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脂质A作为细菌内毒素(LPS)启动外周血白细胞产生促凝血活性的生物活性部分。

Lipid A as the biologically active moiety in bacterial endotoxin (LPS)-initiated generation of procoagulant activity by peripheral blood leukocytes.

作者信息

Niemetz J, Morrison D C

出版信息

Blood. 1977 Jun;49(6):947-56.

PMID:324538
Abstract

Preparations of rabbit or human leukocytes, when incubated with bacterial endotoxins (lipopolysaccharides, LPS) are stimulated to generate a procoagulant-tissue factor activity (TFa). As LPS has been shown to consist of specific repeating oligosaccharide side chains (O-antigen) linked to a central polysaccharide core region that is, in turn, linked to the lipid region of the molecule (lipid A), we have examined the biochemical requirement of the LPS necessary for generation of TFa. Using preparations of LPS from mutant strains of bacteria, which contain varying amounts of polysaccharide in relation to lipid A, we have demonstrated that activity is associated with the lipid A region of the LPS molecule. These observations have been confirmed using isolated lipid A, which is a potent stimulator of TFa, as well as a native protoplasmic polysaccharide that is both devoid of lipid A and without detectable TFa stimulatory activity. Modification of LPS by treatment with mild alkali abrogated its capacity to stimulate TFa generation. In addition, such altered preparations of LPS partially inhibit the stimulatory effect of native LPS. Similarly, treatment of LPS (or lipid A) with the antibiotic polymyxin B substantially inhibited the stimulatory effect of LPS.

摘要

兔或人白细胞制剂在与细菌内毒素(脂多糖,LPS)一起孵育时,会被刺激产生促凝血组织因子活性(TFa)。由于已表明LPS由与中心多糖核心区域相连的特定重复寡糖侧链(O抗原)组成,而该核心区域又与分子的脂质区域(脂质A)相连,我们研究了产生TFa所需的LPS的生化要求。使用来自细菌突变株的LPS制剂,这些制剂中脂质A相关的多糖含量各不相同,我们证明活性与LPS分子的脂质A区域相关。使用分离的脂质A(一种有效的TFa刺激剂)以及既不含脂质A也无可检测到的TFa刺激活性的天然原生质多糖,证实了这些观察结果。用温和碱处理对LPS进行修饰消除了其刺激TFa产生的能力。此外,这种改变后的LPS制剂部分抑制了天然LPS的刺激作用。同样,用抗生素多粘菌素B处理LPS(或脂质A)可大幅抑制LPS的刺激作用。

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