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Procoagulant Activity of Human Mononuclear Leukocytes: Dissociation of the Effect of Mitogens on Procoagulant Activity and Mitogen-Stimulated Lymphocyte Proliferation

机译:人单核白细胞的促凝血活性:丝裂原对促凝血活性和丝裂原刺激的淋巴细胞增殖的影响的分离。

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Summary: The role of mononuclear cells in generating procoagulant activity was examined by incubating Ficoll-Hypaque-separated mononuclear leukocytes with or without mitogens (phytohemagglutinin, pokeweed mitogen, and concanavalin A). The procoagulant activity was assayed by a modification of a one-stage plasma recalcification time. Significant procoagulant activity developed after 24 hr incubation and was dose dependent; mitogens alone had no effect on the clotting tune. The increase in activity was paralleled by the increase in tritiated thymidine incorporation into replicating DNA. However, mitomycin C had little inhibitory effect on the development of procoagulant activity, whereas thymidine incorporation was inhibited. The major procoagulant activity was associated with intact cells and not the conditioned supernatant. The removal of adherent mononuclear cells (mostly monocytes) by polystyrene bead columns abolished the procoagulant activity, whereas purification of mononuclear leukocyte populations for monocytes markedly increased the activity as compared to purified lymphocytes. The procoagulant activity was shown to act by the extrinsic limb of the coagulation sequence because substitution factor VII-deficient plasma for normal plasma resulted in marked depression of procoagulant activity, whereas factor VIII-deficient plasma resulted in a clotting tune only minimally longer than normal plasma. Thus, although procoagulant activity in cultures of mononuclear cells is stimulated by the mitogen reagent, these studies suggest that the activity may not be the result of the mitogenic effect on lymphocytes per se. Whether it is a direct effect of the mitogen on the adherent cell or is an effect of a contaminant of the mitogen reagent, such as endotoxin, remains to be determined.Speculation: Fibrin formation is an important component of inflammatory responses. This study shows that mononuclear leukocytes can be activated to stimulate the formation of fibrin. This suggests that mononuclear leukocytes may play a key role in the deposition of fibrin in inflammatory responses.
机译:简介:通过孵育有或没有丝裂原(植物血凝素,商陆有丝分裂原和伴刀豆球蛋白A)的Ficoll-Hypaque分离的单核白细胞,检查了单核细胞在产生促凝活性中的作用。通过改变一阶段血浆再钙化时间来测定促凝活性。孵育24小时后,产生了显着的促凝血活性,并具有剂量依赖性。单独的促分裂原对凝血调节没有影响。活性的增加与tri代胸苷掺入复制DNA中的增加平行。然而,丝裂霉素C对促凝活性的发展几乎没有抑制作用,而胸苷的掺入被抑制。主要的促凝活性与完整细胞有关,与条件上清液无关。用聚苯乙烯珠柱除去粘附的单核细胞(主要是单核细胞)消除了促凝活性,而与纯化的淋巴细胞相比,单核白细胞的单核细胞群体纯化显着提高了活性。已显示凝血活性由凝血序列的外在肢体发挥作用,因为正常血浆中缺乏凝血因子VII的血浆会导致凝血活性明显降低,而凝血因子VIII缺乏的血浆会导致凝血时间仅比正常血浆短。因此,尽管有丝分裂原试剂刺激了单核细胞培养物中的促凝活性,但这些研究表明该活性可能不是对淋巴细胞本身的有丝分裂作用的结果。究竟是丝裂原对粘附细胞的直接作用还是丝裂原试剂的污染物(例如内毒素)的作用尚待确定。推测:纤维蛋白的形成是炎症反应的重要组成部分。这项研究表明,单核白细胞可以被激活以刺激血纤蛋白的形成。这表明单核白细胞可能在炎症反应中纤维蛋白的沉积中起关键作用。

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