Cohen I, Gerrard J M, White J G
J Cell Biol. 1982 Jun;93(3):775-87. doi: 10.1083/jcb.93.3.775.
We explored the retraction or contraction of platelet-fibrin clots under isometric conditions. In the presence of micromolar calcium clots of normal platelet-rich plasma developed tension at an initial rate of 0.1 to 0.2 g/min per cm2 (initial cross-sectional area). Electron microscopy of clots fixed after attaining a force of 1.6 g/cm2 revealed platelets with elongated bodies and pseudopods in close apposition to fibrin strands which were oriented in cablelike fashion in the direction of tension. The development of tension could not be explained simply on the basis of platelet-platelet association and interaction alone. First, factor XIII-dependent cross-linking of fibrin fibers was critical to normal isometric contraction. Second, tension decreased linearly, rather than exponentially, when the platelet count in the platelet-fibrin clot was decreased, suggesting that platelets must be interacting with another component (i.e. fibrin). Thrombasthenic platelets, deficient in fibrinogen receptors, failed to develop tension or to align fibrin strands or pseudopods in the clot. Platelet-fibrin clots treated with vincristine to disassemble microtubules or cytochalasin B to disrupt microfilaments failed to develop tension and relaxed if these agents were added after tension had developed. Relaxation under these conditions, however, was not associated with loss of orientation of fibrin strands. Our findings suggest that platelet-fibrin interaction in clots under isometric conditions leads to orientation of fibrin strands and platelets in the direction of force generation. Tension develops as platelets simultaneously attach to and spread along fibrin strands, and contract. The contraction draws some fibrin into platelet-fibrin clumps and aligns other strands in the long axis of tension. The achievement and maintenance of maximum tension appears to depend on the development of platelet-fibrin attachments and extension of platelet bodies and long pseudopods containing bundles of microfilaments and microtubules along the oriented fibrin fibers.
我们研究了等长条件下血小板 - 纤维蛋白凝块的回缩或收缩情况。在存在微摩尔浓度钙的情况下,正常富含血小板血浆的凝块以每平方厘米0.1至0.2克/分钟的初始速率(初始横截面积)产生张力。当达到1.6克/平方厘米的力后固定凝块进行电子显微镜观察,结果显示血小板具有细长的主体和伪足,与纤维蛋白丝紧密相邻,这些纤维蛋白丝在张力方向上呈索状排列。张力的产生不能仅简单地基于血小板 - 血小板的结合和相互作用来解释。首先,因子XIII依赖的纤维蛋白纤维交联对于正常的等长收缩至关重要。其次,当血小板 - 纤维蛋白凝块中的血小板计数减少时,张力呈线性下降,而不是指数下降,这表明血小板必须与另一种成分(即纤维蛋白)相互作用。缺乏纤维蛋白原受体的血小板无力症血小板无法产生张力,也无法使凝块中的纤维蛋白丝或伪足排列整齐。用长春新碱破坏微管或用细胞松弛素B破坏微丝处理的血小板 - 纤维蛋白凝块无法产生张力,并且如果在张力产生后添加这些药物,凝块会松弛。然而,在这些条件下的松弛与纤维蛋白丝的排列方向丧失无关。我们的研究结果表明,等长条件下凝块中的血小板 - 纤维蛋白相互作用导致纤维蛋白丝和血小板在力产生的方向上排列。随着血小板同时附着在纤维蛋白丝上并沿其铺展和收缩,张力产生。收缩将一些纤维蛋白吸入血小板 - 纤维蛋白团块中,并使其他纤维蛋白丝在张力的长轴方向上排列整齐。最大张力的实现和维持似乎取决于血小板 - 纤维蛋白附着的形成以及血小板主体和含有微丝和微管束的长伪足沿着定向纤维蛋白纤维的延伸。