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基于空间转录组学分析依赖区域的肝缺血再灌注损伤小鼠模型。

Spatial transcriptomics analysis of zone-dependent hepatic ischemia-reperfusion injury murine model.

机构信息

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.

出版信息

Commun Biol. 2023 Feb 18;6(1):194. doi: 10.1038/s42003-023-04564-0.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2856/9938905/6b5e65de1041/42003_2023_4564_Fig1_HTML.jpg

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