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T细胞活化。IV。MHC I类分子、白细胞介素-2受体和白细胞介素-4受体分子之间功能联系的证据。

T-cell activation. IV. Evidence for a functional linkage between MHC class I, interleukin-2 receptor, and interleukin-4 receptor molecules.

作者信息

Hansen N Q, Tscherning T, Claesson M H

机构信息

Department of Medical Anatomy A, Panum Institute, University of Copenhagen, Denmark.

出版信息

Cytokine. 1991 Jan;3(1):35-41. doi: 10.1016/1043-4666(91)90008-2.

Abstract

The aim of the present work was to study regulatory interactions between MHC class I molecules and the interleukin (IL)-2, IL-3, and IL-4 receptors and functional interactions between the receptors for IL-2 and IL-4. Our major observations were: (1) quiescent splenic T cells exposed to specific anti-MHC class I antibodies become responsive to IL-2 and IL-4 stimulation; (2) T-cell clones (CTLL-2 and HT-1) grown at high cell density or low IL-2 concentrations become refractory to IL-2 and IL-4 stimulation. After exposure to anti-class I antibodies the refractory cells recover responsiveness to lymphokine-induced proliferation; (3) IL-2 receptor expression is non-inducible in class I-negative T-lymphoma cells, but is inducible following class I gene transfection of the cells; (4) exposure of T-cells and clones to IL-2 receptor antibody increases the responsiveness to IL-4 stimulation; (5) IL-2 and IL-4 act synergistically at low and substimulatory lymphokine levels; and (6) IL-3 responsiveness of hemopoietic cells is not influenced by exposure to anti-MHC class I antibody. It is concluded that class I molecules are of importance for the functional expression of the receptors for IL-2 and IL-4 and that these receptors are functionally interrelated.

摘要

本研究的目的是探讨MHC I类分子与白细胞介素(IL)-2、IL-3和IL-4受体之间的调节相互作用,以及IL-2和IL-4受体之间的功能相互作用。我们的主要观察结果如下:(1)暴露于特异性抗MHC I类抗体的静止脾T细胞对IL-2和IL-4刺激变得有反应;(2)在高细胞密度或低IL-2浓度下生长的T细胞克隆(CTLL-2和HT-1)对IL-2和IL-4刺激变得不敏感。在暴露于抗I类抗体后,难治性细胞恢复对淋巴因子诱导增殖的反应性;(3)IL-2受体表达在I类阴性T淋巴瘤细胞中不可诱导,但在细胞进行I类基因转染后可诱导;(4)T细胞和克隆暴露于IL-2受体抗体可增加对IL-4刺激的反应性;(5)IL-2和IL-4在低水平和亚刺激水平的淋巴因子作用下具有协同作用;(6)造血细胞对IL-3的反应性不受暴露于抗MHC I类抗体的影响。结论是I类分子对IL-2和IL-4受体的功能表达很重要,并且这些受体在功能上相互关联。

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