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本文引用的文献

1
Primary Cilium-Mediated Retinal Pigment Epithelium Maturation Is Disrupted in Ciliopathy Patient Cells.原发性纤毛介导的视网膜色素上皮细胞成熟在纤毛病患者细胞中被破坏。
Cell Rep. 2018 Jan 2;22(1):189-205. doi: 10.1016/j.celrep.2017.12.038.
2
Cilia - The sensory antennae in the eye.纤毛——眼睛中的感觉触角。
Prog Retin Eye Res. 2017 Sep;60:144-180. doi: 10.1016/j.preteyeres.2017.05.001. Epub 2017 May 11.
3
The Meckel syndrome- associated protein MKS1 functionally interacts with components of the BBSome and IFT complexes to mediate ciliary trafficking and hedgehog signaling.与梅克尔综合征相关的蛋白MKS1与BBSome和IFT复合体的成分发生功能相互作用,以介导纤毛运输和刺猬信号通路。
PLoS One. 2017 Mar 14;12(3):e0173399. doi: 10.1371/journal.pone.0173399. eCollection 2017.
4
Mechanisms for nonmitotic activation of Aurora-A at cilia.纤毛上极光激酶A(Aurora-A)的非有丝分裂激活机制。
Biochem Soc Trans. 2017 Feb 8;45(1):37-49. doi: 10.1042/BST20160142.
5
The IN/OUT assay: a new tool to study ciliogenesis.入/出检测:一种研究纤毛发生的新工具。
Cilia. 2016 Aug 4;5:23. doi: 10.1186/s13630-016-0044-2. eCollection 2016.
6
Cilium assembly and disassembly.纤毛的组装与拆卸。
Nat Cell Biol. 2016 Jun 28;18(7):711-7. doi: 10.1038/ncb3370.
7
The cilia-regulated proteasome and its role in the development of ciliopathies and cancer.纤毛调节的蛋白酶体及其在纤毛病和癌症发展中的作用。
Cilia. 2016 Jun 10;5:14. doi: 10.1186/s13630-016-0035-3. eCollection 2016.
8
CPAP promotes timely cilium disassembly to maintain neural progenitor pool.持续气道正压通气(CPAP)促进纤毛及时解体以维持神经祖细胞池。
EMBO J. 2016 Apr 15;35(8):803-19. doi: 10.15252/embj.201593679. Epub 2016 Feb 29.
9
Mechanism of ciliary disassembly.纤毛拆卸机制。
Cell Mol Life Sci. 2016 May;73(9):1787-802. doi: 10.1007/s00018-016-2148-7. Epub 2016 Feb 11.
10
Cellular Mechanisms of Ciliary Length Control.纤毛长度控制的细胞机制
Cells. 2016 Jan 29;5(1):6. doi: 10.3390/cells5010006.

Bardet-Biedl 综合征蛋白在组织成熟过程中调节纤毛解体。

Bardet-Biedl Syndrome proteins regulate cilia disassembly during tissue maturation.

机构信息

Cilia Cell Biology, Institute of Molecular Physiology, Johannes-Gutenberg University, 55128, Mainz, Germany.

Institute of Developmental Biology and Neurobiology, Johannes-Gutenberg University, 55128, Mainz, Germany.

出版信息

Cell Mol Life Sci. 2019 Feb;76(4):757-775. doi: 10.1007/s00018-018-2966-x. Epub 2018 Nov 16.

DOI:10.1007/s00018-018-2966-x
PMID:30446775
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11105770/
Abstract

Primary cilia are conserved organelles that mediate cellular communication crucial for organogenesis and homeostasis in numerous tissues. The retinal pigment epithelium (RPE) is a ciliated monolayer in the eye that borders the retina and is vital for visual function. Maturation of the RPE is absolutely critical for visual function and the role of the primary cilium in this process has been largely ignored to date. We show that primary cilia are transiently present during RPE development and that as the RPE matures, primary cilia retract, and gene expression of ciliary disassembly components decline. We observe that ciliary-associated BBS proteins protect against HDAC6-mediated ciliary disassembly via their recruitment of Inversin to the base of the primary cilium. Inhibition of ciliary disassembly components was able to rescue ciliary length defects in BBS deficient cells. This consequently affects ciliary regulation of Wnt signaling. Our results shed light onto the mechanisms by which cilia-mediated signaling facilitates tissue maturation.

摘要

初级纤毛是保守的细胞器,介导细胞通讯,对于许多组织的器官发生和内稳态至关重要。视网膜色素上皮(RPE)是眼睛中的纤毛单层,位于视网膜边缘,对视觉功能至关重要。RPE 的成熟对于视觉功能绝对关键,而初级纤毛在这个过程中的作用迄今为止在很大程度上被忽视了。我们表明,初级纤毛在 RPE 发育过程中短暂存在,并且随着 RPE 的成熟,初级纤毛缩回,并且纤毛解体成分的基因表达下降。我们观察到,纤毛相关的 BBS 蛋白通过将 Inversin 募集到初级纤毛的基部来防止 HDAC6 介导的纤毛解体。抑制纤毛解体成分能够挽救 BBS 缺陷细胞中的纤毛长度缺陷。这继而影响 Wnt 信号的纤毛调节。我们的结果揭示了纤毛介导的信号传导促进组织成熟的机制。