Gelfanov V, Lai Y G, Gelfanova V, Dong J Y, Su J P, Liao N S
Institute of Molecular Biology, Academia Sinica, Taipei, Taiwan, 2epublic of China.
J Immunol. 1995 Jul 1;155(1):76-82.
The CD8+CD4- (CD8+) murine small intestinal intraepithelial lymphocytes (IELs) contain two subpopulations, one expressing alpha alpha-CD8 homodimers and another alpha beta-CD8 heterodimers. In this study, plate-bound anti-TCR beta-chain (TCR-beta) mAb alone or combined with anti-CD28 mAb is used as a model system to study activation requirement of these two CD8+ IEL subsets. In contrast to CD8+ lymph node (LN) cells that require both TCR and CD28 triggering for activation, alpha beta-CD8+ IELs proliferate and produce IL-2 and IFN-gamma when stimulated with anti-TCR-beta mAb alone, and soluble CTLA-4 Ig has no effect on their responses. On the other hand, alpha alpha-CD8+ IELs neither make IL-2 or IFN-gamma nor proliferate even when both stimuli are provided. However, alpha alpha-CD8+ IELs are capable of proliferation in both CD8+ IEL subsets is lower than in CD8+ LN cells, which contributes to the weaker and delayed response of CD8+ IELs.
CD8⁺CD4⁻(CD8⁺)小鼠小肠上皮内淋巴细胞(IEL)包含两个亚群,一个表达αα-CD8同二聚体,另一个表达αβ-CD8异二聚体。在本研究中,单独的板结合抗TCRβ链(TCR-β)单克隆抗体或与抗CD28单克隆抗体联合使用作为模型系统,以研究这两个CD8⁺IEL亚群的激活需求。与需要TCR和CD28触发才能激活的CD8⁺淋巴结(LN)细胞不同,单独用抗TCR-β单克隆抗体刺激时,αβ-CD8⁺IEL会增殖并产生IL-2和IFN-γ,可溶性CTLA-4 Ig对其反应没有影响。另一方面,即使提供两种刺激,αα-CD8⁺IEL既不产生IL-2或IFN-γ也不增殖。然而,αα-CD8⁺IEL能够在两种刺激下增殖,两个CD8⁺IEL亚群的增殖能力均低于CD8⁺LN细胞,这导致CD8⁺IEL的反应较弱且延迟。