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组胺对人白细胞介素-2和干扰素-γ基因表达的双重调控:激活与抑制

Dual control of human interleukin-2 and interferon-gamma gene expression by histamine: activation and suppression.

作者信息

Arad G, Nussinovich R, Na'amad M, Kaempfer R

机构信息

Department of Molecular Virology, Hebrew University Hadassah-Medical School, Jerusalem, Israel.

出版信息

Cell Immunol. 1996 May 25;170(1):149-55. doi: 10.1006/cimm.1996.0145.

DOI:10.1006/cimm.1996.0145
PMID:8660811
Abstract

Histamine is considered to be an activator of cells with suppressive capacity. In agreement with this concept, we show that histamine elicits a strong inhibition of the induced expression of interleukin-2 (IL-2) and interferon-gamma (IFN-gamma) genes. However, our experiments reveal a novel property of histamine: early in the induction process, it strongly stimulates expression of these two genes in cultured human peripheral blood mononuclear cells (PBMC). The histamine-mediated superinduction of IL-2 mRNA is seen also in a Th cell line, showing that such cells respond directly to histamine. In the course of mitogenic induction, a 20-fold stimulation by histamine is converted into an equally strong inhibition. The response of a PBMC population to histamine thus undergoes a remarkable change following T cell activation. The dual effect of histamine can be blocked by the H2 histamine receptor antagonist cimetidine, while the early activation by histamine is mimicked by the H2 agonist impromidine, showing that both activation and inhibition of IL-2 and IFN-gamma gene expression by histamine are exerted via this receptor. These results support the concept that histamine, released during an immune response, exerts opposite regulatory effects by first activating cells able to express the IL-2 and IFN-gamma genes and only then suppressive cells that become responsive to histamine more slowly, but once activated shut off the expression of these genes.

摘要

组胺被认为是具有抑制能力的细胞的激活剂。与这一概念一致,我们发现组胺能强烈抑制白细胞介素-2(IL-2)和干扰素-γ(IFN-γ)基因的诱导表达。然而,我们的实验揭示了组胺的一种新特性:在诱导过程早期,它能强烈刺激培养的人外周血单个核细胞(PBMC)中这两种基因的表达。在Th细胞系中也观察到组胺介导的IL-2 mRNA超诱导,表明此类细胞可直接对组胺作出反应。在有丝分裂诱导过程中,组胺20倍的刺激作用会转变为同样强烈的抑制作用。因此,PBMC群体对组胺的反应在T细胞激活后会发生显著变化。组胺的双重作用可被H2组胺受体拮抗剂西咪替丁阻断,而组胺的早期激活作用可被H2激动剂英普咪定模拟,这表明组胺对IL-2和IFN-γ基因表达的激活和抑制作用均通过该受体发挥。这些结果支持了这样一种概念,即在免疫反应过程中释放的组胺通过首先激活能够表达IL-2和IFN-γ基因的细胞,然后才激活对组胺反应较慢但一旦激活就会关闭这些基因表达的抑制性细胞,从而发挥相反的调节作用。

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