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vol.2 número3DISEÑO DE UN ESPACIO SENSORIAL PARA LA ESTIMULACIÓN TEMPRANA DE NIÑOS CON MULTIDÉFICITMECHANICAL CHARACTERIZATION OF CELLS AND TISSUES AT THE MICRO SCALE índice de autoresíndice de assuntospesquisa de artigos
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Revista Ingeniería Biomédica

versão impressa ISSN 1909-9762

Resumo

GARCIA QUIROZ, Felipe et al. ISOLATION OF HUMAN BONE MARROW MESENCHYMAL STEM CELLS AND EVALUATION OF THEIR OSTEOGENIC POTENTIAL. Rev. ing. biomed. [online]. 2008, vol.2, n.3, pp.48-55. ISSN 1909-9762.

Human bone marrow mesenchymal stem cells (hBMSCs) comprise a cell population capable of self-renewal and multilineage differentiation commonly isolated from bone marrow aspirates of large bones. Their osteogenic potential has been extensively exploited for the biological evaluation of scaffolds or biomaterials with applications in bone tissue engineering. This work aimed to isolate hBMSCs from femoral heads of patients undergoing total hip arthroplasty and to evaluate their osteogenic potential. Briefly, the trabecular bone was extracted and mechanically disaggregated; the released cells were cultured and non-adherent cells were removed after 4 days. The osteogenic potential was evaluated at the fifth passage after 14 and 20 days of induction, comparing cultures with and without osteogenic supplements, via Alizarin red staining and the quantification of the gene expression levels of the osteogenic markers collagen type I, osteonectin and bone sialoprotein through real-time RT-PCR. The obtained hBMSCs presented a stable undifferentiated phenotype after prolonged cell culture, matrix mineralization capabilities and expression of osteoblast phenotype upon osteogenic induction. The three markers were up-regulated in cultures under osteogenic conditions and 2 fold differences in their expression levels were found to be significant for the onset of the differentiation process. The obtained hBMSCs may have applications on the in vitro evaluation of the osteoinductivity of different biomaterials, bioactive molecules or tissue engineering scaffolds.

Palavras-chave : Cell differentiation; Mesenchymal stem cells; Mineralization; Osteogenic markers; Tissue engineering.

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