A requirement for CARMA1 in TCR-induced NF-κB activation

被引:262
作者
Wang, DH
You, Y
Case, SM
McAllister-Lucas, LM
Wang, L
DiStefano, PS
Nuñez, G
Bertin, J
Lin, X [1 ]
机构
[1] SUNY Buffalo, Dept Microbiol, Sch Med & Biomed Sci, Buffalo, NY 14214 USA
[2] Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Sch Med, Ctr Comprehens Canc, Ann Arbor, MI 48109 USA
[4] Millennium Pharmaceut Inc, Cambridge, MA 02139 USA
关键词
D O I
10.1038/ni824
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Stimulation of the T cell receptor (TCR) complex initiates multiple signaling cascades that lead to the activation of several transcription factors, including the NF-kappaB family members. Although various proximal signaling components of the TCR have been intensively studied, the distal components that mediate TCR-induced NF-kappaB activation remain largely unknown. Using a somatic mutagenesis approach, we cloned a CARMA1-deficient T cell line. Deficiency in CARMA1 (originally known as CARDII) resulted in selectively impaired activation of NF-kappaB induced by the TCR and a consequent defect in interleukin-2 (IL-2) production. Reconstitution of the CARMA1-deficient cells with CARMA1 fully rescued this signaling defect. Together, our results show that CARMA1 is an essential signaling component that mediates TCR-induced NF-kappaB activation.
引用
收藏
页码:830 / 835
页数:6
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