表观遗传学
间充质干细胞
神经发生的表观遗传调控
生物
小RNA
DNA甲基化
细胞生物学
祖细胞
干细胞
组蛋白
细胞命运测定
细胞分化
转录因子
基因表达
遗传学
基因
染色质重塑
作者
Gang Fu,Aishu Ren,Yu Qiu,Yi Zhang
出处
期刊:Current stem cell research & therapy
[Bentham Science]
日期:2016-03-03
卷期号:11 (3): 235-246
被引量:24
标识
DOI:10.2174/1574888x10666150528153313
摘要
Mesenchymal stem cells (MSCs) are multipotent progenitors that have the abilities of self-renewal and multiple direction differentiation. The osteogenic potential of MSCs holds great promise for bone defect repair and bone disease treatment. For a long time studies about osteogenic differentiation of MSCs have emphasized on the effect of extrinsic regulators and the corresponding transcription factors controlling cell fate. In fact, cell fate is determined by lineage specific gene expression that is regulated more specifically by epigenetic mechanism. Over the last decade, some progress has been made in epigenetic researches of MSCs osteogenic differentiation. DNA methylation, histone modifications and microRNA (miRNA) are all verified important mechanisms regulating MSCs differentiation. Epigenetic regulation might provide novel treatment targets for promoting bone formation. In this review, we will summarize the recent advance about the epigenetic mechanism that control MSCs commitment to osteoblasts and the potential clinical application of MSCs epigenetics in future.
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