Xynos I D, Edgar A J, Buttery L D, Hench L L, Polak J M
Department of Histochemistry, Imperial College School of Science, Technology and Medicine, London, W12 ONN, United Kingdom.
Biochem Biophys Res Commun. 2000 Sep 24;276(2):461-5. doi: 10.1006/bbrc.2000.3503.
Bioglass 45S5 is an osteoproductive material, which resorbs by releasing its constitutive ions into solution. Treatment with the ionic products of Bioglass 45S5 dissolution in DMEM for 4 days increased human osteoblast proliferation to 155% of control. Two days after treatment, differential gene expression was analyzed by cDNA microarrays. Expression of a potent osteoblast mitogenic growth factor, insulin-like growth factor II (IGF-II), was increased to 290%. Additionally, there was a 168% increase in the concentration of unbound IGF-II protein in the conditioned media of treated osteoblasts. Expression levels of IGFBP-3, an IGF-II carrier protein, metalloproteinase-2 and cathepsin-D were also increased to 200, 340, and 310% of control levels, respectively. Metalloproteinase-2 and cathepsin-D are proteases that cleave IGF-II from its carrier proteins, resulting in the release of the unbound biologically active IGF-II. We suggest that the stimulatory effect of the ionic products of Bioglass 45S5 dissolution on osteoblast proliferation may be mediated by IGF-II.
生物活性玻璃45S5是一种具有成骨作用的材料,它通过将其组成离子释放到溶液中而发生吸收。用生物活性玻璃45S5在DMEM中溶解的离子产物处理4天,可使人类成骨细胞增殖增加至对照的155%。处理两天后,通过cDNA微阵列分析差异基因表达。一种强效的成骨细胞有丝分裂生长因子,即胰岛素样生长因子II(IGF-II)的表达增加至290%。此外,处理后的成骨细胞条件培养基中未结合的IGF-II蛋白浓度增加了168%。IGF-II载体蛋白IGFBP-3、金属蛋白酶-2和组织蛋白酶-D的表达水平也分别增加至对照水平的200%、340%和310%。金属蛋白酶-2和组织蛋白酶-D是将IGF-II从其载体蛋白上切割下来的蛋白酶,导致未结合的生物活性IGF-II释放。我们认为,生物活性玻璃45S5溶解的离子产物对成骨细胞增殖的刺激作用可能是由IGF-II介导的。