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血小板活化因子与γ干扰素在刺激人单核细胞产生白细胞介素-1中的相互作用。

Interaction of platelet-activating factor with interferon-gamma in the stimulation of interleukin-1 production by human monocytes.

作者信息

Barthelson R, Valone F

机构信息

Department of Medicine, University of California-San Francisco.

出版信息

J Allergy Clin Immunol. 1990 Aug;86(2):193-201. doi: 10.1016/s0091-6749(05)80066-1.

Abstract

Platelet-activating factor (PAF) produces both early and late inflammatory responses in vivo. The late and persistent responses to PAF may result from the production of cytokines, such as interleukin-1 (IL-1). The effects of PAF on IL-1 release by human monocytes were studied with PAF alone and in combination with interferon-gamma. These studies involved the use of D10.G4.1 cells in a proliferation assay to determine the actual concentration of active IL-1 in monocyte supernatant and pellet fractions. These studies confirmed that PAF stimulates IL-1 release at two different ranges of PAF concentrations, 100 fM to 1 pM and 100 pM to 1 nM. PAF inhibited IL-1 release at 1 or 10 pM. PAF effects on IL-1 release were specific to the form of PAF that is biologically active in most system; (S)-PAF and lyso-PAF had no effect. When monocytes were incubated with both PAF and interferon-gamma, IL-1 release was greatly stimulated at the same two ranges of PAF concentrations, 100 fM to 1 pM and 100 pM to 1 nM of PAF. PAF and interferon-gamma interacted synergistically to enhance significantly the release of IL-1.

摘要

血小板活化因子(PAF)在体内可引发早期和晚期炎症反应。PAF引发的晚期持续性反应可能是由细胞因子如白细胞介素-1(IL-1)的产生所致。我们使用单独的PAF以及PAF与干扰素-γ联合使用,研究了PAF对人单核细胞释放IL-1的影响。这些研究涉及在增殖试验中使用D10.G4.1细胞,以确定单核细胞上清液和沉淀部分中活性IL-1的实际浓度。这些研究证实,PAF在两个不同的PAF浓度范围(100 fM至1 pM和100 pM至1 nM)刺激IL-1释放。PAF在1或10 pM时抑制IL-1释放。PAF对IL-1释放的影响特定于在大多数系统中具有生物活性的PAF形式;(S)-PAF和溶血PAF没有影响。当单核细胞与PAF和干扰素-γ一起孵育时,在相同的两个PAF浓度范围(100 fM至1 pM和100 pM至1 nM的PAF)下,IL-1释放受到极大刺激。PAF和干扰素-γ协同相互作用,显著增强IL-1的释放。

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