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白血病抑制因子在人单核细胞中诱导白细胞介素-8以及单核细胞趋化和激活因子:受γ干扰素的差异调节。

Leukemia inhibitory factor induces interleukin-8 and monocyte chemotactic and activating factor in human monocytes: differential regulation by interferon-gamma.

作者信息

Musso T, Badolato R, Longo D L, Gusella G L, Varesio L

机构信息

PRI/DynCorp, NCI-FCRDC, Biological Carcinogenesis and Development Program, MD 21702-1201, USA.

出版信息

Blood. 1995 Sep 1;86(5):1961-7.

PMID:7655023
Abstract

Leukemia inhibitory factor (LIF) is a cytokine released at the site of injuries where there is a recruitment of monocytes and polymorphonuclear cells. We analyzed the effect of LIF on human monocytes, which are a major source of chemotactic factors. We showed that supernatants of monocytes treated with LIF (50 ng/mL) for 18 hours had chemotactic activity for neutrophils and monocytes that was neutralized by anti-interleukin-8 (anti-IL-8) and anti-monocyte chemotactic and activating factor (anti-MCAF) neutralizing antibodies. Northern blot analysis showed induction of IL-8 and MCAF RNA in monocytes treated with LIF. Both IL-8 and MCAF mRNA were induced within 3 hours of stimulation. IL-8 and MCAF mRNAs expression peaked at 6 hours and 18 hours, respectively. Interferon-gamma (IFN-gamma), a potent monocyte activator, inhibited IL-8 induction by LIF. On the contrary, IFN-gamma by itself induced MCAF and did not affect the LIF-induced MCAF. These results indicate that LIF released at the site of injury by inducing IL-8 and MCAF can play an important role in recruiting leukocytes and that IFN-gamma can differentially regulate this recruitment.

摘要

白血病抑制因子(LIF)是一种在损伤部位释放的细胞因子,损伤部位会募集单核细胞和多形核细胞。我们分析了LIF对人单核细胞的作用,单核细胞是趋化因子的主要来源。我们发现,用LIF(50 ng/mL)处理18小时的单核细胞培养上清液对中性粒细胞和单核细胞具有趋化活性,这种活性可被抗白细胞介素-8(抗IL-8)和抗单核细胞趋化和激活因子(抗MCAF)中和抗体所中和。Northern印迹分析显示,用LIF处理的单核细胞中IL-8和MCAF RNA被诱导表达。IL-8和MCAF mRNA在刺激后3小时内均被诱导表达。IL-8和MCAF mRNA表达分别在6小时和18小时达到峰值。γ干扰素(IFN-γ)是一种有效的单核细胞激活剂,可抑制LIF诱导的IL-8表达。相反,IFN-γ自身可诱导MCAF表达,且不影响LIF诱导的MCAF表达。这些结果表明,损伤部位释放的LIF通过诱导IL-8和MCAF在白细胞募集中发挥重要作用,且IFN-γ可对这种募集进行差异性调节。

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