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Sptan1 通过粘着斑信号在耳蜗毛细胞形态和功能中的基本作用。

Essential Role of Sptan1 in Cochlear Hair Cell Morphology and Function Via Focal Adhesion Signaling.

机构信息

Department of Otolaryngology-Head and Neck Surgery, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, 200233, China.

Otolaryngology Institute of Shanghai Jiao Tong University, Shanghai, 200233, China.

出版信息

Mol Neurobiol. 2022 Jan;59(1):386-404. doi: 10.1007/s12035-021-02551-2. Epub 2021 Oct 27.

Abstract

Hearing loss is the most common human sensory deficit. Hearing relies on stereocilia, inserted into the cuticular plate of hair cells (HCs), where they play an important role in the perception of sound and its transmission. Although numerous genes have been associated with hearing loss, the function of many hair cell genes has yet to be elucidated. Herein, we focused on nonerythroid spectrin αII (SPTAN1), abundant in the cuticular plate, surrounding the rootlets of stereocilia and along the plasma membrane. Interestingly, mice with HC-specific Sptan1 knockout exhibited rapid deafness, abnormal formation of stereocilia and cuticular plates, and loss of HCs from middle and apical turns of the cochlea during early postnatal stages. Additionally, Sptan1 deficiency led to the decreased spreading of House Ear Institute-Organ of Corti 1 cells, and induced abnormal formation of focal adhesions and integrin signaling in mouse HCs. Altogether, our findings highlight SPTAN1 as a critical molecule for HC stereocilia morphology and auditory function via regulation of focal adhesion signaling.

摘要

听力损失是最常见的人类感觉缺陷。听力依赖于纤毛中的静纤毛,插入毛细胞(HCs)的表皮板中,在声音感知及其传递中发挥重要作用。尽管许多基因与听力损失有关,但许多毛细胞基因的功能仍有待阐明。在此,我们重点研究非红系血影蛋白 αII(SPTAN1),它在表皮板中丰富,环绕静纤毛的根和沿质膜分布。有趣的是,具有 HC 特异性 Sptan1 敲除的小鼠在出生后早期表现出快速耳聋、静纤毛和表皮板的异常形成以及耳蜗中部和顶部转 HC 的丧失。此外,Sptan1 缺乏导致 House Ear Institute-Organ of Corti 1 细胞的扩散减少,并诱导小鼠 HCs 中焦点黏附形成和整合素信号的异常。总之,我们的研究结果强调了 SPTAN1 作为一个关键分子,通过调节焦点黏附信号,对 HC 静纤毛形态和听觉功能具有重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16bf/8786805/ebb5dd0ce186/12035_2021_2551_Fig1_HTML.jpg

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