Department of Orthopedics, Affiliated Kunshan Hospital of Jiangsu University, 91 West Qianjin Road, Suzhou, Jiangsu, 215300, China.
Acta Biochim Pol. 2023 Dec 7;70(4):735-744. doi: 10.18388/abp.2020_6756.
Gaseous hydrogen sulfide (H2S) can function as a signaling molecule similar to nitric oxide or carbon monoxide under physiological conditions, ultimately exerting anti-inflammatory, anti-apoptotic, and antioxidant activities. Many studies have investigated the role of H2S in a variety of biological contexts, and both endogenous H2S and H2S donors have been leveraged as tools for fundamental biomedical research, and it has been suggested that they may provide value for the design of novel therapeutic strategies in the years to come. Ferroptotic cell death is a distinct programmed cell death resulting from excessive lipid peroxidation in an iron-dependent manner, and is characterized by high levels of iron accumulation, reactive oxygen species (ROS) production, and peroxidation of cellular lipids. Several recent studies have revealed a close relationship between ferroproteins and their precursors, H2S, and the enzymes that produce them. This review summarizes the current information pertaining to the relationship between ferroptosis and H2S, with a particular focus on the underlying mechanisms and biological applications of this knowledge.
气态硫化氢 (H2S) 在生理条件下可以作为类似一氧化氮或一氧化碳的信号分子,最终发挥抗炎、抗凋亡和抗氧化作用。许多研究已经探讨了 H2S 在各种生物背景下的作用,内源性 H2S 和 H2S 供体都被用作基础生物医学研究的工具,并且有人认为它们可能为未来设计新型治疗策略提供价值。铁死亡是一种独特的程序性细胞死亡,是铁依赖性的脂质过氧化过度导致的,其特征是铁积累水平高、活性氧 (ROS) 产生和细胞脂质过氧化。最近的几项研究揭示了铁蛋白及其前体、H2S 和产生它们的酶之间的密切关系。本综述总结了铁死亡与 H2S 之间关系的最新信息,特别关注这方面知识的潜在机制和生物学应用。