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酿脓链球菌致热外毒素A(SpeA)和C(SpeC)可刺激RAW 264.7巨噬细胞中诱导型一氧化氮合酶(iNOS)蛋白的产生。

Streptococcal pyrogenic exotoxins A (SpeA) and C (SpeC) stimulate the production of inducible nitric oxide synthase (iNOS) protein in RAW 264.7 macrophages.

作者信息

Christ E A, Meals E, English B K

机构信息

Department of Pediatrics, University of Tennessee, Memphis, USA.

出版信息

Shock. 1997 Dec;8(6):450-3.

PMID:9421860
Abstract

Streptococcal pyrogenic exotoxins A (SpeA) and C (SpeC) are members of a family of superantigens produced by group A streptococci that appear to play a key role in the pathogenesis of streptococcal toxic shock syndrome. Since it is known that nitric oxide (NO) and tumor necrosis factor (TNF) are largely responsible for the shock and multiple organ dysfunction of Gram-negative sepsis, we hypothesized that SpeA and/or SpeC could trigger the production of inducible nitric oxide synthase (iNOS) and/or TNF by murine macrophages. We exposed RAW 264.7 macrophages to increasing concentrations of SpeA or SpeC alone and in combination with recombinant murine interferon-gamma (rIFN gamma) for 16-24 h. We found that both SpeA and SpeC triggered iNOS production in the presence of low concentrations of rIFN gamma, while neither provoked iNOS accumulation in the absence of rIFN gamma. Neither SpeA nor SpeC (with or without rIFN gamma) reproducibly induced TNF production by these murine macrophages. These data indicate that two streptococcal exotoxins up-regulate iNOS production by murine macrophages and suggest that nitric oxide production may play an important role in the pathogenesis of streptococcal toxic shock syndrome.

摘要

A组链球菌产生的超抗原家族成员链球菌致热外毒素A(SpeA)和C(SpeC)似乎在链球菌中毒性休克综合征的发病机制中起关键作用。由于已知一氧化氮(NO)和肿瘤坏死因子(TNF)在很大程度上导致革兰氏阴性菌败血症的休克和多器官功能障碍,我们推测SpeA和/或SpeC可能会触发小鼠巨噬细胞产生诱导型一氧化氮合酶(iNOS)和/或TNF。我们将RAW 264.7巨噬细胞单独暴露于浓度不断增加的SpeA或SpeC中,并与重组小鼠干扰素-γ(rIFNγ)联合暴露16至24小时。我们发现,在低浓度rIFNγ存在的情况下,SpeA和SpeC均可触发iNOS的产生,而在没有rIFNγ的情况下,两者均不会引起iNOS的积累。SpeA和SpeC(无论有无rIFNγ)均不能重复诱导这些小鼠巨噬细胞产生TNF。这些数据表明,两种链球菌外毒素可上调小鼠巨噬细胞中iNOS的产生,并提示一氧化氮的产生可能在链球菌中毒性休克综合征的发病机制中起重要作用。

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