Journal of Biomedical Science · 2010 · 100 citations · 41 references
Life SciencesCell BiologyDevelopmental BiologyCell DifferentiationGene ExpressionStem Cell BiologyEmbryonic Stem CellsMesenchymal DifferentiationMesodermal DifferentiationSkeletal DevelopmentStem Cell DifferentiationCell Differentiation PotentialDifferentiationDifferentiation PotentialEmbryonic Stem Cell DifferentiationEmbryonic Stem Cell Epigenetic RegulationHuman Embryonic Stem CellsPrimary Cell CultureTelomerase Reverse Transcriptase
To overcome loss of stem-like properties and spontaneous differentiation those hinder the expansion and application of human mesenchymal stem cells (hMSCs), we have clonally isolated permanent and stable human MSC lines by ectopic overexpression of primary cell cultures of hMSCs with HPV 16 E6E7 and human telomerase reverse transcriptase (hTERT) genes. These cells were found to have a differentiation potential far beyond the ordinary hMSCs. They expressed trophoectoderm and germline specific markers upon differentiation with BMP4 and retinoic acid, respectively. Furthermore, they displayed higher osteogenic and neural differentiation efficiency than primary hMSCs or hMSCs expressed HPV16 E6E7 alone with a decrease in methylation level as proven by a global CpG island methylation profile analysis. Notably, the demethylated CpG islands were highly associated with development and differentiation associated genes. Principal component analysis further pointed out the expression profile of the cells converged toward embryonic stem cells. These data demonstrate these cells not only are a useful tool for the studies of cell differentiation both for the mesenchymal and neurogenic lineages, but also provide a valuable source of cells for cell therapy studies in animal models of skeletal and neurological disorders.
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