Eichhorn M, Prospero T D, Heussler V T, Dobbelaere D A
Nuclear Research Centre, Institute for Genetics, Karlsruhe, FRG.
J Exp Med. 1993 Sep 1;178(3):769-76. doi: 10.1084/jem.178.3.769.
We have analyzed the effect of antibodies (Abs) directed against major histocompatibility complex (MHC) class II Abs on the proliferation of Theileria parva-infected (Tpi) T cells. Anti-MHC class II Abs exert a direct effect on Tpi T cells causing an acute block in their proliferation. The inhibition does not involve apoptosis and is also entirely reversible. The rapid arrest of DNA synthesis caused by anti-MHC class II Abs is not due to interference with the state of activation of the T cells since the transcriptional activator NF-kappa B remains activated in arrested cells. In addition, interleukin 2 (IL-2), IL-2R, and c-myc gene expression are also unaffected. By analyzing the cell-cycle phase distribution of inhibited cells, it could be shown that cells in all phases of the cell cycle are inhibited. The signal transduction pathway that results in inhibition was shown to be independent of protein kinase C and extracellular Ca2+. Tyrosine kinase inhibitors, however, partly reduced the level of inhibition and, conversely, phosphatase inhibitors enhanced it. The possible relevance of this phenomenon in other systems is discussed.
我们分析了针对主要组织相容性复合体(MHC)II类抗体的抗体(Abs)对感染泰勒虫(Tpi)的T细胞增殖的影响。抗MHC II类抗体对Tpi T细胞产生直接作用,导致其增殖急性受阻。这种抑制不涉及细胞凋亡,并且完全可逆。抗MHC II类抗体引起的DNA合成快速停滞并非由于干扰T细胞的激活状态,因为转录激活因子NF-κB在停滞的细胞中仍保持激活状态。此外,白细胞介素2(IL-2)、IL-2受体和c-myc基因表达也未受影响。通过分析受抑制细胞的细胞周期阶段分布,可以发现细胞周期各阶段的细胞均受到抑制。导致抑制的信号转导途径显示独立于蛋白激酶C和细胞外Ca2+。然而,酪氨酸激酶抑制剂部分降低了抑制水平,相反,磷酸酶抑制剂则增强了抑制作用。本文讨论了这一现象在其他系统中的可能相关性。