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泛素修饰酶与炎性小体的调控

Ubiquitin-Modifying Enzymes and Regulation of the Inflammasome.

作者信息

Kattah Michael G, Malynn Barbara A, Ma Averil

机构信息

Department of Medicine, University of California, San Francisco, San Francisco, CA 94143-0358, USA.

Department of Medicine, University of California, San Francisco, San Francisco, CA 94143-0358, USA.

出版信息

J Mol Biol. 2017 Nov 10;429(22):3471-3485. doi: 10.1016/j.jmb.2017.10.001. Epub 2017 Oct 13.

Abstract

Ubiquitin and ubiquitin-modifying enzymes play critical roles in a wide variety of intracellular signaling pathways. Inflammatory signaling cascades downstream of TNF, TLR agonists, antigen receptor cross-linking, and cytokine receptors, all rely on ubiquitination events to direct subsequent immune responses. In the past several years, inflammasome activation and subsequent signal transduction have emerged as an excellent example of how ubiquitin signals control inflammatory responses. Inflammasomes are multiprotein signaling complexes that ultimately lead to caspase activation and release of the interleukin-1 (IL-1) family members, IL-1β and IL-18. Inflammasome activation is critical for the host's defense against pathogens, but dysregulation of inflammasomes may contribute to the pathogenesis of multiple diseases. Ultimately, understanding how various ubiquitin interacting proteins control inflammatory signaling cascades could provide new pathways for therapeutic intervention. Here we review specific ubiquitin-modifying enzymes and ubiquitination events that orchestrate inflammatory responses, with an emphasis on the NLRP3 inflammasome.

摘要

泛素和泛素修饰酶在多种细胞内信号通路中发挥关键作用。肿瘤坏死因子(TNF)、Toll样受体(TLR)激动剂、抗原受体交联以及细胞因子受体下游的炎症信号级联反应,均依赖泛素化事件来指导后续的免疫反应。在过去几年中,炎性小体激活及随后的信号转导已成为泛素信号如何控制炎症反应的一个绝佳范例。炎性小体是多蛋白信号复合物,最终导致半胱天冬酶激活以及白细胞介素-1(IL-1)家族成员IL-1β和IL-18的释放。炎性小体激活对于宿主抵御病原体至关重要,但炎性小体的失调可能导致多种疾病的发病机制。最终,了解各种泛素相互作用蛋白如何控制炎症信号级联反应可为治疗干预提供新途径。在此,我们综述了协调炎症反应的特定泛素修饰酶和泛素化事件,重点关注NLRP3炎性小体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2958/5675782/41d1abc7faa1/nihms912754f1.jpg

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