Wang Donghai, You Yun, Case Sara M, McAllister-Lucas Linda M, Wang Lin, DiStefano Peter S, Nuñez Gabriel, Bertin John, Lin Xin
Department of Microbiology, School of Medicine and Biomedical Sciences, University at Buffalo, SUNY, Buffalo, NY 14214, USA.
Nat Immunol. 2002 Sep;3(9):830-5. doi: 10.1038/ni824. Epub 2002 Aug 5.
Stimulation of the T cell receptor (TCR) complex initiates multiple signaling cascades that lead to the activation of several transcription factors, including the NF-kappa B family members. Although various proximal signaling components of the TCR have been intensively studied, the distal components that mediate TCR-induced NF-kappa B 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-kappa B 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-kappa B activation.
T细胞受体(TCR)复合物的刺激会启动多个信号级联反应,这些反应会导致包括NF-κB家族成员在内的多种转录因子的激活。尽管TCR的各种近端信号成分已得到深入研究,但介导TCR诱导的NF-κB激活的远端成分仍基本未知。我们采用体细胞诱变方法克隆了一株CARMA1缺陷的T细胞系。CARMA1(最初称为CARDII)的缺陷导致TCR诱导的NF-κB激活选择性受损,进而导致白细胞介素-2(IL-2)产生缺陷。用CARMA1重建CARMA1缺陷细胞可完全挽救这种信号缺陷。总之,我们的结果表明CARMA1是介导TCR诱导的NF-κB激活的必需信号成分。