Abstract
Mechanical stimulation influences stem cell differentiation and may therefore provide improved lineage specification control for clinical applications. Low-frequency oscillatory mechanical stimulation (0.01 Hz) has recently been shown to suppress adipogenic differentiation of mesenchymal stem cells, indicating that the range of effective stimulation frequencies is not limited to those associated with locomotion, circulation, and respiration. We hypothesized that low-frequency mechanical stimulation (0.01 Hz) can also promote osteogenic cell differentiation of myoblastic C2C12 cells in combination with BMP-2. Results indicate that low-frequency mechanical stimulation can significantly enhance osteogenic gene expression, provided that differentiation is initiated by a priming period involving BMP-2 alone. Subsequent application of low-frequency mechanical stimulation appears to act synergistically with continued BMP-2 exposure to promote osteogenic differentiation of C2C12 cells and can even partially compensate for the removal of BMP-2. These effects may be mediated by the ERK and Wnt signalling pathways. Osteogenic induction of C2C12 cells by low-frequency mechanical stimulation is therefore critically dependent upon previous exposure to growth factors, and the timing of superimposed BMP-2 and mechanical stimuli can sensitively influence osteogenesis. These insights may provide a technically simple means for control of stem cell differentiation in cell-based therapies, particularly for the enhancement of differentiation toward desired lineages.
Highlights
Stem cell differentiation to bone is important to growth, development, and tissue maintenance; understanding of the cellular processes underlying osteogenesis is necessary for the development of cell-based therapies
C2C12 cells cultured in osteogenic medium for 6, 24, and 48 hours began differentiating towards an osteoblast-like phenotype. qPCR analysis indicated significant changes in Runx2, Osx, alkaline phosphatase (Alp), Col1a1, Osteopontin, and bone Gla protein after 48 hours of induction with bone morphogenetic proteins (BMPs)-2 (Figure 2)
Previous studies have shown that BMP-2 induces osteogenesis through upregulation of the key transcription factors Runx2 [22] and Osx (Osterix) [23, 24]
Summary
Stem cell differentiation to bone is important to growth, development, and tissue maintenance; understanding of the cellular processes underlying osteogenesis is necessary for the development of cell-based therapies. Growth factor stimulation of stem cells is an initiating event which activates transcription factors that subsequently drive lineage specification. Bone-inducing agents [1] called bone morphogenetic proteins (BMPs) [2, 3] comprise a superfamily of growth factors that drive bone differentiation and adult bone maintenance. Among the BMP superfamily, BMP-2 is known to have a critical role in inducing osteogenic differentiation of mesenchymal stem cells [4]. It has been established that the time course and duration of growth factor stimulation can have important effects on differentiation [6], and BMP-2 efficacy is dose dependent [7]
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