生物
脂肪生成
转录因子
间充质干细胞
间质细胞
转录组
细胞分化
基因表达谱
调节器
细胞生物学
微阵列分析技术
表型
转录调控
基因表达调控
基因表达
癌症研究
基因
遗传学
作者
Jeroen van de Peppel,Tanja Strini,Julia Tilburg,Hans V. Westerhoff,André J. van Wijnen,Johannes P.T.M. van Leeuwen
标识
DOI:10.1016/j.stemcr.2017.02.018
摘要
Age-related skeletal degeneration in patients with osteoporosis is characterized by decreased bone mass and occurs concomitant with an increase in bone marrow adipocytes. Using microarray expression profiling with high temporal resolution, we identified gene regulatory events in early stages of osteogenic and adipogenic lineage commitment of human mesenchymal stromal cells (hMSCs). Data analysis revealed three distinct phases when cells adopt a committed expression phenotype: initiation of differentiation (0-3 hr, phase I), lineage acquisition (6-24 hr, phase II), and early lineage progression (48-96 hr, phase III). Upstream regulator analysis identified 34 transcription factors (TFs) in phase I with a role in hMSC differentiation. Interestingly, expression levels of identified TFs did not always change and indicate additional post-transcriptional regulatory mechanisms. Functional analysis revealed that forced expression of IRF2 enhances osteogenic differentiation. Thus, IRF2 and other early-responder TFs may control osteogenic cell fate of MSCs and should be considered in mechanistic models that clarify bone-anabolic changes during clinical progression of osteoporosis.
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