The Ca2+-activated Cl- channel Ano1 controls microvilli length and membrane surface area in the oocyte

被引:19
|
作者
Courjaret, Raphael [1 ]
Hodeify, Rawad [1 ]
Hubrack, Satanay [1 ]
Ibrahim, Awab [1 ,2 ]
Dib, Maya [1 ]
Daas, Sahar [1 ,3 ]
Machaca, Khaled [1 ]
机构
[1] Educ City Qatar Fdn, Weill Cornell Med Coll Qatar, Dept Physiol & Biophys, Luqta St,POB 24144, Doha 24144, Qatar
[2] Univ S Alabama, Dept Pediat, 1700 Ctr St, Mobile, AL 36604 USA
[3] Qatar Cardiovasc Res Ctr, Qatar Sci & Technol Pk, Doha 26999, Qatar
关键词
Ano1; Microvilli; ERM; Xenopus oocyte; Moesin; XENOPUS-LAEVIS OOCYTES; ERM PROTEINS; CHLORIDE CHANNEL; PLASMA-MEMBRANE; FOLLICLE CELLS; IMAGE-ANALYSIS; BRUSH-BORDER; CA2+; MOESIN; INTERNALIZATION;
D O I
10.1242/jcs.188367
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ca2+-activated Cl- channels (CaCCs) play important physiological functions in epithelia and other tissues. In frog oocytes the CaCC Ano1 regulates resting membrane potential and the block to polyspermy. Here, we show that Ano1 expression increases the oocyte surface, revealing a novel function for Ano1 in regulating cell morphology. Confocal imaging shows that Ano1 increases microvilli length, which requires ERM-protein-dependent linkage to the cytoskeleton. A dominant-negative form of the ERM protein moesin precludes the Ano1-dependent increase in membrane area. Furthermore, both full-length and the truncated dominant-negative forms of moesin co-localize with Ano1 to the microvilli, and the two proteins co-immunoprecipitate. The Ano1-moesin interaction limits Ano1 lateral membrane mobility and contributes to microvilli scaffolding, therefore stabilizing larger membrane structures. Collectively, these results reveal a newly identified role for Ano1 in shaping the plasma membrane during oogenesis, with broad implications for the regulation of microvilli in epithelia.
引用
收藏
页码:2548 / 2558
页数:11
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