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Receptor-targeted, magneto-mechanical stimulation of osteogenic differentiation of human bone marrow-derived mesenchymal stem cells

Receptor-targeted, magneto-mechanical stimulation of osteogenic differentiation of human bone marrow-derived mesenchymal stem cells Thumbnail


Abstract

Mechanical cues are employed to promote stem cell differentiation and functional tissue formation in tissue engineering and regenerative medicine. We have developed a Magnetic Force Bioreactor (MFB) that delivers highly targeted local forces to cells at a pico-newton level, utilizing magnetic micro- and nano-particles to target cell surface receptors. In this study, we investigated the effects of magnetically targeting and actuating specific two mechanical-sensitive cell membrane receptors-platelet-derived growth factor receptor a (PDGFRa) and integrin a?ß3. It was found that a higher mineral-to-matrix ratio was obtained after three weeks of magneto-mechanical stimulation coupled with osteogenic medium culture by initially targeting PDGFRa compared with targeting integrin a?ß3 and non-treated controls. Moreover, different initiation sites caused a differentiated response profile when using a 2-day-lagged magneto-mechanical stimulation over culture periods of 7 and 12 days). However, both resulted in statistically higher osteogenic marker genes expression compared with immediate magneto-mechanical stimulation. These results provide insights into important parameters for designing appropriate protocols for ex vivo induced bone formation via magneto-mechanical actuation.

Acceptance Date Sep 5, 2013
Publication Date Sep 23, 2013
Journal International Journal of Molecular Sciences
Print ISSN 1661-6596
Publisher MDPI
Pages 19276 - 19293
DOI https://doi.org/10.3390/ijms140919276
Keywords bone marrow cells, cell differentiation, cell membrane, cells, cultured, humans, integrin alphavbeta3, magnetic fields, magnetite nanoparticles, mechanotransduction, cellular, mesenchymal stromal cells, oligopeptides, osteogenesis, receptor, platelet-der
Publisher URL http://dx.doi.org/10.3390/ijms140919276

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