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PDGF-BB initiates vascular smooth muscle-like phenotype differentiation of human bone marrow mesenchymal stem cells in vitro / 中华整形外科杂志
Article em Zh | WPRIM | ID: wpr-314219
Biblioteca responsável: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the feasibility of human bone marrow mesenchymal stem cells (hBMSCs) in vitro differentiation into vascular smooth muscle cells with induction of platelet-derived growth Factor BB (PDGF-BB).</p><p><b>METHODS</b>Bone marrow mesenchymal stem cells of adult healthy donors were separated from iliac crest aspiration and expanded in DMEM-LG medium. Cells at passage 1 were transferred to EGM-2 medium containing PDGF-BB (20 ng/ml) and cultured for 14 days. The expression of SM alpha-actin, SM calponin, SMMHC and SM 22alpha were detected by immunofluorescence and observed with fluorescence microscope. mRNA expression of SMalpha-actin, SM calponin, SMMHC as well as SM 22alpha was analyzed by RT-PCR. The method of Western-Blot was applied to determine protein expression of SM 22alpha. Cells with induction were observed for the expression of SM alpha-actin,SM calponin,SMMHC by FACs analysis.</p><p><b>RESULTS</b>With the induction of PDGF-BB, the morphology of cells changed to a spindle fibroblastic appearance. By fluorescence microscope observation, expression of SM alpha-actin, SM calponin and SMMHC was found intracellularly in PDGF-BB treated hBMSCs at 14 days. Western-Blot detection confirmed SM 22alpha expression by 14 days induction. RT-PCR of characteristic vascular smooth muscle cells related genes, such as SM alpha-actin, SM calponin, SMMHC and SM 22alpha revealed differentiation of vascular smooth muscle cells phenotype in monolayer culture upon stimulation with PDGF-BB for 14 days. The positive expression of SM alpha-actin, SM calponin and SMMHC in induced cells was significantly higher than that in non-induced cells (P < 0.05, n=3).</p><p><b>CONCLUSION</b>These results suggested hBMSCs could be differentiated into vascular smooth muscle cell phenotype with PDGF-BB induction in vitro.</p>
Assuntos
Texto completo: 1 Índice: WPRIM Assunto principal: Farmacologia / Fator de Crescimento Derivado de Plaquetas / Células da Medula Óssea / Diferenciação Celular / Células Cultivadas / Proteínas Proto-Oncogênicas c-sis / Biologia Celular / Engenharia Tecidual / Células-Tronco Mesenquimais / Métodos Limite: Adult / Humans Idioma: Zh Revista: Chinese Journal of Plastic Surgery Ano de publicação: 2007 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Assunto principal: Farmacologia / Fator de Crescimento Derivado de Plaquetas / Células da Medula Óssea / Diferenciação Celular / Células Cultivadas / Proteínas Proto-Oncogênicas c-sis / Biologia Celular / Engenharia Tecidual / Células-Tronco Mesenquimais / Métodos Limite: Adult / Humans Idioma: Zh Revista: Chinese Journal of Plastic Surgery Ano de publicação: 2007 Tipo de documento: Article