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Lysis of antibody-coated cells by platelets

机译:血小板裂解抗体包被的细胞

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摘要

Antibody-coated erythrocytes are lysed by murine C5- whole blood but not by plasma separated from such blood. The lytic activity has been shown to derive from platelets that attach to sensitized cells probably through membrane receptors for C3b. Whole blood or platelet-rich plasma (prp) obtained from mice that have been treated with purified cobra venom factor has little or no activity unless it is fortified with fresh C5- plasma. Lysis is observed only if the reactants are incubated at 37 degrees C and mechanical shaking is practiced, at least intermittently, throughout the period of incubation. Adherence of platelets and subsequent lysis are mediated by antibodies of a variety of immunoglobulin classes, including those that fail to mediate complement-dependent lysis. Platelet-mediated lysis is limited to cells to which the platelets adhere; 51Cr labeled, unsensitized cells that are mixed with prp and sensitized, unlabeled cells do not release 51Cr. Normal murine lymphoid cells and ascites tumor cells of mice, rats, and guinea pigs were apparently unaffected by sensitization and incubation with prp. However, because adherence of platelets to these sensitized cells was not observed, it is not clear whether the cells are resistant to the lytic action of platelets or whether the conditions of incubation were unfavorable for the attachment of platelets to the surfaces of nucleated cells. The significance of the lytic reaction described here is not known but may lie in antibody mediated release of microbicidal substances from platelets.
机译:抗体包被的红细胞被鼠C5全血溶解,而不被从这种血液中分离的血浆溶解。已经显示出裂解活性源自血小板,该血小板可能通过C3b的膜受体附着在致敏细胞上。除非已经用新鲜的C5-血浆强化,否则从用纯化的眼镜蛇毒因子治疗的小鼠获得的全血或富含血小板的血浆(prp)几乎没有活性。仅在将反应物在37摄氏度下温育并且在整个温育期间至少间歇地进行机械摇动的情况下,才能观察到裂解。血小板的粘附和随后的裂解是由多种免疫球蛋白类型的抗体介导的,包括那些不能介导补体依赖性裂解的抗体。血小板介导的裂解仅限于血小板粘附的细胞。与prp混合的51Cr标记的未敏化细胞和未标记的敏化的细胞不会释放51Cr。小鼠,大鼠和豚鼠的正常鼠淋巴样细胞和腹水肿瘤细胞显然不受prp致敏和孵育的影响。然而,由于未观察到血小板粘附于这些致敏细胞,因此尚不清楚细胞是否对血小板的溶解作用有抵抗力或温育条件是否不利于血小板粘附于有核细胞表面。此处描述的裂解反应的重要性尚不清楚,但可能在于抗体介导的血小板中杀菌物质的释放。

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