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通过单个等位基因的激活来调控白细胞介素-4的表达。

Regulation of IL-4 expression by activation of individual alleles.

作者信息

Rivière I, Sunshine M J, Littman D R

机构信息

Molecular Pathogenesis Program, Skirball Institute of Biomolecular Medicine, New York University Medical Center, New York 10016, USA.

出版信息

Immunity. 1998 Aug;9(2):217-28. doi: 10.1016/s1074-7613(00)80604-4.

Abstract

To study the in vivo role of IL-4-expressing cells, we developed a strategy to tag these cells, by generating mice in which one IL-4 allele was replaced with a cDNA encoding the human CD2 (huCD2) cell-surface molecule. Expression of the huCD2 reporter was, like IL-4, restricted to the appropriately polarized T helper 2 cells. However, most of the cells expressed only the IL-4 or the targeted allele. Analysis of the frequency of monoallelic versus biallelic expression suggests that the activation of each individual allele is regulated by a stochastic process whose probability can be augmented by increasing the strength of signal delivered through the TCR. Allele-specific activation may be a general feature of cytokine regulation that contributes to the functional diversity within T helper cell subpopulations.

摘要

为了研究表达白细胞介素-4(IL-4)的细胞在体内的作用,我们开发了一种标记这些细胞的策略,即通过构建小鼠,将其中一个IL-4等位基因替换为编码人类CD2(huCD2)细胞表面分子的cDNA。与IL-4一样,huCD2报告基因的表达仅限于适当极化的辅助性T细胞2型(Th2)细胞。然而,大多数细胞仅表达IL-4或靶向等位基因。单等位基因与双等位基因表达频率的分析表明,每个单个等位基因的激活受随机过程调控,通过增加经由T细胞受体传递的信号强度,该过程的概率可被提高。等位基因特异性激活可能是细胞因子调节的一个普遍特征,有助于辅助性T细胞亚群内的功能多样性。

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