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克隆性T细胞群体中单细胞细胞因子基因表达的异质性。

Heterogeneity of single cell cytokine gene expression in clonal T cell populations.

作者信息

Bucy R P, Panoskaltsis-Mortari A, Huang G Q, Li J, Karr L, Ross M, Russell J H, Murphy K M, Weaver C T

机构信息

Department of Pathology, University of Alabama at Birmingham 35233.

出版信息

J Exp Med. 1994 Oct 1;180(4):1251-62. doi: 10.1084/jem.180.4.1251.

Abstract

T helper type 0 (Th0), Th1, and Th2 CD4+ T cell clones derived from a T cell receptor alpha/beta (TCR-alpha/beta) transgenic mouse were activated by antigen presented on "artificial" antigen-presenting cells that expressed or lacked the costimulatory molecule B7-1, and were analyzed for single cell cytokine mRNA expression by in situ hybridization. There was significant heterogeneity in the frequency of T cells that expressed individual cytokine mRNAs within each clonal population, suggesting that transcriptional control of each of the cytokine genes was not coordinate within an individual cell. The majority of antigen-stimulated Th1 cells expressed mRNA for interferon gamma (IFN-gamma), but far fewer cells in the same population expressed interleukin 2 (IL-2). Similarly, the frequency of IL-4-expressing cells was greater than that of IL-5- or IL-10-expressing cells in the same Th2 population, but the difference in expression frequencies was more variable between clones. The expression frequencies of each of the cytokines was quite heterogeneous in the antigen-activated Th0 population. The principal effect of increased antigen on the activation of individual cytokine genes in each of the clonal populations was to increase recruitment of mRNA-positive cells, with little or no effect on the level of cytokine mRNA expression in individual positive cells. The effects of B7 costimulation were variable depending on the cytokine gene analyzed. B7 costimulation markedly increased the frequency and the level of IL-2 mRNA expression in individual positive cells in the Th1 and Th0 populations, with less effect on the recruitment and single cell expression level of IFN-gamma. IL-4 frequencies were modestly increased by B7 costimulation of the Th2 clones, but there was no detectable increase in single cell IL-4 expression level. The observed patterns of cytokine mRNA expression favor a model of T cell activation in which all-or-none, rather than graded, responses of cytokine genes are dominant.

摘要

从表达T细胞受体α/β(TCR-α/β)的转基因小鼠获得的辅助性T细胞0型(Th0)、Th1和Th2 CD4 + T细胞克隆,由表达或缺乏共刺激分子B7-1的“人工”抗原呈递细胞呈递的抗原激活,并通过原位杂交分析单细胞细胞因子mRNA表达。每个克隆群体中表达单个细胞因子mRNA的T细胞频率存在显著异质性,这表明每个细胞因子基因的转录控制在单个细胞内并非协同进行。大多数抗原刺激的Th1细胞表达干扰素γ(IFN-γ)的mRNA,但同一群体中表达白细胞介素2(IL-2)的细胞要少得多。同样,在同一Th2群体中,表达IL-4的细胞频率高于表达IL-5或IL-10的细胞频率,但不同克隆之间表达频率的差异更具变异性。在抗原激活的Th0群体中,每种细胞因子的表达频率非常不均一。抗原增加对每个克隆群体中单个细胞因子基因激活的主要作用是增加mRNA阳性细胞的募集,对单个阳性细胞中细胞因子mRNA表达水平几乎没有影响。B7共刺激的作用因所分析的细胞因子基因而异。B7共刺激显著增加了Th1和Th0群体中单个阳性细胞中IL-2 mRNA表达的频率和水平,对IFN-γ的募集和单细胞表达水平影响较小。B7共刺激Th2克隆适度增加了IL-4频率,但单细胞IL-4表达水平没有可检测到的增加。观察到的细胞因子mRNA表达模式支持一种T细胞激活模型,其中细胞因子基因的全或无反应而非分级反应占主导地位。

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