Laboratory of Molecular Cell Biology, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi, Japan.
Endocr J. 2012;59(8):641-52. doi: 10.1507/endocrj.ej12-0148. Epub 2012 May 19.
The NF-κB pathway is a central signaling pathway for inflammatory and immune responses, and aberrant NF-κB signaling is implicated multiple disorders, such as cancer and autoimmune, chronic inflammatory and metabolic diseases. NF-κB is regulated by various post-translational modifications, including phosphorylation and multiple ubiquitinations. We determined that LUBAC (linear ubiquitin chain assembly complex), composed of SHARPIN, HOIL-IL and HOIP, generates a novel type of Met1-linked linear polyubiquitin chain and specifically regulates the canonical NF-κB pathway via the linear ubiquitination of NEMO and RIP1. In the absence of LUBAC components, NF-κB signaling was attenuated and induced apoptosis and inflammation. Many studies on the pathophysiological functions of LUBAC, such as in B cell development, innate immune response, carcinogenesis, and osteogenesis, have been performed recently. This review summarizes these new findings on LUBAC- and linear ubiquitination-mediated NF-κB regulation and their implications in disorders.
NF-κB 通路是炎症和免疫反应的核心信号通路,异常的 NF-κB 信号通路与多种疾病相关,如癌症、自身免疫性疾病、慢性炎症和代谢性疾病。NF-κB 受到多种翻译后修饰的调控,包括磷酸化和多种泛素化。我们发现 LUBAC(线性泛素链组装复合物)由 SHARPIN、HOIL-IL 和 HOIP 组成,可生成一种新型的 Met1 连接的线性多泛素链,并通过 NEMO 和 RIP1 的线性泛素化特异性调节经典的 NF-κB 通路。在缺乏 LUBAC 成分的情况下,NF-κB 信号通路减弱,并诱导细胞凋亡和炎症。最近对 LUBAC 的病理生理学功能进行了许多研究,如 B 细胞发育、先天免疫反应、致癌作用和成骨作用。本综述总结了 LUBAC 和线性泛素化介导的 NF-κB 调节的这些新发现及其在疾病中的意义。