Endothelial cell‐derived extracellular vesicles induce pro‐angiogenic responses in mesenchymal stem cells

血管生成 间充质干细胞 细胞生物学 血管内皮生长因子 脐静脉 内皮干细胞 成纤维细胞生长因子 生物 碱性成纤维细胞生长因子 伤口愈合 人脐静脉内皮细胞 癌症研究 化学 生长因子 免疫学 受体 体外 生物化学 血管内皮生长因子受体
作者
Hüseyin Abdik,Oğuz Kaan Kırbaş,Batuhan Turhan Bozkurt,Ezgi Avşar Abdik,Taha Bartu Hayal,Fikrettin Şahin,Pakize Neslihan Taşlı
出处
期刊:FEBS Open Bio [Wiley]
卷期号:14 (5): 740-755 被引量:1
标识
DOI:10.1002/2211-5463.13650
摘要

Angiogenesis is a central component of vital biological processes such as wound healing, tissue nourishment, and development. Therefore, angiogenic activities are precisely maintained with secreted factors such as angiopoietin‐1 (Ang1), fibroblast growth factor (FGF), and vascular endothelial growth factor (VEGF). As an element of intracellular communication, extracellular vesicles (EVs)—particularly EVs of vascular origin—could have key functions in maintaining angiogenesis. However, the functions of EVs in the control of angiogenesis have not been fully studied. In this study, human umbilical vein endothelial cell line (HUVEC)‐derived small EVs (<200 nm; HU‐sEVs) were investigated as a potential pro‐angiogenic agent. Treating mesenchymal stem cells (MSCs) and mature HUVEC cells with HU‐sEVs induced their tube formation under in vitro conditions and significantly increased the expression of angiogenesis‐related genes, such as Ang1 , VEGF , Flk‐1 (VEGF receptor 2), Flt‐1 (VEGF receptor 1), and vWF (von Willebrand Factor), in a dose‐dependent manner. These results indicate that HU‐sEVs take part in angiogenesis activities in physiological systems, and suggest endothelial EVs as a potential therapeutic candidate for the treatment of angiogenesis‐related diseases.

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