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      Paxillin-dependent regulation of apical-basal polarity in mammary gland morphogenesis

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          ABSTRACT

          Establishing apical-basal epithelial cell polarity is fundamental for mammary gland duct morphogenesis during mammalian development. While the focal adhesion adapter protein paxillin is a well-characterized regulator of mesenchymal cell adhesion signaling, F-actin cytoskeleton remodeling and single cell migration, its role in epithelial tissue organization and mammary gland morphogenesis in vivo has not been investigated. Here, using a newly developed paxillin conditional knockout mouse model with targeted ablation in the mammary epithelium, in combination with ex vivo three-dimensional organoid and acini cultures, we identify new roles for paxillin in the establishment of apical-basal epithelial cell polarity and lumen formation, as well as mammary gland duct diameter and branching. Paxillin is shown to be required for the integrity and apical positioning of the Golgi network, Par complex and the Rab11/MyoVb trafficking machinery. Paxillin depletion also resulted in reduced levels of apical acetylated microtubules, and rescue experiments with the HDAC6 inhibitor tubacin highlight the central role for paxillin-dependent regulation of HDAC6 activity and associated microtubule acetylation in controlling epithelial cell apical-basal polarity and tissue branching morphogenesis.

          Abstract

          Summary: During mammary gland morphogenesis, paxillin regulates HDAC6 activity and microtubule acetylation to control cell polarization, cell shape and ductal branching.

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          Author and article information

          Journal
          Development
          Development
          DEV
          develop
          Development (Cambridge, England)
          The Company of Biologists Ltd
          0950-1991
          1477-9129
          1 May 2019
          1 May 2019
          1 May 2020
          : 146
          : 9
          : dev174367
          Affiliations
          [1 ] Department of Cell and Developmental Biology, State University of New York Upstate Medical University , 750 East Adams Street, Syracuse, NY 13210, USA
          [2 ] Department of Neuroscience and Physiology, State University of New York Upstate Medical University , 505 Irving Ave, Syracuse, NY 13210, USA
          Author notes
          [*]

          Present address: Dana-Farber Cancer Institute, Harvard Medical School, 450 Brookline Ave, Boston, MA 02115, USA

          [‡]

          Present address: Division of Hematology, Department of Medicine, Brigham and Women's Hospital, 75 Francis St, Boston, MA 02115, USA.

          [§ ]Author for correspondence ( turnerce@ 123456upstate.edu )
          Author information
          http://orcid.org/0000-0002-7210-4007
          Article
          PMC6526716 PMC6526716 6526716 DEV174367
          10.1242/dev.174367
          6526716
          30967426
          fe81ef16-d30f-4db0-a3b6-1851205877d0
          © 2019. Published by The Company of Biologists Ltd
          History
          : 28 November 2018
          : 3 April 2019
          Funding
          Funded by: National Institutes of Health, http://dx.doi.org/10.13039/100000002;
          Award ID: RO1 GM047607
          Categories
          Research Article

          Cell polarity,Tubulin acetylation,Extracellular matrix,Focal adhesions,Vesicle trafficking,Cytoskeleton

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