Suda Y, Kirikae T, Shiyama T, Yasukochi T, Kirikae F, Nakano M, Rietschel E T, Kusumoto S
Faculty of Science, Osaka University, Japan.
Biochem Biophys Res Commun. 1995 May 25;210(3):678-85. doi: 10.1006/bbrc.1995.1713.
The S-form lipopolysaccharide (LPS) was effectively separated from a native preparation of smooth-type Salmonella abortus equi LPS by means of the centrifugal partition chromatography (CPC). To clarify the mechanisms by which LPS activates macrophages, CPC-separated S-form LPS was assessed for its ability to induce the secretion of tumor necrosis factor-alpha (TNF-alpha) by murine macrophage-like J774.1 cells in comparison with other fractions of LPS which lacks most of O-polysaccharides. LPS dose-response and time-kinetics studies showed that serum factor(s) regulated especially the onset of TNF-alpha secretion in stimulation with S-form LPS. These results strongly suggest that the native (unfractionated) LPS activates macrophages in both O-polysaccharide/serum-dependent and -independent pathways.
通过离心分配色谱法(CPC)从光滑型马流产沙门氏菌脂多糖(LPS)的天然制剂中有效分离出S型脂多糖。为阐明LPS激活巨噬细胞的机制,将CPC分离的S型LPS与缺乏大部分O-多糖的LPS其他组分相比较,评估其诱导鼠巨噬细胞样J774.1细胞分泌肿瘤坏死因子-α(TNF-α)的能力。LPS剂量反应和时间动力学研究表明,血清因子尤其调节S型LPS刺激中TNF-α分泌的起始。这些结果有力地表明,天然(未分级)LPS通过O-多糖/血清依赖性和非依赖性途径激活巨噬细胞。