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Uncoupling apical constriction from tissue invagination
Apical constriction is a widely utilized cell shape change linked to folding, bending and invagination of polarized epithelia. It remains unclear how apical constriction is regulated spatiotemporally during tissue invagination and how this cellular process contributes to tube formation in different...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5338918/ https://www.ncbi.nlm.nih.gov/pubmed/28263180 http://dx.doi.org/10.7554/eLife.22235 |
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author | Chung, SeYeon Kim, Sangjoon Andrew, Deborah J |
author_facet | Chung, SeYeon Kim, Sangjoon Andrew, Deborah J |
author_sort | Chung, SeYeon |
collection | PubMed |
description | Apical constriction is a widely utilized cell shape change linked to folding, bending and invagination of polarized epithelia. It remains unclear how apical constriction is regulated spatiotemporally during tissue invagination and how this cellular process contributes to tube formation in different developmental contexts. Using Drosophila salivary gland (SG) invagination as a model, we show that regulation of folded gastrulation expression by the Fork head transcription factor is required for apicomedial accumulation of Rho kinase and non-muscle myosin II, which coordinate apical constriction. We demonstrate that neither loss of spatially coordinated apical constriction nor its complete blockage prevent internalization and tube formation, although such manipulations affect the geometry of invagination. When apical constriction is disrupted, compressing force generated by a tissue-level myosin cable contributes to SG invagination. We demonstrate that fully elongated polarized SGs can form outside the embryo, suggesting that tube formation and elongation are intrinsic properties of the SG. DOI: http://dx.doi.org/10.7554/eLife.22235.001 |
format | Online Article Text |
id | pubmed-5338918 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53389182017-03-10 Uncoupling apical constriction from tissue invagination Chung, SeYeon Kim, Sangjoon Andrew, Deborah J eLife Cell Biology Apical constriction is a widely utilized cell shape change linked to folding, bending and invagination of polarized epithelia. It remains unclear how apical constriction is regulated spatiotemporally during tissue invagination and how this cellular process contributes to tube formation in different developmental contexts. Using Drosophila salivary gland (SG) invagination as a model, we show that regulation of folded gastrulation expression by the Fork head transcription factor is required for apicomedial accumulation of Rho kinase and non-muscle myosin II, which coordinate apical constriction. We demonstrate that neither loss of spatially coordinated apical constriction nor its complete blockage prevent internalization and tube formation, although such manipulations affect the geometry of invagination. When apical constriction is disrupted, compressing force generated by a tissue-level myosin cable contributes to SG invagination. We demonstrate that fully elongated polarized SGs can form outside the embryo, suggesting that tube formation and elongation are intrinsic properties of the SG. DOI: http://dx.doi.org/10.7554/eLife.22235.001 eLife Sciences Publications, Ltd 2017-03-06 /pmc/articles/PMC5338918/ /pubmed/28263180 http://dx.doi.org/10.7554/eLife.22235 Text en © 2017, Chung et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Chung, SeYeon Kim, Sangjoon Andrew, Deborah J Uncoupling apical constriction from tissue invagination |
title | Uncoupling apical constriction from tissue invagination |
title_full | Uncoupling apical constriction from tissue invagination |
title_fullStr | Uncoupling apical constriction from tissue invagination |
title_full_unstemmed | Uncoupling apical constriction from tissue invagination |
title_short | Uncoupling apical constriction from tissue invagination |
title_sort | uncoupling apical constriction from tissue invagination |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5338918/ https://www.ncbi.nlm.nih.gov/pubmed/28263180 http://dx.doi.org/10.7554/eLife.22235 |
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