Department of Cell and Developmental Biology, University of Pennsylvania School of Medicine, Philadelphia, PA, USA.
Blood. 2011 Apr 28;117(17):4609-14. doi: 10.1182/blood-2010-07-297671. Epub 2011 Jan 19.
We determined the sequence of events and identified and quantitatively characterized the mobility of moving structures present during the early stages of fibrin-clot formation from the beginning of polymerization to the gel point. Three complementary techniques were used in parallel: spinning-disk confocal microscopy, transmission electron microscopy, and turbidity measurements. At the beginning of polymerization the major structures were monomers, whereas at the middle of the lag period there were monomers, oligomers, protofibrils (defined as structures that consisted of more than 8 monomers), and fibers. At the end of the lag period, there were primarily monomers and fibers, giving way to mainly fibers at the gel point. Diffusion rates were calculated from 2 different results, one based on sizes and another on the velocity of the observed structures, with similar results in the range of 3.8-0.1 μm²/s. At the gel point, the diffusion coefficients corresponded to very large, slow-moving structures and individual protofibrils. The smallest moving structures visible by confocal microscopy during fibrin polymerization were identified as protofibrils with a length of approximately 0.5 μm. The sequence of early events of clotting and the structures present are important for understanding hemostasis and thrombosis.
我们确定了事件的顺序,并鉴定和定量描述了纤维蛋白凝块形成早期从聚合开始到凝胶点期间存在的运动结构的迁移性。三种互补技术同时使用:旋转盘共聚焦显微镜、透射电子显微镜和浊度测量。在聚合开始时,主要结构是单体,而在滞后期的中间阶段,有单体、低聚物、原纤维(定义为由超过 8 个单体组成的结构)和纤维。在滞后期末期,主要是单体和纤维,在凝胶点时主要是纤维。扩散速率是根据 2 个不同的结果计算得出的,一个基于结构的大小,另一个基于观察到的结构的速度,在 3.8-0.1 μm²/s 的范围内得到了相似的结果。在凝胶点,扩散系数对应于非常大的、移动缓慢的结构和单个原纤维。在纤维蛋白聚合过程中通过共聚焦显微镜可见的最小运动结构被鉴定为长度约为 0.5 μm 的原纤维。凝血和存在的结构的早期事件的顺序对于理解止血和血栓形成很重要。