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Specification of the patterning of a ductal tree during branching morphogenesis of the submandibular gland

The development of ductal structures during branching morphogenesis relies on signals that specify ductal progenitors to set up a pattern for the ductal network. Here, we identify cellular asymmetries defined by the F-actin cytoskeleton and the cell adhesion protein ZO-1 as the earliest determinants...

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Autores principales: Walker, Janice L., Wang, Weihao, Lin, Edith, Romisher, Alison, Bouchie, Meghan P., Bleaken, Brigid, Menko, A. Sue, Kukuruzinska, Maria A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801450/
https://www.ncbi.nlm.nih.gov/pubmed/33432003
http://dx.doi.org/10.1038/s41598-020-79650-y
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author Walker, Janice L.
Wang, Weihao
Lin, Edith
Romisher, Alison
Bouchie, Meghan P.
Bleaken, Brigid
Menko, A. Sue
Kukuruzinska, Maria A.
author_facet Walker, Janice L.
Wang, Weihao
Lin, Edith
Romisher, Alison
Bouchie, Meghan P.
Bleaken, Brigid
Menko, A. Sue
Kukuruzinska, Maria A.
author_sort Walker, Janice L.
collection PubMed
description The development of ductal structures during branching morphogenesis relies on signals that specify ductal progenitors to set up a pattern for the ductal network. Here, we identify cellular asymmetries defined by the F-actin cytoskeleton and the cell adhesion protein ZO-1 as the earliest determinants of duct specification in the embryonic submandibular gland (SMG). Apical polarity protein aPKCζ is then recruited to the sites of asymmetry in a ZO-1-dependent manner and collaborates with ROCK signaling to set up apical-basal polarity of ductal progenitors and further define the path of duct specification. Moreover, the motor protein myosin IIB, a mediator of mechanical force transmission along actin filaments, becomes localized to vertices linking the apical domains of multiple ductal epithelial cells during the formation of ductal lumens and drives duct maturation. These studies identify cytoskeletal, junctional and polarity proteins as the early determinants of duct specification and the patterning of a ductal tree during branching morphogenesis of the SMG.
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spelling pubmed-78014502021-01-12 Specification of the patterning of a ductal tree during branching morphogenesis of the submandibular gland Walker, Janice L. Wang, Weihao Lin, Edith Romisher, Alison Bouchie, Meghan P. Bleaken, Brigid Menko, A. Sue Kukuruzinska, Maria A. Sci Rep Article The development of ductal structures during branching morphogenesis relies on signals that specify ductal progenitors to set up a pattern for the ductal network. Here, we identify cellular asymmetries defined by the F-actin cytoskeleton and the cell adhesion protein ZO-1 as the earliest determinants of duct specification in the embryonic submandibular gland (SMG). Apical polarity protein aPKCζ is then recruited to the sites of asymmetry in a ZO-1-dependent manner and collaborates with ROCK signaling to set up apical-basal polarity of ductal progenitors and further define the path of duct specification. Moreover, the motor protein myosin IIB, a mediator of mechanical force transmission along actin filaments, becomes localized to vertices linking the apical domains of multiple ductal epithelial cells during the formation of ductal lumens and drives duct maturation. These studies identify cytoskeletal, junctional and polarity proteins as the early determinants of duct specification and the patterning of a ductal tree during branching morphogenesis of the SMG. Nature Publishing Group UK 2021-01-11 /pmc/articles/PMC7801450/ /pubmed/33432003 http://dx.doi.org/10.1038/s41598-020-79650-y Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Walker, Janice L.
Wang, Weihao
Lin, Edith
Romisher, Alison
Bouchie, Meghan P.
Bleaken, Brigid
Menko, A. Sue
Kukuruzinska, Maria A.
Specification of the patterning of a ductal tree during branching morphogenesis of the submandibular gland
title Specification of the patterning of a ductal tree during branching morphogenesis of the submandibular gland
title_full Specification of the patterning of a ductal tree during branching morphogenesis of the submandibular gland
title_fullStr Specification of the patterning of a ductal tree during branching morphogenesis of the submandibular gland
title_full_unstemmed Specification of the patterning of a ductal tree during branching morphogenesis of the submandibular gland
title_short Specification of the patterning of a ductal tree during branching morphogenesis of the submandibular gland
title_sort specification of the patterning of a ductal tree during branching morphogenesis of the submandibular gland
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801450/
https://www.ncbi.nlm.nih.gov/pubmed/33432003
http://dx.doi.org/10.1038/s41598-020-79650-y
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