Schubert J, Uciechowski P, Zielinska-Skowronek M, Tietjen C, Leo R, Schmidt R E
Abteilung Immunologie und Transfusionsmedizin, Zentrum Innere Medizin, Medizinische Hochschule, Hannover, Germany.
J Immunol. 1992 Jun 15;148(12):3814-9.
In these studies, the role of glycosylphosphatidylinositol (GPI)-anchored surface molecules during T cell activation was investigated in fresh T cells and T cell lines obtained from patients with paroxysmal nocturnal hemoglobinuria. For control, GPI-expressing T cells of the same patients were used. Unstimulated GPI- T cells exhibited significantly reduced surface expression of the activation Ag CD45R0, compared with GPI+ T cells. In addition, in measurements of proliferation, IFN-gamma production, and induction of second messengers such as cytoplasmic Ca2+, CD48- lymphocytes showed a similar response to TCR-specific stimulation, compared with CD48+ lymphocytes. In contrast, stimulation with the lectin PHA produced a decreased response of CD48- lymphocytes in these functions. In addition, stimulation with cross-linked CD59 mAb increased the proliferation of GPI-molecule expressing CD48+ T cell lines only. From these data, it can be concluded that GPI-anchored surface molecules play an important role in T lymphocyte activation.
在这些研究中,对来自阵发性夜间血红蛋白尿患者的新鲜T细胞和T细胞系中糖基磷脂酰肌醇(GPI)锚定的表面分子在T细胞活化过程中的作用进行了研究。作为对照,使用了同一患者表达GPI的T细胞。与GPI+T细胞相比,未受刺激的GPI-T细胞活化抗原CD45R0的表面表达显著降低。此外,在增殖、IFN-γ产生以及诸如细胞质Ca2+等第二信使诱导的测量中,与CD48+淋巴细胞相比,CD48-淋巴细胞对TCR特异性刺激表现出相似的反应。相反,用凝集素PHA刺激在这些功能中使CD48-淋巴细胞的反应降低。此外,用交联的CD59单克隆抗体刺激仅增加了表达GPI分子的CD48+T细胞系的增殖。从这些数据可以得出结论,GPI锚定的表面分子在T淋巴细胞活化中起重要作用。