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Mesenchymal Stem Cells Ameliorated Glucolipotoxicity in HUVECs through TSG-6

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 μM palmitic acid was used to i...

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Autores principales: An, Xingxing, Li, Lan, Chen, Younan, Luo, Ai, Ni, Zuyao, Liu, Jingping, Yuan, Yujia, Shi, Meimei, Chen, Bo, Long, Dan, Cheng, Jingqiu, Lu, Yanrong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4848939/
https://www.ncbi.nlm.nih.gov/pubmed/27043548
http://dx.doi.org/10.3390/ijms17040483
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author An, Xingxing
Li, Lan
Chen, Younan
Luo, Ai
Ni, Zuyao
Liu, Jingping
Yuan, Yujia
Shi, Meimei
Chen, Bo
Long, Dan
Cheng, Jingqiu
Lu, Yanrong
author_facet An, Xingxing
Li, Lan
Chen, Younan
Luo, Ai
Ni, Zuyao
Liu, Jingping
Yuan, Yujia
Shi, Meimei
Chen, Bo
Long, Dan
Cheng, Jingqiu
Lu, Yanrong
author_sort An, Xingxing
collection PubMed
description 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 μM 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-α 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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spelling pubmed-48489392016-05-04 Mesenchymal Stem Cells Ameliorated Glucolipotoxicity in HUVECs through TSG-6 An, Xingxing Li, Lan Chen, Younan Luo, Ai Ni, Zuyao Liu, Jingping Yuan, Yujia Shi, Meimei Chen, Bo Long, Dan Cheng, Jingqiu Lu, Yanrong Int J Mol Sci Article 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 μM 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-α 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. MDPI 2016-04-01 /pmc/articles/PMC4848939/ /pubmed/27043548 http://dx.doi.org/10.3390/ijms17040483 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
An, Xingxing
Li, Lan
Chen, Younan
Luo, Ai
Ni, Zuyao
Liu, Jingping
Yuan, Yujia
Shi, Meimei
Chen, Bo
Long, Dan
Cheng, Jingqiu
Lu, Yanrong
Mesenchymal Stem Cells Ameliorated Glucolipotoxicity in HUVECs through TSG-6
title Mesenchymal Stem Cells Ameliorated Glucolipotoxicity in HUVECs through TSG-6
title_full Mesenchymal Stem Cells Ameliorated Glucolipotoxicity in HUVECs through TSG-6
title_fullStr Mesenchymal Stem Cells Ameliorated Glucolipotoxicity in HUVECs through TSG-6
title_full_unstemmed Mesenchymal Stem Cells Ameliorated Glucolipotoxicity in HUVECs through TSG-6
title_short Mesenchymal Stem Cells Ameliorated Glucolipotoxicity in HUVECs through TSG-6
title_sort mesenchymal stem cells ameliorated glucolipotoxicity in huvecs through tsg-6
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4848939/
https://www.ncbi.nlm.nih.gov/pubmed/27043548
http://dx.doi.org/10.3390/ijms17040483
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