Berg-Brown Nancy N, Gronski Matthew A, Jones Russell G, Elford Alisha R, Deenick Elissa K, Odermatt Bernhard, Littman Dan R, Ohashi Pamela S
Ontario Cancer Institute, University Health Network, 610 University Ave., Toronto, M5G 2M9 Canada.
J Exp Med. 2004 Mar 15;199(6):743-52. doi: 10.1084/jem.20031022.
Understanding the pathways that signal T cell tolerance versus activation is key to regulating immunity. Previous studies have linked CD28 and protein kinase C-theta (PKCtheta) as a potential signaling pathway that influences T cell activation. Therefore, we have compared the responses of T cells deficient for CD28 and PKCtheta in vivo and in vitro. Here, we demonstrate that the absence of PKCtheta leads to the induction of T cell anergy, with a phenotype that is comparable to the absence of CD28. Further experiments examined whether PKCtheta triggered other CD28-dependent responses. Our data show that CD4 T cell-B cell cooperation is dependent on CD28 but not PKCtheta, whereas CD28 costimulatory signals that augment proliferation can be uncoupled from signals that regulate anergy. Therefore, PKCtheta relays a defined subset of CD28 signals during T cell activation and is critical for the induction of activation versus tolerance in vivo.
了解介导T细胞耐受与激活的信号通路是调节免疫的关键。以往的研究将CD28和蛋白激酶C-θ(PKCθ)联系起来,作为影响T细胞激活的潜在信号通路。因此,我们比较了体内和体外缺乏CD28和PKCθ的T细胞的反应。在此,我们证明PKCθ的缺失会导致T细胞无反应性的诱导,其表型与CD28缺失时相当。进一步的实验研究了PKCθ是否触发其他依赖CD28的反应。我们的数据表明,CD4 T细胞与B细胞的合作依赖于CD28而非PKCθ,而增强增殖的CD28共刺激信号可以与调节无反应性的信号分离。因此,PKCθ在T细胞激活过程中传递特定的CD28信号子集,并且对于体内激活与耐受的诱导至关重要。