首页> 美国卫生研究院文献>The Journal of Experimental Medicine >Mechanisms of Ly2 suppressor cell activity. Activation of an Ly1 I-J+ cell is required to transduce the suppressive signal
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Mechanisms of Ly2 suppressor cell activity. Activation of an Ly1 I-J+ cell is required to transduce the suppressive signal

机译:Ly2抑制细胞活性的机制。 Ly1 I-J +细胞的激活需要转导抑制信号

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摘要

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)
机译:Ly1-2 + T细胞分泌的无细胞产物(Ly2 TsF)可以抑制耗尽Ly2 + T细胞的脾细胞对绵羊红细胞(SRBC)的体外反应。仅当受体细胞与构成Ly2 TsF的细胞共享主要的组织相容性复合物(MHC)连接的多态性基因时,该抑制因子才表达生物活性。从测定培养物中去除Ly1 I-J +细胞消除了Ly2 TsF抑制这些培养物的能力,但是我们可以用衍生自它们的I-J +可溶因子代替测定培养物中对I-J +细胞的需要。我们调查了由Ly2 TsF在体外激活I-J +细胞所涉及的细胞相互作用。我们已经能够在消耗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。该分子不仅不能结合抗原,而且是抗原非特异性的,因为它可以被无关特异性的Ly2 TsF诱导。为了替换测定培养物中Ly1 I-J +细胞的活性,由Ly2 TsF诱导的体外产生I-J +分子诱导的细胞必须共享与Ly2 TsF连接到MHC的遗传多态性,以及与之相关的遗传多态性。与靶细胞结合的Igh-V基因复合物。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区相连的遗传多态性。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。该I-J +分子用于将抗原特异性抑制分子聚焦在靶细胞上。该抑制性复合物在受体细胞表面上的识别事件受抑制性复合物的I-J +分子限制的Igh-V连接基因控制。由于抑制Ly2 TsF活性所需的I-J +分子不能替代激活Lys TsiF的T细胞因子Ly1 TsiF所需的I-J +分子,因此这种抑制物的相互作用仅限于抑制电路的抑制物效应相。抑制器单元电路(摘要截断为400字)

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