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白细胞介素-10抑制脂多糖刺激的单核细胞产生前列腺素E2。

IL-10 inhibits prostaglandin E2 production by lipopolysaccharide-stimulated monocytes.

作者信息

Niiro H, Otsuka T, Kuga S, Nemoto Y, Abe M, Hara N, Nakano T, Ogo T, Niho Y

机构信息

First Department of Internal Medicine, Faculty of Medicine, Kyushu University, Fukuoka, Japan.

出版信息

Int Immunol. 1994 Apr;6(4):661-4. doi: 10.1093/intimm/6.4.661.

Abstract

Since IL-10 has recently been shown to exhibit pleiotropic effects on human monocytes, it was of interest to determine the effect of this cytokine on prostaglandin E2 (PGE2) production by monocytes. Recombinant IL-10 (rIL-10) did not significantly affect PGE2 production by lipopolysaccharide (LPS)-unstimulated monocytes, but efficiently inhibited PGE2 production by LPS-stimulated monocytes. The inhibition by rIL-10 was achieved in a dose-dependent manner. Recombinant IL-4 also inhibited PGE2 production at the same degree as rIL-10. Viral IL-10 inhibited PGE2 production by monocytes in a similar fashion as did human rIL-10. Endogenously produced IL-10 was also shown to inhibit PGE2 production by LPS-stimulated monocytes. Kinetic studies showed that the inhibition by rIL-10 on PGE2 production was observed at least 3 h after LPS stimulation. Taken together, these results indicate that IL-10 may play an important role in modulating immunological responses via down-regulation of PGE2 production by monocytes.

摘要

由于最近研究表明白细胞介素-10(IL-10)对人单核细胞具有多效性作用,因此确定这种细胞因子对单核细胞产生前列腺素E2(PGE2)的影响很有意义。重组IL-10(rIL-10)对脂多糖(LPS)未刺激的单核细胞产生PGE2的过程没有显著影响,但能有效抑制LPS刺激的单核细胞产生PGE2。rIL-10的抑制作用呈剂量依赖性。重组IL-4也能以与rIL-10相同的程度抑制PGE2的产生。病毒IL-10抑制单核细胞产生PGE2的方式与人类rIL-10类似。内源性产生的IL-10也被证明能抑制LPS刺激的单核细胞产生PGE2。动力学研究表明,rIL-10对PGE2产生的抑制作用至少在LPS刺激后3小时才观察到。综上所述,这些结果表明IL-10可能通过下调单核细胞产生PGE2在调节免疫反应中发挥重要作用。

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