Mesenchymal Stem Cells Potentiate the Vasculogenic Capacity of Endothelial Colony-Forming Cells under Hyperglycemic Conditions

被引:5
作者
Lee, Hyunsook [1 ,2 ]
Huh, Yang-Hoon [3 ]
Kang, Kyu-Tae [1 ,2 ]
机构
[1] Duksung Womens Univ, Coll Pharm, Seoul 01369, South Korea
[2] Duksung Womens Univ, Duksung Innovat Drug Ctr, Seoul 01369, South Korea
[3] Korea Basic Sci Inst, Electron Microscopy Res Ctr, Ochang 28119, South Korea
来源
LIFE-BASEL | 2022年 / 12卷 / 04期
基金
新加坡国家研究基金会;
关键词
diabetes; hyperglycemia; vasculogenesis; endothelial colony-forming cells; mesenchymal stem cells; IN-VIVO; PROGENITOR CELLS; DIABETES-MELLITUS; VASCULATURE; ROBUST;
D O I
10.3390/life12040469
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Many studies have demonstrated a reduced number and vasculogenic capacity of endothelial colony-forming cells (ECFCs) in diabetic patients. However, whether the vasculogenic capacity of ECFCs is recovered or not when combined with pericyte precursors, mesenchymal stem cells (MSCs), under hyperglycemic conditions has not been studied. Thus, we investigated the role of MSCs in ECFC-mediated vascular formation under high-glucose conditions. The ECFCs and MSCs were treated with normal glucose (5 mM; NG) or high glucose (30 mM; HG) for 7 days. The cell viability, proliferation, migration, and tube formation of ECFCs were reduced in HG compared to NG. Interestingly, the ECFC+MSC combination after HG treatment formed tubular structures similar to NG-treated ECFCs+MSCs. An in vivo study using a diabetic mouse model revealed that the number of perfused vessels formed by HG-treated ECFCs+MSCs in diabetic mice was comparable with that of NG-treated ECFCs+MSCs in normal mice. Electron microscopy revealed that the ECFCs+MSCs formed pericyte-covered perfused blood vessels, while the ECFCs alone did not form perfused vessels when injected into the mice. Taken together, MSCs potentiate the vasculogenic capacity of ECFCs under hyperglycemic conditions, suggesting that the combined delivery of ECFCs+MSCs can be a promising strategy to build a functional microvascular network to repair vascular defects in diabetic ischemic regions.
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页数:14
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