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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...

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Autores principales: Witkowski, Travis A., Li, Bin, Andersen, Jason G., Kumar, Bhavna, Mroz, Edmund A., Rocco, James W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2023
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.
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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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