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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...

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Autores principales: Sahu, Aresh, Karmakar, Susnata, Halder, Sudipta, Ghosh, Gaurab, Acharjee, Sayan, Dasgupta, Purbasa, Ghosh, Ritabrata, Deshpande, Girish, Prasad, Mohit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
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.
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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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