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Effect of Titanium Surface Roughness on MG63 Oseteblast-Like Cell Differentiation and Response to 1,25-Dihydroxyvitamin D3

机译:钛表面粗糙度对mG63成纤维细胞样细胞分化及对1,25-二羟维生素D3反应的影响

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Surface roughness has been shown to affect cell differentiation and local factor production of MG63 osteoblast-like cells. The first specific aim of this study was to examine whether surface roughness alters the response of MG63 cells to circulating systemic hormones like 1,25-(OH)2D3 (1,25). Unalloyed titanium (Ti) disks were pretreated with HF/HNO3 (PT) and then machined and acid-etched (MA). Ti disks were also sandblasted (SB), sandblasted and acid- etched (CA), or plasma-sprayed with Ti particles (PS). The surfaces, from smoothest to roughest, were: PT, MA, CA, SB, and PS. MG63 cells were cultured to confluence on standard tissue culture polystyrene (plastic) or the Ti surfaces and then treated for 24 hours with either 10(exp -8)M or 10(exp -7)M 1,25-(OH) 2D3 or vehicle (control). Cellular response was measured by assaying cell number, cell layer alkaline phosphatase specific activity, and the production of osteocalcin, latent transforming growth factor-beta (LTGFbeta), and prostaglandin E2 (PGE2). Alkaline phosphatase specific activity was affected by surface roughness; as the surface became rougher, the cultures showed a significant increase in alkaline phosphatase specific activity. Addition of 1, 25-(OH)2D3 to the cultures caused a dose-dependent stimulation of alkaline phosphatase specific activity which was synergistic with the effect caused by surface roughness alone. 1,25-(OH)2D3 also caused a synergistic increase in osteocalcin production, as well as local factor (LTGFbeta and PGE2) production, on the rougher CA, SB and PS surfaces, but had no effect on the cultures grown on the smoother surfaces. The inhibitory effect of surface roughness on cell number was not affected by 1,25-(OH)2D3, except on the SB surface.

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