SIRT2 通过去乙酰化调节小胶质细胞中高迁移率基团蛋白 B1 的核质穿梭和降解。

IF 4.5 2区 生物学 Q2 CELL BIOLOGY
Wan-Qun Xing, Xian-ji Piao, Qi Han, Hui-Ying Shi, Wen-Cong Wu, Fan Si, Jing-Jing Lu, Tie-Zhong Zhou, Jing-Ru Guo, Shi-Ze Li, Bin Xu
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引用次数: 0

摘要

高迁移率基团蛋白 B1(HMGB1)是一种致病性炎症反应,可介导癫痫、脓毒性休克、缺血、脑外伤、帕金森病、阿尔茨海默病和质谱分析等一系列疾病。HMGB1 在无菌和感染性损伤期间促进炎症反应,并在疾病的发展过程中起着至关重要的作用。从细胞核调动到细胞质是活化的免疫细胞释放 HMGB1 的第一个重要步骤。在这里,我们证明了 Sirtuin 2(SIRT2)与 HMGB1 的物理相互作用,并在核定位信号位置的 43 个赖氨酸残基上对 HMGB1 进行去乙酰化,从而加强了其与 HMGB1 的相互作用,并使 HMGB1 定位于细胞质中。这些发现首次揭示了影响 HMGB1 及其降解的 SIRT2 核质穿梭作用,从而为神经炎症的治疗揭示了新的治疗靶点和途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SIRT2 regulates high mobility group protein B1 nucleoplasmic shuttle and degradation via deacetylation in microglia

High mobility group protein B1 (HMGB1) acts as a pathogenic inflammatory response to mediate ranges of conditions such as epilepsy, septic shock, ischemia, traumatic brain injury, Parkinson's disease, Alzheimer's disease and mass spectrometry. HMGB1 promotes inflammation during sterile and infectious damage and plays a crucial role in disease development. Mobilization from the nucleus to the cytoplasm is the first important step in the release of HMGB1 from activated immune cells. Here, we demonstrated that Sirtuin 2 (SIRT2) physically interacts with and deacetylates HMGB1 at 43 lysine residue at nuclear localization signal locations, strengthening its interaction with HMGB1 and causing HMGB1 to be localized in the cytoplasm. These discoveries are the first to shed light on the SIRT2 nucleoplasmic shuttle, which influences HMGB1 and its degradation, hence revealing novel therapeutic targets and avenues for neuroinflammation treatment.

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来源期刊
CiteScore
14.70
自引率
0.00%
发文量
256
审稿时长
1 months
期刊介绍: The Journal of Cellular Physiology publishes reports of high biological significance in areas of eukaryotic cell biology and physiology, focusing on those articles that adopt a molecular mechanistic approach to investigate cell structure and function. There is appreciation for the application of cellular, biochemical, molecular and in vivo genetic approaches, as well as the power of genomics, proteomics, bioinformatics and systems biology. In particular, the Journal encourages submission of high-interest papers investigating the genetic and epigenetic regulation of proliferation and phenotype as well as cell fate and lineage commitment by growth factors, cytokines and their cognate receptors and signal transduction pathways that influence the expression, integration and activities of these physiological mediators. Similarly, the Journal encourages submission of manuscripts exploring the regulation of growth and differentiation by cell adhesion molecules in addition to the interplay between these processes and those induced by growth factors and cytokines. Studies on the genes and processes that regulate cell cycle progression and phase transition in eukaryotic cells, and the mechanisms that determine whether cells enter quiescence, proliferate or undergo apoptosis are also welcomed. Submission of papers that address contributions of the extracellular matrix to cellular phenotypes and physiological control as well as regulatory mechanisms governing fertilization, embryogenesis, gametogenesis, cell fate, lineage commitment, differentiation, development and dynamic parameters of cell motility are encouraged. Finally, the investigation of stem cells and changes that differentiate cancer cells from normal cells including studies on the properties and functions of oncogenes and tumor suppressor genes will remain as one of the major interests of the Journal.
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