Adipogenic Differentiation of Human Mesenchymal Stromal Cells Is Down-Regulated by microRNA-369-5p and Up-Regulated by microRNA-371

被引:82
作者
Bork, Simone [1 ,2 ]
Horn, Patrick [1 ]
Castoldi, Mirco [3 ]
Hellwig, Isabelle [1 ]
Ho, Anthony D. [1 ]
Wagner, Wolfgang [1 ,4 ]
机构
[1] Heidelberg Univ, Dept Med 5, Heidelberg, Germany
[2] Heidelberg Acad Sci & Humanities, Heidelberg, Germany
[3] Heidelberg Univ, Dept Pediat Oncol Hematol & Immunol, Heidelberg, Germany
[4] Rhein Westfal TH Aachen, Sch Med, Helmholtz Inst Biomed Engn, D-52074 Aachen, Germany
关键词
HUMAN BONE-MARROW; STEM-CELLS; GENE-EXPRESSION; OSTEOGENIC DIFFERENTIATION; ADIPOCYTE DIFFERENTIATION; ADIPOSE-TISSUE; PROLIFERATION; METHYLATION; CULTURE; HETEROGENEITY;
D O I
10.1002/jcp.22557
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Long-term culture of human mesenchymal stromal cells (MSC) has implications on their proliferation and differentiation potential and we have demonstrated that this is associated with up-regulation of the five microRNAs miR-29c, miR-369-5p, miR-371, miR-499, and let-7f. In this study, we examined the role of these senescence-associated microRNAs for cellular aging and differentiation of MSC. Proliferation was reduced upon transfection with miR-369-5p, miR-371, and miR-499. Adipogenic differentiation was impaired by miR-369-5p whereas it was highly increased by miR-371. This was accompanied by respective gene expression changes of some adipogenic key molecules (adiponectin and fatty acid-binding protein 4 [FABP4]). Furthermore luciferase reporter assay indicated that FABP4 is a direct target of miR-369-5p. Microarray analysis upon adipogenic or osteogenic differentiation revealed down-regulation of several microRNAs albeit miR-369-5p and miR-371 were not affected. Expression of the de novo DNA methyltransferases DNMT3A and DNMT3B was up-regulated by transfection of miR-371 whereas expression of DNMT3A was down-regulated by miR-369-5p. In summary, we identified miR-369-5p and miR-371 as antagonistic up-stream regulators of adipogenic differentiation and this might be indirectly mediated by epigenetic modifications. J. Cell. Physiol. 226: 2226-2234, 2011. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:2226 / 2234
页数:9
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