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间充质干细胞增强高血糖条件下内皮祖细胞的血管生成能力。

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

作者信息

Lee Hyunsook, Huh Yang-Hoon, Kang Kyu-Tae

机构信息

College of Pharmacy, Duksung Women's University, Seoul 01369, Korea.

Duksung Innovative Drug Center, Duksung Women's University, Seoul 01369, Korea.

出版信息

Life (Basel). 2022 Mar 23;12(4):469. doi: 10.3390/life12040469.

Abstract

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.

摘要

许多研究表明,糖尿病患者体内内皮祖细胞(ECFCs)的数量减少且血管生成能力降低。然而,在高血糖条件下,当ECFCs与周细胞前体细胞——间充质干细胞(MSCs)联合时,其血管生成能力是否恢复尚未得到研究。因此,我们研究了MSCs在高糖条件下对ECFC介导的血管形成中的作用。将ECFCs和MSCs分别用正常葡萄糖(5 mM;NG)或高糖(30 mM;HG)处理7天。与NG相比,HG处理后ECFCs的细胞活力、增殖、迁移和管腔形成能力均降低。有趣的是,HG处理后的ECFC+MSC组合形成的管状结构与NG处理的ECFCs+MSCs相似。一项使用糖尿病小鼠模型的体内研究表明,HG处理的ECFCs+MSCs在糖尿病小鼠中形成的灌注血管数量与NG处理的ECFCs+MSCs在正常小鼠中形成的数量相当。电子显微镜显示,ECFCs+MSCs形成了被周细胞覆盖的灌注血管,而单独注射ECFCs时,注入小鼠体内后未形成灌注血管。综上所述,MSCs在高血糖条件下增强了ECFCs的血管生成能力,这表明联合递送ECFCs+MSCs可能是构建功能性微血管网络以修复糖尿病缺血区域血管缺陷的一种有前景的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a26/9028253/279a31caa696/life-12-00469-g001.jpg

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