Sengupta Soma, George Manju, Miller Katharine K, Naik Khurram, Chou Jonathan, Cheatham Mary Ann, Dallos Peter, Naramura Mayumi, Band Hamid, Zheng Jing
Department of Communication Sciences and Disorders, Hugh Knowles Center, Northwestern University, Evanston, Illinois 60208, USA.
J Biol Chem. 2009 Jul 24;284(30):20121-9. doi: 10.1074/jbc.M109.025668. Epub 2009 Jun 1.
Cadherin 23 (CDH23), a transmembrane protein localized near the tips of hair cell stereocilia in the mammalian inner ear, is important for delivering mechanical signals to the mechano-electric transducer channels. To identify CDH23-interacting proteins, a membrane-based yeast two-hybrid screen of an outer hair cell (OHC) cDNA library was performed. EHD4, a member of the C-terminal EH domain containing a protein family involved in endocytic recycling, was identified as a potential interactor. To confirm the interaction, we first demonstrated the EHD4 mRNA expression in hair cells using in situ hybridization. Next, we showed that EHD4 co-localizes and co-immunoprecipitates with CDH23 in mammalian cells. Interestingly, the co-immunoprecipitation was found to be calcium-sensitive. To investigate the role of EHD4 in hearing, compound action potentials were measured in EHD4 knock-out (KO) mice. Although EHD4 KO mice have normal hearing sensitivity, analysis of mouse cochlear lysates revealed a 2-fold increase in EHD1, but no increase in EHD2 or EHD3, in EHD4 KO cochleae compared with wild type, suggesting that a compensatory increase in EHD1 levels may account for the absence of a hearing defect in EHD4 KO mice. Taken together, these data indicate that EHD4 is a novel CDH23-interacting protein that could regulate CDH23 trafficking/localization in a calcium-sensitive manner.
钙黏蛋白23(CDH23)是一种跨膜蛋白,定位于哺乳动物内耳毛细胞静纤毛尖端附近,对于将机械信号传递给机械电换能通道至关重要。为了鉴定与CDH23相互作用的蛋白,我们对外毛细胞(OHC)cDNA文库进行了基于膜的酵母双杂交筛选。EHD4是含C末端EH结构域的蛋白家族成员,参与内吞再循环,被鉴定为潜在的相互作用蛋白。为了证实这种相互作用,我们首先通过原位杂交证明了EHD4 mRNA在毛细胞中的表达。接下来,我们表明EHD4在哺乳动物细胞中与CDH23共定位并共免疫沉淀。有趣的是,发现共免疫沉淀对钙敏感。为了研究EHD4在听力中的作用,我们在EHD4基因敲除(KO)小鼠中测量了复合动作电位。尽管EHD4基因敲除小鼠具有正常的听力敏感性,但对小鼠耳蜗裂解物的分析显示,与野生型相比,EHD4基因敲除耳蜗中的EHD1增加了2倍,但EHD2或EHD3没有增加,这表明EHD1水平的代偿性增加可能解释了EHD4基因敲除小鼠没有听力缺陷的原因。综上所述,这些数据表明EHD4是一种新型的与CDH23相互作用的蛋白,它可以以钙敏感的方式调节CDH23的运输/定位。