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Ly2抑制性细胞活性的机制。转导抑制信号需要激活Ly1 I-J+细胞。

Mechanisms of Ly2 suppressor cell activity. Activation of an Ly1 I-J+ cell is required to transduce the suppressive signal.

作者信息

Flood P M, Louie D C

出版信息

J Exp Med. 1984 May 1;159(5):1413-28. doi: 10.1084/jem.159.5.1413.

Abstract

A cell-free product secreted by Ly1-2+ T cells (Ly2 TsF) can suppress the in vitro response to sheep erythrocytes (SRBC) of spleen cells depleted of Ly2+ T cells. This suppressor factor expresses biological activity only when the acceptor cells share major histocompatibility complex (MHC)-linked polymorphic genes with the cells that made the Ly2 TsF. Removal of Ly1 I-J+ cells from the assay culture abrogates the ability of Ly2 TsF to suppress these cultures, but we can replace the need for the I-J+ cells in the assay culture with an I-J+ soluble factor derived from them. We investigated the cellular interactions involved in the activation of I-J+ cells by Ly2 TsF in vitro. We have been able to induce the production of an I-J+ molecule needed for Ly2 TsF activity in a 48-h intermediate culture of B cell-depleted Ly1 spleen cells, Ly2 TsF, and antigen. This molecule not only fails to bind antigen, but is also antigen nonspecific in that it can be induced by Ly2 TsF of irrelevant specificities. In order to replace the activity of the Ly1 I-J+ cell in the assay culture, the cell induced by Ly2 TsF to produce the I-J+ molecule in vitro must share genetic polymorphisms linked to the MHC with the Ly2 TsF, and genetic polymorphisms linked to the Igh-V gene complex with the target cell. In order for Ly2 TsF to induce cells of the primary culture to produce the I-J+ molecule, Ly2 TsF must share genetic polymorphisms linked to the IE region of the MHC with the Ly1 I-J+ cell producing the I-J+ molecule. These results indicate that the suppressive mechanism of Ly2 TsF involves the interaction with an Ly1 I-J+ molecule. This I-J+ molecule serves to focus the antigen-specific suppressor molecule on the target cell. The recognition event of this suppressive complex on the surface of the acceptor cell is controlled by Igh-V-linked genes restricted by the I-J+ molecule of the suppressor complex. This suppressor interaction is confined to the suppressor effector phase of the suppressor circuit since the I-J+ molecules needed for by Ly2 TsF activity do not substitute for the I-J+ molecules needed for the activity of Ly1 TsiF , a T cell factor that initiates the suppressor cell circuit.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

Ly1-2+ T细胞分泌的一种无细胞产物(Ly2 TsF)能够抑制去除Ly2+ T细胞的脾细胞对绵羊红细胞(SRBC)的体外反应。这种抑制因子只有在受体细胞与产生Ly2 TsF的细胞共享主要组织相容性复合体(MHC)连锁的多态性基因时才表达生物活性。从检测培养物中去除Ly1 I-J+细胞会消除Ly2 TsF抑制这些培养物的能力,但我们可以用源自它们的I-J+可溶性因子来替代检测培养物中对I-J+细胞的需求。我们研究了体外Ly2 TsF激活I-J+细胞所涉及的细胞间相互作用。我们已经能够在去除B细胞的Ly1脾细胞、Ly2 TsF和抗原的48小时中间培养物中诱导产生Ly2 TsF活性所需的I-J+分子。这种分子不仅不能结合抗原,而且在抗原方面是非特异性的,因为它可以由不相关特异性的Ly2 TsF诱导产生。为了替代检测培养物中Ly1 I-J+细胞的活性,体外被Ly2 TsF诱导产生I-J+分子的细胞必须与Ly2 TsF共享与MHC连锁的遗传多态性,并与靶细胞共享与Igh-V基因复合体连锁的遗传多态性。为了使Ly2 TsF诱导原代培养细胞产生I-J+分子,Ly2 TsF必须与产生I-J+分子的Ly1 I-J+细胞共享与MHC的IE区域连锁的遗传多态性。这些结果表明,Ly2 TsF的抑制机制涉及与Ly1 I-J+分子的相互作用。这种I-J+分子用于将抗原特异性抑制分子聚焦于靶细胞。受体细胞表面这种抑制复合物的识别事件由抑制复合物的I-J+分子限制的与Igh-V连锁的基因控制。这种抑制相互作用仅限于抑制回路的抑制效应阶段,因为Ly2 TsF活性所需的I-J+分子不能替代启动抑制细胞回路的T细胞因子Ly1 TsiF活性所需的I-J+分子。(摘要截取自400字)

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