Mørland B
Thromb Haemost. 1979 Dec 21;42(4):1207-16.
Collagen was incubated with cells or media fractions of mouse peritoneal macrophage cultures, and its aggregating effect on human platelets was tested. Incubation with lysates of cultured cells completely abolished the normal collagen-induced platelet aggregation, while incubation with media fractions only caused partial inhibition. The latter inhibition was more pronounced after macrophage phagocytosis of latex particles, while endocytosis of endotoxin had no effect. Corresponding macrophage cultures were also tested for specific collagenase activity, using 14C-glycine labelled collagen as substrate. Collagenase activity was found in the culture media fractions only, and the enzyme activity could be enhanced by endocytosis of latex as well as endotoxin. It appears that the effect of macrophage lysates and media on collagen-platelet interaction cannot be ascribed only to secretion of collagenase from macrophages.
将胶原蛋白与小鼠腹腔巨噬细胞培养物的细胞或培养基组分一起孵育,并测试其对人血小板的聚集作用。与培养细胞的裂解物孵育完全消除了正常胶原蛋白诱导的血小板聚集,而与培养基组分孵育仅引起部分抑制。巨噬细胞吞噬乳胶颗粒后,后者的抑制作用更明显,而内毒素的内吞作用则没有影响。还使用14C-甘氨酸标记的胶原蛋白作为底物,对相应的巨噬细胞培养物进行了特异性胶原酶活性测试。仅在培养基组分中发现了胶原酶活性,并且乳胶和内毒素的内吞作用均可增强酶活性。看来巨噬细胞裂解物和培养基对胶原蛋白-血小板相互作用的影响不能仅归因于巨噬细胞分泌胶原酶。