| Literature DB >> 34793116 |
Xianyun Wang1,2,3,4,5, Shiqi Hu4,5, Junlang Li4,5, Dashuai Zhu4,5, Zhenzhen Wang4,5, Jhon Cores4,5, Ke Cheng4,5, Gang Liu2,3, Ke Huang4,5.
Abstract
Mesenchymal stem cells (MSCs) repair injured tissues mainly through their paracrine actions. One of the important paracrine components of MSC secretomes is the extracellular vesicle (EV). The therapeutic potential of MSC-EVs has been established in various cardiac injury preclinical models. However, the large-scale production of EVs remains a challenge. We sought to develop a scale-up friendly method to generate a large number of therapeutic nanovesicles from MSCs by extrusion. Those extruded nanovesicles (NVs) are miniature versions of MSCs in terms of surface marker expression. The yield of NVs is 20-fold more than that of EVs. In vitro, cell-based assays demonstrated the myocardial protective effects and therapeutic potential of NVs. Intramyocardial delivery of NVs in the injured heart after ischemia-reperfusion led to a reduction in scar sizes and preservation of cardiac functions. Such therapeutic benefits are similar to those injected with natural EVs from the same MSC parental cells. In addition, NV therapy promoted angiogenesis and proliferation of cardiomyocytes in the post-injury heart. In summary, extrusion is a highly efficient method to generate a large quantity of therapeutic NVs that can potentially replace extracellular vesicles in regenerative medicine applications.Entities:
Keywords: extracellular vesicles; extrusion; ischemia reperfusion injury; mesenchymal stem cell; nanovesicles
Mesh:
Year: 2021 PMID: 34793116 DOI: 10.1021/acsami.1c08044
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229