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T-bet在CD4和CD8 T细胞的TH1谱系定向分化及IFN-γ产生中的不同作用。

Distinct effects of T-bet in TH1 lineage commitment and IFN-gamma production in CD4 and CD8 T cells.

作者信息

Szabo Susanne J, Sullivan Brandon M, Stemmann Claudia, Satoskar Abhay R, Sleckman Barry P, Glimcher Laurie H

机构信息

Department of Immunology and Infectious Diseases, Harvard School of Public Health, Boston, MA 02115, USA.

出版信息

Science. 2002 Jan 11;295(5553):338-42. doi: 10.1126/science.1065543.

Abstract

T-bet is a member of the T-box family of transcription factors that appears to regulate lineage commitment in CD4 T helper (TH) lymphocytes in part by activating the hallmark TH1 cytokine, interferon-gamma (IFN-gamma). IFN-gamma is also produced by natural killer (NK) cells and most prominently by CD8 cytotoxic T cells, and is vital for the control of microbial pathogens. Although T-bet is expressed in all these cell types, it is required for control of IFN-gamma production in CD4 and NK cells, but not in CD8 cells. This difference is also apparent in the function of these cell subsets. Thus, the regulation of a single cytokine, IFN-gamma, is controlled by distinct transcriptional mechanisms within the T cell lineage.

摘要

T-bet是T-box转录因子家族的成员,它似乎部分通过激活标志性的辅助性T细胞1型(TH1)细胞因子γ干扰素(IFN-γ)来调节CD4辅助性T(TH)淋巴细胞的谱系定向。IFN-γ也由自然杀伤(NK)细胞产生,在CD8细胞毒性T细胞中产生最为显著,并且对控制微生物病原体至关重要。尽管T-bet在所有这些细胞类型中都有表达,但它是CD4和NK细胞中控制IFN-γ产生所必需的,而在CD8细胞中则不是。这种差异在这些细胞亚群的功能中也很明显。因此,单一细胞因子IFN-γ的调节是由T细胞谱系内不同的转录机制控制的。

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