Adipose-derived mesenchymal stem cells ameliorate hyperglycemia through regulating hepatic glucose metabolism in type 2 diabetic rats

被引:52
作者
Xie, Min [1 ]
Hao, Hao Jie [2 ]
Cheng, Yu [1 ]
Xie, Zong Yan [1 ]
Yin, Ya Qi [1 ]
Zhang, Qi [1 ]
Gao, Jie Qing [1 ]
Liu, Hong Yu [3 ]
Mu, Yi Ming [1 ]
Han, Wei Dong [2 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Dept Endocrinol, Beijing 100853, Peoples R China
[2] Chinese Peoples Liberat Army Gen Hosp, Inst Basic Med Sci, Coll Life Sci, Beijing 100853, Peoples R China
[3] Chinese Peoples Liberat Army Gen Hosp, Dept Neurosurg, Beijing 100853, Peoples R China
关键词
Mesenchymal stem cells; Hyperglycemia; Insulin resistance; Type 2 diabetes mellitus; Liver; ACTIVATED PROTEIN-KINASE; INSULIN-RESISTANCE; GLUCONEOGENESIS; STRATEGY; PATHWAY; MICE; HEPATOCYTES; MECHANISM; LIVER;
D O I
10.1016/j.bbrc.2016.12.125
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
Infusion of mesenchymal stem cells (MSCs) has been identified in the rapid alleviation in hyperglycemia of diabetic individuals, but the mechanism involved has not been adequately explained by these cells' potential role in modulating system insulin sensitivity and islet regeneration. In this study, we demonstrated adipose-derived mesenchymal stem cells (ASCs) produced significantly lower blood glucose via promoting hepatic glycogen synthesis and inhibiting hepatic glucose production within 24 h after infusion in T2DM rats. In vitro, HepG2 cells treated with palmitate (PA) were used as a model of hepatic glucose metabolism disorder to confirm that ASCs stimulates the phosphorylation of hepatic AMP-activated protein kinase (AMPK) to restores hepatic glucose metabolism in type 2 diabetes. In summary, this study indicated that ASCs improve hyperglycemia via regulating hepatic glucose metabolism. Additionally, the effect of ASCs on hepatic glucose metabolism depended on the AMPK signaling pathway. Thus, this is the new research of the molecular mechanisms of MSCs administration to improve glucose metabolism, and it may indicate a new treatment target of MSCs in T2DM. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:435 / 441
页数:7
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