Zhou Yaqi, Xiang Yaxuan, Liu Sijie, Li Chenyao, Dong Jiaheng, Kong Xiangrui, Ji Xinying, Cheng Xiaoxia, Zhang Lei
School of Basic Medical Sciences, Henan University, Kaifeng, 475004, China.
Department of Pathology, the Second People's Hospital of Jiaozuo; The First Affiliated Hospital of Henan Polytechnic University, Jiaozuo, 454000, China.
Cell Death Discov. 2024 Apr 29;10(1):200. doi: 10.1038/s41420-024-01957-w.
Receptor-interacting protein kinase 3 (RIPK3), a member of the receptor-interacting protein kinase (RIPK) family with serine/threonine protein kinase activity, interacts with RIPK1 to generate necrosomes, which trigger caspase-independent programmed necrosis. As a vital component of necrosomes, RIPK3 plays an indispensable role in necroptosis, which is crucial for human life and health. In addition, RIPK3 participates in the pathological process of several infections, aseptic inflammatory diseases, and tumors (including tumor-promoting and -suppressive activities) by regulating autophagy, cell proliferation, and the metabolism and production of chemokines/cytokines. This review summarizes the recent research progress of the regulators of the RIPK3 signaling pathway and discusses the potential role of RIPK3/necroptosis in the aetiopathogenesis of various diseases. An in-depth understanding of the mechanisms and functions of RIPK3 may facilitate the development of novel therapeutic strategies.
受体相互作用蛋白激酶3(RIPK3)是具有丝氨酸/苏氨酸蛋白激酶活性的受体相互作用蛋白激酶(RIPK)家族成员,它与RIPK1相互作用形成坏死小体,进而触发不依赖半胱天冬酶的程序性坏死。作为坏死小体的重要组成部分,RIPK3在坏死性凋亡中发挥着不可或缺的作用,而坏死性凋亡对人类生命和健康至关重要。此外,RIPK3通过调节自噬、细胞增殖以及趋化因子/细胞因子的代谢和产生,参与多种感染、无菌性炎症疾病和肿瘤的病理过程(包括促进肿瘤和抑制肿瘤的活性)。本文综述了RIPK3信号通路调节因子的最新研究进展,并讨论了RIPK3/坏死性凋亡在各种疾病发病机制中的潜在作用。深入了解RIPK3的机制和功能可能有助于开发新的治疗策略。