Banerjee Arnob, Banks Alexander S, Nawijn Martijn C, Chen X Peter, Rothman Paul B
Integrated Program in Molecular, Cellular, and Biophysical Studies, Columbia College of Physicians and Surgeons, New York, NY 10032, USA.
J Immunol. 2002 May 1;168(9):4277-81. doi: 10.4049/jimmunol.168.9.4277.
Recent studies have suggested that signaling initiated by the activation of Ag receptors and signaling activated through cytokine receptors may be regulated by a common set of inhibitory proteins. Suppressor of cytokine signaling 3 (SOCS-3), which has previously been demonstrated to inhibit cytokine signaling, is induced on TCR ligation. Overexpression of SOCS-3 can inhibit transcription driven by the IL-2 promoter in response to T cell activation. This inhibitory activity correlates with the suppression of calcineurin-dependent dephosphorylation and activation of the IL-2 promoter binding transcription factor, NFATp. Infection of primary murine T cells with a retrovirus encoding SOCS-3 blocks their IL-2 production in response to activation. Interestingly, SOCS-3 was found to coimmunoprecipitate with the catalytic subunit of calcineurin. These studies suggest that SOCS-3 may regulate T cell function as part of a negative feedback loop.
最近的研究表明,由抗原受体激活引发的信号传导以及通过细胞因子受体激活的信号传导可能受一组共同的抑制性蛋白调控。细胞因子信号传导抑制因子3(SOCS-3)此前已被证明可抑制细胞因子信号传导,在TCR连接时被诱导产生。SOCS-3的过表达可抑制IL-2启动子在T细胞激活时驱动的转录。这种抑制活性与钙调神经磷酸酶依赖性去磷酸化的抑制以及IL-2启动子结合转录因子NFATp的激活相关。用编码SOCS-3的逆转录病毒感染原代小鼠T细胞可阻断其在激活时的IL-2产生。有趣的是,发现SOCS-3可与钙调神经磷酸酶的催化亚基进行共免疫沉淀。这些研究表明,SOCS-3可能作为负反馈回路的一部分来调节T细胞功能。