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

间充质干细胞 微泡 炎症 干细胞 细胞生物学 医学 生物 免疫学 小RNA 内科学 生物化学 基因
作者
Jinsong Zhang,Ruyi Lin,Yingyu Li,Jiawen Wang,Huiqing Ding,Pan-Feng Fang,Yingzhi Huang,Jing Shi,Jianqing Gao,Tianyuan Zhang
出处
期刊:Biotechnology Journal [Wiley]
卷期号:19 (2): e2300174-e2300174 被引量:19
标识
DOI:10.1002/biot.202300174
摘要

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 9 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.
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