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首页> 外文期刊>Lipids in Health Disease >Induction of calcification by serum depletion in cell culture: a model for focal calcification in aortas related to atherosclerosis
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Induction of calcification by serum depletion in cell culture: a model for focal calcification in aortas related to atherosclerosis

机译:在细胞培养中通过血清消耗诱导钙化:与动脉粥样硬化相关的主动脉局灶性钙化模型

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Background Since aortic calcification has been shown to initiate in the lower zone of well-thickened plaques (LZP) adjacent to the aortic media of rabbits fed supplemental cholesterol diets, a restricted supply of serum to vascular cells could play a role in vascular calcification. This study was designed to use a cell culture model to support this hypothesis. Results Rabbit aortic smooth muscle cells were grown to confluence in a culture media containing 10 % fetal bovine serum (FBS). The confluent cells were then exposed to the media for 2 hrs with or without serum at a Ca × P ion product range of 4.5–9.4 mM2. In contrast to the cells cultured in the presence of FBS, confluent cells in its absence displayed marked mineral-positive alizarin red staining and infrared absorption of mineral phosphate. A kinetic parameter C1/2 was used to designate the concentration of serum or its protein constituents needed to reduce the deposition of Ca and P by half. The C1/2 for FBS and rabbit serum was 0.04–0.07 % The C1/2 value for rabbit serum proteins was 13.5 μg/ml corresponding to the protein concentration in 0.06 % of serum. This C1/2 was markedly smaller than 86.2 μg/ml for bovine serum albumin present in 0.37 % serum (p < 0.05). Serum depletion also caused marked membrane translocation as evidenced through a specific apoptosis dye uptake by cells. The proteomic analysis of calcifying vesicles, which can be released by serum depletion, revealed several calcification-related proteins. Conclusion The aortic smooth muscle cell culture model suggests that serum depletion may play a role in the initiation of aortic calcification. The serum exhibits remarkable ability to inhibit cell-mediated calcification.
机译:背景技术由于已经显示主动脉钙化在邻近补充胆固醇饮食的兔子的主动脉介质附近的厚壁斑块(LZP)的下部区域开始,因此限制向血管细胞的血清供应可能在血管钙化中起作用。本研究旨在使用细胞培养模型来支持这一假设。结果兔主动脉平滑肌细胞在含有10%胎牛血清(FBS)的培养基中生长至汇合。然后在有或没有血清的情况下,将融合细胞暴露于培养基中2小时,Ca×P离子产物的范围为4.5–9.4 mM2。与在FBS存在下培养的细胞相反,在不存在FBS的情况下,融合细胞表现出明显的矿物质阳性茜素红染色和矿物质磷酸盐的红外吸收。使用动力学参数C1 / 2来指定将Ca和P沉积减少一半所需的血清或其蛋白成分的浓度。 FBS和兔血清的C1 / 2为0.04-0.07%。兔血清蛋白的C1 / 2值为13.5μg/ ml,对应于0.06%血清中的蛋白质浓度。对于存在于0.37%血清中的牛血清白蛋白,该C1 / 2显着小于86.2μg/ ml(p <0.05)。血清耗竭也会引起明显的膜移位,这通过细胞摄取特定的凋亡染料来证明。钙化囊泡的蛋白质组学分析可通过血清消耗而释放,揭示了几种钙化相关蛋白。结论主动脉平滑肌细胞培养模型表明,血清消耗可能与主动脉钙化的开始有关。血清表现出显着的抑制细胞介导的钙化的能力。

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