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本文引用的文献

1
THE PREPARATION OF I-131-LABELLED HUMAN GROWTH HORMONE OF HIGH SPECIFIC RADIOACTIVITY.高比放射性碘-131标记人生长激素的制备
Biochem J. 1963 Oct;89(1):114-23. doi: 10.1042/bj0890114.
2
Genetic control of Propionibacterium acnes-induced protection of mice against Babesia microti.痤疮丙酸杆菌诱导小鼠对微小巴贝斯虫产生保护性免疫的遗传控制
Infect Immun. 1982 Jan;35(1):52-7. doi: 10.1128/iai.35.1.52-57.1982.
3
Genetic control of susceptibility to Salmonella typhimurium in mice: role of the LPS gene.
J Immunol. 1980 Jan;124(1):20-4.
4
Macrophages in resistance to rickettsial infection: susceptibility to lethal effects of Rickettsia akari infection in mouse strains with defective macrophage function.巨噬细胞在抵抗立克次体感染中的作用:巨噬细胞功能缺陷的小鼠品系对红恙虫病立克次体感染致死效应的易感性。
Cell Immunol. 1980 Sep 1;54(2):487-90. doi: 10.1016/0008-8749(80)90229-4.
5
Genetic control of the susceptibility of C3HeB/FeJ mice to Salmonella typhimurium is regulated by a locus distinct from known salmonella response genes.C3HeB/FeJ小鼠对鼠伤寒沙门氏菌易感性的遗传控制由一个与已知沙门氏菌反应基因不同的基因座调控。
J Immunol. 1983 Dec;131(6):2613-5.
6
Modulation of macrophage Ia-expression by lipopolysaccharide. I. Induction of Ia expression in vivo.脂多糖对巨噬细胞Ia表达的调节。I. 体内Ia表达的诱导
J Immunol. 1984 Oct;133(4):1825-35.
7
Mouse chromosome 1 Ity locus regulates microbicidal activity of isolated peritoneal macrophages against a diverse group of intracellular and extracellular bacteria.小鼠1号染色体上的Ity基因座调节分离的腹膜巨噬细胞对多种细胞内和细胞外细菌的杀菌活性。
J Immunol. 1985 Jul;135(1):544-7.
8
Evidence for separate genetic defects in C3H/HeJ and C3HeB/FeJ mice, that affect susceptibility to gram-negative infections.C3H/HeJ和C3HeB/FeJ小鼠中存在影响革兰氏阴性菌感染易感性的不同遗传缺陷的证据。
J Immunol. 1985 Jun;134(6):4118-22.
9
Protection of C3H/HeJ mice from lethal Salmonella typhimurium LT2 infection by immunization with lipopolysaccharide-lipid A-associated protein complexes.通过用脂多糖-脂质A相关蛋白复合物免疫来保护C3H/HeJ小鼠免受致死性鼠伤寒沙门氏菌LT2感染。
Infect Immun. 1986 Oct;54(1):1-8. doi: 10.1128/iai.54.1.1-8.1986.
10
Mouse genetic locus Lps influences susceptibility to Neisseria meningitidis infection.小鼠基因位点Lps影响对脑膜炎奈瑟菌感染的易感性。
Infect Immun. 1988 Aug;56(8):1950-5. doi: 10.1128/iai.56.8.1950-1955.1988.

脂多糖在革兰氏阴性菌感染期间诱导Ia表达中的作用。

Role of lipopolysaccharide in induction of Ia expression during infection with gram-negative bacteria.

作者信息

Marshall N E, Ziegler H K

机构信息

Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia 30322.

出版信息

Infect Immun. 1989 May;57(5):1556-60. doi: 10.1128/iai.57.5.1556-1560.1989.

DOI:10.1128/iai.57.5.1556-1560.1989
PMID:2496032
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC313313/
Abstract

Lipopolysaccharide (LPS), a major component of the outer membrane of gram-negative bacteria, is known to be a potent modulator of many host immune functions, including the expression of products of the class II major histocompatibility locus (Ia molecules) by macrophages. LPS-mediated Ia induction is controlled by the lps gene. We sought to determine the role of LPS in the induction of Ia expression during infection with gram-negative bacteria. To address this question, we tested a simple prediction: if LPS is the primary determinant of Ia induction during gram-negative infection, then the Ia response to intraperitoneal injection of these organisms should be under the control of the lps gene. We found that while both LPS-responder and LPS-low-responder mice showed strong Ia responses to injection of either a gram-positive bacterium (Listeria monocytogenes) or concanavalin A, only the LPS-responder mice responded strongly to gram-negative organisms or to LPS alone. We interpret these results as strong evidence for the role of LPS as the primary determinant of Ia induction by gram-negative bacteria.

摘要

脂多糖(LPS)是革兰氏阴性菌外膜的主要成分,已知它是许多宿主免疫功能的有效调节剂,包括巨噬细胞对II类主要组织相容性位点产物(Ia分子)的表达。LPS介导的Ia诱导由lps基因控制。我们试图确定LPS在革兰氏阴性菌感染期间Ia表达诱导中的作用。为了解决这个问题,我们测试了一个简单的预测:如果LPS是革兰氏阴性菌感染期间Ia诱导的主要决定因素,那么腹腔注射这些细菌后Ia的反应应该受lps基因的控制。我们发现,虽然LPS反应者和LPS低反应者小鼠对注射革兰氏阳性菌(单核细胞增生李斯特菌)或伴刀豆球蛋白A均表现出强烈的Ia反应,但只有LPS反应者小鼠对革兰氏阴性菌或单独的LPS有强烈反应。我们将这些结果解释为LPS作为革兰氏阴性菌诱导Ia的主要决定因素的有力证据。