School of Traditional Chinese Medicine, Capital Medical University, Beijing, 100069, China.
Department of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, 100069, China.
Commun Biol. 2023 Feb 18;6(1):194. doi: 10.1038/s42003-023-04564-0.
Hepatic ischemia-reperfusion (I/R) injury is a common complication in liver transplantation. The connection between I/R-induced injury response and liver heterogeneity has yet to be fully understood. In this study, we converge histopathological examination with spatial transcriptomics to dissect I/R injury patterns and their associated molecular changes, which reveal that the pericentral zones are most sensitive to I/R injury in terms of histology, transcriptomic changes, and cell type dynamics. Bioinformatic analysis of I/R injury-related pathways predicts that celastrol can protect against liver I/R injury by inducing ischemic pre-conditioning, which is experimentally validated. Mechanistically, celastrol likely implements its protective effect against I/R injury by activating HIF1α signaling and represents a potential strategy for resolving liver I/R.
肝缺血再灌注(I/R)损伤是肝移植中的一种常见并发症。I/R 诱导的损伤反应与肝异质性之间的联系尚未被完全理解。在这项研究中,我们将组织病理学检查与空间转录组学相结合,以剖析 I/R 损伤模式及其相关的分子变化,结果表明,就组织学、转录组变化和细胞类型动力学而言,中央区周围组织对 I/R 损伤最为敏感。对与 I/R 损伤相关途径的生物信息学分析表明,藜芦碱通过诱导缺血预适应来保护肝脏免受 I/R 损伤,这一预测得到了实验验证。从机制上讲,藜芦碱可能通过激活 HIF1α 信号来实现其对 I/R 损伤的保护作用,代表了解决肝 I/R 的一种潜在策略。