Sun Xiaofang, Tang Daolin
Key Laboratory for Major Obstetric Diseases of Guangdong Province; Key Laboratory of Reproduction and Genetics of Guangdong Higher Education Institutes; The Third Affiliated Hospital of Guangzhou Medical University; Guangzhou, Guangdong China.
Department of Surgery; University of Pittsburgh Cancer Institute; University of Pittsburgh; Pittsburgh, PA USA.
Autophagy. 2014 Oct 1;10(10):1873-6. doi: 10.4161/auto.32184. Epub 2014 Aug 13.
HMGB1 (high mobility group box 1) is a multifunctional, ubiquitous protein located inside and outside cells that plays a critical role in various physiological and pathological processes including cell development, differentiation, inflammation, immunity, metastasis, metabolism, and death. Increasing evidence demonstrates that HMGB1-dependent autophagy promotes chemotherapy resistance, sustains tumor metabolism requirements and T cell survival, prevents polyglutamine aggregates and excitotoxicity, and protects against endotoxemia, bacterial infection, and ischemia-reperfusion injury in vitro or in vivo. In contrast, HMGB1 may not be required for autophagy in some organs such as the liver and heart. Understanding HMGB1-dependent and -independent autophagy in more detail will provide insight into the integrated stress response and guide HMGB1-based therapeutic intervention.
高迁移率族蛋白B1(HMGB1)是一种多功能、广泛存在于细胞内外的蛋白质,在包括细胞发育、分化、炎症、免疫、转移、代谢和死亡等多种生理和病理过程中发挥关键作用。越来越多的证据表明,HMGB1依赖性自噬促进化疗耐药性,维持肿瘤代谢需求和T细胞存活,防止多聚谷氨酰胺聚集和兴奋性毒性,并在体外或体内预防内毒素血症、细菌感染和缺血再灌注损伤。相比之下,在肝脏和心脏等某些器官中,自噬可能不需要HMGB1。更详细地了解HMGB1依赖性和非依赖性自噬将有助于深入了解综合应激反应,并指导基于HMGB1的治疗干预。