Preparation of Engineered Extracellular Vesicles Derived from Human Umbilical Cord Mesenchymal Stem Cells with Ultrasonication for Skin Rejuvenation

被引:57
|
作者
Wang, Lixue [1 ,2 ,3 ]
Abhange, Komal K. [4 ]
Wen, Yi [4 ]
Chen, Yundi [4 ]
Xue, Fei [4 ]
Wang, Guosheng [4 ]
Tong, Jinlong [3 ]
Zhu, Chuandong [3 ]
He, Xia [1 ,2 ]
Wan, Yuan [4 ]
机构
[1] Nanjing Med Univ, Affiliated Canc Hosp, Dept Radiotherapy, Jiangsu Canc Hosp, Nanjing 210009, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Affiliated Canc Hosp, Jiangsu Inst Canc Res, Nanjing 210009, Jiangsu, Peoples R China
[3] Nanjing Univ Chinese Med, Hosp Nanjing 2, Dept Radiotherapy, Nanjing 210003, Jiangsu, Peoples R China
[4] SUNY Binghamton, Pq Lab Micro Nano BiomeDx, Dept Biomed Engn, Binghamton, NY 13902 USA
来源
ACS OMEGA | 2019年 / 4卷 / 27期
关键词
DERMAL FIBROBLAST; EXOSOMES; ANGIOGENESIS; MECHANISMS; DRUG; MODULATION; PATHWAY; REPAIR;
D O I
10.1021/acsomega.9b03561
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Extracellular vesicles (EVs) are lipid-bilayer-enclosed vesicles of submicron size that are secreted by various cells. As mediators of intercellular communication, EVs can alter the physiological state of recipient cells by delivering encapsulated proteins and nucleic acids. Incontestably, growing evidence has shown important biological roles and the clinical relevance of EVs. The use of stem cell-derived EVs as a cell-free therapeutic modality for skin treatment has emerged as a promising application in dermatology. However, the moderate isolation efficiency of prevalent ultracentrifugation and low secretion rate make the massive low-cost production of EVs difficult. Here, we report development of engineered EVs (eEV) derived from human umbilical cord mesenchymal stem cells (hucMSCs) for skin treatment. Ultrasonication was used to shear intact hucMSCs for only 1 min, followed by regular centrifugation and filtration for producing nanoscale eEVs. This approach has similar to 20-fold higher yield and similar to 100-fold faster production than that of naturally secreted EVs (nsEV), while the production cost decreased to less than 10%. The eEVs have similar morphology, size distribution, and typical protein markers compared to nsEVs. Moreover, in vitro, both nsEVs and eEVs promote the proliferation and migration of dermal fibroblasts and increase in the expression of collagen, elastin, and fibronectin, whereas the matrix metalloproteinases-1 (MMP-1) and MMP-3 production can be significantly reduced. The wound-healing study in mice showed that both nsEVs and eEVs promote wound recovery in comparison with the controls. In sum, our results indicate that hucMSC-derived eEVs prepared by ultrasonication potentially can be used to increase skin extracellular matrix and enhance skin rejuvenation.
引用
收藏
页码:22638 / 22645
页数:8
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