PLGA公司
伤口愈合
脂肪组织
血管生成
小RNA
再生(生物学)
化学
新生血管
癌症研究
细胞生物学
体外
医学
免疫学
生物
生物化学
基因
作者
Huiyu Peng,Fangzhou Du,Jingwen Wang,Yue Wu,Wei Qian,Aoying Chen,Yuhan Duan,Shuaiguang Shi,Jingzhong Zhang,Shuang Yu
出处
期刊:Pharmaceutics
[MDPI AG]
日期:2024-08-23
卷期号:16 (9): 1113-1113
标识
DOI:10.3390/pharmaceutics16091113
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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