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从脂肪组织来源的间充质干细胞中分离和表征外泌体。

Isolation and characterization of exosomes from adipose tissue-derived mesenchymal stem cells.

机构信息

Department of Anatomy, Faculty of Veterinary Sciences, University of León-Universidad de León, León, España.

Institute of Biomedicine (IBIOMED), University of León-Universidad de León, León, España.

出版信息

J Anat. 2021 May;238(5):1203-1217. doi: 10.1111/joa.13365. Epub 2020 Dec 29.

Abstract

Mesenchymal stem cells (MSCs) are the subject of intense research as they are a potential therapeutic tool for several clinical applications. The new MSCs action models are focused on the use of MSC-derived secretome which contains several growth factors, cytokines, microRNAs, and extracellular vesicles such as exosomes. Exosomes have recently emerged as a component with great potential involved as mediators in cellular communication. The isolation and identification of exosomes has made it possible for them to be used in cell-free therapies. The purposes of this study are: (i) to detect exosomes released into adipose-derived MSC conditioned cell culture medium, (ii) to identify exosome morphology, and (iii) to carry out a complete characterization of said exosomes. Moreover, it is aimed at determining which method for exosome isolation would be best to use. Precipitation has been identified as a highly useful method of exosome isolation since it provides higher efficiency and purity values than other methods. A broad characterization of the exosomes present in the MSC-conditioned medium was also carried out. This work fills a gap in the existing literature on bioactive molecules which have attracted a great deal of interest due to their potential use in cellular therapies.

摘要

间充质干细胞(MSCs)是目前研究的热点,因为它们是几种临床应用的潜在治疗工具。新的 MSCs 作用模型集中在使用 MSC 衍生的分泌组,其中包含几种生长因子、细胞因子、microRNAs 和细胞外囊泡,如外泌体。外泌体最近作为一种具有巨大潜力的成分出现,作为细胞间通讯的介质。外泌体的分离和鉴定使其能够用于无细胞治疗。本研究的目的是:(i)检测脂肪来源的 MSC 条件培养基中释放的外泌体,(ii)鉴定外泌体的形态,(iii)对所述外泌体进行全面表征。此外,还旨在确定哪种外泌体分离方法最适合使用。沉淀已被确定为一种非常有用的外泌体分离方法,因为它比其他方法提供更高的效率和纯度值。还对 MSC 条件培养基中存在的外泌体进行了广泛的表征。这项工作填补了现有生物活性分子文献中的空白,由于其在细胞治疗中的潜在用途,这些生物活性分子引起了极大的关注。

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