Senften Mathias, Schwander Martin, Kazmierczak Piotr, Lillo Concepcion, Shin Jung-Bum, Hasson Tama, Géléoc Gwenaëlle S G, Gillespie Peter G, Williams David, Holt Jeffrey R, Müller Ulrich
Department of Cell Biology, The Scripps Research Institute, Institute for Childhood and Neglected Disease, La Jolla, California 92037, USA.
J Neurosci. 2006 Feb 15;26(7):2060-71. doi: 10.1523/JNEUROSCI.4251-05.2006.
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.
哺乳动物内耳的毛细胞是将声音引起的振动转化为电信号的机械感受器。调节毛细胞机械敏感细胞器(即毛束)发育和功能的分子机制目前尚不清楚。我们在此将两种与耳聋和毛束缺陷相关的基因产物原钙黏蛋白15(PCDH15)和肌球蛋白VIIa(MYO7A)联系到一条共同途径中。我们发现PCDH15与MYO7A结合,并且这两种蛋白在毛束中以重叠模式表达。在MYO7A缺陷小鼠中,PCDH15的定位受到干扰;而在PCDH15缺陷小鼠中,MYO7A的定位受到干扰。与MYO7A一样,PCDH15对耳蜗和前庭毛细胞中毛束的发育至关重要,可控制毛束的形态发生和极性。PCDH15缺陷小鼠的耳蜗和前庭毛细胞在机械转导方面也存在缺陷。总之,我们的研究结果表明,PCDH15和MYO7A共同协作来调节机械敏感毛束的发育和功能。