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Regulation of apical constriction via microtubule- and Rab11-dependent apical transport during tissue invagination

The formation of an epithelial tube is a fundamental process for organogenesis. During Drosophila embryonic salivary gland (SG) invagination, Folded gastrulation (Fog)-dependent Rho-associated kinase (Rok) promotes contractile apical myosin formation to drive apical constriction. Microtubules (MTs)...

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Autores principales: Le, Thao Phuong, Chung, SeYeon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8101490/
https://www.ncbi.nlm.nih.gov/pubmed/33788621
http://dx.doi.org/10.1091/mbc.E21-01-0021
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author Le, Thao Phuong
Chung, SeYeon
author_facet Le, Thao Phuong
Chung, SeYeon
author_sort Le, Thao Phuong
collection PubMed
description The formation of an epithelial tube is a fundamental process for organogenesis. During Drosophila embryonic salivary gland (SG) invagination, Folded gastrulation (Fog)-dependent Rho-associated kinase (Rok) promotes contractile apical myosin formation to drive apical constriction. Microtubules (MTs) are also crucial for this process and are required for forming and maintaining apicomedial myosin. However, the underlying mechanism that coordinates actomyosin and MT networks still remains elusive. Here, we show that MT-dependent intracellular trafficking regulates apical constriction during SG invagination. Key components involved in protein trafficking, such as Rab11 and Nuclear fallout (Nuf), are apically enriched near the SG invagination pit in a MT-dependent manner. Disruption of the MT networks or knockdown of Rab11 impairs apicomedial myosin formation and apical constriction. We show that MTs and Rab11 are required for apical enrichment of the Fog ligand and the continuous distribution of the apical determinant protein Crumbs (Crb) and the key adherens junction protein E-Cadherin (E-Cad) along junctions. Targeted knockdown of crb or E-Cad in the SG disrupts apical myosin networks and results in apical constriction defects. Our data suggest a role of MT- and Rab11-dependent intracellular trafficking in regulating actomyosin networks and cell junctions to coordinate cell behaviors during tubular organ formation.
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spelling pubmed-81014902021-07-16 Regulation of apical constriction via microtubule- and Rab11-dependent apical transport during tissue invagination Le, Thao Phuong Chung, SeYeon Mol Biol Cell Articles The formation of an epithelial tube is a fundamental process for organogenesis. During Drosophila embryonic salivary gland (SG) invagination, Folded gastrulation (Fog)-dependent Rho-associated kinase (Rok) promotes contractile apical myosin formation to drive apical constriction. Microtubules (MTs) are also crucial for this process and are required for forming and maintaining apicomedial myosin. However, the underlying mechanism that coordinates actomyosin and MT networks still remains elusive. Here, we show that MT-dependent intracellular trafficking regulates apical constriction during SG invagination. Key components involved in protein trafficking, such as Rab11 and Nuclear fallout (Nuf), are apically enriched near the SG invagination pit in a MT-dependent manner. Disruption of the MT networks or knockdown of Rab11 impairs apicomedial myosin formation and apical constriction. We show that MTs and Rab11 are required for apical enrichment of the Fog ligand and the continuous distribution of the apical determinant protein Crumbs (Crb) and the key adherens junction protein E-Cadherin (E-Cad) along junctions. Targeted knockdown of crb or E-Cad in the SG disrupts apical myosin networks and results in apical constriction defects. Our data suggest a role of MT- and Rab11-dependent intracellular trafficking in regulating actomyosin networks and cell junctions to coordinate cell behaviors during tubular organ formation. The American Society for Cell Biology 2021-05-01 /pmc/articles/PMC8101490/ /pubmed/33788621 http://dx.doi.org/10.1091/mbc.E21-01-0021 Text en © 2021 Le and Chung. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. https://creativecommons.org/licenses/by-nc-sa/3.0/This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License.
spellingShingle Articles
Le, Thao Phuong
Chung, SeYeon
Regulation of apical constriction via microtubule- and Rab11-dependent apical transport during tissue invagination
title Regulation of apical constriction via microtubule- and Rab11-dependent apical transport during tissue invagination
title_full Regulation of apical constriction via microtubule- and Rab11-dependent apical transport during tissue invagination
title_fullStr Regulation of apical constriction via microtubule- and Rab11-dependent apical transport during tissue invagination
title_full_unstemmed Regulation of apical constriction via microtubule- and Rab11-dependent apical transport during tissue invagination
title_short Regulation of apical constriction via microtubule- and Rab11-dependent apical transport during tissue invagination
title_sort regulation of apical constriction via microtubule- and rab11-dependent apical transport during tissue invagination
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8101490/
https://www.ncbi.nlm.nih.gov/pubmed/33788621
http://dx.doi.org/10.1091/mbc.E21-01-0021
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