Department of Digestive Diseases, The Affiliated Changsha Central Hospital, Hengyang Medical School, University of South China, 161 Shaoshan Road, Changsha City, 410000, People's Republic of China.
Immunol Res. 2023 Dec;71(6):800-813. doi: 10.1007/s12026-023-09400-5. Epub 2023 Jun 9.
Ubiquitination (or ubiquitylation) and de-ubiquitination, which are both post-translational modifications (PTMs) of proteins, have become a research hotspot in recent years. Some ubiquitinated or de-ubiquitinated signaling proteins have been found to promote or suppress innate immunity through Toll-like receptor (TLR), RIG-like receptor (RIG-I-like receptor, RLR), NOD-like receptor (NLR), and the cyclic guanosine monophosphate (GMP)-adenosine monophosphate (AMP) synthase (cGAS)-STING pathway. This article aimed to provide a review on the role of ubiquitination and de-ubiquitination, especially ubiquitin ligase enzymes and de-ubiquitinating enzymes, in the above four pathways. We hope that our work can contribute to the research and development of treatment strategies for innate immunity-related diseases such as inflammatory bowel disease.
泛素化(或 ubiquitylation)和去泛素化,都是蛋白质的翻译后修饰(PTMs),近年来已成为研究热点。一些泛素化或去泛素化的信号蛋白已被发现通过 Toll 样受体(TLR)、RIG 样受体(RLR)、NOD 样受体(NLR)和环鸟苷酸(GMP)-腺苷酸(AMP)合酶(cGAS)-STING 途径促进或抑制固有免疫。本文旨在综述泛素化和去泛素化,特别是泛素连接酶和去泛素化酶,在上述四条通路中的作用。我们希望我们的工作能为炎症性肠病等与固有免疫相关疾病的治疗策略的研究和开发做出贡献。