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Three-dimensional reconstruction of fibrin clot networks from stereoscopic intermediate voltage electron microscope images and analysis of branching.

机译:从立体中压电子显微镜图像和分支分析对纤维蛋白凝块网络进行三维重建。

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摘要

Fibrin polymerizes to produce branching fibers forming a three-dimensional network, which has been difficult to visualize by conventional microscopy. Three-dimensional images of whole clots at high resolution were obtained from stereo-pair intermediate-voltage electron micrographs. Computer software was developed to produce three-dimensional reconstructions of the networks in the form of a pattern of links that connect branching junctions. Network parameters were measured and analyzed to characterize the clots quantitatively. Models in which all links were moved to the origin, while preserving their orientation, allowed visualization of some network parameters and facilitated comparison of networks. Fibrin clots formed in three different conditions were analyzed and compared by these methods. Clots formed in 0.20 M saline buffer consist of fibers of uniform size, and most of the branching junctions consist of three links. Fibrin clots formed in 0.05 M saline buffer are made up of very large diameter fiber bundles with far fewer branching junctions and correspondingly longer links. Clots formed in 0.40 M saline buffer consist of very fine fibers with numerous branching junctions and very short links. In summary, the extent of lateral aggregation is directly related to the distance between branching junctions and inversely related to the total number of branching junctions. These observations must be considered in defining possible mechanisms of fibrin branching.
机译:纤维蛋白聚合以产生形成三维网络的支化纤维,这很难通过常规显微镜观察到。从立体对中压电子显微照片获得高分辨率的整个血凝块的三维图像。开发了计算机软件,以连接分支结的链接形式生成网络的三维重构。测量并分析网络参数以定量表征血块。将所有链接移至原点的模型,同时保留其方向,可以可视化某些网络参数并促进网络比较。用这些方法分析并比较了在三种不同条件下形成的纤维蛋白凝块。在0.20 M盐水缓冲液中形成的凝块由大小均一的纤维组成,大多数分支结由三个链节组成。在0.05 M盐水缓冲液中形成的纤维蛋白凝块由直径非常大的纤维束组成,其束缚连接点少得多,链节也相应更长。在0.40 M盐水缓冲液中形成的凝块由非常细的纤维组成,具有许多分支结和非常短的链节。总之,横向聚集的程度与分支结之间的距离直接相关,而与分支结的总数成反比。在定义纤维蛋白分支的可能机制时必须考虑这些观察结果。

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