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首页> 外文期刊>The journal of immunology >Toll-Like Receptor 4-MD-2 Complex Mediates the Signal Transduction Induced by Flavolipin, an Amino Acid-Containing Lipid Unique to Flavobacterium meningosepticum
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Toll-Like Receptor 4-MD-2 Complex Mediates the Signal Transduction Induced by Flavolipin, an Amino Acid-Containing Lipid Unique to Flavobacterium meningosepticum

机译:类似Toll的受体4-MD-2复合物介导黄病毒素(一种脑膜炎黄杆菌特有的含氨基酸的脂质)诱导的信号传导

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Flavolipin, an amino acid-containing lipid isolated from Flavobacterium meningosepticum , induces many immune responses. It has been shown that flavolipin does not induce an immune response of macrophages derived from C3H/HeJ mice, which possess a point mutation in Toll-like receptor 4 (TLR4). To determine whether TLR4 or the molecular complex of TLR4 and TLR4 association molecule MD-2 mediates the flavolipin signal, flavolipin responsiveness was examined by measuring NF-κB activation in Ba/F3 cells and Ba/F3 transfectants expressing TLR4 or both TLR4 and MD-2. Flavolipin-induced NF-κB activation was detected in the cells expressing both TLR4 and MD-2, but not in the other cells. Expression of CD14 in the transfectant expressing both TLR4 and MD-2 increased the sensitivity to flavolipin. Furthermore, flavolipin stereoisomers were chemically synthesized, and their abilities to induce NF-κB activation were examined. ( R )-Flavolipin, in which the configuration of the lipid moiety is R, induced NF-κB activation via the TLR4-MD-2 complex, but ( S )-flavolipin did not. In this study, we demonstrated the involvement of TLR4-MD-2 and CD14 in flavolipin signaling and the importance of the ( R )-configuration of the flavolipin lipid moiety for the induction of an immune response via TLR4-MD-2.
机译:黄病毒素是一种从脑膜炎黄杆菌中分离的含氨基酸脂质,可诱导许多免疫反应。已经显示黄酮磷脂不诱导衍生自C3H / HeJ小鼠的巨噬细胞的免疫应答,所述巨噬细胞在Toll样受体4(TLR4)中具有点突变。为了确定TLR4或TLR4和TLR4缔合分子MD-2的分子复合物是否介导黄素信号,通过测量表达TLR4的Ba / F3细胞和Ba / F3转染子或TLR4和MD-两者中的NF-κB活化来检查黄素反应性。 2。在表达TLR4和MD-2的细胞中均检测到黄素诱导的NF-κB活化,而在其他细胞中均未检测到。在同时表达TLR4和MD-2的转染子中CD14的表达增加了对黄素的敏感性。此外,化学合成了黄酮磷脂立体异构体,并检测了它们诱导NF-κB活化的能力。 (R)-黄酮素,其中脂质部分的构型是R,通过TLR4-MD-2复合物诱导NF-κB活化,而(S)-黄素磷脂没有。在这项研究中,我们证明了TLR4-MD-2和CD14参与黄素类脂蛋白信号传导,以及黄素类脂素脂质部分的(R)-构型对于通过TLR4-MD-2诱导免疫反应的重要性。

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