| Literature DB >> 24928442 |
Supyong Hwang1, Seul-Ki Park2, Ha Yeon Lee1, Seong Who Kim3, Jung Shin Lee4, Eun Kyung Choi5, Dalsan You6, Choung-Soo Kim7, Nayoung Suh8.
Abstract
Human mesenchymal stem cells (hMSCs) have self-renewal and differentiation capabilities but the regulatory mechanisms of MSC fate determination remain poorly understood. Here, we aimed to identify microRNAs enriched in hMSCs that modulate differentiation commitments. Microarray analysis revealed that miR-140-5p is commonly enriched in undifferentiated hMSCs from various tissue sources. Moreover, bioinformatic analysis and luciferase reporter assay validated that miR-140-5p directly represses bone morphogenic protein 2 (BMP2). Furthermore, blocking miR-140-5p in hMSCs increased the expression of BMP signaling components and critical regulators of osteogenic differentiation. We propose that miR-140-5p functionally inhibits osteogenic lineage commitment in undifferentiated hMSCs.Entities:
Keywords: Bone morphogenic protein 2; Differentiation; Human mesenchymal stem cells; Osteogenic lineage commitment; miR-140-5p
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Year: 2014 PMID: 24928442 DOI: 10.1016/j.febslet.2014.05.048
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124