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从脑膜败血黄杆菌中分离出的脂多糖A的生物学特性。

Biological properties of lipid A isolated from Flavobacterium meningosepticum.

作者信息

Tanamoto K, Kato H, Haishima Y, Azumi S

机构信息

Division of Microbiology, National Institute of Health Sciences, Tokyo 158-8501, Japan.

出版信息

Clin Diagn Lab Immunol. 2001 May;8(3):522-7. doi: 10.1128/CDLI.8.3.522-527.2001.

Abstract

The biological properties of the lipid A from Flavobacterium meningosepticum, which we recently isolated and whose complete chemical structure has been determined (H. Kato, T. Iida, Y. Haishima, A. Tanaka, and K. Tanamoto. J. Bacteriol. 180:3891--3899, 1998), were studied. The lipid A exhibited generally moderate activity compared to Salmonella enterica subsp. enterica serovar abortus equi lipopolysaccharide (LPS) used as a control in the assay systems tested; lethal toxicity in galactosamine-sensitized mice, mitogenicity in mouse spleen cells, induction of tumor necrosis factor alpha (TNF-alpha) release from mouse peritoneal macrophages and J774-1 mouse macrophage-like and human THP-1 line cells, nitric oxide induction activity from J774-1 cells, and Limulus gelation activity. The moderate activity of the F. meningosepticum lipid A may be explained by its unique fatty acid composition and the lack of a phosphate group in position 4'. It is noteworthy that the lipid A apparently induced TNF-alpha release from peritoneal macrophages in LPS-unresponsive C3H/HeJ mice and that the activation was suppressed by the LPS-specific antagonist, succinylated lipid A precursor. Significant splenocyte mitogenicity in C3H/HeJ mice was also observed with the lipid A. Taken together with the previous results concerning Porphyromonas gingivalis lipid A, which has a high level of structural similarity to the lipid A of F. meningosepticum, and the induction of TNF-alpha release in macrophages from C3H/HeJ mice, the lipid A of F. meningosepticum, which has novel fatty acids, may possibly play an role for the activation of C3H/HeJ macrophages.

摘要

我们最近分离出了脑膜炎败血黄杆菌的脂多糖A,并确定了其完整的化学结构(H. Kato、T. Iida、Y. Haishima、A. Tanaka和K. Tanamoto。《细菌学杂志》180:3891 - 3899,1998年),并对其生物学特性进行了研究。与在测试的分析系统中用作对照的肠炎沙门氏菌亚种肠炎血清型马流产脂多糖(LPS)相比,该脂多糖A的活性总体适中;在半乳糖胺致敏小鼠中的致死毒性、对小鼠脾细胞的促有丝分裂活性、从小鼠腹腔巨噬细胞以及J774 - 1小鼠巨噬细胞样细胞和人THP - 1细胞系诱导肿瘤坏死因子α(TNF - α)释放、J774 - 1细胞的一氧化氮诱导活性以及鲎试剂凝胶化活性。脑膜炎败血黄杆菌脂多糖A的适度活性可能由其独特的脂肪酸组成以及4'位缺乏磷酸基团来解释。值得注意的是,该脂多糖A明显能诱导LPS无反应性的C3H/HeJ小鼠腹腔巨噬细胞释放TNF - α,并且这种激活被LPS特异性拮抗剂琥珀酰化脂多糖前体所抑制。用该脂多糖A还观察到C3H/HeJ小鼠中有显著的脾细胞促有丝分裂活性。结合先前关于牙龈卟啉单胞菌脂多糖A的结果(其与脑膜炎败血黄杆菌的脂多糖A具有高度的结构相似性)以及在C3H/HeJ小鼠巨噬细胞中诱导TNF - α释放的情况,具有新型脂肪酸的脑膜炎败血黄杆菌脂多糖A可能在激活C3H/HeJ巨噬细胞中发挥作用。

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本文引用的文献

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