4.5 Article

MicroRNA expression profile during adipogenic differentiation in mouse embryonic stem cells

期刊

PHYSIOLOGICAL GENOMICS
卷 43, 期 10, 页码 611-620

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/physiolgenomics.00116.2010

关键词

CGR8 cells; adipogenesis; microRNA microarray

资金

  1. German Academic Exchange Service
  2. German National Academic Foundation
  3. German Research Council [DFG NA418]

向作者/读者索取更多资源

Knelangen JM, van der Hoek MB, Kong WC, Owens JA, Fischer B, Navarrete Santos A. MicroRNA expression profile during adipogenic differentiation in mouse embryonic stem cells. Physiol Genomics 43: 611-620, 2011. First published January 18, 2011; doi:10.1152/physiolgenomics.00116.2010.-Pluripotent embryonic stem cells (ESC) have the potential to differentiate into any cell type of the three germ layers. Differentiation processes depend on genetic and epigenetic factors. The guidance of cell fate determination by microRNAs (miRs) seems important for embryonic development and cell lineage decisions. MiRs are short, single-stranded, noncoding RNA molecules that regulate through posttranscriptional modulation, a subset of target genes involved in cell differentiation and specific cell function. We have used microarray profiling of miRs in the mouse embryonic stem cell line CGR8. Comparison of the miR profiles of undifferentiated stem cells with mesodermal progenitors cells (day 5), preadipocytes (day 10), and adipocytes (day 21) showed that the expression level of 129 miRs changed (twofold) during adipogenic differentiation. We identified 10 clusters of differentially expressed miRs, which contain putative markers and regulators of mesodermal differentiation and cell fate determination into adipocytes. Notably, the adipocyte-specific miRs 143 and 103 were upregulated from day 10 onward. We have therefore demonstrated and characterized the dynamic profile of miR expression during murine adipogenic differentiation in vitro, including the initial differentiation from ESC via mesenchymal progenitors up to adipocytes. Our findings and experimental approach provide a suitable system to directly interrogate the role of miRs during adipogenic differentiation of embryonic stem cells.

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