Adipose-Derived Stem-Cell-Membrane-Coated PLGA-PEI Nanoparticles Promote Wound Healing via Efficient Delivery of miR-21

被引:0
|
作者
Peng, Huiyu [1 ,2 ]
Du, Fangzhou [2 ]
Wang, Jingwen [2 ]
Wu, Yue [2 ]
Wei, Qian [1 ,2 ]
Chen, Aoying [1 ,2 ]
Duan, Yuhan [1 ,2 ]
Shi, Shuaiguang [1 ,2 ]
Zhang, Jingzhong [1 ,2 ,3 ]
Yu, Shuang [1 ,2 ,3 ]
机构
[1] Univ Sci & Technol China, Sch Biomed Engn Suzhou, Div Life Sci & Med, Hefei 230026, Peoples R China
[2] Chinese Acad Sci, Suzhou Inst Biomed Engn & Technol, Suzhou 215163, Peoples R China
[3] Xuzhou Med Univ, Sch Med Imaging, Xuzhou 221004, Peoples R China
基金
中国国家自然科学基金;
关键词
biomimetic nanoparticles; microRNA delivery; PLGA-PEI; stem cell; wound repair; SIRNA DELIVERY; MOLECULAR-WEIGHT; EXOSOMES; ANGIOGENESIS; DNA; POLYETHYLENIMINE; CHALLENGES; DRUGS; RNA;
D O I
10.3390/pharmaceutics16091113
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
miRNAs have been shown to be involved in the regulation of a variety of physiological and pathological processes, but their use in the treatment of diseases is still limited due to their instability. Biomimetic nanomaterials combine nanomaterials with cellular components that are readily modifiable and biocompatible, making them an emerging miRNA delivery vehicle. In this study, adipose-derived MSC membranes were wrapped around PLGA-PEI loaded with miR-21 through co-extrusion and later transplanted into C57BL/6 mice wounds. The wound-healing rate, epithelialization, angiogenesis, and collagen deposition were assessed after treatment and corroborated in vitro. Our study demonstrated that m/NP/miR-21 can promote wound healing in terms of epithelialization, dermal reconstruction, and neovascularization, and it can regulate the corresponding functions of keratinocytes, fibroblasts, and vascular endothelial cells. m/NP/miR-21 can inhibit the expression of PTEN, a gene downstream of miR-21, and increase the phosphorylation activation of AKT, which can then regulate the functions of fibroblasts. In conclusion, this provides a new approach to therapy for skin wounds using microRNA transporters and biomimetic nanoparticles.
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页数:21
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