Kimura M, Yamashita M, Kubo M, Iwashima M, Shimizu C, Tokoyoda K, Chiba J, Taniguchi M, Katsumata M, Nakayama T
Department of Molecular Immunology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana Chuo-ku, Chiba 260-8670, Japan.
Int Immunol. 2000 Jun;12(6):817-24. doi: 10.1093/intimm/12.6.817.
Clonal anergy is one of the mechanisms that may account for self tolerance induced in T cells in the periphery. In this study we used the well-documented system of in vivo administration of a superantigen, staphylococcal enterotoxin B (SEB), to induce a state of hyporesponsiveness (anergy) in murine peripheral T cells to decipher the intracellular biochemical basis for this process. The TCR-induced Ca response of in vitro activated T cells was found to be impaired with significant defects in the phosphorylation of phospholipase C-gamma 1. Experiments with calcium ionophore and newly established transgenic mouse lines that express an active form of calcineurin suggested that in vivo SEB-induced anergy is established and/or maintained by a selective impairment in the TCR-induced activation of the Ca/calcineurin pathway.
克隆无能是外周T细胞诱导自身耐受的机制之一。在本研究中,我们使用了文献记载充分的体内给予超抗原——葡萄球菌肠毒素B(SEB)的系统,来诱导小鼠外周T细胞低反应性(无能)状态,以阐明该过程的细胞内生化基础。我们发现,体外活化的T细胞的TCR诱导的Ca反应受损,磷脂酶C-γ1的磷酸化存在显著缺陷。使用钙离子载体的实验以及新建立的表达活性形式钙调神经磷酸酶的转基因小鼠品系表明,体内SEB诱导的无能是由TCR诱导的Ca/钙调神经磷酸酶途径激活的选择性损伤所建立和/或维持的。