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The cGAS-STING pathway as a therapeutic target in inflammatory diseases.cGAS-STING 通路作为炎症性疾病的治疗靶点。
Nat Rev Immunol. 2021 Sep;21(9):548-569. doi: 10.1038/s41577-021-00524-z. Epub 2021 Apr 8.
2
Beyond K48 and K63: non-canonical protein ubiquitination.超越 K48 和 K63:非典型蛋白泛素化。
Cell Mol Biol Lett. 2021 Jan 5;26(1):1. doi: 10.1186/s11658-020-00245-6.
3
Linkage-specific ubiquitin chain formation depends on a lysine hydrocarbon ruler.连接特异性泛素链的形成依赖于赖氨酸疏水规则。
Nat Chem Biol. 2021 Mar;17(3):272-279. doi: 10.1038/s41589-020-00696-0. Epub 2020 Dec 7.
4
TRIM32 regulates mitochondrial mediated ROS levels and sensitizes the oxidative stress induced cell death.TRIM32调节线粒体介导的活性氧水平,并使氧化应激诱导的细胞死亡敏感化。
Cell Signal. 2020 Dec;76:109777. doi: 10.1016/j.cellsig.2020.109777. Epub 2020 Sep 10.
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PDLIM7 Synergizes With PDLIM2 and p62/Sqstm1 to Inhibit Inflammatory Signaling by Promoting Degradation of the p65 Subunit of NF-κB.PDLIM7 与 PDLIM2 和 p62/Sqstm1 协同作用,通过促进 NF-κB p65 亚基的降解来抑制炎症信号。
Front Immunol. 2020 Aug 4;11:1559. doi: 10.3389/fimmu.2020.01559. eCollection 2020.
6
Autoantibodies targeting TRIM72 compromise membrane repair and contribute to inflammatory myopathy.针对 TRIM72 的自身抗体损害了膜修复,并导致炎性肌病。
J Clin Invest. 2020 Aug 3;130(8):4440-4455. doi: 10.1172/JCI131721.
7
TRIM9 overexpression promotes uterine leiomyoma cell proliferation and inhibits cell apoptosis via NF-κB signaling pathway.TRIM9 过表达通过 NF-κB 信号通路促进子宫肌瘤细胞增殖并抑制细胞凋亡。
Life Sci. 2020 Sep 15;257:118101. doi: 10.1016/j.lfs.2020.118101. Epub 2020 Jul 15.
8
Molecular mechanisms and cellular functions of cGAS-STING signalling.cGAS-STING 信号转导的分子机制和细胞功能。
Nat Rev Mol Cell Biol. 2020 Sep;21(9):501-521. doi: 10.1038/s41580-020-0244-x. Epub 2020 May 18.
9
The Tripartite Nexus: Autophagy, Cancer, and Tripartite Motif-Containing Protein Family Members.三方关系:自噬、癌症与含三联基序蛋白家族成员
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10
The Role of Mitochondria in Inflammation: From Cancer to Neurodegenerative Disorders.线粒体在炎症中的作用:从癌症到神经退行性疾病
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TRIMs:在核因子κB通路不同步骤的选择性募集——炎症激活或消退的决定因素

TRIMs: selective recruitment at different steps of the NF-κB pathway-determinant of activation or resolution of inflammation.

作者信息

Roy Milton, Singh Rajesh

机构信息

Department of Biochemistry, Faculty of Science, The MS University of Baroda, Vadodara, Gujarat, 390002, India.

Institute for Cell Engineering, The Johns Hopkins University School of Medicine, 733 North Broadway, MRB 731, Baltimore, MD, 21205, USA.

出版信息

Cell Mol Life Sci. 2021 Sep;78(17-18):6069-6086. doi: 10.1007/s00018-021-03900-z. Epub 2021 Jul 20.

DOI:10.1007/s00018-021-03900-z
PMID:34283248
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11072854/
Abstract

TNF-α-induced NF-κB pathway is an essential component of innate and adaptive immune pathway, and it is tightly regulated by various post-translational modifications including ubiquitination. Oscillations in NF-κB activation and temporal gene expression are emerging as critical determinants of inflammatory response, however, the regulators of unique outcomes in different patho-physiological conditions are not well understood. Tripartite Motif-containing proteins (TRIMs) are RING domain-containing E3 ligases involved in the regulation of cellular homeostasis, metabolism, cell death, inflammation, and host defence. Emerging reports suggest that TRIMs are recruited at different steps of TNF-α-induced NF-κB pathway and modulate via their E3 ligase activity. TRIMs show synergy and antagonism in the regulation of the NF-κB pathway and also regulate it in a feedback manner. TRIMs also regulate pattern recognition receptors (PRRs) mediated inflammatory pathways and may have evolved to directly regulate a specific arm of immune signalling. The review emphasizes TRIM-mediated ubiquitination and modulation of TNF-α-regulated temporal and NF-κB signaling and its possible impact on unique transcriptional and functional outcomes.

摘要

肿瘤坏死因子-α(TNF-α)诱导的核因子-κB(NF-κB)信号通路是固有免疫和适应性免疫通路的重要组成部分,并且受到包括泛素化在内的各种翻译后修饰的严格调控。NF-κB激活和基因表达随时间的振荡正成为炎症反应的关键决定因素,然而,在不同病理生理条件下产生独特结果的调节因子尚未得到充分了解。含三联基序蛋白(TRIMs)是含RING结构域的E3连接酶,参与细胞稳态、代谢、细胞死亡、炎症和宿主防御的调节。新出现的报道表明,TRIMs在TNF-α诱导的NF-κB信号通路的不同步骤中被招募,并通过其E3连接酶活性进行调节。TRIMs在NF-κB信号通路的调节中表现出协同作用和拮抗作用,并且还以反馈方式对其进行调节。TRIMs还调节模式识别受体(PRRs)介导的炎症信号通路,并且可能已经进化到直接调节免疫信号的特定分支。本综述强调TRIM介导的泛素化以及对TNF-α调节的时间和NF-κB信号的调节及其对独特转录和功能结果的可能影响。