Mori K, Shioi A, Jono S, Nishizawa Y, Morii H
Second Department of Internal Medicine, Osaka City University Medical School, Osaka, Japan.
FEBS Lett. 1998 Aug 14;433(1-2):19-22. doi: 10.1016/s0014-5793(98)00870-9.
To investigate the role of matrix Gla protein (MGP), which can bind mineral ions through gamma-carboxylated glutamic acid residues, in vascular calcification, we examined the expression of MGP in an in vitro calcification model by using bovine vascular smooth muscle cells (BVSMC). The expression of MGP mRNA was decreased during BVSMC calcification and its levels were inversely correlated with the quantities of BVSMC calcification. MGP mRNA expression was restored to the level of uncalcified control by inhibiting BVSMC calcification with bisphosphonates. These data suggest that the expression of MGP gene is modulated in the development of vascular calcification.
为研究可通过γ-羧化谷氨酸残基结合矿物质离子的基质Gla蛋白(MGP)在血管钙化中的作用,我们利用牛血管平滑肌细胞(BVSMC)在体外钙化模型中检测了MGP的表达。在BVSMC钙化过程中,MGP mRNA的表达降低,其水平与BVSMC钙化量呈负相关。通过用双膦酸盐抑制BVSMC钙化,MGP mRNA表达恢复到未钙化对照的水平。这些数据表明,在血管钙化发展过程中,MGP基因的表达受到调节。