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不同CC趋化因子诱导的辅助性T细胞细胞因子产生增强作用。

Differential CC chemokine-induced enhancement of T helper cell cytokine production.

作者信息

Karpus W J, Lukacs N W, Kennedy K J, Smith W S, Hurst S D, Barrett T A

机构信息

Department of Pathology, Northwestern University Institute for Neuroscience, Chicago, IL 60611, USA.

出版信息

J Immunol. 1997 May 1;158(9):4129-36.

PMID:9126972
Abstract

Chemokines are a family of small m.w. cytokines that induce chemotaxis and chemokinesis of leukocytes. These molecules are ligands for seven-transmembrane, Gi protein-linked receptors that induce a signaling cascade in human T cells and provide costimulation for T cell activation, in addition to participating in transendothelial migration of leukocytes. To address the role of chemokines in the regulation of Th cell cytokine production, we utilized an OVA-specific TCR transgenic (Tg+) model. Cells stimulated through the TCR and incubated in the presence of macrophage inflammatory protein-1alpha (MIP-1alpha) showed enhanced IFN-gamma production, whereas cells incubated in the presence of monocyte chemotactic protein-1 (MCP-1) showed enhanced IL-4 production. Similar results were obtained whether TCR Tg+ T cells were stimulated with anti-CD3 mAb or OVA peptide. Primary stimulation of T cells in the presence of chemokines, followed by secondary stimulation and tertiary stimulation with anti-TCR clonotype mAb alone (no exogenous chemokines), revealed an enhanced IFN-gamma production for MIP-1alpha stimulation and IL-4 production for MCP-1 stimulation. Naive Tg+ T cells, obtained from Tg+ mice crossed to RAG-1-deficient mice, showed enhanced IFN-gamma production when incubated with MIP-1alpha and enhanced IL-4 production when incubated with MCP-1. These results suggest CC chemokines play a role in regulating naive Th cell cytokine production, in addition to regulating leukocyte trafficking.

摘要

趋化因子是一类低分子量的细胞因子家族,可诱导白细胞的趋化性和化学增活现象。这些分子是七跨膜、与Gi蛋白偶联受体的配体,除了参与白细胞的跨内皮迁移外,还能在人T细胞中诱导信号级联反应,并为T细胞活化提供共刺激。为了研究趋化因子在Th细胞细胞因子产生调节中的作用,我们使用了一种OVA特异性TCR转基因(Tg+)模型。通过TCR刺激并在巨噬细胞炎性蛋白-1α(MIP-1α)存在下孵育的细胞,其IFN-γ产生增强,而在单核细胞趋化蛋白-1(MCP-1)存在下孵育的细胞,其IL-4产生增强。无论TCR Tg+ T细胞是用抗CD3单克隆抗体还是OVA肽刺激,都得到了类似的结果。在趋化因子存在下对T细胞进行初次刺激,然后单独用抗TCR克隆型单克隆抗体(无外源性趋化因子)进行二次刺激和三次刺激,结果显示MIP-1α刺激可增强IFN-γ产生,MCP-1刺激可增强IL-4产生。从与RAG-1缺陷小鼠杂交的Tg+小鼠获得的初始Tg+ T细胞,与MIP-1α孵育时IFN-γ产生增强,与MCP-1孵育时IL-4产生增强。这些结果表明,CC趋化因子除了调节白细胞迁移外,还在调节初始Th细胞细胞因子产生中发挥作用。

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