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铁过载抑制 ATDC5 细胞的钙化和分化。

Iron overload inhibits calcification and differentiation of ATDC5 cells.

机构信息

Department of Biological Sciences, Tokyo Institute of Technology, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8501, Japan.

出版信息

J Biochem. 2012 Jan;151(1):109-14. doi: 10.1093/jb/mvr124. Epub 2011 Oct 11.

Abstract

There is a little information about the effects of iron overload on cartilage metabolism. In the present study, we examined the effects of excess iron on the differentiation and mineralization of cultured chondrocytes, ATDC5 cells. We used ferric ammonium citrate (FAC) as a ferric ion donor and desferrioxamine (DFO) as a ferric ion chelator. Neither chemical affected the production of proteoglycan, a marker of an early stage of ATDC5 differentiation. In contrast, FAC inhibited the deposition of calcium, a late-stage event in chondrocyte differentiation, by ATDC5 cells in a dose-dependent manner, and DFO accelerated it. Energy dispersive X-ray spectroscopy/scanning electron microscope analysis revealed that the levels of iron and calcium in cells treated with FAC were increased and decreased, respectively. Furthermore, FAC inhibited the expression of matrix metalloproteinase 13 mRNA, another marker of late-stage chondrocyte differentiation. In addition, we found that the heavy and light chains of ferritin were expressed specifically at a late stage of ATDC5 differentiation, and the levels of both proteins were enhanced by the addition of iron. These results suggest that iron overload might give rise to osteopenia and arthritis by inhibiting chondrocyte differentiation and mineralization.

摘要

关于铁过载对软骨代谢影响的信息较少。在本研究中,我们研究了过量铁对培养软骨细胞(ATDC5 细胞)分化和矿化的影响。我们使用柠檬酸铁铵(FAC)作为铁离子供体,去铁胺(DFO)作为铁离子螯合剂。这两种化学物质均不影响蛋白聚糖的产生,蛋白聚糖是 ATDC5 分化早期的标志物。相比之下,FAC 以剂量依赖的方式抑制 ATDC5 细胞钙的沉积,钙的沉积是软骨细胞分化的晚期事件,而 DFO 则加速了钙的沉积。能谱 X 射线/扫描电子显微镜分析显示,用 FAC 处理的细胞中铁和钙的水平分别增加和减少。此外,FAC 抑制基质金属蛋白酶 13 mRNA 的表达,基质金属蛋白酶 13 mRNA 是软骨细胞分化晚期的另一个标志物。此外,我们发现铁蛋白的重链和轻链在 ATDC5 分化的晚期特异性表达,并且这两种蛋白的水平都因铁的添加而增强。这些结果表明,铁过载可能通过抑制软骨细胞分化和矿化导致骨质疏松症和关节炎。

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