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阳离子铁蛋白诱导血小板聚集的电子显微镜观察

Electron microscopic observations on platelet aggregation induced by cationized ferritin.

作者信息

Yamazaki H, Suzuki H, Yamamoto N, Tanoue K

出版信息

Blood. 1984 Feb;63(2):439-47.

PMID:6419796
Abstract

Washed and gel-filtered human platelets were dose-dependently aggregated by the addition of cationized ferritin (CF). Ca++ and plasma factors were not necessary to induce the aggregation. Immediately after the addition of CF, CF particles were attached to the surface of platelets that showed discoid form, as observed electron microscopically. Some platelets were connected to each other through the CF particles located on their membranes. After the addition of CF, the following was observed: at 15 sec after, platelets showed a round form and were aggregated to each other; at 3 min after, centralization of granules was clearly seen and the aggregates increased their size during the time course; at 3-5 min after, the CF-connected aggregates were found locally. Around the aggregates, other platelets were aggregated, though not through the membrane-located CF. Observing with a lumiaggregometer, the aggregation showed a biphasic curve associated with adenosine triphosphate (ATP) release. The second part of aggregation curve was inhibited by PGI2, PGE1, aspirin, N-ethylmaleimide, and apyrase. The first part of the aggregation curve was inhibited only by heparin. Neuraminidase treatment also inhibited the aggregation dose-dependently. These findings suggest that neutralization of the platelet surface negative charge by a positively charged macromolecule can trigger platelet aggregation, which is followed by the release reaction.

摘要

经洗涤和凝胶过滤的人血小板通过添加阳离子铁蛋白(CF)呈剂量依赖性聚集。诱导聚集不需要钙离子和血浆因子。添加CF后立即在电子显微镜下观察到,CF颗粒附着在呈盘状的血小板表面。一些血小板通过位于其膜上的CF颗粒相互连接。添加CF后,观察到以下情况:添加后15秒,血小板呈圆形并相互聚集;添加后3分钟,颗粒明显集中,聚集物在该时间段内尺寸增大;添加后3至5分钟,发现CF连接的聚集物局部存在。在聚集物周围,其他血小板也聚集在一起,尽管不是通过位于膜上的CF。用发光聚集仪观察,聚集呈现与三磷酸腺苷(ATP)释放相关的双相曲线。聚集曲线的第二部分受到前列环素(PGI2)、前列腺素E1(PGE1)、阿司匹林、N-乙基马来酰亚胺和腺苷三磷酸双磷酸酶的抑制。聚集曲线的第一部分仅受到肝素的抑制。神经氨酸酶处理也呈剂量依赖性地抑制聚集。这些发现表明,带正电荷的大分子中和血小板表面负电荷可引发血小板聚集,随后发生释放反应。

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