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Grhl3 promotes retention of epidermal cells under endocytic stress to maintain epidermal architecture in zebrafish
Epithelia such as epidermis cover large surfaces and are crucial for survival. Maintenance of tissue homeostasis by balancing cell proliferation, cell size, and cell extrusion ensures epidermal integrity. Although the mechanisms of cell extrusion are better understood, how epithelial cells that roun...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8496789/ https://www.ncbi.nlm.nih.gov/pubmed/34570762 http://dx.doi.org/10.1371/journal.pgen.1009823 |
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author | Phatak, Mandar Kulkarni, Shruti Miles, Lee B. Anjum, Nazma Dworkin, Sebastian Sonawane, Mahendra |
author_facet | Phatak, Mandar Kulkarni, Shruti Miles, Lee B. Anjum, Nazma Dworkin, Sebastian Sonawane, Mahendra |
author_sort | Phatak, Mandar |
collection | PubMed |
description | Epithelia such as epidermis cover large surfaces and are crucial for survival. Maintenance of tissue homeostasis by balancing cell proliferation, cell size, and cell extrusion ensures epidermal integrity. Although the mechanisms of cell extrusion are better understood, how epithelial cells that round up under developmental or perturbed genetic conditions are reintegrated in the epithelium to maintain homeostasis remains unclear. Here, we performed live imaging in zebrafish embryos to show that epidermal cells that round up due to membrane homeostasis defects in the absence of goosepimples/myosinVb (myoVb) function, are reintegrated into the epithelium. Transcriptome analysis and genetic interaction studies suggest that the transcription factor Grainyhead-like 3 (Grhl3) induces the retention of rounded cells by regulating E-cadherin levels. Moreover, Grhl3 facilitates the survival of MyoVb deficient embryos by regulating cell adhesion, cell retention, and epidermal architecture. Our analyses have unraveled a mechanism of retention of rounded cells and its importance in epithelial homeostasis. |
format | Online Article Text |
id | pubmed-8496789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-84967892021-10-08 Grhl3 promotes retention of epidermal cells under endocytic stress to maintain epidermal architecture in zebrafish Phatak, Mandar Kulkarni, Shruti Miles, Lee B. Anjum, Nazma Dworkin, Sebastian Sonawane, Mahendra PLoS Genet Research Article Epithelia such as epidermis cover large surfaces and are crucial for survival. Maintenance of tissue homeostasis by balancing cell proliferation, cell size, and cell extrusion ensures epidermal integrity. Although the mechanisms of cell extrusion are better understood, how epithelial cells that round up under developmental or perturbed genetic conditions are reintegrated in the epithelium to maintain homeostasis remains unclear. Here, we performed live imaging in zebrafish embryos to show that epidermal cells that round up due to membrane homeostasis defects in the absence of goosepimples/myosinVb (myoVb) function, are reintegrated into the epithelium. Transcriptome analysis and genetic interaction studies suggest that the transcription factor Grainyhead-like 3 (Grhl3) induces the retention of rounded cells by regulating E-cadherin levels. Moreover, Grhl3 facilitates the survival of MyoVb deficient embryos by regulating cell adhesion, cell retention, and epidermal architecture. Our analyses have unraveled a mechanism of retention of rounded cells and its importance in epithelial homeostasis. Public Library of Science 2021-09-27 /pmc/articles/PMC8496789/ /pubmed/34570762 http://dx.doi.org/10.1371/journal.pgen.1009823 Text en © 2021 Phatak et al 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/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Phatak, Mandar Kulkarni, Shruti Miles, Lee B. Anjum, Nazma Dworkin, Sebastian Sonawane, Mahendra Grhl3 promotes retention of epidermal cells under endocytic stress to maintain epidermal architecture in zebrafish |
title | Grhl3 promotes retention of epidermal cells under endocytic stress to maintain epidermal architecture in zebrafish |
title_full | Grhl3 promotes retention of epidermal cells under endocytic stress to maintain epidermal architecture in zebrafish |
title_fullStr | Grhl3 promotes retention of epidermal cells under endocytic stress to maintain epidermal architecture in zebrafish |
title_full_unstemmed | Grhl3 promotes retention of epidermal cells under endocytic stress to maintain epidermal architecture in zebrafish |
title_short | Grhl3 promotes retention of epidermal cells under endocytic stress to maintain epidermal architecture in zebrafish |
title_sort | grhl3 promotes retention of epidermal cells under endocytic stress to maintain epidermal architecture in zebrafish |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8496789/ https://www.ncbi.nlm.nih.gov/pubmed/34570762 http://dx.doi.org/10.1371/journal.pgen.1009823 |
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