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GPS2对Ubc13介导的泛素化的抑制作用调控B细胞发育的多个阶段。

Inhibition of Ubc13-mediated Ubiquitination by GPS2 Regulates Multiple Stages of B Cell Development.

作者信息

Lentucci Claudia, Belkina Anna C, Cederquist Carly T, Chan Michelle, Johnson Holly E, Prasad Sherry, Lopacinski Amanda, Nikolajczyk Barbara S, Monti Stefano, Snyder-Cappione Jennifer, Tanasa Bogdan, Cardamone M Dafne, Perissi Valentina

机构信息

From the Departments of Biochemistry.

the Flow Cytometry Core Facility, Boston University School of Medicine, Boston, Massachusetts 02118 and.

出版信息

J Biol Chem. 2017 Feb 17;292(7):2754-2772. doi: 10.1074/jbc.M116.755132. Epub 2016 Dec 30.

Abstract

Non-proteolytic ubiquitin signaling mediated by Lys ubiquitin chains plays a critical role in multiple pathways that are key to the development and activation of immune cells. Our previous work indicates that GPS2 (G-protein Pathway Suppressor 2) is a multifunctional protein regulating TNFα signaling and lipid metabolism in the adipose tissue through modulation of Lys ubiquitination events. However, the full extent of GPS2-mediated regulation of ubiquitination and the underlying molecular mechanisms are unknown. Here, we report that GPS2 is required for restricting the activation of TLR and BCR signaling pathways and the AKT/FOXO1 pathway in immune cells based on direct inhibition of Ubc13 enzymatic activity. Relevance of this regulatory strategy is confirmed by B cell-targeted deletion of GPS2, resulting in developmental defects at multiple stages of B cell differentiation. Together, these findings reveal that GPS2 genomic and non-genomic functions are critical for the development and cellular homeostasis of B cells.

摘要

由赖氨酸泛素链介导的非蛋白水解性泛素信号在免疫细胞发育和激活的多个关键途径中发挥着关键作用。我们之前的研究表明,GPS2(G蛋白途径抑制因子2)是一种多功能蛋白,通过调节赖氨酸泛素化事件来调控脂肪组织中的TNFα信号和脂质代谢。然而,GPS2介导的泛素化调控的全貌及其潜在分子机制尚不清楚。在此,我们报告称,基于对Ubc13酶活性的直接抑制,GPS2是免疫细胞中限制TLR和BCR信号通路以及AKT/FOXO1通路激活所必需的。通过对B细胞进行GPS2靶向缺失,证实了这种调控策略的相关性,这导致B细胞分化多个阶段出现发育缺陷。总之,这些发现揭示了GPS2的基因组和非基因组功能对于B细胞的发育和细胞内稳态至关重要。

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