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Germline soma communication mediated by gap junction proteins regulates epithelial morphogenesis
Gap junction (GJ) proteins, the primary constituents of GJ channels, are conserved determinants of patterning. Canonically, a GJ channel, made up of two hemi-channels contributed by the neighboring cells, facilitates transport of metabolites/ions. Here we demonstrate the involvement of GJ proteins d...
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/PMC8330916/ https://www.ncbi.nlm.nih.gov/pubmed/34343194 http://dx.doi.org/10.1371/journal.pgen.1009685 |
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author | Sahu, Aresh Karmakar, Susnata Halder, Sudipta Ghosh, Gaurab Acharjee, Sayan Dasgupta, Purbasa Ghosh, Ritabrata Deshpande, Girish Prasad, Mohit |
author_facet | Sahu, Aresh Karmakar, Susnata Halder, Sudipta Ghosh, Gaurab Acharjee, Sayan Dasgupta, Purbasa Ghosh, Ritabrata Deshpande, Girish Prasad, Mohit |
author_sort | Sahu, Aresh |
collection | PubMed |
description | Gap junction (GJ) proteins, the primary constituents of GJ channels, are conserved determinants of patterning. Canonically, a GJ channel, made up of two hemi-channels contributed by the neighboring cells, facilitates transport of metabolites/ions. Here we demonstrate the involvement of GJ proteins during cuboidal to squamous epithelial transition displayed by the anterior follicle cells (AFCs) from Drosophila ovaries. Somatically derived AFCs stretch and flatten when the adjacent germline cells start increasing in size. GJ proteins, Innexin2 (Inx2) and Innexin4 (Inx4), functioning in the AFCs and germline respectively, promote the shape transformation by modulating calcium levels in the AFCs. Our observations suggest that alterations in calcium flux potentiate STAT activity to influence actomyosin-based cytoskeleton, possibly resulting in disassembly of adherens junctions. Our data have uncovered sequential molecular events underlying the cuboidal to squamous shape transition and offer unique insight into how GJ proteins expressed in the neighboring cells contribute to morphogenetic processes. |
format | Online Article Text |
id | pubmed-8330916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-83309162021-08-04 Germline soma communication mediated by gap junction proteins regulates epithelial morphogenesis Sahu, Aresh Karmakar, Susnata Halder, Sudipta Ghosh, Gaurab Acharjee, Sayan Dasgupta, Purbasa Ghosh, Ritabrata Deshpande, Girish Prasad, Mohit PLoS Genet Research Article Gap junction (GJ) proteins, the primary constituents of GJ channels, are conserved determinants of patterning. Canonically, a GJ channel, made up of two hemi-channels contributed by the neighboring cells, facilitates transport of metabolites/ions. Here we demonstrate the involvement of GJ proteins during cuboidal to squamous epithelial transition displayed by the anterior follicle cells (AFCs) from Drosophila ovaries. Somatically derived AFCs stretch and flatten when the adjacent germline cells start increasing in size. GJ proteins, Innexin2 (Inx2) and Innexin4 (Inx4), functioning in the AFCs and germline respectively, promote the shape transformation by modulating calcium levels in the AFCs. Our observations suggest that alterations in calcium flux potentiate STAT activity to influence actomyosin-based cytoskeleton, possibly resulting in disassembly of adherens junctions. Our data have uncovered sequential molecular events underlying the cuboidal to squamous shape transition and offer unique insight into how GJ proteins expressed in the neighboring cells contribute to morphogenetic processes. Public Library of Science 2021-08-03 /pmc/articles/PMC8330916/ /pubmed/34343194 http://dx.doi.org/10.1371/journal.pgen.1009685 Text en © 2021 Sahu 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 Sahu, Aresh Karmakar, Susnata Halder, Sudipta Ghosh, Gaurab Acharjee, Sayan Dasgupta, Purbasa Ghosh, Ritabrata Deshpande, Girish Prasad, Mohit Germline soma communication mediated by gap junction proteins regulates epithelial morphogenesis |
title | Germline soma communication mediated by gap junction proteins regulates epithelial morphogenesis |
title_full | Germline soma communication mediated by gap junction proteins regulates epithelial morphogenesis |
title_fullStr | Germline soma communication mediated by gap junction proteins regulates epithelial morphogenesis |
title_full_unstemmed | Germline soma communication mediated by gap junction proteins regulates epithelial morphogenesis |
title_short | Germline soma communication mediated by gap junction proteins regulates epithelial morphogenesis |
title_sort | germline soma communication mediated by gap junction proteins regulates epithelial morphogenesis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8330916/ https://www.ncbi.nlm.nih.gov/pubmed/34343194 http://dx.doi.org/10.1371/journal.pgen.1009685 |
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