Wang Fei, Huang Huiming, Wei Xuejiao, Tan Peng, Wang Zhuguo, Hu Zhongdong
School of Chinese Materia Medica, Beijing University of Chinese Medicine, 100029, Beijing, China.
Modern Research Center for Traditional Chinese Medicine, Beijing Research Institute of Chinese Medicine, Beijing University of Chinese Medicine, 100029, Beijing, China.
Cell Death Discov. 2024 Mar 4;10(1):112. doi: 10.1038/s41420-024-01891-x.
Intestinal ischemia-reperfusion (I/R) is a multifaceted pathological process, and there is a lack of clear treatment for intestinal I/R injury. During intestinal I/R, oxidative stress and inflammation triggered by cells can trigger a variety of cell death mechanisms, including apoptosis, autophagy, pyroptosis, ferroptosis, and necrosis. These cell death processes can send a danger signal for the body to be damaged and prevent intestinal I/R injury. Therefore, identifying key regulatory molecules or markers of these cell death mechanisms when intestinal I/R injury occurs may provide valuable information for the treatment of intestinal I/R injury. This paper reviews the regulatory molecules and potential markers that may be involved in regulating cell death during intestinal I/R and elaborates on the cell death mechanism of intestinal I/R injury at the molecular level to provide a theoretical basis for discovering new molecules or markers regulating cell death during intestinal I/R injury and provides ideas for drug development for the treatment of intestinal I/R injury.
肠缺血再灌注(I/R)是一个多方面的病理过程,目前缺乏针对肠I/R损伤的明确治疗方法。在肠I/R过程中,细胞引发的氧化应激和炎症可触发多种细胞死亡机制,包括凋亡、自噬、焦亡、铁死亡和坏死。这些细胞死亡过程可发出身体受损的危险信号,预防肠I/R损伤。因此,在肠I/R损伤发生时识别这些细胞死亡机制的关键调节分子或标志物,可能为肠I/R损伤的治疗提供有价值的信息。本文综述了可能参与调节肠I/R过程中细胞死亡的调节分子和潜在标志物,并在分子水平上阐述了肠I/R损伤的细胞死亡机制,为发现调节肠I/R损伤时细胞死亡的新分子或标志物提供理论依据,并为治疗肠I/R损伤的药物开发提供思路。