Mesenchymal Stem Cells Ameliorated Glucolipotoxicity in HUVECs through TSG-6

被引:24
|
作者
An, Xingxing [1 ,2 ]
Li, Lan [1 ,2 ]
Chen, Younan [1 ,2 ,3 ]
Luo, Ai [4 ]
Ni, Zuyao [5 ]
Liu, Jingping [1 ,2 ]
Yuan, Yujia [1 ,2 ]
Shi, Meimei [1 ,2 ]
Chen, Bo [1 ,2 ]
Long, Dan [1 ,2 ]
Cheng, Jingqiu [1 ,2 ]
Lu, Yanrong [1 ,2 ]
机构
[1] Minist Hlth, Key Lab Transplant Engn & Immunol, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Hosp, Chengdu 610041, Peoples R China
[3] Curtin Univ, CHIRI Biosci, Sch Biomed Sci, GPO Box U1987, Perth, WA 6845, Australia
[4] Sichuan Neolife Stem Cell Biotech Inc, Chengdu 610041, Peoples R China
[5] Univ Toronto, Donnelly Ctr Cellular & Biomol Res, Toronto, ON M5S 3E1, Canada
基金
中国国家自然科学基金;
关键词
HUVECs; MSCs; glucolipotoxicity; inflammation; tumor necrosis factor-alpha stimulated protein 6 (TSG-6); FREE FATTY-ACIDS; STEM/PROGENITOR CELLS; PANCREATIC-ISLETS; OXIDATIVE STRESS; KAPPA-B; APOPTOSIS; LIPOTOXICITY; MECHANISMS; EXPOSURE; PATHWAY;
D O I
10.3390/ijms17040483
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
Glucolipotoxicity is one of the critical causal factors of diabetic complications. Whether mesenchymal stem cells (MSCs) have effects on glucolipotoxicity in human umbilical vein endothelial cells (HUVECs) and mechanisms involved are unclear. Thirty mM glucose plus 100 mu M palmitic acid was used to induce glucolipotoxicity in HUVECs. MSCs and HUVECs were co-cultured at the ratio of 1: 5 via Transwell system. The mRNA expressions of inflammatory factors were detected by RT-qPCR. The productions of reactive oxygen species (ROS), cell cycle and apoptosis were analyzed by flow cytometry. The tumor necrosis factor-alpha stimulated protein 6 (TSG-6) was knockdown in MSCs by RNA interference. High glucose and palmitic acid remarkably impaired cell viability and tube formation capacity, as well as increased the mRNA expression of inflammatory factors, ROS levels, and cell apoptosis in HUVECs. MSC co-cultivation ameliorated these detrimental effects in HUVECs, but no effect on ROS production. Moreover, TSG-6 was dramatically up-regulated by high glucose and fatty acid stimulation in both MSCs and HUVECs. TSG-6 knockdown partially abolished the protection mediated by MSCs. MSCs had protective effects on high glucose and palmitic acid induced glucolipotoxicity in HUVECs, and TSG-6 secreted by MSCs was likely to play an important role in this process.
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页码:1 / 14
页数:14
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