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白细胞介素2介导克隆的小鼠细胞毒性T淋巴细胞系中裂解活性的诱导。

Interleukin 2-mediated induction of lytic activity in a cloned murine CTL line.

作者信息

Howe R C, Milstone D S, Ratliff T L, Russell J H

出版信息

J Immunol. 1985 Apr;134(4):2414-8.

PMID:2579143
Abstract

We have analyzed the ability of interleukin 2 (IL 2) to induce lytic activity within a cloned murine H-2Dd-specific CTL line. Weakly lytic CTL harvested 6 to 7 days after previous stimulation with irradiated DBA/2J spleen cells and conditioned medium from secondary MLC (MLC SN) could be reactivated to high antigen-specific lytic activity with highly purified gibbon IL 2 or E. coli-produced human recombinant DNA IL 2. Dose-response curves with IL 2 and MLC SN suggest that IL 2 may be the principal detectable activity in MLC SN that is active on these CTL. Doses of IL 2 or MLC SN that were saturating for the induction of lytic activity were suboptimal for the expression of DNA synthesis measured by 3HTdR incorporation. This is consistent with a mechanism in which different threshold IL 2 concentrations are required to induce these two biologic responses. Finally, we show that IFN-gamma has little effect on the expression of lytic activity either alone or in combination with IL 2 in this bioassay.

摘要

我们分析了白细胞介素2(IL-2)在克隆的小鼠H-2Dd特异性CTL系中诱导溶解活性的能力。先前用经辐照的DBA/2J脾细胞和来自二次混合淋巴细胞培养(MLC)的条件培养基(MLC SN)刺激6至7天后收获的低溶解活性CTL,可用高度纯化的长臂猿IL-2或大肠杆菌产生的人重组DNA IL-2重新激活至高抗原特异性溶解活性。IL-2和MLC SN的剂量反应曲线表明,IL-2可能是MLC SN中对这些CTL有活性的主要可检测活性。诱导溶解活性达到饱和的IL-2或MLC SN剂量,对于通过3HTdR掺入测量的DNA合成表达而言并非最佳。这与一种机制一致,即诱导这两种生物学反应需要不同阈值的IL-2浓度。最后,我们表明在该生物测定中,单独或与IL-2联合使用时,IFN-γ对溶解活性的表达几乎没有影响。

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