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Hsa-miR-654-5p regulates osteogenic differentiation of human bone marrow mesenchymal stem cells by repressing bone morphogenetic protein 2 / 南方医科大学学报
Journal of Southern Medical University ; (12): 291-295, 2012.
Artículo en Chino | WPRIM | ID: wpr-267614
ABSTRACT
<p><b>OBJECTIVE</b>To study the effect of hsa-miR-654-5p in repressing bone morphogenetic protein 2 (BMP2) mRNA and protein in human bone marrow mesenchymal stem cells (hBMSCs), and explore its regulatory role in osteogenic differentiation of hBMSCs.</p><p><b>METHODS</b>hBMSCs in the 4th passage were cultured for 16 h and transfected with hsa-miR-654-5p followed by further culture for 48 h. qRT-PCR and Western blotting were performed to detect the expressions of BMP2 mRNA and protein. Dual-luciferase?reporter gene assay was employed to examine the repression of the BMP2 gene.</p><p><b>RESULTS</b>BMP2 mRNA and protein expressions were significantly down-regulated in hBMSCs with hsa-miR-654-5p overexpression. Dualluci-ferase reporter gene assay indicated that the predicted target site of BMP2 was repressed directly by hsa-miR-654-5p, but this repression did not occur at the mutant predicted target site of BMP2.</p><p><b>CONCLUSION</b>hsa-miR-654-5p can directly repress the mRNA and protein expressions of BMP2 by binding to a specific target site. The changes in hsa-miR-654-5p can play an important role in osteogenic differentiation regulation of hBMSCs.</p>
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Osteoblastos / Osteogénesis / ARN Mensajero / Células de la Médula Ósea / Transfección / Diferenciación Celular / Células Cultivadas / Regulación de la Expresión Génica / Biología Celular / MicroARNs Límite: Humanos Idioma: Chino Revista: Journal of Southern Medical University Año: 2012 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Osteoblastos / Osteogénesis / ARN Mensajero / Células de la Médula Ósea / Transfección / Diferenciación Celular / Células Cultivadas / Regulación de la Expresión Génica / Biología Celular / MicroARNs Límite: Humanos Idioma: Chino Revista: Journal of Southern Medical University Año: 2012 Tipo del documento: Artículo