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异二聚体封端蛋白是静纤毛长度和宽度调节所必需的。

Heterodimeric capping protein is required for stereocilia length and width regulation.

作者信息

Avenarius Matthew R, Krey Jocelyn F, Dumont Rachel A, Morgan Clive P, Benson Connor B, Vijayakumar Sarath, Cunningham Christopher L, Scheffer Deborah I, Corey David P, Müller Ulrich, Jones Sherri M, Barr-Gillespie Peter G

机构信息

Oregon Hearing Research Center and Vollum Institute, Oregon Health and Science University, Portland, OR.

Department of Special Education and Communication Disorders, University of Nebraska-Lincoln, Lincoln, NE.

出版信息

J Cell Biol. 2017 Nov 6;216(11):3861-3881. doi: 10.1083/jcb.201704171. Epub 2017 Sep 12.

Abstract

Control of the dimensions of actin-rich processes like filopodia, lamellipodia, microvilli, and stereocilia requires the coordinated activity of many proteins. Each of these actin structures relies on heterodimeric capping protein (CAPZ), which blocks actin polymerization at barbed ends. Because dimension control of the inner ear's stereocilia is particularly precise, we studied the CAPZB subunit in hair cells. CAPZB, present at ∼100 copies per stereocilium, concentrated at stereocilia tips as hair cell development progressed, similar to the CAPZB-interacting protein TWF2. We deleted specifically in hair cells using , which eliminated auditory and vestibular function. -null stereocilia initially developed normally but later shortened and disappeared; surprisingly, stereocilia width decreased concomitantly with length. CAPZB2 expressed by in utero electroporation prevented normal elongation of vestibular stereocilia and irregularly widened them. Together, these results suggest that capping protein participates in stereocilia widening by preventing newly elongating actin filaments from depolymerizing.

摘要

对富含肌动蛋白的突起(如丝状伪足、片状伪足、微绒毛和静纤毛)的尺寸控制需要多种蛋白质的协同活动。这些肌动蛋白结构中的每一种都依赖于异二聚体封端蛋白(CAPZ),它能阻止肌动蛋白在带刺末端的聚合。由于内耳静纤毛的尺寸控制特别精确,我们研究了毛细胞中的CAPZB亚基。每个静纤毛中约有100个CAPZB拷贝,随着毛细胞发育的进行,它集中在静纤毛顶端,这与与CAPZB相互作用的蛋白TWF2类似。我们使用在毛细胞中特异性缺失,这消除了听觉和前庭功能。缺失CAPZB的静纤毛最初正常发育,但后来缩短并消失;令人惊讶的是,静纤毛宽度随着长度的减小而同时减小。通过子宫内电穿孔表达的CAPZB2阻止了前庭静纤毛的正常伸长并使其不规则增宽。总之,这些结果表明封端蛋白通过阻止新伸长的肌动蛋白丝解聚而参与静纤毛增宽。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb04/5674897/baf16ca5985a/JCB_201704171_Fig1.jpg

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