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CRP制剂的血小板抑制作用归因于一种共同分离出的低分子量因子。

Platelet inhibitory effects of CRP preparations are due to a co-isolating low molecular weight factor.

作者信息

Fiedel B A, Potempa L A, Frenzke M E, Simpson R M, Gewurz H

出版信息

Immunology. 1982 Jan;45(1):15-22.

Abstract

We previously reported that C-reactive protein (CRP), an acute phase reactant, inhibits platelet activation through an effect upon a factor(s) critical to ADP-mediated secondary wave platelet aggregation but independent of a direct effect upon platelet contractile elements. However, a role for an accessory factor in this inhibitory effect became of concern because of an inconsistency in the effects of CRP preparations upon the platelet: inhibition was lost upon storage and CRP preparations differed, on a weight basis, in inhibitory capacity and sensitivity to the presence of the CRP ligand C-polysaccharide (CPS(. The studies presented herein were thus intended to assess whether an accessory factor was involved in the inhibition of platelet activation observed with CRP. We report that the activity of the inhibitory CRP preparations resulted from association with a low molecular weight factor (LMF) with an apparent nominal molecular weight of 8300-12,500 and an A280:A260 ratio of approximately 0.4. Purified CRP did not inhibit platelet responsiveness but CRP with associated LMF (CRP-LMF) did. Moreover, the inhibitory capacity of CRP-LMF but not LMF was substantially reversed in the presence of CPS. These studies indicate that the platelet inhibitory properties of CRP preparations result from and are contingent upon the presence of a co-isolating low molecular weight factor.

摘要

我们之前报道过,急性期反应物C反应蛋白(CRP)通过作用于对ADP介导的血小板二次聚集至关重要的一个或多个因子来抑制血小板活化,但与对血小板收缩元件的直接作用无关。然而,由于CRP制剂对血小板的作用存在不一致性,一种辅助因子在这种抑制作用中的作用受到关注:储存后抑制作用丧失,并且基于重量,CRP制剂在抑制能力和对CRP配体C多糖(CPS)存在的敏感性方面存在差异。因此,本文提出的研究旨在评估是否存在一种辅助因子参与了用CRP观察到的血小板活化抑制作用。我们报告,抑制性CRP制剂的活性源于与一种低分子量因子(LMF)的结合,该因子的表观标称分子量为8300 - 12,500,A280:A260比值约为0.4。纯化的CRP不抑制血小板反应性,但与LMF相关的CRP(CRP-LMF)则可以。此外,在CPS存在的情况下,CRP-LMF而非LMF的抑制能力被显著逆转。这些研究表明,CRP制剂的血小板抑制特性源于并取决于一种共同分离的低分子量因子的存在。

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本文引用的文献

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C-reactive protein: a molecule composed of subunits.C反应蛋白:一种由亚基组成的分子。
Proc Natl Acad Sci U S A. 1965 Aug;54(2):558-66. doi: 10.1073/pnas.54.2.558.

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