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1型(胰岛素依赖型)糖尿病中抗单链DNA抗体的抗血小板特性。

Anti platelet property of anti-single-stranded DNA antibodies in type 1 (insulin-dependent) diabetes mellitus.

作者信息

Triolo G, Palumbo A A, Giardina E, Davi G, Triolo G

机构信息

Department of Internal Medicine, University of Palermo, Italy.

出版信息

Diabetes Res. 1994;26(2):79-87.

PMID:7554728
Abstract

Nineteen of 50 sera from children with type 1 (insulin-dependent) diabetes mellitus showed anti-platelet reactivity. This reactivity was significantly associated with the presence of proteoglycan cross-reactive anti-ssDNA antibodies. As well as DNA-anti-DNA interaction, increasing salt concentration of the dilution buffer caused a decrease in the binding of positive sera to platelets. Purified ssDNA inhibited also the anti-platelet reactivity of anti-ssDNA positive sera. The addition of purified IgG from anti-ssDNA positive but not from anti-ssDNA negative sera to washed platelets caused an increased collagen-induced platelet aggregation similar to that obtained with the addition of polycationic agents. It may be suggested that ionic interaction between anti-negative charged molecule antibodies (such as anti-ssDNA antibodies) and platelet surface negative charges may be a pathophysiological mechanism contributing to the altered platelet function observed in diabetes.

摘要

在50名1型(胰岛素依赖型)糖尿病患儿的血清中,有19份显示出抗血小板反应性。这种反应性与蛋白聚糖交叉反应性抗单链DNA抗体的存在显著相关。除了DNA与抗DNA的相互作用外,稀释缓冲液盐浓度的增加会导致阳性血清与血小板的结合减少。纯化的单链DNA也抑制了抗单链DNA阳性血清的抗血小板反应性。将抗单链DNA阳性血清而非抗单链DNA阴性血清中的纯化IgG添加到洗涤过的血小板中,会导致胶原诱导的血小板聚集增加,类似于添加聚阳离子剂时的情况。可以推测,抗带负电荷分子抗体(如抗单链DNA抗体)与血小板表面负电荷之间的离子相互作用可能是导致糖尿病中观察到的血小板功能改变的一种病理生理机制。

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