Clarke N, Collins M
Br J Exp Pathol. 1969 Apr;50(2):153-7.
Human chorion cells have been broken open and separated into “nuclear”, “mitochondrial”, “microsomal” and soluble fractions by differential centrifugation in the cold. Minute quantities of the homogenate and individual cell fractions were immediately tested for their fibrinolytic activity on fibrin plates with and without plasminogen, and also in the presence of streptokinase, ε-aminocaproic acid or Triton X-100. With the technique employed, no direct fibrinolysis was produced by the homogenate or cell fractions. In the presence of streptokinase the homogenate and cell fractions led to marked fibrinolysis indicating the presence of cellular proactivator activity. Comparison of the intracellular fractions indicated that the greatest proactivator activity was associated with the “microsomal fraction”. The streptokinase-induced proactivator activity was partly inhibited by certain concentrations of ε-aminocaproic acid.
人绒毛膜细胞已被破碎,并通过在低温下进行差速离心分离成“细胞核”、“线粒体”、“微粒体”和可溶性部分。立即对微量的匀浆和各个细胞部分在有和没有纤溶酶原的情况下以及在存在链激酶、ε-氨基己酸或曲拉通X-100的情况下在纤维蛋白平板上的纤溶活性进行了测试。采用该技术,匀浆或细胞部分未产生直接的纤维蛋白溶解作用。在链激酶存在的情况下,匀浆和细胞部分导致明显的纤维蛋白溶解,表明存在细胞前激活剂活性。细胞内部分的比较表明,最大的前激活剂活性与“微粒体部分”相关。链激酶诱导的前激活剂活性被一定浓度的ε-氨基己酸部分抑制。