诱导多能干细胞
细胞培养
间充质干细胞
同源盒蛋白纳米
细胞
成纤维细胞
成纤维细胞生长因子
成体干细胞
重编程
胚状体
SOX2
再生医学
作者
Chunhui Xu,Jianjie Jiang,Virginie Sottile,Jim McWhir,Jane S. Lebkowski,Melissa K. Carpenter
出处
期刊:Stem Cells
[Wiley]
日期:2004-11-01
卷期号:22 (6): 972-980
被引量:175
标识
DOI:10.1634/stemcells.22-6-972
摘要
Human embryonic stem cells (hESCs) have the potential to generate multiple cell types and hold promise for future therapeutic applications. Although undifferentiated hESCs can proliferate indefinitely, hESC derivatives significantly downregulate telomerase and have limited replication potential. In this study we examine whether the replicative lifespan of hESC derivatives can be extended by ectopic expression of human telomerase reverse transcriptase (hTERT), the catalytic component of the telomerase complex. To this end, we have derived HEF1 cells, a fibroblast-like cell type, differentiated from hESCs. Infection of HEF1 cells with a retrovirus expressing hTERT extends their replicative capacity, resulting in immortal human HEF1-hTERT cells. HEF1-hTERT cells can be used to produce conditioned medium (CM) capable of supporting hESC growth under feeder-free conditions. Cultures maintained in HEF1-CM show characteristics similar to mouse embryonic fibroblast CM control cultures, including morphology, surface marker and transcription factor expression, telomerase activity, differentiation, and karyotypic stability. In addition, HEF1-hTERT cells have the capacity to differentiate into cells of the osteogenic lineage. These results suggest that immortalized cell lines can be generated from hESCs and that cells derived from hESCs can be used to support their own growth, creating a genotypically homogeneous system for the culture of hESCs.
科研通智能强力驱动
Strongly Powered by AbleSci AI