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干扰素β或γ对人肺泡巨噬细胞体外新蝶呤生物合成及色氨酸降解的影响:与脂多糖的协同作用

Effects of interferons beta or gamma on neopterin biosynthesis and tryptophan degradation by human alveolar macrophages in vitro: synergy with lipopolysaccharide.

作者信息

Meyer K C, Cornwell R, Carlin J M, Powers C, Irizarry A, Byrne G I, Borden E C

机构信息

Department of Medicine, University of Wisconsin, Madison.

出版信息

Am J Respir Cell Mol Biol. 1992 Jun;6(6):639-46. doi: 10.1165/ajrcmb/6.6.639.

Abstract

Interferons can induce neopterin biosynthesis and tryptophan degradation in monocytic cells. Indoleamine 2,3-dioxygenase (IDO), an inducible cellular enzyme, metabolizes tryptophan to N-formyl-L-kynurenine. Tryptophan degradation has been linked to interferon-mediated inhibition of replication by intracellular pathogens and inhibition of cancer cell proliferation. We evaluated the ability of the recombinant human interferons beta ser and gamma to stimulate neopterin production and tryptophan degradation in vitro by alveolar macrophages (AM) obtained from normal volunteers by bronchoalveolar lavage. Additionally, because other biologic response modifiers such as lipopolysaccharide (LPS) can also stimulate monocytic cells to produce increased amounts of neopterin and degrade tryptophan, we evaluated the effects of LPS on interferon-induced neopterin production and tryptophan degradation by AM. Both interferon-gamma (IFN-gamma) and interferon-beta (IFN-beta) induced neopterin production and tryptophan degradation by AM with corresponding inhibition of intracellular replication by Chlamydia psittaci in AM, but IFN-gamma was a more potent inducer of these responses than IFN-beta. LPS enhanced neopterin production and tryptophan degradation by interferon-exposed cells. This effect was particularly evident at lower concentrations of interferon, and LPS synergy was more pronounced with IFN-beta than IFN-gamma. Concentrations of LPS that alone had no stimulatory effect on tryptophan degradation synergistically enhanced the induction of IDO activity by lower concentrations of interferon. These studies suggest that IFN-gamma stimulates human AM to produce neopterin and degrade tryptophan more potently than IFN-beta, and that low concentrations of LPS can synergistically enhance such effects of interferons on tissue macrophage metabolism.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

干扰素可诱导单核细胞中蝶呤生物合成及色氨酸降解。吲哚胺2,3-双加氧酶(IDO)是一种可诱导的细胞酶,可将色氨酸代谢为N-甲酰基-L-犬尿氨酸。色氨酸降解与干扰素介导的细胞内病原体复制抑制及癌细胞增殖抑制有关。我们评估了重组人β型和γ型干扰素刺激通过支气管肺泡灌洗从正常志愿者获得的肺泡巨噬细胞(AM)体外产生蝶呤及降解色氨酸的能力。此外,由于其他生物反应调节剂如脂多糖(LPS)也可刺激单核细胞产生更多蝶呤并降解色氨酸,我们评估了LPS对干扰素诱导的AM蝶呤产生及色氨酸降解的影响。γ干扰素(IFN-γ)和β干扰素(IFN-β)均可诱导AM产生蝶呤及降解色氨酸,并相应抑制鹦鹉热衣原体在AM中的细胞内复制,但IFN-γ比IFN-β更有效地诱导这些反应。LPS增强了经干扰素处理的细胞的蝶呤产生及色氨酸降解。这种效应在较低浓度的干扰素时尤为明显,且LPS与IFN-β的协同作用比与IFN-γ的更显著。单独对色氨酸降解无刺激作用的LPS浓度可协同增强较低浓度干扰素对IDO活性的诱导。这些研究表明,IFN-γ比IFN-β更有效地刺激人AM产生蝶呤及降解色氨酸,且低浓度的LPS可协同增强干扰素对组织巨噬细胞代谢的此类作用。(摘要截短至250字)

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