Garcia Sergio G, Sanroque-Muñoz Marta, Clos-Sansalvador Marta, Font-Morón Miriam, Monguió-Tortajada Marta, Borràs Francesc E, Franquesa Marcella
REMAR-IGTP Group, Health Science research Institute Germans Trias i Pujol (IGTP), Can Ruti Campus, Badalona 08916, Spain.
Department of Cell Biology, Physiology and Immunology, Universitat Autònoma de Barcelona (UAB), Bellaterra 08193, Spain.
Extracell Vesicles Circ Nucl Acids. 2024 May 14;5(2):201-220. doi: 10.20517/evcna.2023.76. eCollection 2024.
Mesenchymal stromal cell-derived extracellular vesicles (MSC-EVs) have been reported to hold great potential as cell-free therapies due to their low immunogenicity and minimal toxicity. However, the large doses of MSC-EVs that are required for their clinical application highlight the urgency of finding a large-scale system for MSC-EV manufacture. In this study, we aimed to set up a hollow fiber bioreactor system for the continuous homogenous production of functional and high-quality MSC-EVs. MSC lines from two donors were immortalized (iMSC) and inoculated into hollow fiber bioreactors. Throughout 4 weeks, conditioned medium was daily harvested. iMSC-EVs were purified and characterized for content, immunophenotype, size, and functionality and compared to 2D cultured iMSC. The iMSC inoculated into the bioreactor remained viable during the whole culture period, and they maintained their MSC phenotype at the end of EV production. Our results showed that the bioreactor system allows to obtain 3D-cultured iMSC-derived EVs (3D-EVs) that are comparable to flask (2D)-cultured iMSC-derived EVs (2D-EVs) in terms of protein and lipid content, size, and phenotype. We also confirm that 3D-derived EVs exhibit comparable functionality to 2D-EVs, showing pro-angiogenic potential in a dose-dependent manner. These findings suggest that setting up a hollow fiber bioreactor system inoculating immortalized MSC lines facilitates the large-scale, functional, and high-quality production of iMSC-EVs. Our results emphasize the great potential of this production methodology to standardize EV production in the pursuit of clinical applications.
间充质基质细胞衍生的细胞外囊泡(MSC-EVs)因其低免疫原性和最小毒性,作为无细胞疗法具有巨大潜力。然而,其临床应用所需的大剂量MSC-EVs凸显了寻找大规模MSC-EV生产系统的紧迫性。在本研究中,我们旨在建立一个中空纤维生物反应器系统,用于连续均匀地生产功能性和高质量的MSC-EVs。将来自两名供体的间充质干细胞系进行永生化处理(iMSC),并接种到中空纤维生物反应器中。在整个4周期间,每天收集条件培养基。对iMSC-EVs进行纯化,并对其含量、免疫表型、大小和功能进行表征,并与二维培养的iMSC进行比较。接种到生物反应器中的iMSC在整个培养期间保持存活,并在EV生产结束时维持其MSC表型。我们的结果表明,该生物反应器系统能够获得在蛋白质和脂质含量、大小和表型方面与培养瓶(二维)培养的iMSC衍生的EVs(2D-EVs)相当的三维培养的iMSC衍生的EVs(3D-EVs)。我们还证实,3D衍生的EVs与2D-EVs具有相当的功能,以剂量依赖的方式显示出促血管生成潜力。这些发现表明,建立一个接种永生化MSC系的中空纤维生物反应器系统有助于大规模、功能性和高质量地生产iMSC-EVs。我们的结果强调了这种生产方法在追求临床应用中标准化EV生产的巨大潜力。