Preparation of therapy-grade extracellular vesicles from adipose tissue to promote diabetic wound healing

伤口愈合 脂肪组织 胶原酶 血管生成 体内 炎症 纳米粒子跟踪分析 污渍 体外 慢性伤口 医学 细胞生物学 小RNA 癌症研究 化学 微泡 免疫学 生物 生物技术 内科学 生物化学 基因
作者
Chuqiao Pan,Peng Xu,Yi Zheng,Yikai Wang,Chuhsin Chen,Shibo Fu,Zibo Liu,Yahong Chen,Ke Xue,Qimin Zhou,Kai Li
出处
期刊:Frontiers in Bioengineering and Biotechnology [Frontiers Media SA]
卷期号:11 被引量:1
标识
DOI:10.3389/fbioe.2023.1129187
摘要

Background: Treatment of diabetic wounds is a major challenge in clinical practice. Extracellular vesicles (EVs) from adipose-derived stem cells have shown effectiveness in diabetic wound models. However, obtaining ADSC-EVs requires culturing vast numbers of cells, which is hampered by the need for expensive equipment and reagents, extended time cost, and complicated procedures before commercialization. Therefore, methods to extract EVs from discarded tissue need to be developed, for immediate application during surgery. For this reason, mechanical, collagenase-digestive, and constant in-vitro-collective methods were designed and compared for preparing therapy-grade EVs directly from adipose tissue. Methods: Characteristics and quantities of EVs were detected by transmission electron microscopy, nanoparticle tracking analysis, and Western blotting firstly. To investigate the biological effects of EVs on diabetic wound healing, angiogenesis, proliferation, migration, and inflammation-regulation assays were then evaluated in vitro, along with a diabetic wound healing mouse model in vivo. To further explore the potential therapeutic mechanism of EVs, miRNA expression profile of EVs were also identified and analyzed. Results: The adipose tissue derived EVs (AT-EVs) were showed to qualify ISEV identification by nanoparticle tracking analysis and Western blotting and the AT-EVs yield from three methods was equal. EVs also showed promoting effects on biological processes related to diabetic wound healing, which depend on fibroblasts, keratinocytes, endothelial cells, and macrophages both in vitro and in vivo. We also observed enrichment of overlapping or unique miRNAs originate from different types of AT-EVs associated with diabetic wound healing for further investigation. Conclusion: After comparative analyses, a mechanical method was proposed for preparing immediate clinical applicable EVs from adipose tissue that would result in reduced preparation time and lower cost, which could have promising application potential in treating diabetic wounds.
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