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叉头框蛋白 O3(FOXO3):调节缺血再灌注损伤的关键因子。

The forkhead box O3 (FOXO3): a key player in the regulation of ischemia and reperfusion injury.

机构信息

Department of Biochemistry and Molecular Biology, Jiamusi University School of Basic Medical Sciences, Jiamusi, 154000, Heilongjiang, People's Republic of China.

Department Epidemiology and Health Statistics, Jiamusi University School of Public Health, Jiamusi, 154000, Heilongjiang, People's Republic of China.

出版信息

Cell Mol Life Sci. 2023 Mar 20;80(4):102. doi: 10.1007/s00018-023-04755-2.

Abstract

Forkhead box O3 is a protein encoded by the FOXO3 gene expressed throughout the body. FOXO3 could play a crucial role in longevity and many other pathologies, such as Alzheimer's disease, glioblastoma, and stroke. This study is a comprehensive review of the expression of FOXO3 under ischemia and reperfusion (IR) and the molecular mechanisms of its regulation and function. We found that the expression level of FOXO3 under ischemia and IR is tissue-specific. Specifically, the expression level of FOXO3 is increased in the lung and intestinal epithelial cells after IR. However, FOXO3 is downregulated in the kidney after IR and in the skeletal muscles following ischemia. Interestingly, both increased and decreased FOXO3 expression have been reported in the brain, liver, and heart following IR. Nevertheless, these contribute to stimulating ischemia and reperfusion injury via the induction of inflammatory response, apoptosis, autophagy, mitophagy, pyroptosis, and oxidative damage. These results suggest that FOXO3 could play protective effects in some organs and detrimental effects in others against IR injury. Most importantly, these findings indicate that controlling FOXO3 expression, genetically or pharmacologically, could contribute to preventing or treating ischemia and reperfusion damage.

摘要

叉头框蛋白 O3 是一种由 FOXO3 基因编码的蛋白质,在全身表达。FOXO3 可能在长寿和许多其他病理学中发挥关键作用,如阿尔茨海默病、神经胶质瘤和中风。本研究对缺血再灌注(IR)下 FOXO3 的表达及其调控和功能的分子机制进行了全面综述。我们发现,IR 下 FOXO3 的表达水平具有组织特异性。具体来说,IR 后肺和肠上皮细胞中 FOXO3 的表达水平增加。然而,IR 后肾脏中 FOXO3 的表达下调,以及缺血后骨骼肌中 FOXO3 的表达下调。有趣的是,IR 后大脑、肝脏和心脏中 FOXO3 的表达增加和减少都有报道。然而,这些都有助于通过诱导炎症反应、细胞凋亡、自噬、线粒体自噬、细胞焦亡和氧化损伤来刺激缺血再灌注损伤。这些结果表明,FOXO3 可能对某些器官的 IR 损伤具有保护作用,而对其他器官则具有有害作用。最重要的是,这些发现表明,控制 FOXO3 的表达,无论是通过遗传还是药理学手段,都可能有助于预防或治疗缺血再灌注损伤。

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