安普克
脂肪组织
间充质干细胞
内分泌学
碳水化合物代谢
内科学
葡萄糖摄取
新陈代谢
胰岛素
AMP活化蛋白激酶
糖原
生物
蛋白激酶A
化学
医学
激酶
生物化学
细胞生物学
作者
Min Xie,Hao Jie Hao,Yu Cheng,Zong Yan Xie,Ya Qi Yin,Qi Zhang,Jie Gao,Hong Yu Liu,Yi Ming Mu,Wei Han
标识
DOI:10.1016/j.bbrc.2016.12.125
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.
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