Apelin/APJ signaling in hypoxia-related diseases

被引:51
作者
He, Lu [1 ]
Xu, Jin [1 ]
Chen, Linxi [1 ]
Li, Lanfang [1 ]
机构
[1] Univ South China, Inst Pharm & Pharmacol, Learning Key Lab Pharmacoprote, Hunan Prov Cooperat Innovat Ctr Mol Target New Dr, Hengyang 421001, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Apelin/APJ; Hypoxia/hypoxia-inducible factor-1 alpha; Hypoxia-related diseases; ENDOTHELIAL GROWTH-FACTOR; RETINAL MULLER CELLS; PULMONARY-HYPERTENSION; TRANSDUCTION PATHWAY; VASCULAR DEVELOPMENT; ENDOGENOUS LIGAND; ANGIOGENIC FACTOR; ADIPOSE-TISSUE; FACTOR; 1-ALPHA; APJ RECEPTOR;
D O I
10.1016/j.cca.2015.09.029
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
The regulatory peptide apelin is the endogenous ligand for the orphan G protein-coupled receptor APJ. Apelin and APJ exist in a variety of tissues, with special status in the heart, lung and tumors. Consequently, the apelin/APJ system exerts a broad range of activities that affect multiple organ systems. Accumulating evidence indicates that the expressions of apelin and APJ are significantly augmented by hypoxia through the hypoxia-inducible factor-1 alpha (HIF-l alpha.) signaling pathway. Increased apelin promotes cellular proliferation, migration and survival, therefore regulating angiogenesis. In addition, the pre-administration of exogenous apelin is involved in the occurrence and development of hypoxia-induced pathological diseases. The purpose of this article is to review the properties of the apelin/APJ system, which is affected by hypoxic conditions, and the regulation of apelin/APJ signaling in hypoxia-associated disorders. Thus, the apelin/APJ system may be a potential therapeutic target in hypoxia-related diseases. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:191 / 198
页数:8
相关论文
共 92 条
[91]   APELIN IN EPIRETINAL FIBROVASCULAR MEMBRANES OF PATIENTS WITH RETINOPATHY OF PREMATURITY AND THE CHANGES AFTER INTRAVITREAL BEVACIZUMAB [J].
Zhang, Yan ;
Jiang, Yan-rong ;
Lu, Qiang ;
Yin, Hong ;
Tao, Yong .
RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, 2013, 33 (03) :613-620
[92]   Binding of ALX40-4C to APJ, a CNS-based receptor, inhibits its utilization as a co-receptor by HIV-1 [J].
Zhou, NM ;
Fang, JH ;
Acheampong, E ;
Mukhtar, M ;
Pomerantz, RJ .
VIROLOGY, 2003, 312 (01) :196-203