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外被体复合物成员 EXOC5 对于毛细胞和螺旋神经节神经元的存活以及听力的维持是必需的。

Exocyst Complex Member EXOC5 Is Required for Survival of Hair Cells and Spiral Ganglion Neurons and Maintenance of Hearing.

机构信息

Department of Biology, College of Natural Sciences, Kyungpook National University, Daegu, 41566, Republic of Korea.

School of Life Sciences, BK21 Plus KNU Creative BioResearch Group, Kyungpook National University, Daegu, 41566, Republic of Korea.

出版信息

Mol Neurobiol. 2018 Aug;55(8):6518-6532. doi: 10.1007/s12035-017-0857-z. Epub 2018 Jan 11.

DOI:10.1007/s12035-017-0857-z
PMID:29327200
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6984595/
Abstract

The exocyst, an octameric protein complex consisting of Exoc1 through Exoc8, was first determined to regulate exocytosis by targeting vesicles to the plasma membrane in yeast to mice. In addition to this fundamental role, the exocyst complex has been implicated in other cellular processes. In this study, we investigated the role of the exocyst in cochlear development and hearing by targeting EXOC5, a central exocyst component. Deleting Exoc5 in the otic epithelium with widely used Cre lines resulted in early lethality. Thus, we generated two different inner ear-specific Exoc5 knockout models by crossing Gfi1 mice with Exoc5 mice for hair cell-specific deletion (Gfi1;Exoc5) and by in utero delivery of rAAV-iCre into the otocyst of embryonic day 12.5 for deletion throughout the otic epithelium (rAAV2/1-iCre;Exoc5). Gfi1;Exoc5 mice showed relatively normal hair cell morphology until postnatal day 20, after which hair cells underwent apoptosis accompanied by disorganization of stereociliary bundles, resulting in progressive hearing loss. rAAV2/1-iCre;Exoc5 mice exhibited abnormal neurite morphology, followed by apoptotic degeneration of spiral ganglion neurons (SGNs) and hair cells, which led to profound and early-onset hearing loss. These results demonstrate that Exoc5 is essential for the normal development and survival of cochlear hair cells and SGNs, as well as the functional maintenance of hearing.

摘要

外泌体(exocyst),由 Exoc1 到 Exoc8 八个蛋白组成的八聚体蛋白复合物,最初在酵母到小鼠中被确定通过将囊泡靶向质膜来调节胞吐作用。除了这个基本作用外,外泌体复合物还被牵连到其他细胞过程中。在这项研究中,我们通过靶向 EXOC5(外泌体复合物的一个核心成分)来研究外泌体在耳蜗发育和听力中的作用。使用广泛使用的 Cre 线在耳上皮细胞中删除 Exoc5 导致早期死亡。因此,我们通过将 Gfi1 小鼠与 Exoc5 小鼠杂交,生成了两种不同的内耳特异性 Exoc5 敲除模型,用于毛细胞特异性缺失(Gfi1;Exoc5)和通过在胚胎第 12.5 天将 rAAV-iCre 递送到卵囊中来实现整个耳上皮的缺失(rAAV2/1-iCre;Exoc5)。Gfi1;Exoc5 小鼠表现出相对正常的毛细胞形态,直到出生后第 20 天,之后毛细胞发生凋亡,伴随着静纤毛束的紊乱,导致进行性听力损失。rAAV2/1-iCre;Exoc5 小鼠表现出异常的神经突形态,随后螺旋神经节神经元 (SGNs) 和毛细胞发生凋亡变性,导致严重和早期的听力损失。这些结果表明 Exoc5 对于耳蜗毛细胞和 SGNs 的正常发育和存活以及听力的功能维持是必不可少的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9be7/6984595/cb5bdf2f8d1f/nihms-1035976-f0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9be7/6984595/a4816d2518a0/nihms-1035976-f0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9be7/6984595/f8bf003bcc65/nihms-1035976-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9be7/6984595/a18fbc68f250/nihms-1035976-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9be7/6984595/83fa0acc4723/nihms-1035976-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9be7/6984595/1228960dc976/nihms-1035976-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9be7/6984595/cb5bdf2f8d1f/nihms-1035976-f0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9be7/6984595/a4816d2518a0/nihms-1035976-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9be7/6984595/45bb6b244375/nihms-1035976-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9be7/6984595/97de384bc766/nihms-1035976-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9be7/6984595/398b25a1ce65/nihms-1035976-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9be7/6984595/f8bf003bcc65/nihms-1035976-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9be7/6984595/a18fbc68f250/nihms-1035976-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9be7/6984595/83fa0acc4723/nihms-1035976-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9be7/6984595/1228960dc976/nihms-1035976-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9be7/6984595/cb5bdf2f8d1f/nihms-1035976-f0009.jpg

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