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兔主动脉体外矿化抑制剂及其在生物矿化中的作用。

Inhibitors of in vitro mineralization from rabbit aorta and their role in biomineralization.

作者信息

Tandon C D, Aggarwal S, Forouzandeh M, Jethi R K

机构信息

Department of Biochemistry, Panjab University, Chandigarh, India.

出版信息

J Cell Biochem. 1998 Mar 1;68(3):287-97.

PMID:9518256
Abstract

Mineralization of aorta is known to occur late in life and appears to be a pathological phenomenon. In vitro studies revealed that the matrix prepared from the thoracic aorta pieces after their extraction with 3% Na2HPO4 and 0.1 mM CaCl2 were mineralized under physiological conditions of temperature, pH, and ionic strength of the media to form matrix-bound mineral phase resembling hydroxyapatite in nature. However, the matrix identically prepared from the unextracted rabbits aortae failed to mineralize under identical assay conditions. The addition of the aorta extract in the assay system inhibited the above mineralization process. Standard biochemical techniques, e.g., dialysis, ion exchange, and molecular sieve chromatography, sodium dodecyl sulfate-polyacrylamide gel electrophoresis, and amino acid analysis by high-performance liquid chromatography were employed to isolate, purify, and characterize the potent inhibitory biomolecules from the aorta extract. The inhibitory activity of the aorta extract was found to be primarily due to the presence of three biomolecules having molecular weights of 66, 45, and 27-29 kDa. The above inhibitory biomolecules loosely associated with aorta may be involved in the control of calcification associated with arteriosclerosis.

摘要

已知主动脉矿化在生命后期发生,且似乎是一种病理现象。体外研究表明,从胸主动脉碎片中用3% Na2HPO4和0.1 mM CaCl2提取后制备的基质,在温度、pH值和培养基离子强度的生理条件下发生矿化,形成本质上类似于羟基磷灰石的与基质结合的矿化相。然而,从未提取的兔主动脉中同样制备的基质在相同的检测条件下未能矿化。在检测系统中添加主动脉提取物会抑制上述矿化过程。采用标准生化技术,如透析、离子交换、分子筛色谱、十二烷基硫酸钠-聚丙烯酰胺凝胶电泳以及高效液相色谱法进行氨基酸分析,以从主动脉提取物中分离、纯化和鉴定有效的抑制性生物分子。发现主动脉提取物的抑制活性主要归因于存在三种分子量分别为66、45和27 - 29 kDa的生物分子。上述与主动脉松散结合的抑制性生物分子可能参与了与动脉硬化相关的钙化控制。

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