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中性粒细胞介导的抗体依赖性和免疫复合物触发的细胞毒性中涉及的不同激活途径。

Different activation pathways involved in antibody-dependent and immune-complexes-triggered cytotoxicity mediated by neutrophils.

作者信息

Geffner J R, Giordano M, Serebrinsky G, Isturiz M A

机构信息

Instituto de Investigaciones Hematológicas, Academia Nacional de Medicina, Buenos Aires, Argentina.

出版信息

Clin Exp Immunol. 1988 Dec;74(3):471-6.

Abstract

We have shown previously that normal human neutrophils triggered by immune complexes displayed significant levels of cytotoxicity towards non-sensitized target cells (non-specific cytotoxicity-NSC) (Geffner, J. R. et al. 1987). Despite the fact that NSC and antibody-dependent cellular cytotoxicity (ADCC) are both mediated through neutrophil Fc gamma R and require the activation of the respiratory burst, the cytolytic mechanisms involved in each case appear to be different. In order to analyse the pathways of activation involved in the induction of NSC and ADCC, we studied here some of the metabolic requirements associated with each cytotoxic function. Our results suggest that ADCC is dependent on Na+/H+ antiporter activity, de novo protein synthesis, availability of external Ca2+ and calmodulin activity, activation of phospholipase C and activation of protein kinase C. On the other hand, NSC appears to be dependent on availability of external Ca2+ and calmodulin activity and activation of phospholipase A2. These results indicate that different pathways of activation are involved in the induction of neutrophil-mediated ADCC and NSC.

摘要

我们之前已经表明,由免疫复合物触发的正常人中性粒细胞对未致敏靶细胞表现出显著水平的细胞毒性(非特异性细胞毒性-NSC)(杰夫纳,J.R.等人,1987年)。尽管NSC和抗体依赖性细胞毒性(ADCC)均通过中性粒细胞FcγR介导且都需要呼吸爆发的激活,但每种情况下涉及的细胞溶解机制似乎有所不同。为了分析参与NSC和ADCC诱导的激活途径,我们在此研究了与每种细胞毒性功能相关的一些代谢需求。我们的结果表明,ADCC依赖于Na+/H+反向转运体活性、从头蛋白质合成、细胞外Ca2+的可用性和钙调蛋白活性、磷脂酶C的激活以及蛋白激酶C的激活。另一方面,NSC似乎依赖于细胞外Ca2+的可用性和钙调蛋白活性以及磷脂酶A2的激活。这些结果表明,中性粒细胞介导的ADCC和NSC的诱导涉及不同的激活途径。

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Inhibition of phospholipase.磷脂酶的抑制作用。
Br Med Bull. 1983 Jul;39(3):260-4. doi: 10.1093/oxfordjournals.bmb.a071830.
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Am J Physiol. 1984 Apr;246(4 Pt 2):R409-38. doi: 10.1152/ajpregu.1984.246.4.R409.

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