微泡
微流控
基因工程
纳米技术
间质细胞
材料科学
吞吐量
计算生物学
生物
小RNA
计算机科学
癌症研究
遗传学
基因
电信
无线
作者
Junjie Huang,Hanxu Chen,Zhiqiang Luo,Min Nie,Jinglin Wang,Ling Lü,Yuanjin Zhao
出处
期刊:PubMed
日期:2025-03-05
被引量:1
标识
DOI:10.1021/acsnano.5c01773
摘要
Stromal cell-derived exosomes have demonstrated their value in the field of biomedical engineering. However, the low production and specific requirements of different diseases limited the practical efficacy of these exosomes and restricted their wider applications. Here, we presented a method to culture genetically engineered mesenchymal stromal cells (MSC) that overexpressed the hepatocyte growth factor (HGF) in microfluidics and harvest mass HGF overexpressed exosomes for wound healing. The microfluidic chips were featured with herringbone grooves and micropillar arrays, where sufficient fluidic mechanical stimuli and efficient nutrient delivery were promoted by a turbulent vortex. It was demonstrated that the production of exosomes was much higher than by the traditional flask cell culture, along with higher HGF content. In addition, the MSCHGF-secreted exosomes were applied for wound healing in diabetic rat model, showing superior angiogenesis, cell migration, and immune modulation capabilities. These features indicated that the genetically engineered MSCHGF exosomes from high-throughput herringbone microfluidics possess great potential for wound healing and related biomedical applications.
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