CECS/AFM, I-STEM, 91100 Corbeil-Essonnes, France.
INSERM/ UEVE UMR 861, Paris Saclay Univ I-STEM, 91100 Corbeil-Essonnes, France.
Cells. 2019 Nov 26;8(12):1523. doi: 10.3390/cells8121523.
Substantial variations in differentiation properties have been reported among human pluripotent cell lines (hPSC), which could affect their utility and clinical safety. We characterized the variable osteogenic capacity observed between different human pluripotent stem cell lines. By focusing on the miRNA expression profile, we demonstrated that the osteogenic differentiation propensity of human pluripotent stem cell lines could be associated with the methylation status and the expression of miRNAs from the imprinted locus. More specifically, quantitative analysis of the expression of six different miRNAs of that locus prospectively identified human embryonic stem cells and human-induced pluripotent stem cells with differential osteogenic differentiation capacities. At the molecular and functional levels, we showed that these miRNAs modulated the expression of the activin receptor type 2B and the downstream signal transduction, which impacted osteogenesis. In conclusion, miRNAs of the imprinted locus appear to have both a predictive value and a functional impact in determining the osteogenic fate of human pluripotent stem cells.
已报道人类多能干细胞系(hPSC)之间存在分化特性的显著差异,这可能影响它们的应用和临床安全性。我们描述了不同人类多能干细胞系之间观察到的可变成骨能力。通过关注 miRNA 表达谱,我们证明人类多能干细胞系的成骨分化倾向可能与印记基因座的甲基化状态和 miRNA 的表达相关。更具体地说,对该基因座中六个不同 miRNA 的定量分析,前瞻性地鉴定了具有不同成骨分化能力的人胚胎干细胞和人诱导多能干细胞。在分子和功能水平上,我们表明这些 miRNA 调节了激活素受体 2B 的表达及其下游信号转导,从而影响成骨。总之,印记基因座的 miRNA 似乎在预测人类多能干细胞的成骨命运方面具有预测价值和功能影响。