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T细胞受体下调控制病毒特异性CD8+ T细胞反应。

TCR down-regulation controls virus-specific CD8+ T cell responses.

作者信息

Bonefeld Charlotte Menné, Haks Mariëlle, Nielsen Bodil, von Essen Marina, Boding Lasse, Hansen Ann Kathrine, Larsen Jeppe Madura, Odum Niels, Krimpenfort Paul, Kruisbeek Ada, Christensen Jan Pravsgaard, Thomsen Allan Randrup, Geisler Carsten

机构信息

Department of International Health, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.

出版信息

J Immunol. 2008 Dec 1;181(11):7786-99. doi: 10.4049/jimmunol.181.11.7786.

Abstract

The CD3gamma di-leucine-based motif plays a central role in TCR down-regulation. However, little is understood about the role of the CD3gamma di-leucine-based motif in physiological T cell responses. In this study, we show that the expansion in numbers of virus-specific CD8(+) T cells is impaired in mice with a mutated CD3gamma di-leucine-based motif. The CD3gamma mutation did not impair early TCR signaling, nor did it compromise recruitment or proliferation of virus-specific T cells, but it increased the apoptosis rate of the activated T cells by increasing down-regulation of the antiapoptotic molecule Bcl-2. This resulted in a 2-fold reduction in the clonal expansion of virus-specific CD8(+) T cells during the acute phase of vesicular stomatitis virus and lymphocytic choriomeningitis virus infections. These results identify an important role of CD3gamma-mediated TCR down-regulation in virus-specific CD8(+) T cell responses.

摘要

基于双亮氨酸基序的CD3γ在TCR下调中起核心作用。然而,对于基于双亮氨酸基序的CD3γ在生理性T细胞应答中的作用了解甚少。在本研究中,我们发现,具有突变的基于双亮氨酸基序的CD3γ的小鼠中,病毒特异性CD8(+) T细胞数量的扩增受损。CD3γ突变不损害早期TCR信号传导,也不影响病毒特异性T细胞的募集或增殖,但通过增加抗凋亡分子Bcl-2的下调来提高活化T细胞的凋亡率。这导致在水疱性口炎病毒和淋巴细胞性脉络丛脑膜炎病毒感染急性期,病毒特异性CD8(+) T细胞的克隆扩增减少了2倍。这些结果确定了CD3γ介导的TCR下调在病毒特异性CD8(+) T细胞应答中的重要作用。

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