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不同激活程度下人血小板之间的破裂力

Rupture Forces among Human Blood Platelets at different Degrees of Activation.

作者信息

Nguyen Thi-Huong, Palankar Raghavendra, Bui Van-Chien, Medvedev Nikolay, Greinacher Andreas, Delcea Mihaela

机构信息

Nanostructure Group, ZIK HIKE - Center for Innovation Competence, Humoral Immune Reactions in Cardiovascular Diseases, University of Greifswald, 17489 Greifswald, Germany.

Institute for Immunology and Transfusion Medicine, University Medicine Greifswald, 17475 Greifswald, Germany.

出版信息

Sci Rep. 2016 May 5;6:25402. doi: 10.1038/srep25402.

Abstract

Little is known about mechanics underlying the interaction among platelets during activation and aggregation. Although the strength of a blood thrombus has likely major biological importance, no previous study has measured directly the adhesion forces of single platelet-platelet interaction at different activation states. Here, we filled this void first, by minimizing surface mediated platelet-activation and second, by generating a strong adhesion force between a single platelet and an AFM cantilever, preventing early platelet detachment. We applied our setup to measure rupture forces between two platelets using different platelet activation states, and blockade of platelet receptors. The rupture force was found to increase proportionally to the degree of platelet activation, but reduced with blockade of specific platelet receptors. Quantification of single platelet-platelet interaction provides major perspectives for testing and improving biocompatibility of new materials; quantifying the effect of drugs on platelet function; and assessing the mechanical characteristics of acquired/inherited platelet defects.

摘要

关于血小板在激活和聚集过程中相互作用的力学机制,人们了解甚少。尽管血栓的强度可能具有重要的生物学意义,但此前尚无研究直接测量不同激活状态下单血小板与血小板相互作用的粘附力。在此,我们首先通过最小化表面介导的血小板激活,其次通过在单个血小板与原子力显微镜(AFM)悬臂之间产生强大的粘附力以防止血小板早期脱离,填补了这一空白。我们应用该装置测量了处于不同激活状态的两个血小板之间的破裂力,以及血小板受体的阻断情况。结果发现,破裂力与血小板激活程度成正比增加,但随着特定血小板受体的阻断而降低。单血小板与血小板相互作用的量化为测试和改善新材料的生物相容性、量化药物对血小板功能的影响以及评估获得性/遗传性血小板缺陷的力学特性提供了重要视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c64b/4857101/2e98a6b80e22/srep25402-f1.jpg

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