间充质干细胞
生物过程
克隆(Java方法)
间质细胞
生物
细胞生物学
细胞培养
免疫分型
转基因
原电池
细胞疗法
转导(生物物理学)
计算生物学
干细胞
转基因生物
再生医学
细胞
细胞生长
细胞分化
多能干细胞
转录组
基因
电池类型
胚胎干细胞
自分泌信号
免疫学
组织工程
功能基因组学
电穿孔
遗传学
作者
Janina Burk,Heidrun Holland,Anne F. Lauermann,Tobias May,Philipp Siedlaczek,Verena Charwat,Cornelia Kasper
摘要
Abstract Multipotent mesenchymal stromal cells (MSC) and MSC‐derived products have emerged as promising therapeutic tools. To fully exploit their potential, further mechanistic studies are still necessary and bioprocessing needs to be optimized, which requires an abundant supply of functional MSC for basic research. To address this need, here we used a novel technology to establish a human adipose‐derived MSC line with functional characteristics representative of primary MSC. Primary MSC were isolated and subjected to lentiviral transduction with a library of expansion genes. Clonal cell lines were generated and evaluated on the basis of their morphology, immunophenotype, and proliferation potential. One clone (K5 iMSC) was then selected for further characterization. This clone had integrated a specific transgene combination including genes involved in stemness and maintenance of adult stem cells. Favorably, the K5 iMSC showed cell characteristics resembling juvenile MSC, as they displayed a shorter cell length and enhanced migration and proliferation compared with the non‐immortalized original primary MSC ( p < 0.05). Still, their immunophenotype and differentiation potential corresponded to the original primary MSC and the MSC definition criteria, and cytogenetic analyses revealed no clonal aberrations. We conclude that the technology used is applicable to generate functional MSC lines for basic research and possible future bioprocessing applications.
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