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血小板铺展和黏附的时间分辨微波成像和电磁层析成像测量

Time-resolved MIET measurements of blood platelet spreading and adhesion.

作者信息

Zelená Anna, Isbaner Sebastian, Ruhlandt Daja, Chizhik Anna, Cassini Chiara, Klymchenko Andrey S, Enderlein Jörg, Chizhik Alexey, Köster Sarah

机构信息

Institute for X-Ray Physics, University of Göttingen, Friedrich-Hund-Platz 1, 37077 Göttingen, Germany.

出版信息

Nanoscale. 2020 Nov 7;12(41):21306-21315. doi: 10.1039/d0nr05611a. Epub 2020 Oct 19.

Abstract

Human blood platelets are non-nucleated fragments of megakaryocytes and of high importance for early hemostasis. To form a blood clot, platelets adhere to the blood vessel wall, spread and attract other platelets. Despite the importance for biomedicine, the exact mechanism of platelet spreading and adhesion to surfaces remains elusive. Here, we employ metal-induced energy transfer (MIET) imaging with a leaflet-specific fluorescent membrane probe to quantitatively determine, with nanometer resolution and in a time-resolved manner, the height profile of the basal and the apical platelet membrane above a rigid substrate during platelet spreading. We observe areas, where the platelet membrane approaches the substrate particularly closely and these areas are stable on a time scale of minutes. Time-resolved MIET measurements reveal distinct behaviors of the outermost rim and the central part of the platelets, respectively. Our findings quantify platelet adhesion and spreading and improve our understanding of early steps in blood clotting. Furthermore, the results of this study demonstrate the potential of MIET for simultaneous imaging of two close-by membranes and thus three-dimensional reconstruction of the cell shape.

摘要

人类血小板是巨核细胞的无核碎片,对早期止血至关重要。为了形成血凝块,血小板会黏附于血管壁,铺展并吸引其他血小板。尽管对生物医学很重要,但血小板铺展和黏附于表面的确切机制仍不清楚。在这里,我们使用金属诱导能量转移(MIET)成像技术,结合小叶特异性荧光膜探针,以纳米分辨率并在时间分辨的方式下,定量测定血小板铺展过程中刚性底物上方基底和顶端血小板膜的高度轮廓。我们观察到血小板膜特别接近底物的区域,这些区域在数分钟的时间尺度上是稳定的。时间分辨的MIET测量分别揭示了血小板最外缘和中心部分的不同行为。我们的研究结果量化了血小板的黏附和铺展,增进了我们对血液凝固早期步骤的理解。此外,本研究结果证明了MIET在同时成像两个相邻膜从而进行细胞形状三维重建方面的潜力。

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