间充质干细胞
微泡
哈卡特
旁分泌信号
干细胞
细胞
细胞生长
细胞生物学
癌症研究
伤口愈合
生物
免疫学
小RNA
细胞培养
生物化学
遗传学
基因
受体
作者
Shijie Liu,Mingyao Meng,Han Shen,Hui Gao,Yiyi Zhao,Yang� Yang,Zhuying Lin,Lirong Yang,Kai Zhu,Rui Han,Wenwen Huang,Runqing Wang,Lili Yang,Sheng Wang,Lin Li,Xiaodan Wang,Zongliu Hou,Li-Wei Liao,Yang Li
标识
DOI:10.1089/rej.2020.2313
摘要
Umbilical cord mesenchymal stem cells (UCMSCs) have been identified as a potentially ideal cell type for use in regenerative therapeutic contexts owing to their excellent paracrine secretory abilities and other desirable properties. Previous work has shown that stem cell-derived exosomes can effectively reduce skin aging, but few studies have specifically focused on the role of UCMSC-derived exosomes in this context. In this study, we isolated exosomes derived from UCMSCs grown in a three-dimensional culture system and explored their ability to modulate the photo-aging of HaCaT keratinocytes. Cell viability and proliferation were assessed using CCK8 assay, whereas wound healing and transwell assays were used to assess cell migratory capabilities. UVB irradiation (60 mJ/cm2) was used to induce photo-aging of HaCaT cells. TUNEL and SA-β-Gal staining were used to explore HaCaT cell apoptosis and senescence, respectively, whereas real-time quantitative PCR was used to assess the expression of relevant genes at the mRNA level. We found that UCMSC-derived exosomes were able to enhance normal HaCaT cell proliferation and migration while also inhibiting UVB-induced damage to these cells. These exosomes also reduced HaCaT cell apoptosis and senescence, increasing collagen type I expression and reducing matrix metalloproteinase (MMP1) expression in photo-aged HaCaT cells. Together, these findings indicate that UCMSC-derived exosomes have the potential to be used therapeutically to suppress skin aging.
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