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S型脂多糖(LPS),而非脂质A或R化学型LPS,可在维生素D3分化的THP-1细胞中诱导白细胞介素-6的产生。

S-form lipopolysaccharide (LPS), but not lipid A or R-chemo-type LPS, induces interleukin-6 production in vitamin D3-differentiated THP-1 cells.

作者信息

Suda Y, Aoyama K, Arimoto K, Tamura T, Kusumoto S

机构信息

Graduate School of Science, Osaka University, Osaka, Toyonaka, 560-0043, Japan.

出版信息

Biochem Biophys Res Commun. 1999 Apr 13;257(2):327-32. doi: 10.1006/bbrc.1999.0464.

Abstract

Bacterial lipopolysaccharide (LPS) induces the production of various inflammatory cytokines and the inducibility is considered attributable to the glycolipid part of LPS called lipid A. We report an in vitro model in which lipid A is not necessarily a minimal structure for the LPS activity. Vitamin D3-differentiated THP-1 cells, cultured human monocytic leukemia cells, produced a high level of interleukin-6 (IL-6) by stimulating LPS from Escherichia coli O111:B4, but not by stimulating synthetic E. coli-type lipid A (compound 506), E. coli Re mutant LPS (ReLPS), or alkali-treated LPS. The induction by LPS was inhibited by the anti-CD14 antibodies or by the synthetic lipid A precursor (compound 406). An alkali-treated LPS or compound 506 partially inhibited the LPS-induced IL-6 production. These facts suggest that lipid A alone is not sufficient for the IL-6-inducing activity, but the polysaccharide part in LPS contributes or acts as a co-factor for activation of differentiated THP-1 cells.

摘要

细菌脂多糖(LPS)可诱导多种炎性细胞因子的产生,这种诱导能力被认为归因于LPS中名为脂质A的糖脂部分。我们报道了一种体外模型,在该模型中脂质A不一定是LPS活性的最小结构。经维生素D3分化的THP-1细胞(培养的人单核细胞白血病细胞)通过刺激来自大肠杆菌O111:B4的LPS产生高水平的白细胞介素-6(IL-6),但不通过刺激合成的大肠杆菌型脂质A(化合物506)、大肠杆菌Re突变体LPS(ReLPS)或碱处理的LPS产生IL-6。LPS的诱导作用被抗CD14抗体或合成脂质A前体(化合物406)抑制。碱处理的LPS或化合物506部分抑制LPS诱导的IL-6产生。这些事实表明,仅脂质A不足以产生诱导IL-6的活性,但LPS中的多糖部分有助于或作为激活分化的THP-1细胞的辅助因子发挥作用。

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