Apelin Enhances Brown Adipogenesis and Browning of White Adipocytes

被引:88
作者
Than, Aung [1 ]
He, Hui Ling [1 ]
Chua, Si Hui [1 ]
Xu, Dan [2 ]
Sun, Lei [2 ]
Leow, Melvin Khee-Shing [3 ]
Chen, Peng [1 ]
机构
[1] Nanyang Technol Univ, Sch Chem & Biomed Engn, Bioengn Program, 70 Nanyang Dr, Singapore 637457, Singapore
[2] Duke NUS Grad Med Sch, Singapore 169857, Singapore
[3] Tan Tock Seng Hosp, Endocrine & Diabet Clin, Singapore 308433, Singapore
基金
新加坡国家研究基金会;
关键词
ADIPOSE-TISSUE; UNCOUPLING PROTEIN; INSULIN-RESISTANCE; TRANSCRIPTIONAL CONTROL; GLUCOSE-HOMEOSTASIS; PPAR-GAMMA; FAT; EXPRESSION; RECEPTOR; DIFFERENTIATION;
D O I
10.1074/jbc.M115.643817
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Brown adipose tissue expends energy in the form of heat via the mitochondrial uncoupling protein UCP1. Recent studies showed that brown adipose tissue is present in adult humans and may be exploited for its anti-obesity and anti-diabetes actions. Apelin is an adipocyte-derived hormone that plays important roles in energy metabolism. Here, we report that apelin-APJ signaling promotes brown adipocyte differentiation by increasing the expressions of brown adipogenic and thermogenic transcriptional factors via the PI3K/Akt and AMPK signaling pathways. It is also found that apelin relieves the TNF alpha inhibition on brown adipogenesis. In addition, apelin increases the basal activity of brown adipocytes, as evidenced by the increased PGC1 alpha and UCP1 expressions, mitochondrial biogenesis, and oxygen consumption. Finally, we provide both in vitro and in vivo evidence that apelin is able to increase the brown-like characteristics in white adipocytes. This study, for the first time, reveals the brown adipogenic and browning effects of apelin and suggests a potential therapeutic route to combat obesity and related metabolic disorders.
引用
收藏
页码:14679 / 14691
页数:13
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