Literature DB >> 29327200

Exocyst Complex Member EXOC5 Is Required for Survival of Hair Cells and Spiral Ganglion Neurons and Maintenance of Hearing.

Byeonghyeon Lee1,2, Jeong-In Baek3,4, Hyehyun Min5, Seung-Hyun Bae1, Kyeonghye Moon5,6, Min-A Kim1,2, Ye-Ri Kim1,2, Ben Fogelgren7, Joshua H Lipschutz4,8, Kyu-Yup Lee9, Jinwoong Bok10,11,12, Un-Kyung Kim13,14.   

Abstract

The exocyst, an octameric protein complex consisting of Exoc1 through Exoc8, was first determined to regulate exocytosis by targeting vesicles to the plasma membrane in yeast to mice. In addition to this fundamental role, the exocyst complex has been implicated in other cellular processes. In this study, we investigated the role of the exocyst in cochlear development and hearing by targeting EXOC5, a central exocyst component. Deleting Exoc5 in the otic epithelium with widely used Cre lines resulted in early lethality. Thus, we generated two different inner ear-specific Exoc5 knockout models by crossing Gfi1Cre mice with Exoc5f/f mice for hair cell-specific deletion (Gfi1Cre/+;Exoc5f/f) and by in utero delivery of rAAV-iCre into the otocyst of embryonic day 12.5 for deletion throughout the otic epithelium (rAAV2/1-iCre;Exoc5f/f). Gfi1Cre/+;Exoc5f/f mice showed relatively normal hair cell morphology until postnatal day 20, after which hair cells underwent apoptosis accompanied by disorganization of stereociliary bundles, resulting in progressive hearing loss. rAAV2/1-iCre;Exoc5f/f mice exhibited abnormal neurite morphology, followed by apoptotic degeneration of spiral ganglion neurons (SGNs) and hair cells, which led to profound and early-onset hearing loss. These results demonstrate that Exoc5 is essential for the normal development and survival of cochlear hair cells and SGNs, as well as the functional maintenance of hearing.

Entities:  

Keywords:  Cochlea; Exoc5; Exocyst; Hearing loss; Spiral ganglion

Mesh:

Substances:

Year:  2018        PMID: 29327200      PMCID: PMC6984595          DOI: 10.1007/s12035-017-0857-z

Source DB:  PubMed          Journal:  Mol Neurobiol        ISSN: 0893-7648            Impact factor:   5.590


  64 in total

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2.  Interaction of 14-3-3 with signaling proteins is mediated by the recognition of phosphoserine.

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Journal:  Cell       Date:  1996-03-22       Impact factor: 41.582

3.  Mutant rab8 Impairs docking and fusion of rhodopsin-bearing post-Golgi membranes and causes cell death of transgenic Xenopus rods.

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Journal:  Mol Biol Cell       Date:  2001-08       Impact factor: 4.138

4.  The Ral/exocyst effector complex counters c-Jun N-terminal kinase-dependent apoptosis in Drosophila melanogaster.

Authors:  Maria Balakireva; Carine Rossé; Johanna Langevin; Yu-chen Chien; Michel Gho; Geneviève Gonzy-Treboul; Stéphanie Voegeling-Lemaire; Sandra Aresta; Jean-Antoine Lepesant; Yohanns Bellaiche; Michael White; Jacques Camonis
Journal:  Mol Cell Biol       Date:  2006-09-25       Impact factor: 4.272

5.  Generation of hair cells in neonatal mice by β-catenin overexpression in Lgr5-positive cochlear progenitors.

Authors:  Fuxin Shi; Lingxiang Hu; Albert S B Edge
Journal:  Proc Natl Acad Sci U S A       Date:  2013-08-05       Impact factor: 11.205

6.  Rab8b GTPase, a protein transport regulator, is an interacting partner of otoferlin, defective in a human autosomal recessive deafness form.

Authors:  Paulina Heidrych; Ulrike Zimmermann; Andreas Bress; Carsten M Pusch; Peter Ruth; Markus Pfister; Marlies Knipper; Nikolaus Blin
Journal:  Hum Mol Genet       Date:  2008-09-04       Impact factor: 6.150

7.  Sec6/8 complex is recruited to cell-cell contacts and specifies transport vesicle delivery to the basal-lateral membrane in epithelial cells.

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Journal:  Cell       Date:  1998-05-29       Impact factor: 41.582

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Authors:  C Clayton Hazelett; David Sheff; Charles Yeaman
Journal:  Mol Biol Cell       Date:  2011-10-19       Impact factor: 4.138

9.  Association of hearing impairment with chronic kidney disease: a cross-sectional study of the Korean general population.

Authors:  Young Joon Seo; Sang Baek Ko; Tae Hyung Ha; Tae Hoon Gong; Jeong Pyo Bong; Dong-Joon Park; Sang Yoo Park
Journal:  BMC Nephrol       Date:  2015-09-16       Impact factor: 2.388

10.  Atp6v0a4 knockout mouse is a model of distal renal tubular acidosis with hearing loss, with additional extrarenal phenotype.

Authors:  Elizabeth E Norgett; Zoe J Golder; Beatriz Lorente-Cánovas; Neil Ingham; Karen P Steel; Fiona E Karet Frankl
Journal:  Proc Natl Acad Sci U S A       Date:  2012-08-07       Impact factor: 11.205

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Journal:  Front Genet       Date:  2019-09-19       Impact factor: 4.599

2.  Conditional Loss of the Exocyst Component Exoc5 in Retinal Pigment Epithelium (RPE) Results in RPE Dysfunction, Photoreceptor Cell Degeneration, and Decreased Visual Function.

Authors:  Bärbel Rohrer; Manas R Biswal; Elisabeth Obert; Yujing Dang; Yanhui Su; Xiaofeng Zuo; Ben Fogelgren; Altaf A Kondkar; Glenn P Lobo; Joshua H Lipschutz
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