4.7 Article

Physical and functional interaction between protocadherin 15 and myosin VIIa in mechanosensory hair cells

期刊

JOURNAL OF NEUROSCIENCE
卷 26, 期 7, 页码 2060-2071

出版社

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.4251-05.2006

关键词

hair cell; deafness; mechanotransduction; PCDH15; MY07A; cochlea

资金

  1. NEI NIH HHS [EY07042, EY12598, R01 EY007042] Funding Source: Medline
  2. NIDCD NIH HHS [R01 DC005439, DC002368, DC005965, DC006183, DC005439, DC003279, R01 DC005439-04, DC007704] Funding Source: Medline

向作者/读者索取更多资源

Hair cells of the mammalian inner ear are the mechanoreceptors that convert sound-induced vibrations into electrical signals. The molecular mechanisms that regulate the development and function of the mechanically sensitive organelle of hair cells, the hair bundle, are poorly defined. We link here two gene products that have been associated with deafness and hair bundle defects, protocadherin 15 (PCDH15) and myosin VIIa (MYO7A), into a common pathway. We show that PCDH15 binds to MYO7A and that both proteins are expressed in an overlapping pattern in hair bundles. PCDH15 localization is perturbed in MYO7A-deficient mice, whereas MYO7A localization is perturbed in PCDH15-deficient mice. Like MYO7A, PCDH15 is critical for the development of hair bundles in cochlear and vestibular hair cells, controlling hair bundle morphogenesis and polarity. Cochlear and vestibular hair cells from PCDH15-deficient mice also show defects in mechanotransduction. Together, our findings suggest that PCDH15 and MYO7A cooperate to regulate the development and function of the mechanically sensitive hair bundle.

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