| Literature DB >> 27381991 |
Guang-Yang Liu1, Jin Liu1, You-Liang Wang2, Yang Liu1, Yong Shao2, Yan Han3, Ya-Ru Qin1, Feng-Jun Xiao1, Peng-Fei Li1, Lan-Jun Zhao1, En-Yan Gu1, Si-Yu Chen1, Li-Hua Gao2, Chu-Tse Wu1, Xian-Wen Hu4, Hai-Feng Duan5.
Abstract
UNLABELLED: : Adipose-derived mesenchymal stem cells (AD-MSCs) have been shown to ameliorate hyperglycemia in diabetic animals and individuals. However, little is known about whether AD-MSCs affect lipid metabolism. Here we have demonstrated for the first time that AD-MSC infusion can significantly suppress the increase in body weight and remarkably improve dyslipidemia in db/db obese mice and diet-induced obesity mice. Induction of white fat tissue "browning" and activation of adenosine monophosphate-activated protein kinase and its downstream hormone-sensitive lipase in adipose tissue contribute to the antiobesity and lipid-lowering effects. Thus, AD-MSC infusion holds great therapeutic potential for dyslipidemia and associated cardiovascular diseases. SIGNIFICANCE: Mesenchymal stem cells (MSCs) are considered one of the most promising types of stem cells for translational application because of their rich tissue sources, multilineage differentiation capacity, and easy amplification in vitro and unique immunobiological properties. This study demonstrated that adipose-derived MSCs (AD-MSCs) infusion can significantly suppress the increase in body weight and remarkably improve dyslipidemia in obese mice. Induction of white fat tissue "browning" and activation of adenosine monophosphate-activated protein kinase and its downstream hormone-sensitive lipase in adipose tissue were demonstrated to contribute to the antiobesity and lipid-lowering effects. Thus, AD-MSC infusion holds great therapeutic potential for dyslipidemia. ©AlphaMed Press.Entities:
Keywords: Adenosine monophosphate-activated protein kinase; Adipose-derived mesenchymal stem cell; Anti-obesity; Lipid metabolism
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Year: 2016 PMID: 27381991 PMCID: PMC4996437 DOI: 10.5966/sctm.2015-0239
Source DB: PubMed Journal: Stem Cells Transl Med ISSN: 2157-6564 Impact factor: 6.940