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中心体卫星加速母中心体重塑以促进纤毛发生。

Centriolar satellites expedite mother centriole remodeling to promote ciliogenesis.

机构信息

MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, United Kingdom.

Department of Biochemistry and Biophysics, Cardiovascular Research Institute, University of California, San Francisco, United States.

出版信息

Elife. 2023 Feb 15;12:e79299. doi: 10.7554/eLife.79299.

DOI:10.7554/eLife.79299
PMID:36790165
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9998092/
Abstract

Centrosomes are orbited by centriolar satellites, dynamic multiprotein assemblies nucleated by Pericentriolar material 1 (PCM1). To study the requirement for centriolar satellites, we generated mice lacking PCM1, a crucial component of satellites. mice display partially penetrant perinatal lethality with survivors exhibiting hydrocephalus, oligospermia, and cerebellar hypoplasia, and variably expressive phenotypes such as hydronephrosis. As many of these phenotypes have been observed in human ciliopathies and satellites are implicated in cilia biology, we investigated whether cilia were affected. PCM1 was dispensable for ciliogenesis in many cell types, whereas multiciliated ependymal cells and human retinal pigmented epithelial 1 (RPE1) cells showed reduced ciliogenesis. RPE1 cells displayed reduced docking of the mother centriole to the ciliary vesicle and removal of CP110 and CEP97 from the distal mother centriole, indicating compromised early ciliogenesis. Similarly, ependymal cells exhibited reduced removal of CP110 from basal bodies in vivo. We propose that PCM1 and centriolar satellites facilitate efficient trafficking of proteins to and from centrioles, including the departure of CP110 and CEP97 to initiate ciliogenesis, and that the threshold to trigger ciliogenesis differs between cell types.

摘要

中心体被中心粒卫星环绕,中心粒卫星是由中心粒周围物质 1(PCM1)引发的动态多蛋白组装体。为了研究中心粒卫星的需求,我们生成了缺乏 PCM1 的小鼠,PCM1 是卫星的关键组成部分。这些小鼠表现出部分穿透性的围产期致死性,幸存者表现出脑积水、少精症和小脑发育不良,以及表达可变的表型,如肾积水。由于许多这些表型在人类纤毛病中都有观察到,并且卫星与纤毛生物学有关,我们研究了纤毛是否受到影响。在许多细胞类型中,PCM1 对纤毛发生不是必需的,而 多纤毛室管膜细胞和人视网膜色素上皮 1(RPE1)细胞显示出纤毛发生减少。RPE1 细胞显示母中心粒与纤毛泡的对接减少,以及 CP110 和 CEP97 从母中心粒远端去除减少,表明早期纤毛发生受损。同样,脑室管膜细胞在体内显示出 CP110 从基底体去除减少。我们提出,PCM1 和中心粒卫星促进蛋白质向中心粒和从中心粒的有效运输,包括 CP110 和 CEP97 的离开以启动纤毛发生,并且触发纤毛发生的阈值在不同细胞类型之间不同。

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