Berg Martina, Zavazava Nicholas
Department of Internal Medicine, University of Iowa Hospitals and Clinics and VA Medical Center, Iowa City, IA 52242, USA.
J Leukoc Biol. 2008 Apr;83(4):853-63. doi: 10.1189/jlb.0107065. Epub 2007 Dec 27.
CD28 and CTLA-4 are the critical costimulatory receptors that predominantly determine the outcome of T cell stimulation, with CD28 promoting positive costimulation and CTLA-4 inducing inhibitory signals. Blockage of the B7-CD28/CTLA-4 pathway leads to transplantation tolerance. However, the exact mechanism of the inhibitory function of CTLA-4 remains elusive. Here, we investigated the influence of CTLA-4 expression on CD28 using CTLA-4-transfected Jurkat T cells as well as primary T cells. Up-regulation of CTLA-4 induced abrogation of IL-2 production, indicating an anergic phenotype of CTLA-4(high) T cells. Besides the negative signaling function of CTLA-4, we show for the first time that CTLA-4 expression promotes the down-regulation of CD28 on the T cell surface as a result of enhanced internalization and degradation of CD28. These data suggest that apart from the established competition for B7.1 and B7.2 by CTLA-4, inhibition of T cells by CTLA-4 might be additionally explained by reduction of CD28 on the cell surface, which might impede T cell response to stimulation. Our data provide a previously unrecognized mechanism for T cell regulation.
CD28和CTLA-4是主要决定T细胞刺激结果的关键共刺激受体,其中CD28促进正向共刺激,而CTLA-4诱导抑制性信号。阻断B7-CD28/CTLA-4通路可导致移植耐受。然而,CTLA-4抑制功能的确切机制仍不清楚。在此,我们使用转染CTLA-4的Jurkat T细胞以及原代T细胞研究了CTLA-4表达对CD28的影响。CTLA-4的上调导致IL-2产生的废除,表明CTLA-4(高表达)T细胞呈无反应性表型。除了CTLA-4的负向信号传导功能外,我们首次表明,由于CD28内化和降解增强,CTLA-4表达促进了T细胞表面CD28的下调。这些数据表明,除了已确定的CTLA-4对B7.1和B7.2的竞争外,CTLA-4对T细胞的抑制作用可能还可以通过细胞表面CD28的减少来解释,这可能会阻碍T细胞对刺激的反应。我们的数据提供了一种以前未被认识的T细胞调节机制。