Literature DB >> 28746879

Daple Coordinates Planar Polarized Microtubule Dynamics in Ependymal Cells and Contributes to Hydrocephalus.

Maki Takagishi1, Masato Sawada2, Shinya Ohata3, Naoya Asai4, Atsushi Enomoto5, Kunihiko Takahashi6, Liang Weng5, Kaori Ushida5, Hosne Ara5, Shigeyuki Matsui6, Kozo Kaibuchi7, Kazunobu Sawamoto8, Masahide Takahashi9.   

Abstract

Motile cilia in ependymal cells, which line the cerebral ventricles, exhibit a coordinated beating motion that drives directional cerebrospinal fluid (CSF) flow and guides neuroblast migration. At the apical cortex of these multi-ciliated cells, asymmetric localization of planar cell polarity (PCP) proteins is required for the planar polarization of microtubule dynamics, which coordinates cilia orientation. Daple is a disheveled-associating protein that controls the non-canonical Wnt signaling pathway and cell motility. Here, we show that Daple-deficient mice present hydrocephalus and their ependymal cilia lack coordinated orientation. Daple regulates microtubule dynamics at the anterior side of ependymal cells, which in turn orients the cilial basal bodies required for the directional cerebrospinal fluid flow. These results demonstrate an important role for Daple in planar polarity in motile cilia and provide a framework for understanding the mechanisms and functions of planar polarization in the ependymal cells.
Copyright © 2017 The Author(s). Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Daple; cilia; ependymal cell; hydrocephalus; planar cell polarity

Mesh:

Substances:

Year:  2017        PMID: 28746879     DOI: 10.1016/j.celrep.2017.06.089

Source DB:  PubMed          Journal:  Cell Rep            Impact factor:   9.423


  25 in total

1.  DAPLE orchestrates apical actomyosin assembly from junctional polarity complexes.

Authors:  Arthur Marivin; Rachel Xi-Yeen Ho; Mikel Garcia-Marcos
Journal:  J Cell Biol       Date:  2022-04-07       Impact factor: 10.539

2.  MT1-MMP deficiency leads to defective ependymal cell maturation, impaired ciliogenesis, and hydrocephalus.

Authors:  Zhixin Jiang; Jin Zhou; Xin Qin; Huiling Zheng; Bo Gao; Xinguang Liu; Guoxiang Jin; Zhongjun Zhou
Journal:  JCI Insight       Date:  2020-05-07

3.  Bi-allelic mutations of CCDC88C are a rare cause of severe congenital hydrocephalus.

Authors:  Gaia Ruggeri; Andrew E Timms; Chi Cheng; Avery Weiss; Peter Kollros; Teresa Chapman; Hannah Tully; Ghayda M Mirzaa
Journal:  Am J Med Genet A       Date:  2018-01-17       Impact factor: 2.802

4.  Hydrocephalus in mouse B3glct mutants is likely caused by defects in multiple B3GLCT substrates in ependymal cells and subcommissural organ.

Authors:  Sanjiv Neupane; June Goto; Steven J Berardinelli; Atsuko Ito; Robert S Haltiwanger; Bernadette C Holdener
Journal:  Glycobiology       Date:  2021-09-09       Impact factor: 4.313

5.  Multi-omic analysis elucidates the genetic basis of hydrocephalus.

Authors:  Andrew T Hale; Lisa Bastarache; Diego M Morales; John C Wellons; David D Limbrick; Eric R Gamazon
Journal:  Cell Rep       Date:  2021-05-04       Impact factor: 9.423

6.  Dendrites with specialized glial attachments develop by retrograde extension using SAX-7 and GRDN-1.

Authors:  Elizabeth R Cebul; Ian G McLachlan; Maxwell G Heiman
Journal:  Development       Date:  2020-02-17       Impact factor: 6.862

Review 7.  New insights into regulation and function of planar polarity in the inner ear.

Authors:  Basile Tarchini; Xiaowei Lu
Journal:  Neurosci Lett       Date:  2019-07-08       Impact factor: 3.197

8.  Daple coordinates organ-wide and cell-intrinsic polarity to pattern inner-ear hair bundles.

Authors:  Kimberly Siletti; Basile Tarchini; A J Hudspeth
Journal:  Proc Natl Acad Sci U S A       Date:  2017-12-11       Impact factor: 11.205

9.  Neuropathological hallmarks of fetal hydrocephalus linked to CCDC88C pathogenic variants.

Authors:  Annie Laquerriere; Pascale Saugier-Veber; Florent Marguet; Myriam Vezain; Pascale Marcorelles; Séverine Audebert-Bellanger; Kévin Cassinari; Nathalie Drouot; Pascal Chambon; Bruno J Gonzalez; Arie Horowitz
Journal:  Acta Neuropathol Commun       Date:  2021-06-06       Impact factor: 7.801

10.  Multiple PDZ domain protein maintains patterning of the apical cytoskeleton in sensory hair cells.

Authors:  Amandine Jarysta; Basile Tarchini
Journal:  Development       Date:  2021-07-21       Impact factor: 6.862

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