Indiana University School of Medicine, Department of Medical and Molecular Genetics, Indianapolis, Indiana 46202, USA.
J Biomed Opt. 2010 Jan-Feb;15(1):016020. doi: 10.1117/1.3322676.
Thrombus development in mouse mesenteric vessels following laser-induced injury was monitored by high-resolution, near-real-time, two-photon, intravital microscopy. In addition to the use of fluorescently tagged fibrin(ogen) and platelets, plasma was labeled with fluorescently tagged dextran. Because blood cells exclude the dextran in the single plane, blood cells appear as black silhouettes. Thus, in addition to monitoring the accumulation of platelets and fibrin in the thrombus, the protocol detects the movement and incorporation of unlabeled cells in and around it. The developing thrombus perturbs the blood flow near the thrombus surface, which affects the incorporation of platelets and blood cells into the structure. The hemodynamic effects and incorporation of blood cells lead to the development of thrombi with heterogeneous domain structures. Additionally, image processing algorithms and simulations were used to quantify structural features of developing thrombi. This analysis suggests a novel mechanism to stop the growth of developing thrombus.
通过高分辨率、近实时、双光子、活体显微镜监测激光诱导损伤后小鼠肠系膜血管中的血栓形成。除了使用荧光标记的纤维蛋白原和血小板外,还使用荧光标记的葡聚糖标记血浆。由于血细胞在单个平面上排斥葡聚糖,因此血细胞呈现为黑色轮廓。因此,除了监测血栓中血小板和纤维蛋白的积累外,该方案还检测未标记细胞在血栓内外的运动和掺入。正在形成的血栓会扰乱血栓表面附近的血流,这会影响血小板和血细胞掺入到结构中。血液动力学效应和血细胞的掺入导致血栓具有异质结构域。此外,还使用图像处理算法和模拟来量化正在形成的血栓的结构特征。该分析提出了一种阻止正在形成的血栓生长的新机制。