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新发病机制:Apelin/APJ系统对细胞凋亡的调控

Novel pathogenesis: regulation of apoptosis by Apelin/APJ system.

作者信息

Liu Jiaqi, Liu Meiqing, Chen Linxi

机构信息

Institute of Pharmacy and Pharmacology, Learning Key Laboratory for Pharmacoproteomics, University of South China, Hengyang 421001, China.

出版信息

Acta Biochim Biophys Sin (Shanghai). 2017 Jun 1;49(6):471-478. doi: 10.1093/abbs/gmx035.

Abstract

Apelin is the endogenous peptide APJ receptor, while APJ is a member of the G protein-coupled receptors family. Recent evidence strongly suggests that Apelin/APJ system influences apoptosis in various diseases through different signal pathways. In this review, we discuss the possible mechanisms by which the Apelin/APJ system inhibits apoptosis, including the phosphatidylinositol-3-kinase (PI3K)/Akt, ERK1/2, caspase signaling, and autophagy pathway. We also summarize the role of Apelin/APJ system in apoptosis in myocardial ischemia-reperfusion (I/R) injury, pulmonary artery hypertension, retinal neovascular disease, acute renal injury, skeletal homeostasis, and gastrointestinal diseases. Apelin/APJ system decreases myocardial infarction size and alleviates myocardial I/R injury by inhibiting cardiomyocytes apoptosis. However, Apelin/APJ system improves pulmonary artery hypertension via increasing apoptosis. Apelin/APJ system exerts neuroprotective effect by blocking apoptosis and participates in the recovery of retinal neovascular disease by suppressing apoptosis. Apelin/APJ system also shows anti-apoptotic effect against acute renal injury and plays a role in regulating skeletal homeostasis. In gastrointestinal disease, Apelin/APJ system plays a potential physiological role in gastrointestinal cytoprotection by regulating apoptosis. We hope that a better understanding of the Apelin/APJ system will help to discover new disease pathogenesis and find possible therapeutic targets of the Apelin/APJ system essential for various diseases.

摘要

Apelin是内源性肽APJ受体,而APJ是G蛋白偶联受体家族的成员。最近的证据有力地表明,Apelin/APJ系统通过不同的信号通路影响各种疾病中的细胞凋亡。在本综述中,我们讨论了Apelin/APJ系统抑制细胞凋亡的可能机制,包括磷脂酰肌醇-3-激酶(PI3K)/Akt、ERK1/2、半胱天冬酶信号传导和自噬途径。我们还总结了Apelin/APJ系统在心肌缺血再灌注(I/R)损伤、肺动脉高压、视网膜新生血管疾病、急性肾损伤、骨骼稳态和胃肠道疾病中的细胞凋亡中的作用。Apelin/APJ系统通过抑制心肌细胞凋亡来减小心肌梗死面积并减轻心肌I/R损伤。然而,Apelin/APJ系统通过增加细胞凋亡来改善肺动脉高压。Apelin/APJ系统通过阻断细胞凋亡发挥神经保护作用,并通过抑制细胞凋亡参与视网膜新生血管疾病的恢复。Apelin/APJ系统对急性肾损伤也显示出抗凋亡作用,并在调节骨骼稳态中发挥作用。在胃肠道疾病中,Apelin/APJ系统通过调节细胞凋亡在胃肠道细胞保护中发挥潜在的生理作用。我们希望对Apelin/APJ系统有更好的了解将有助于发现新的疾病发病机制,并找到对各种疾病至关重要的Apelin/APJ系统的可能治疗靶点。

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