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脂肪组织来源间充质干细胞的条件培养基可逆转细胞模型中的胰岛素抵抗

Conditioned Media From Adipose Tissue Derived Mesenchymal Stem Cells Reverse Insulin Resistance in Cellular Models.

作者信息

Shree Nitya, Bhonde Ramesh R

机构信息

School of Regenerative Medicine, GKVK Post, Bellary Road, Bangalore, India.

出版信息

J Cell Biochem. 2017 Aug;118(8):2037-2043. doi: 10.1002/jcb.25777. Epub 2017 Jan 10.

Abstract

The link between insulin resistance (IR) and type 2 diabetes has been recognized for a long time. Type 2 diabetes is often associated with basal hyperinsulinemia, reduced sensitivity to insulin, and disturbances in insulin release. There are evidences showing the reversal of IR by mesenchymal stem cells. However, the effect of conditioned media from adipose derived mesenchymal stem cells (ADSCs-CM) in reversal of IR has not been established. We established an insulin resistant model of 3T3L1 and C2C12 cells and treated with ADSCs-CM. 2-NBDG (2-[N-[7-Nitrobenz-2-oxa-1,3-diazol-4-yl]Amino]-2-Deoxyglucose) uptake was performed to assess improvement in glucose uptake. Genes involved in glucose transport and in inflammation were also analysed. Western blot for glucose transporter-4 and Akt was performed to evaluate translocation of Glut4 and insulin signaling respectively. We found that the ADSCs-CM treated cells restored insulin, stimulated glucose uptake as compared to the untreated control indicating the insulin sensitizing effect of the CM. The treated cells also showed inhibition adipogenesis in 3T3L1 cells and significant reduction of intramuscular triglyceride accumulation in C2C12 cells. Gene expressions studies revealed the drastic upregulation of GLUT4 gene and significant reduction in IL6 and PAI1 gene in both 3T3L1 and C2C12 cells, indicating possible mechanism of glucose uptake with concomitant decrease in inflammation. Enhancement of GLUT4 and phospho Akt protein expression seems to be responsible for the increment in glucose uptake and enhanced insulin signaling, respectively. Our study revealed for the first time that ADSCs-CM acts as an alternative insulin sensitizer providing stem cell solution to IR. J. Cell. Biochem. 118: 2037-2043,2017. © 2016 Wiley Periodicals, Inc.

摘要

胰岛素抵抗(IR)与2型糖尿病之间的联系早已为人所知。2型糖尿病常伴有基础高胰岛素血症、胰岛素敏感性降低以及胰岛素释放紊乱。有证据表明间充质干细胞可逆转IR。然而,脂肪来源的间充质干细胞条件培养基(ADSCs-CM)在逆转IR方面的作用尚未明确。我们建立了3T3L1和C2C12细胞的胰岛素抵抗模型,并用ADSCs-CM进行处理。通过2-NBDG(2-[N-[7-硝基苯并-2-恶唑-1,3-二氮杂环丁烷-4-基]氨基]-2-脱氧葡萄糖)摄取来评估葡萄糖摄取的改善情况。还分析了参与葡萄糖转运和炎症的基因。进行葡萄糖转运蛋白-4和Akt的蛋白质印迹分析,分别评估Glut4的转位和胰岛素信号传导。我们发现,与未处理的对照相比,经ADSCs-CM处理的细胞恢复了胰岛素刺激的葡萄糖摄取,表明CM具有胰岛素增敏作用。处理后的细胞在3T3L1细胞中还显示出抑制脂肪生成,在C2C12细胞中显著减少肌内甘油三酯积累。基因表达研究表明,3T3L1和C2C12细胞中GLUT4基因显著上调,IL6和PAI1基因显著下调,这表明葡萄糖摄取的可能机制以及炎症的同时减少。GLUT4和磷酸化Akt蛋白表达的增强似乎分别是葡萄糖摄取增加和胰岛素信号增强的原因。我们的研究首次表明,ADSCs-CM可作为一种替代的胰岛素增敏剂,为IR提供干细胞解决方案。《细胞生物化学杂志》118: 2037 - 2043,2017。© 2016威利期刊公司

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