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