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Magnetic-based multi-layer microparticles for endothelial progenitor cell isolation enrichment and detachment

机译:基于磁性的多层微粒用于内皮祖细胞的分离富集和分离

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摘要

Although endothelial progenitor cells (EPCs) are useful in many applications including cell-based therapies, their use is still limited due to issues associated with cell culture techniques like a low isolation efficiency, use of harmful proteolytic enzymes in cell cultures, and difficulty in ex vivo expansion. Here, we report a tool to simultaneously isolate, enrich, and detach EPCs without the use of harmful chemicals. In particular, we developed magnetic-based multi-layer microparticles (MLMPs) that (1) magnetically isolate EPCs via anti-CD34 antibodies to avoid the use of Ficoll and harsh shear forces; (2) provide a 3D surface for cell attachment and growth; (3) produce sequential releases of growth factors (GFs) to enrich ex vivo expansion of cells; and (4) detach cells without using trypsin. MLMPs were successful in isolating EPCs from a cell suspension and provided a sequential release of GFs for EPC proliferation and differentiation. The cell enrichment profiles indicated steady cell growth on MLMPs in comparison to commercial Cytodex3 microbeads. Further, the cells were detached from MLMPs by lowering the temperature below 32 °C. Results indicate that the MLMPs have potential to be an effective tool towards efficient cell isolation, fast expansion, and non-chemical detachment.
机译:尽管内皮祖细胞(EPC)在包括基于细胞的疗法在内的许多应用中很有用,但由于与细胞培养技术相关的问题,例如分离效率低,在细胞培养中使用有害蛋白水解酶以及难以进行分离等原因,其使用仍然受到限制。体内扩增。在这里,我们报告了一种无需使用有害化学物质即可同时隔离,富集和分离EPC的工具。特别是,我们开发了基于磁性的多层微粒(MLMP),该微粒(1)通过抗CD34抗体磁性分离EPC,以避免使用Ficoll和苛刻的剪切力; (2)为细胞附着和生长提供3D表面; (3)产生生长因子(GFs)的连续释放,以丰富细胞的离体扩增; (4)不使用胰蛋白酶分离细胞。 MLMP成功地从细胞悬液中分离了EPC,并为EPC的增殖和分化提供了GF的顺序释放。与商业Cytodex3微珠相比,细胞富集曲线表明MLMP上的细胞稳定生长。此外,通过将温度降低到32℃以下将细胞与MLMP分离。结果表明,MLMP具有成为有效分离细胞,快速扩增和非化学分离的有效工具的潜力。

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