Genetic insights into the morphogenesis of inner ear hair cells

被引:166
作者
Frolenkov, GI
Belyantseva, IA
Friedman, TB
Griffith, AJ [1 ]
机构
[1] Natl Inst Deafness & Other Commun Disorders, Sect Gene Struct & Funct, NIH, Rockville, MD 20850 USA
[2] Natl Inst Deafness & Other Commun Disorders, Sect Human Genet, Genet Mol Lab, NIH, Rockville, MD 20850 USA
[3] Natl Inst Deafness & Other Commun Disorders, Hearing Sect, Neurootol Branch, NIH, Rockville, MD 20850 USA
关键词
D O I
10.1038/nrg1377
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The mammalian inner ear is a sensory organ that has specialized hair cells that detect sound, as well as orientation and movement of the head. The 'hair' bundle on the apical surface of these cells is a mechanosensitive organelle that consists of precisely organized actin-filled projections known as stereocilia. Alterations in hair-bundle morphogenesis can result in hearing loss, balance defects or both. Positional cloning of genes that underlie hereditary hearing loss, coupled with the characterization of corresponding mouse models, is revealing how hair cells have adapted the molecular mechanisms of intracellular motility and intercellular adhesion for the morphogenesis of their apical surfaces.
引用
收藏
页码:489 / 498
页数:10
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