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[人白细胞介素-2产生的细胞调节]

[Cellular regulation of human interleukin-2 production].

作者信息

Chouaib S, Fradelizi D

出版信息

C R Seances Acad Sci III. 1982 Oct 11;295(5):365-8.

PMID:6817873
Abstract

The mechanism of IL2 production by T lymphocytes has been clearly established in Mice. Previous studies have also suggested that control of IL2 production is similar in the Human. We have observed that a complete depletion of adherent monocytes abrogates IL2 production by T lymphocytes. On the other hands in humane inhibition of IL2 production was also mediated by an excess of monocytes. This inhibition was mediated by soluble products and could be blocked by treatment with indomethacin. PGE2 was identified as one of this, inhibitory monokine. A possible mechanism of this inhibition by PGE2 is suggested. Such inhibition was not observed if the T lymphocyte suspension was irradiated (1000 rad) before addition of PGE2 or excess monocytes. These results suggest that activation of a radiosensitive T cell by monokines is required for the inhibition of IL2 production. A model for the cellular control of human IL2 production is proposed.

摘要

T淋巴细胞产生白细胞介素2(IL2)的机制在小鼠中已得到明确证实。先前的研究也表明,人类中IL2产生的调控与之相似。我们观察到,贴壁单核细胞完全耗竭会消除T淋巴细胞产生IL2的能力。另一方面,在人类中,IL2产生的抑制也由过量的单核细胞介导。这种抑制是由可溶性产物介导的,并且可以通过吲哚美辛处理来阻断。前列腺素E2(PGE2)被确定为其中一种抑制性单核因子。提出了PGE2这种抑制作用的一种可能机制。如果在添加PGE2或过量单核细胞之前对T淋巴细胞悬液进行照射(1000拉德),则不会观察到这种抑制作用。这些结果表明,单核因子激活放射敏感的T细胞是抑制IL2产生所必需的。提出了一个人类IL2产生的细胞调控模型。

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