Ciceri Paola, Elli Francesca, Cappelletti Laura, Tosi Delfina, Savi Federica, Bulfamante Gaetano, Cozzolino Mario
Laboratory of Experimental Nephrology, Department of Health Sciences, San Paolo Hospital, University of Milan, Via A. di Rudinì,8, 20142, Milan, Italy.
Unit of Human Pathology, Department of Health Sciences, University of Milan, Milan, Italy.
Calcif Tissue Int. 2016 Nov;99(5):472-480. doi: 10.1007/s00223-016-0167-x. Epub 2016 Jun 23.
Osteonectin, also termed SPARC, is a noncollagenous protein of bone matrix. Since there are controversial results regarding its role during the process of vascular calcification, we investigated osteonectin expression in our in vitro calcification model. Rat vascular smooth muscle cells (VSMCs) were challenged with high phosphate (5 mmol/L Pi) and analyzed quantifying calcium levels, through immunohistochemical studies, and studying gene expression. We detected a peak of osteonectin expression at day 7 in cell treated with high phosphate. The time course of calcium deposition, reflected the expression of osteonectin, resulting extensively present at day 7. On the contrary, the expression of the mitotic marker Ki-67 had a peak at day 4, showing no correlation between osteonectin and cell proliferation. Moreover, 7 days was the time point in which Cbfα1/RUNX-2 had its maximal expression. Furthermore, ascorbic acid increased osteonectin expression, supporting a procalcifying role for this protein. Next we decided to study osteonectin expression ex vivo in fetal, adult not calcified, and adult calcific vessels. Immunohistochemical studies demonstrated a spread and strong reactivity in VSMCs of a 20-week fetus, confirming that osteonectin may have a potential role in regulation of mitosis and in cell differentiation. In adult not calcified arteries, osteonectin was constitutively expressed and its levels increased in atherosclerotic and in calcified plaques, where it could have a regulatory role in the calcification process. Our in vitro and ex vivo data show osteonectin expression during the calcification process and suggest its potential role as procalcifying factor.
骨连接蛋白,也称为富含半胱氨酸的酸性分泌蛋白(SPARC),是一种骨基质中的非胶原蛋白。由于关于其在血管钙化过程中的作用存在有争议的结果,我们在我们的体外钙化模型中研究了骨连接蛋白的表达。用高磷(5 mmol/L无机磷)刺激大鼠血管平滑肌细胞(VSMC),并通过免疫组织化学研究定量分析钙水平以及研究基因表达。我们检测到在高磷处理的细胞中,第7天时骨连接蛋白表达出现峰值。钙沉积的时间进程反映了骨连接蛋白的表达情况,在第7天时广泛存在。相反,有丝分裂标记物Ki-67的表达在第4天达到峰值,表明骨连接蛋白与细胞增殖之间无相关性。此外,第7天是核心结合因子α1/Runx-2表达最高的时间点。此外,抗坏血酸增加了骨连接蛋白的表达,支持了该蛋白的促钙化作用。接下来我们决定在胎儿、未钙化的成年和成年钙化血管的离体组织中研究骨连接蛋白的表达。免疫组织化学研究表明,在20周胎儿的VSMC中存在广泛且强烈的反应性,证实骨连接蛋白可能在有丝分裂调节和细胞分化中具有潜在作用。在未钙化的成年动脉中,骨连接蛋白呈组成性表达,其水平在动脉粥样硬化斑块和钙化斑块中升高,在这些斑块中它可能在钙化过程中起调节作用。我们的体外和离体数据显示了钙化过程中骨连接蛋白的表达,并提示其作为促钙化因子的潜在作用。