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去泛素化酶与骨重塑

Deubiquitinating Enzymes and Bone Remodeling.

作者信息

Guo Yu-Chen, Zhang Shi-Wen, Yuan Quan

机构信息

State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, China.

出版信息

Stem Cells Int. 2018 Jul 8;2018:3712083. doi: 10.1155/2018/3712083. eCollection 2018.

DOI:10.1155/2018/3712083
PMID:30123285
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6079350/
Abstract

Bone remodeling, which is essential for bone homeostasis, is controlled by multiple factors and mechanisms. In the past few years, studies have emphasized the role of the ubiquitin-dependent proteolysis system in regulating bone remodeling. Deubiquitinases, which are grouped into five families, remove ubiquitin from target proteins and are involved in several cell functions. Importantly, a number of deubiquitinases mediate bone remodeling through regulating differentiation and/or function of osteoblast and osteoclasts. In this review, we review the functions and mechanisms of deubiquitinases in mediating bone remodeling.

摘要

骨重塑对于骨稳态至关重要,它受多种因素和机制的调控。在过去几年中,研究强调了泛素依赖性蛋白水解系统在调节骨重塑中的作用。去泛素化酶分为五个家族,可从靶蛋白上去除泛素,并参与多种细胞功能。重要的是,许多去泛素化酶通过调节成骨细胞和破骨细胞的分化和/或功能来介导骨重塑。在本综述中,我们回顾了去泛素化酶在介导骨重塑中的功能和机制。

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本文引用的文献

1
A20 upregulation during treated HIV disease is associated with intestinal epithelial cell recovery and function.在治疗后的 HIV 疾病中,A20 的上调与肠道上皮细胞的恢复和功能有关。
PLoS Pathog. 2018 Mar 5;14(3):e1006806. doi: 10.1371/journal.ppat.1006806. eCollection 2018 Mar.
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Delineating Crosstalk Mechanisms of the Ubiquitin Proteasome System That Regulate Apoptosis.阐明调节细胞凋亡的泛素蛋白酶体系统的串扰机制。
Front Cell Dev Biol. 2018 Feb 9;6:11. doi: 10.3389/fcell.2018.00011. eCollection 2018.
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Roles of E3 Ubiquitin-Ligases in Nuclear Protein Homeostasis during Plant Stress Responses.E3泛素连接酶在植物应激反应期间核蛋白稳态中的作用
Front Plant Sci. 2018 Feb 8;9:139. doi: 10.3389/fpls.2018.00139. eCollection 2018.
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USP35 regulates mitotic progression by modulating the stability of Aurora B.USP35 通过调节 Aurora B 的稳定性来调控有丝分裂进程。
Nat Commun. 2018 Feb 15;9(1):688. doi: 10.1038/s41467-018-03107-0.
5
CRISPR/Cas9 knockout of USP18 enhances type I IFN responsiveness and restricts HIV-1 infection in macrophages.USP18的CRISPR/Cas9基因敲除增强了巨噬细胞中I型干扰素反应并限制了HIV-1感染。
J Leukoc Biol. 2018 Feb 13;103(6):1225-40. doi: 10.1002/JLB.3MIA0917-352R.
6
C-Terminal Farnesylation of UCH-L1 Plays a Role in Transport of Epstein-Barr Virus Primary Oncoprotein LMP1 to Exosomes.泛素羧基末端水解酶L1(UCH-L1)的C末端法尼基化在爱泼斯坦-巴尔病毒主要癌蛋白潜伏膜蛋白1(LMP1)向细胞外囊泡的转运中起作用。
mSphere. 2018 Feb 7;3(1). doi: 10.1128/mSphere.00030-18. eCollection 2018 Jan-Feb.
7
OTUB1 protein suppresses mTOR complex 1 (mTORC1) activity by deubiquitinating the mTORC1 inhibitor DEPTOR.OTUB1 蛋白通过去泛素化 mTORC1 抑制剂 DEPTOR 来抑制 mTOR 复合物 1(mTORC1)的活性。
J Biol Chem. 2018 Mar 30;293(13):4883-4892. doi: 10.1074/jbc.M117.809533. Epub 2018 Jan 30.
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Ubiquitin carboxyl-terminal hydrolase isozyme L5 inhibits human glioma cell migration and invasion via downregulating SNRPF.泛素羧基末端水解酶同工酶L5通过下调SNRPF抑制人胶质瘤细胞的迁移和侵袭。
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The deubiquitinase USP9X regulates FBW7 stability and suppresses colorectal cancer.去泛素化酶 USP9X 调节 FBW7 的稳定性并抑制结直肠癌。
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