Cordero O J, Salgado F J, Fernández-Alonso C M, Herrera C, Lluis C, Franco R, Nogueira M
Department of Biochemistry, University of Santiago de Compostela, 15706 Santiago de Compostela, Spain.
J Leukoc Biol. 2001 Dec;70(6):920-30.
CD26 is a lymphocyte marker that can anchor adenosine deaminase (ADA) on the T cell surface. We found that ADA is regulated by cytokines on the cell surface during T cell activation. By means of flow cytometry, immunofluorescence, and immunoblotting techniques, we found that interleukin (IL)-2 and IL-12 up-regulate ecto-ADA and CD26 expression. In clear contrast, IL-4 led to down-regulation of lymphocyte surface ADA without modifying the level of CD26. Moreover, neither circulating ADA transcription nor mRNA translation was regulated by cytokines. These results, along with absence of total-ADA modulation, the variable amount of ADA found in purified plasma membranes, and the different effect of Brefeldin A on the surface presence of ADA and CD26 indicated that cytokines regulate the translocation of ADA towards the cell surface through a mechanism not involving CD26. Ecto-ADA protected activated lymphocytes from the toxic effects of extracellular adenosine. Therefore, this cell surface ADA control might constitute part of the fine immunoregulatory mechanism of adenosine-mediated signaling through purinergic receptors in leukocytes.
CD26是一种淋巴细胞标志物,可将腺苷脱氨酶(ADA)锚定在T细胞表面。我们发现,在T细胞活化过程中,ADA在细胞表面受细胞因子调控。通过流式细胞术、免疫荧光和免疫印迹技术,我们发现白细胞介素(IL)-2和IL-12上调胞外ADA和CD26的表达。与之形成鲜明对比的是,IL-4导致淋巴细胞表面ADA下调,而不改变CD26的水平。此外,细胞因子既不调节循环ADA的转录,也不调节mRNA的翻译。这些结果,连同总ADA未受调节、纯化质膜中发现的ADA量可变以及布雷菲德菌素A对ADA和CD26表面存在的不同影响,表明细胞因子通过一种不涉及CD26的机制调节ADA向细胞表面的转运。胞外ADA保护活化的淋巴细胞免受细胞外腺苷的毒性作用。因此,这种细胞表面ADA调控可能构成腺苷通过嘌呤能受体介导的白细胞信号传导精细免疫调节机制的一部分。