Gipc1 has a dual role in Vangl2 trafficking and hair bundle integrity in the inner ear

被引:49
作者
Giese, Arnaud P. [1 ,2 ]
Ezan, Jerome [1 ,2 ]
Wang, Lingyan [3 ]
Lasvaux, Lea [1 ]
Lembo, Frederique [4 ,5 ,6 ,7 ]
Mazzocco, Claire [1 ]
Richard, Elodie [1 ]
Reboul, Jerome [4 ,5 ,6 ,7 ]
Borg, Jean-Paul [4 ,5 ,6 ,7 ]
Kelley, Matthew W. [8 ]
Sans, Nathalie [1 ,2 ]
Brigande, John [3 ]
Montcouquiol, Mireille [1 ,2 ]
机构
[1] Neuroctr Magendie, Inserm U862, Planar Polar & Plast Grp, Bordeaux, France
[2] Univ Bordeaux, F-33000 Bordeaux, France
[3] Oregon Hlth & Sci Univ, Oregon Hearing Res Ctr, Portland, OR 97239 USA
[4] CRCM, INSERM, U1068, F-13009 Marseille, France
[5] Inst J Paoli I Calmettes, F-13009 Marseille, France
[6] Aix Marseille Univ, F-13284 Marseille, France
[7] CNRS, UMR7258, F-75700 Paris, France
[8] NIDCD, Lab Cochlear Dev, NIH, Bethesda, MD USA
来源
DEVELOPMENT | 2012年 / 139卷 / 20期
关键词
Polarity; Traffic; Actin; Cochlea; Van Gogh-like 2; Gipc1; Myosin VI; Planar polarity; Mouse; Rat; PLANAR CELL-POLARITY; NMDA RECEPTOR TRAFFICKING; NEURAL-TUBE DEFECTS; MYOSIN-VI; ASYMMETRIC LOCALIZATION; UNCONVENTIONAL MYOSIN; ENDOCYTIC VESICLES; SENSORY EPITHELIA; MAMMALIAN COCHLEA; GENE-TRANSFER;
D O I
10.1242/dev.074229
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Vangl2 is one of the central proteins controlling the establishment of planar cell polarity in multiple tissues of different species. Previous studies suggest that the localization of the Vangl2 protein to specific intracellular microdomains is crucial for its function. However, the molecular mechanisms that control Vangl2 trafficking within a cell are largely unknown. Here, we identify Gipc1 (GAIP C-terminus interacting protein 1) as a new interactor for Vangl2, and we show that a myosin VI-Gipc1 protein complex can regulate Vangl2 traffic in heterologous cells. Furthermore, we show that in the cochlea of MyoVI mutant mice, Vangl2 presence at the membrane is increased, and that a disruption of Gipc1 function in hair cells leads to maturation defects, including defects in hair bundle orientation and integrity. Finally, stimulated emission depletion microscopy and overexpression of GFP-Vangl2 show an enrichment of Vangl2 on the supporting cell side, adjacent to the proximal membrane of hair cells. Altogether, these results indicate a broad role for Gipc1 in the development of both stereociliary bundles and cell polarization, and suggest that the strong asymmetry of Vangl2 observed in early postnatal cochlear epithelium is mostly a 'tissue' polarity readout.
引用
收藏
页码:3775 / 3785
页数:11
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