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A conserved YAP/Notch/REST network controls the neuroendocrine cell fate in the lungs
The Notch pathway is a conserved cell-cell communication pathway that controls cell fate decisions. Here we sought to determine how Notch pathway activation inhibits the neuroendocrine cell fate in the lungs, an archetypal process for cell fate decisions orchestrated by Notch signaling that has rema...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110333/ https://www.ncbi.nlm.nih.gov/pubmed/35577801 http://dx.doi.org/10.1038/s41467-022-30416-2 |
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author | Shue, Yan Ting Drainas, Alexandros P. Li, Nancy Yanzhe Pearsall, Sarah M. Morgan, Derrick Sinnott-Armstrong, Nasa Hipkins, Susan Q. Coles, Garry L. Lim, Jing Shan Oro, Anthony E. Simpson, Kathryn L. Dive, Caroline Sage, Julien |
author_facet | Shue, Yan Ting Drainas, Alexandros P. Li, Nancy Yanzhe Pearsall, Sarah M. Morgan, Derrick Sinnott-Armstrong, Nasa Hipkins, Susan Q. Coles, Garry L. Lim, Jing Shan Oro, Anthony E. Simpson, Kathryn L. Dive, Caroline Sage, Julien |
author_sort | Shue, Yan Ting |
collection | PubMed |
description | The Notch pathway is a conserved cell-cell communication pathway that controls cell fate decisions. Here we sought to determine how Notch pathway activation inhibits the neuroendocrine cell fate in the lungs, an archetypal process for cell fate decisions orchestrated by Notch signaling that has remained poorly understood at the molecular level. Using intratumoral heterogeneity in small-cell lung cancer as a tractable model system, we uncovered a role for the transcriptional regulators REST and YAP as promoters of the neuroendocrine to non-neuroendocrine transition. We further identified the specific neuroendocrine gene programs repressed by REST downstream of Notch in this process. Importantly, we validated the importance of REST and YAP in neuroendocrine to non-neuroendocrine cell fate switches in both developmental and tissue repair processes in the lungs. Altogether, these experiments identify conserved roles for REST and YAP in Notch-driven inhibition of the neuroendocrine cell fate in embryonic lungs, adult lungs, and lung cancer. |
format | Online Article Text |
id | pubmed-9110333 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91103332022-05-18 A conserved YAP/Notch/REST network controls the neuroendocrine cell fate in the lungs Shue, Yan Ting Drainas, Alexandros P. Li, Nancy Yanzhe Pearsall, Sarah M. Morgan, Derrick Sinnott-Armstrong, Nasa Hipkins, Susan Q. Coles, Garry L. Lim, Jing Shan Oro, Anthony E. Simpson, Kathryn L. Dive, Caroline Sage, Julien Nat Commun Article The Notch pathway is a conserved cell-cell communication pathway that controls cell fate decisions. Here we sought to determine how Notch pathway activation inhibits the neuroendocrine cell fate in the lungs, an archetypal process for cell fate decisions orchestrated by Notch signaling that has remained poorly understood at the molecular level. Using intratumoral heterogeneity in small-cell lung cancer as a tractable model system, we uncovered a role for the transcriptional regulators REST and YAP as promoters of the neuroendocrine to non-neuroendocrine transition. We further identified the specific neuroendocrine gene programs repressed by REST downstream of Notch in this process. Importantly, we validated the importance of REST and YAP in neuroendocrine to non-neuroendocrine cell fate switches in both developmental and tissue repair processes in the lungs. Altogether, these experiments identify conserved roles for REST and YAP in Notch-driven inhibition of the neuroendocrine cell fate in embryonic lungs, adult lungs, and lung cancer. Nature Publishing Group UK 2022-05-16 /pmc/articles/PMC9110333/ /pubmed/35577801 http://dx.doi.org/10.1038/s41467-022-30416-2 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 Shue, Yan Ting Drainas, Alexandros P. Li, Nancy Yanzhe Pearsall, Sarah M. Morgan, Derrick Sinnott-Armstrong, Nasa Hipkins, Susan Q. Coles, Garry L. Lim, Jing Shan Oro, Anthony E. Simpson, Kathryn L. Dive, Caroline Sage, Julien A conserved YAP/Notch/REST network controls the neuroendocrine cell fate in the lungs |
title | A conserved YAP/Notch/REST network controls the neuroendocrine cell fate in the lungs |
title_full | A conserved YAP/Notch/REST network controls the neuroendocrine cell fate in the lungs |
title_fullStr | A conserved YAP/Notch/REST network controls the neuroendocrine cell fate in the lungs |
title_full_unstemmed | A conserved YAP/Notch/REST network controls the neuroendocrine cell fate in the lungs |
title_short | A conserved YAP/Notch/REST network controls the neuroendocrine cell fate in the lungs |
title_sort | conserved yap/notch/rest network controls the neuroendocrine cell fate in the lungs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110333/ https://www.ncbi.nlm.nih.gov/pubmed/35577801 http://dx.doi.org/10.1038/s41467-022-30416-2 |
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