Role of bone morphogenetic protein-9 in the regulation of glucose and lipid metabolism

被引:42
作者
Yang, Min [1 ]
Liang, Zerong [2 ]
Yang, Mengliu [2 ]
Jia, Yanjun [2 ]
Yang, Gangyi [2 ]
He, Yirui [2 ]
Li, Xinrun [2 ]
Gu, Harvest F. [3 ]
Zheng, Hongting [4 ]
Zhu, Zhiming [5 ]
Li, Ling [1 ]
机构
[1] Chongqing Med Univ, Coll Lab Med, Dept Clin Biochem, Key Lab Diagnost Med,Minist Educ, 1 Yixueyuan Rd, Chongqing 400016, Peoples R China
[2] Chongqing Med Univ, Chongqing Clin Res Ctr Geriatr, Affiliated Hosp 2, Dept Endocrinol, Chongqing, Peoples R China
[3] Karolinska Inst, Karolinska Univ Hosp, Dept Clin Sci Intervent & Technol, Stockholm, Sweden
[4] Third Mil Med Univ, Xinqiao Hosp, Dept Endocrinol, Chongqing, Peoples R China
[5] Third Mil Med Univ, Chongqing Inst Hypertens, Daping Hosp, Dept Hypertens & Endocrinol, Chongqing, Peoples R China
关键词
BMP9; metabolism; insulin resistance; cytokine; ELEMENT-BINDING PROTEIN; TRANSCRIPTION FACTOR; INSULIN SENSITIVITY; CELLS; DIFFERENTIATION; EXPRESSION; BMP-9; CYTOKINE; PROMOTER; SREBP-1C;
D O I
10.1096/fj.201802544RR
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
Bone morphogenetic protein (BMP)-9 has been reported to regulate energy balance in vivo. However, the mechanisms underlying BMP9-mediated regulation of energy balance remain incompletely understood. Here, we investigated the role of BMP9 in energy metabolism. In the current study, we found that hepatic BMP9 expression was down-regulated in insulin resistance (IR) mice and in patients who are diabetic. In mice fed a high-fat diet (HFD), the overexpression of hepatic BMP9 improved glucose tolerance and IR. The expression of gluconeogenic genes was down-regulated, whereas the level of insulin signaling molecule phosphorylation was increased in the livers of Adenovirus-BMP9-treated mice and glucosamine-treated hepatocytes. Furthermore, BMP9 overexpression ameliorated triglyceride accumulation and inhibited the expression of lipogenic genes in both human hepatocellular carcinoma HepG2 cells treated with a fatty acid mixture as well as the livers of HFD-fed mice. In hepatocytes isolated from sterol regulatory element-binding protein (SREBP)-1c knockout mice, the effects of BMP9 were ablated. Mechanistically, BMP9 inhibited SREBP-1c expression through the inhibition of liver X receptor response element 1 activity in the SREBP-1c promoter. Taken together, our results show that BMP9 is an important regulator of hepatic glucose and lipid metabolism.-Yang, M., Liang, Z., Yang, M., Jia, Y., Yang, G., He, Y., Li, X., Gu, H. F., Zheng, H., Zhu, Z., Li, L. Role of bone morphogenetic protein-9 in the regulation of glucose and lipid metabolism.
引用
收藏
页码:10077 / 10088
页数:12
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