Hair cells, plasma membrane Ca2+ ATPase and deafness

被引:18
|
作者
Giacomello, Marta [1 ,2 ]
De Mario, Agnese [1 ]
Primerano, Simona [1 ]
Brini, Marisa [3 ]
Carafoli, Ernesto [1 ,3 ]
机构
[1] VIMM, I-35129 Padua, Italy
[2] Univ Padua, Dept Expt Biomed Sci, Padua, Italy
[3] Univ Padua, Dept Biol Chem, Padua, Italy
关键词
Ca2+ homeostasis; Deafness; Hair cells; Stereocilia; CALCIUM-PUMP; HEARING; PMCA2; TRANSDUCTION; CADHERIN-23; MUTATION; MOUSE; DETERMINANTS; BALANCE; LINKS;
D O I
10.1016/j.biocel.2012.02.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hearing relies on the ability of the inner ear to convert sound waves into electrical signals. The main actors in this process are hair cells. Their stereocilia contain a number of specific proteins and a scaffold of actin molecules. They are organized in bundles by tip-link filaments composed of cadherin 23 and protocadherin 15. The bundle is deflected by sound waves leading to the opening of mechano-transduction channels and to the influx of K+ and Ca2+ into the stereocilia. Cadherin 23 and the plasma membrane calcium ATPase isoform 2 (PMCA2) are defective in human and murine cases of deafness. While the involvement of cadherin 23 in deafness/hearing could be expected due to its structural role in the tip-links, that of PMCA2 has been discovered only recently. This review will summarize the structural and functional characteristics of hair cells, focusing on the proteins whose mutations may lead to a deafness phenotype. (c) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:679 / 683
页数:5
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