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阵发性夜间血红蛋白尿症患者来源的正常淋巴细胞和糖基磷脂酰肌醇阴性淋巴细胞的激活差异。

Differences in activation of normal and glycosylphosphatidylinositol-negative lymphocytes derived from patients with paroxysmal nocturnal hemoglobinuria.

作者信息

Schubert J, Uciechowski P, Zielinska-Skowronek M, Tietjen C, Leo R, Schmidt R E

机构信息

Abteilung Immunologie und Transfusionsmedizin, Zentrum Innere Medizin, Medizinische Hochschule, Hannover, Germany.

出版信息

J Immunol. 1992 Jun 15;148(12):3814-9.

PMID:1376342
Abstract

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.

摘要

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。

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