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促进间充质干细胞衍生外泌体的生物发生和分泌。

Boosting the Biogenesis and Secretion of Mesenchymal Stem Cell-Derived Exosomes.

机构信息

Department of Biomedical Engineering, University at Buffalo, The State University of New York, Buffalo, NY 14214, USA.

Division of Pharmacoengineering and Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.

出版信息

Cells. 2020 Mar 9;9(3):660. doi: 10.3390/cells9030660.

Abstract

A limitation of using exosomes to their fullest potential is their limited secretion from cells, a major bottleneck to efficient exosome production and application. This is especially true for mesenchymal stem cells (MSCs), which can self-renew but have a limited expansion capacity, undergoing senescence after only a few passages, with exosomes derived from senescent stem cells showing impaired regenerative capacity compared to young cells. Here, we examined the effects of small molecule modulators capable of enhancing exosome secretion from MSCs. The treatment of MSCs with a combination of N-methyldopamine and norepinephrine robustly increased exosome production by three-fold without altering the ability of the MSC exosomes to induce angiogenesis, polarize macrophages to an anti-inflammatory phenotype, or downregulate collagen expression. These small molecule modulators provide a promising means to increase exosome production by MSCs.

摘要

使用外泌体的一个限制是它们从细胞中分泌的有限性,这是有效生产和应用外泌体的主要瓶颈。对于间充质干细胞(MSCs)来说尤其如此,它们可以自我更新,但扩展能力有限,在经过几次传代后就会衰老,与年轻细胞相比,来自衰老干细胞的外泌体显示出受损的再生能力。在这里,我们研究了能够增强 MSCs 外泌体分泌的小分子调节剂的作用。用 N-甲基多巴胺和去甲肾上腺素联合处理 MSCs,可使外泌体的产生增加三倍,而不改变 MSC 外泌体诱导血管生成、将巨噬细胞极化到抗炎表型或下调胶原蛋白表达的能力。这些小分子调节剂为增加 MSCs 的外泌体产量提供了一种很有前途的方法。

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