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血栓反应蛋白 1 和 2 对于内耳传入突触的形成和功能很重要。

Thrombospondins 1 and 2 are important for afferent synapse formation and function in the inner ear.

机构信息

Department of Otolaryngology - Head and Neck Surgery, Stanford University, Edwards Building, 300 Pasteur Drive, Room R111A, Stanford, CA, 94305-5453, USA.

出版信息

Eur J Neurosci. 2014 Apr;39(8):1256-67. doi: 10.1111/ejn.12486. Epub 2014 Jan 27.

Abstract

Thrombospondins (TSPs) constitute a family of secreted extracellular matrix proteins that have been shown to be involved in the formation of synapses in the central nervous system. In this study, we show that TSP1 and TSP2 are expressed in the cochlea, and offer the first description of their putative roles in afferent synapse development and function in the inner ear. We examined mice with deletions of TSP1, TSP2 and both (TSP1/TSP2) for inner ear development and function. Immunostaining for synaptic markers indicated a significant decrease in the number of formed afferent synapses in the cochleae of TSP2 and TSP1/TSP2 knockout (KO) mice at postnatal day (P)29. In functional studies, TSP2 and TSP1/TSP2 KO mice showed elevated auditory brainstem response (ABR) thresholds as compared with wild-type littermates, starting at P15, with the most severe phenotype being seen for TSP1/TSP2 KO mice. TSP1/TSP2 KO mice also showed reduced wave I amplitudes of ABRs and vestibular evoked potentials, suggesting synaptic dysfunction in both the auditory and vestibular systems. Whereas ABR thresholds in TSP1 KO mice were relatively unaffected at early ages, TSP1/TSP2 KO mice showed the most severe phenotype among all of the genotypes tested, suggesting functional redundancy between the two genes. On the basis of the above results, we propose that TSPs play an important role in afferent synapse development and function of the inner ear.

摘要

血栓反应蛋白(TSPs)构成了一组分泌型细胞外基质蛋白,它们被证明参与了中枢神经系统中突触的形成。在这项研究中,我们表明 TSP1 和 TSP2 在耳蜗中表达,并首次描述了它们在内耳传入突触发育和功能中的潜在作用。我们检查了 TSP1、TSP2 和两者(TSP1/TSP2)缺失的小鼠的内耳发育和功能。突触标记的免疫染色表明,在出生后第 29 天(P29),TSP2 和 TSP1/TSP2 敲除(KO)小鼠耳蜗中的形成传入突触数量显著减少。在功能研究中,与野生型同窝仔相比,TSP2 和 TSP1/TSP2 KO 小鼠的听觉脑干反应(ABR)阈值从 P15 开始升高,其中 TSP1/TSP2 KO 小鼠的表型最为严重。TSP1/TSP2 KO 小鼠的 ABR 和前庭诱发电位的 I 波幅度也降低,提示听觉和前庭系统的突触功能障碍。虽然 TSP1 KO 小鼠的 ABR 阈值在早期相对不受影响,但 TSP1/TSP2 KO 小鼠在所有测试基因型中表现出最严重的表型,表明这两个基因具有功能冗余。基于上述结果,我们提出 TSPs 在内耳传入突触的发育和功能中发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc00/4132060/3e767dfcb927/nihms609192f1.jpg

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