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人类淋巴细胞激活的白细胞介素非依赖途径的证据。

Evidence for an interleukin-independent pathway for human lymphocyte activation.

作者信息

Koretzky G A, Daniele R P, Greene W C, Nowell P C

出版信息

Proc Natl Acad Sci U S A. 1983 Jun;80(11):3444-7. doi: 10.1073/pnas.80.11.3444.

Abstract

Though lectin mitogen stimulation of T-cell proliferation is an interleukin 1- (IL 1), interleukin 2- (IL 2) dependent process, the calcium ionophore A23187 may be able to initiate T-lymphocyte proliferation by an additional pathway. That the action of A23187 is IL 1 independent was demonstrated by its ability to stimulate monocyte-depleted cells without the addition of exogenous IL 1. The IL 2 independence of A23187 was indicated by (i) the inability of exogenous IL 2 to augment A23187-induced proliferation and (ii) the inability of the monoclonal antibody anti-Tac (with specificity for the human IL 2 receptor) to inhibit proliferation mediated by A23187. By contrast, in cultures stimulated with the lectin mitogen phytohemagglutinin, additional IL 2 considerably increased proliferation, whereas anti-Tac routinely caused 60-90% inhibition. Although the ionophore caused some IL 2 production and resulted in IL 2 receptor expression, quantitative studies showed that our results could not be explained by excessive amounts of endogenous IL 2 interfering with the blocking action of the antibody. Therefore, these data suggest that the action of A23187 as a human lymphocyte mitogen may be the result of at least two pathways--one dependent on the interleukin-cell interactions and the other independent of these mediators.

摘要

尽管凝集素丝裂原刺激T细胞增殖是一个依赖白细胞介素1(IL-1)、白细胞介素2(IL-2)的过程,但钙离子载体A23187可能能够通过另一条途径启动T淋巴细胞增殖。A23187的作用不依赖IL-1,这一点可通过其在不添加外源性IL-1的情况下刺激去除单核细胞的细胞的能力得到证明。A23187不依赖IL-2表现在:(i)外源性IL-2无法增强A23187诱导的增殖;(ii)抗Tac单克隆抗体(对人IL-2受体具有特异性)无法抑制A23187介导的增殖。相比之下,在用凝集素丝裂原植物血凝素刺激的培养物中,额外的IL-2可显著增加增殖,而抗Tac通常会导致60%-90%的抑制。尽管离子载体可导致一些IL-2的产生并导致IL-2受体表达,但定量研究表明,我们的结果无法用过量的内源性IL-2干扰抗体的阻断作用来解释。因此,这些数据表明,A23187作为人淋巴细胞丝裂原的作用可能是至少两条途径的结果——一条依赖白细胞介素-细胞相互作用,另一条不依赖这些介质。

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