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白细胞介素2诱导γ-干扰素生成:巨噬细胞和自然杀伤样细胞的参与

Interleukin 2 induces gamma-interferon production: participation of macrophages and NK-like cells.

作者信息

Kawase I, Brooks C G, Kuribayashi K, Olabuenaga S, Newman W, Gillis S, Henney C S

出版信息

J Immunol. 1983 Jul;131(1):288-92.

PMID:6408175
Abstract

Interleukin 2 (IL 2) has been shown to be a potent stimulator of natural killer (NK) cells. In the present studies, partially purified mouse and human IL 2 preparations were also found to induce interferon (IFN) from mouse spleen cells. By the criteria of sensitivity to treatment at pH 2 and failure to be neutralized by a potent anti-alpha, beta IFN serum, the species of IFN produced was of type gamma. Cooperation between two types of cell, a macrophage and an NK-like cell, was required for IFN production by murine spleen cells treated with IL 2. The requirement for macrophages could be replaced with supernatant obtained by incubating macrophages for 24 hr with lymphokine preparations containing IL 2. Interestingly, mature T cells apparently played no role in the process. Furthermore, the beige (bg/bg) mutation, which severely impairs NK cell lytic activity, had no effect on the ability of NK-like cells to participate in IFN production. Cell fractionation experiments revealed no dissociation between the requirements for augmentation of NK cytotoxic activity and for IFN production, and it is concluded that at least a portion of the NK boosting induced by IL 2-containing preparations is mediated through gamma-IFN.

摘要

白细胞介素2(IL-2)已被证明是自然杀伤(NK)细胞的有效刺激剂。在本研究中,还发现部分纯化的小鼠和人IL-2制剂能诱导小鼠脾细胞产生干扰素(IFN)。根据对pH 2处理的敏感性以及不能被高效抗α、β干扰素血清中和的标准,所产生的干扰素类型为γ型。用IL-2处理的小鼠脾细胞产生IFN需要两种细胞(巨噬细胞和NK样细胞)之间的协作。对巨噬细胞的需求可用含有IL-2的淋巴因子制剂与巨噬细胞孵育24小时后获得的上清液替代。有趣的是,成熟T细胞显然在该过程中不起作用。此外,严重损害NK细胞裂解活性的米色(bg/bg)突变对NK样细胞参与IFN产生的能力没有影响。细胞分级分离实验表明,增强NK细胞毒性活性的需求与产生IFN的需求之间没有分离,并且得出结论,含IL-2制剂诱导的至少一部分NK增强是通过γ-干扰素介导的。

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