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本文引用的文献

1
Nek2 activation of Kif24 ensures cilium disassembly during the cell cycle.Nek2对Kif24的激活作用确保了细胞周期中纤毛的解体。
Nat Commun. 2015 Aug 20;6:8087. doi: 10.1038/ncomms9087.
2
Deacetylation of α-tubulin and cortactin is required for HDAC6 to trigger ciliary disassembly.HDAC6触发纤毛解聚需要α-微管蛋白和皮层肌动蛋白的去乙酰化。
Sci Rep. 2015 Aug 6;5:12917. doi: 10.1038/srep12917.
3
Microtubule-depolymerizing kinesins in the regulation of assembly, disassembly, and length of cilia and flagella.微管解聚驱动蛋白在纤毛和鞭毛的组装、解聚及长度调控中的作用
Int Rev Cell Mol Biol. 2015;317:241-65. doi: 10.1016/bs.ircmb.2015.01.008. Epub 2015 Mar 5.
4
Cilia and Diseases.纤毛与疾病
Bioscience. 2014 Dec 1;64(12):1126-1137. doi: 10.1093/biosci/biu174.
5
Actin remodelling factors control ciliogenesis by regulating YAP/TAZ activity and vesicle trafficking.肌动蛋白重塑因子通过调节 YAP/TAZ 活性和囊泡运输来控制纤毛发生。
Nat Commun. 2015 Apr 7;6:6781. doi: 10.1038/ncomms7781.
6
Cilia disassembly with two distinct phases of regulation.纤毛解聚具有两个不同的调控阶段。
Cell Rep. 2015 Mar 24;10(11):1803-10. doi: 10.1016/j.celrep.2015.02.044.
7
Dynein and intraflagellar transport.动力蛋白与鞭毛内运输
Exp Cell Res. 2015 May 15;334(1):26-34. doi: 10.1016/j.yexcr.2015.02.017. Epub 2015 Feb 25.
8
The Microtubule-Depolymerizing Activity of a Mitotic Kinesin Protein KIF2A Drives Primary Cilia Disassembly Coupled with Cell Proliferation.有丝分裂驱动蛋白KIF2A的微管解聚活性驱动初级纤毛解聚并与细胞增殖相关。
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9
The primary cilium undergoes dynamic size modifications during adipocyte differentiation of human adipose stem cells.在人脂肪干细胞的脂肪细胞分化过程中,初级纤毛会经历动态的大小变化。
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10
Ciliary ectosomes: transmissions from the cell's antenna.睫状外泌体:来自细胞“天线”的传递物质
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纤毛拆卸机制。

Mechanism of ciliary disassembly.

作者信息

Liang Yinwen, Meng Dan, Zhu Bing, Pan Junmin

机构信息

MOE Key Laboratory of Protein Sciences, School of Life Sciences, Tsinghua University, Beijing, 100084, China.

Laboratory for Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Qingdao, Shandong, China.

出版信息

Cell Mol Life Sci. 2016 May;73(9):1787-802. doi: 10.1007/s00018-016-2148-7. Epub 2016 Feb 11.

DOI:10.1007/s00018-016-2148-7
PMID:26869233
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11108551/
Abstract

As motile organelles and sensors, cilia play pivotal roles in cell physiology, development and organ homeostasis. Ciliary defects are associated with a class of cilia-related diseases or developmental disorders, termed ciliopathies. Even though the presence of cilia is required for diverse functions, cilia can be removed through ciliary shortening or resorption that necessitates disassembly of the cilium, which occurs normally during cell cycle progression, cell differentiation and in response to cellular stress. The functional significance of ciliary resorption is highlighted in controlling the G1-S transition during cell cycle progression. Internal or external cues that trigger ciliary resorption initiate signaling cascades that regulate several downstream events including depolymerization of axonemal microtubules, dynamic changes in actin and the ciliary membrane, regulation of intraflagellar transport and posttranslational modifications of ciliary proteins. To ensure ciliary resorption, both the active disassembly of the cilium and the simultaneous inhibition of ciliary assembly must be coordinately regulated.

摘要

作为运动细胞器和传感器,纤毛在细胞生理学、发育和器官稳态中发挥着关键作用。纤毛缺陷与一类称为纤毛病的纤毛相关疾病或发育障碍有关。尽管多种功能都需要纤毛的存在,但纤毛可以通过纤毛缩短或吸收而被去除,这需要纤毛的拆卸,通常发生在细胞周期进程、细胞分化以及对细胞应激的反应过程中。纤毛吸收在控制细胞周期进程中的G1-S转换方面的功能意义得到了凸显。触发纤毛吸收的内部或外部信号会启动信号级联反应,调节几个下游事件,包括轴丝微管的解聚、肌动蛋白和纤毛膜的动态变化、鞭毛内运输的调节以及纤毛蛋白的翻译后修饰。为确保纤毛吸收,纤毛的主动拆卸和纤毛组装的同时抑制必须得到协调调节。