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通过p75白细胞介素2受体激活自然杀伤细胞。

Activation of natural killer cells via the p75 interleukin 2 receptor.

作者信息

Phillips J H, Takeshita T, Sugamura K, Lanier L L

机构信息

Becton Dickinson Monoclonal Center, Inc., Mountain View, California 94043.

出版信息

J Exp Med. 1989 Jul 1;170(1):291-6. doi: 10.1084/jem.170.1.291.

Abstract

The IL-2R is composed of at least two subunits, the p55 (CD25/Tac) and p75 glycoproteins. The p75 IL-2R is expressed preferentially on resting human peripheral blood NK cells, but is not detected on substantial proportions of T and B lymphocytes, monocytes, or granulocytes. Anti-p75 IL-2R mAb substantially inhibits the early events associated with NK cell activation by IL-2, including inhibition of cytotoxic activity and induction of the CD69 early activation antigen. While anti-p55 IL-2R mAb alone failed to substantially inhibit the initial events of IL-2 stimulation, maximal inhibition of IL-2-induced cytotoxicity and proliferation was achieved by combining both anti-p55 IL-2R and anti-p75 IL-2R. Collectively, results from the present studies directly implicate the p75 IL-2R as the structure predominantly responsible for IL-2 activation of NK cells.

摘要

白细胞介素-2受体(IL-2R)至少由两个亚基组成,即p55(CD25/Tac)和p75糖蛋白。p75 IL-2R优先表达于静息的人外周血自然杀伤(NK)细胞上,但在相当比例的T淋巴细胞、B淋巴细胞、单核细胞或粒细胞上未检测到。抗p75 IL-2R单克隆抗体(mAb)可显著抑制与IL-2介导的NK细胞激活相关的早期事件,包括抑制细胞毒性活性和诱导CD69早期激活抗原。虽然单独使用抗p55 IL-2R mAb未能显著抑制IL-2刺激的初始事件,但联合使用抗p55 IL-2R和抗p75 IL-2R可实现对IL-2诱导的细胞毒性和增殖的最大抑制。总体而言,本研究结果直接表明p75 IL-2R是主要负责IL-2激活NK细胞的结构。

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