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J Biol Chem. 2009 Jul 24;284(30):20121-9. doi: 10.1074/jbc.M109.025668. Epub 2009 Jun 1.
2
[The experimental study on endoplasmic reticulum stress-participated outer hair cell apoptosis in cadherin 23 gene mutant mice].[钙黏蛋白23基因敲除小鼠内质网应激参与外毛细胞凋亡的实验研究]
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3
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Identifying components of the hair-cell interactome involved in cochlear amplification.确定参与耳蜗放大的毛细胞相互作用组的组成部分。
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Ehd4 is required to attain normal prepubertal testis size but dispensable for fertility in male mice.Ehd4是雄性小鼠达到青春期前正常睾丸大小所必需的,但对生育能力并非不可或缺。
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C-terminal EH-domain-containing proteins: consensus for a role in endocytic trafficking, EH?含C末端EH结构域的蛋白质:内吞运输中作用的共识,EH?
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1
Eps15 Homology Domain Protein 4 (EHD4) is required for Eps15 Homology Domain Protein 1 (EHD1)-mediated endosomal recruitment and fission.Eps15 同源结构域蛋白 4(EHD4)对于 Eps15 同源结构域蛋白 1(EHD1)介导的内体募集和裂变是必需的。
PLoS One. 2020 Sep 23;15(9):e0239657. doi: 10.1371/journal.pone.0239657. eCollection 2020.
2
EHD1 and RUSC2 Control Basal Epidermal Growth Factor Receptor Cell Surface Expression and Recycling.EHD1 和 RUSC2 控制基础表皮生长因子受体的细胞表面表达和再循环。
Mol Cell Biol. 2020 Mar 16;40(7). doi: 10.1128/MCB.00434-19.
3
Cochlear Proteins Associated with Noise-induced Hearing Loss: An Update.与噪声性听力损失相关的耳蜗蛋白:最新进展
Indian J Occup Environ Med. 2018 May-Aug;22(2):60-73. doi: 10.4103/ijoem.IJOEM_43_18.
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Cadherin 23-C Regulates Microtubule Networks by Modifying CAMSAP3's Function.钙黏蛋白 23-C 通过调节 CAMSAP3 的功能来调节微管网络。
Sci Rep. 2016 Jun 28;6:28706. doi: 10.1038/srep28706.
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CSF-1 receptor signalling is governed by pre-requisite EHD1 mediated receptor display on the macrophage cell surface.集落刺激因子-1受体信号传导由巨噬细胞表面上必需的EHD1介导的受体展示所调控。
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Sci Rep. 2016 Feb 17;6:20727. doi: 10.1038/srep20727.
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8
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9
Cyclic nucleotide-gated channel α-3 (CNGA3) interacts with stereocilia tip-link cadherin 23 + exon 68 or alternatively with myosin VIIa, two proteins required for hair cell mechanotransduction.环核苷酸门控通道 α-3(CNGA3)与静纤毛尖端连接黏附蛋白 23 + 外显子 68 相互作用,或者与肌球蛋白 VIIa 相互作用,这两种蛋白都是毛细胞机械转导所必需的。
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10
Eps homology domain endosomal transport proteins differentially localize to the neuromuscular junction.Eps 同源结构域内体运输蛋白在神经肌肉接头处的定位不同。
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本文引用的文献

1
Identifying components of the hair-cell interactome involved in cochlear amplification.确定参与耳蜗放大的毛细胞相互作用组的组成部分。
BMC Genomics. 2009 Mar 25;10:127. doi: 10.1186/1471-2164-10-127.
2
EHD3 regulates early-endosome-to-Golgi transport and preserves Golgi morphology.EHD3调节早期内体到高尔基体的运输并维持高尔基体形态。
J Cell Sci. 2009 Feb 1;122(Pt 3):389-400. doi: 10.1242/jcs.037051. Epub 2009 Jan 12.
3
MAGI-1, a candidate stereociliary scaffolding protein, associates with the tip-link component cadherin 23.MAGI-1是一种候选的静纤毛支架蛋白,与顶端连接成分钙黏蛋白23相关联。
J Neurosci. 2008 Oct 29;28(44):11269-76. doi: 10.1523/JNEUROSCI.3833-08.2008.
4
Mechanisms of EHD/RME-1 protein function in endocytic transport.EHD/RME-1蛋白在胞吞运输中的功能机制。
Traffic. 2008 Dec;9(12):2043-52. doi: 10.1111/j.1600-0854.2008.00834.x. Epub 2008 Oct 14.
5
A role for EHD4 in the regulation of early endosomal transport.EHD4在早期内体运输调控中的作用。
Traffic. 2008 Jun;9(6):995-1018. doi: 10.1111/j.1600-0854.2008.00732.x. Epub 2008 Mar 6.
6
Calcium- and otoferlin-dependent exocytosis by immature outer hair cells.未成熟外毛细胞的钙和 otoferlin 依赖性胞吐作用。
J Neurosci. 2008 Feb 20;28(8):1798-803. doi: 10.1523/JNEUROSCI.4653-07.2008.
7
EHD1 interacts with retromer to stabilize SNX1 tubules and facilitate endosome-to-Golgi retrieval.EHD1与回收蛋白相互作用以稳定SNX1微管并促进从内体到高尔基体的回收。
Traffic. 2007 Dec;8(12):1873-1886. doi: 10.1111/j.1600-0854.2007.00652.x. Epub 2007 Oct 7.
8
Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells.钙黏蛋白23和原钙黏蛋白15相互作用,在感觉毛细胞中形成顶连接丝。
Nature. 2007 Sep 6;449(7158):87-91. doi: 10.1038/nature06091.
9
EHD1 regulates cholesterol homeostasis and lipid droplet storage.EHD1调节胆固醇稳态和脂滴储存。
Biochem Biophys Res Commun. 2007 Jun 8;357(3):792-9. doi: 10.1016/j.bbrc.2007.04.022. Epub 2007 Apr 13.
10
The micromachinery of mechanotransduction in hair cells.毛细胞机械转导的微机械装置。
Annu Rev Neurosci. 2007;30:339-65. doi: 10.1146/annurev.neuro.29.051605.112917.

EHD4和CDH23是耳蜗毛细胞中的相互作用伙伴。

EHD4 and CDH23 are interacting partners in cochlear hair cells.

作者信息

Sengupta Soma, George Manju, Miller Katharine K, Naik Khurram, Chou Jonathan, Cheatham Mary Ann, Dallos Peter, Naramura Mayumi, Band Hamid, Zheng Jing

机构信息

Department of Communication Sciences and Disorders, Hugh Knowles Center, Northwestern University, Evanston, Illinois 60208, USA.

出版信息

J Biol Chem. 2009 Jul 24;284(30):20121-9. doi: 10.1074/jbc.M109.025668. Epub 2009 Jun 1.

DOI:10.1074/jbc.M109.025668
PMID:19487694
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2740438/
Abstract

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.

摘要

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。