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大规模生产间充质干细胞及其外泌体,以有效治疗肺部炎症。

A large-scale production of mesenchymal stem cells and their exosomes for an efficient treatment against lung inflammation.

机构信息

College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, China.

Department of Obstetrics and Gynecology, The First Affiliated Hospital of Ningbo University, Ningbo, China.

出版信息

Biotechnol J. 2024 Feb;19(2):e2300174. doi: 10.1002/biot.202300174.

Abstract

Mesenchymal stem cells (MSCs) and their produced exosomes have demonstrated inherent capabilities of inflammation-guided targeting and inflammatory modulation, inspiring their potential applications as biologic agents for inflammatory treatments. However, the clinical applications of stem cell therapies are currently restricted by several challenges, and one of them is the mass production of stem cells to satisfy the therapeutic demands in the clinical bench. Herein, a production of human amnion-derived MSCs (hMSCs) at a scale of over 1 × 10 cells per batch was reported using a three-dimensional (3D) culture technology based on microcarriers coupled with a spinner bioreactor system. The present study revealed that this large-scale production technology improved the inflammation-guided migration and the inflammatory suppression of hMSCs, without altering their major properties as stem cells. Moreover, these large-scale produced hMSCs showed an efficient treatment against the lipopolysaccharide (LPS)-induced lung inflammation in mice models. Notably, exosomes collected from these large-scale produced hMSCs were observed to inherit the efficient inflammatory suppression capability of hMSCs. The present study showed that 3D culture technology using microcarriers coupled with a spinner bioreactor system can be a promising strategy for the large-scale expansion of hMSCs with improved anti-inflammation capability, as well as their secreted exosomes.

摘要

间充质干细胞(MSCs)及其产生的外泌体具有固有的炎症导向靶向和炎症调节能力,激发了它们作为炎症治疗生物制剂的潜在应用。然而,干细胞疗法的临床应用目前受到几个挑战的限制,其中之一是大量生产干细胞以满足临床需求。在此,报告了一种使用基于微载体的三维(3D)培养技术和搅拌生物反应器系统,以每批超过 1×10 细胞的规模生产人羊膜源性 MSCs(hMSCs)的方法。本研究表明,这种大规模生产技术提高了 hMSCs 的炎症导向迁移和炎症抑制能力,而不会改变其作为干细胞的主要特性。此外,这些大规模生产的 hMSCs 对小鼠模型中的脂多糖(LPS)诱导的肺炎症表现出有效的治疗作用。值得注意的是,从这些大规模生产的 hMSCs 中收集的外泌体被观察到继承了 hMSCs 的有效炎症抑制能力。本研究表明,使用微载体结合搅拌生物反应器系统的 3D 培养技术可能是一种有前途的策略,可用于大规模扩增具有改善抗炎能力的 hMSCs 及其分泌的外泌体。

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