reprogramming and learn how ROCKs control epidermal stem cell renewal. In conditional reprogramming, Y-27632 increased HFK adherence to culture dishes, progression through S, G2 and M phases of the cell cycle, and epidermal stem cell marker levels. Although this correlated with ROCK inhibition by Y-27632, we generated CRISPR–Cas9-mediated HFK ROCK knockouts to test the direct role of ROCK inhibition. Knockout of single ROCK isoforms was insufficient to disrupt ROCK activity or promote HFK propagation without Y-27632. Although ROCK activity was reduced, HFKs with double knockout of ROCK1 and ROCK2 still required Y-27632 to propagate. Y-27632 was the most effective among the ROCK inhibitors we tested at promoting HFK proliferation and epidermal stem cell marker expression. Thus, the ability of Y-27632 to promote an epidermal stem cell state in conditional reprogramming not only depends upon ROCK inhibition but also acts via as-yet-unidentified mechanisms. Epidermal stem cell renewal might in part be regulated by ROCKs, but also involves additional pathways. The Company of Biologists Ltd 2023-09-12 /pmc/articles/PMC10508688/ /pubmed/37698512 http://dx.doi.org/10.1242/jcs.260990 Text en © 2023. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Witkowski, Travis A. Li, Bin Andersen, Jason G. Kumar, Bhavna Mroz, Edmund A. Rocco, James W. Y-27632 acts beyond ROCK inhibition to maintain epidermal stem-like cells in culture |
title | Y-27632 acts beyond ROCK inhibition to maintain epidermal stem-like cells in culture |
title_full | Y-27632 acts beyond ROCK inhibition to maintain epidermal stem-like cells in culture |
title_fullStr | Y-27632 acts beyond ROCK inhibition to maintain epidermal stem-like cells in culture |
title_full_unstemmed | Y-27632 acts beyond ROCK inhibition to maintain epidermal stem-like cells in culture |
title_short | Y-27632 acts beyond ROCK inhibition to maintain epidermal stem-like cells in culture |
title_sort | y-27632 acts beyond rock inhibition to maintain epidermal stem-like cells in culture |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10508688/ https://www.ncbi.nlm.nih.gov/pubmed/37698512 http://dx.doi.org/10.1242/jcs.260990 |
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