Wang Lixue, Abhange Komal K, Wen Yi, Chen Yundi, Xue Fei, Wang Guosheng, Tong Jinlong, Zhu Chuandong, He Xia, Wan Yuan
Department of Radiotherapy, Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research, The Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, Jiangsu 210009, China.
Department of Radiotherapy, The Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, Jiangsu 210003, China.
ACS Omega. 2019 Dec 19;4(27):22638-22645. doi: 10.1021/acsomega.9b03561. eCollection 2019 Dec 31.
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 ∼20-fold higher yield and ∼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.
细胞外囊泡(EVs)是由各种细胞分泌的亚微米大小的脂质双层包裹的囊泡。作为细胞间通讯的介质,EVs可以通过传递封装的蛋白质和核酸来改变受体细胞的生理状态。无可争议的是,越来越多的证据表明EVs具有重要的生物学作用和临床相关性。使用干细胞衍生的EVs作为一种无细胞治疗方式用于皮肤治疗已成为皮肤病学中一个有前景的应用。然而,普遍使用的超速离心法分离效率中等且分泌率低,使得大规模低成本生产EVs变得困难。在此,我们报告了源自人脐带间充质干细胞(hucMSCs)的工程化EVs(eEVs)用于皮肤治疗的研发。使用超声处理仅剪切完整的hucMSCs 1分钟,然后进行常规离心和过滤以产生纳米级eEVs。这种方法的产量比天然分泌的EVs(nsEVs)高约20倍,生产速度快约100倍,同时生产成本降低至不到10%。与nsEVs相比,eEVs具有相似的形态、大小分布和典型的蛋白质标志物。此外,在体外,nsEVs和eEVs都能促进真皮成纤维细胞的增殖和迁移,并增加胶原蛋白、弹性蛋白和纤连蛋白的表达,而基质金属蛋白酶-1(MMP-1)和MMP-3的产生可显著减少。小鼠伤口愈合研究表明,与对照组相比,nsEVs和eEVs都能促进伤口恢复。总之,我们的结果表明,通过超声处理制备的hucMSC衍生的eEVs可能可用于增加皮肤细胞外基质并促进皮肤年轻化。