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首页> 外文期刊>Journal of Nutritional Science and Vitaminology >Low Pyridoxine Concentrations Enhance Lipopolysaccharide-Stimulated Gene Expression of Cyclooxygenase-2 and Inducible Nitric Oxide Synthase in RAW264.7 Cells
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Low Pyridoxine Concentrations Enhance Lipopolysaccharide-Stimulated Gene Expression of Cyclooxygenase-2 and Inducible Nitric Oxide Synthase in RAW264.7 Cells

机译:低的吡ox醇浓度增强RAW264.7细胞中脂多糖刺激的环氧合酶-2和诱导型一氧化氮合酶的基因表达。

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摘要

Pyridoxal (PL) has been shown to suppress lipopolysaccharide (LPS)-induced gene expression of cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS). Commonly used cell culture media contain extremely high concentrations of pyridoxine (PN) compared to total serum levels of vitamin B6. Therefore, we evaluated how physiological concentrations of PN influence LPS-stimulated gene expression of COX-2 and iNOS. The mouse macrophage cell line, RAW264.7, was cultured in PN-free DMEM supplemented with 10% fetal bovine serum (DMEM(?PN+FBS)) for 7 d. Although the level of pyridoxal 5'-phosphate in these cells was decreased by 65%, no change was observed in cell proliferation rate or aspartate aminotransferase activity for 7 d. LPS-induced expression of COX-2 mRNA was compared between DMEM(+FBS) and DMEM(?PN+FBS). COX-2 expression was enhanced by 2.2 or 1.9 times with a 1 or 3 d treatment, respectively; however, no difference was observed at 7 d. PN (0.032-100 μm) added to the DMEM(?PN+FBS) and RAW264.7 cells was cultured in the medium containing each concentration of PN for 1 d. Enhancement of COX-2 and iNOS gene expression was suppressed by PN addition in a concentration-dependent manner. COX-2 and iNOS mRNA were similarly expressed in cells grown in media containing PN at 4 μm or higher. Overall, induction of COX-2 and iNOS by LPS was transiently enhanced when RAW264.7 cells were cultured in physiological PN concentrations.
机译:吡rid醛(PL)已显示抑制脂多糖(LPS)诱导的环氧合酶2(COX-2)和诱导型一氧化氮合酶(iNOS)的基因表达。与血清中维生素B 6 的总水平相比,常用的细胞培养基中吡pyr醇(PN)的浓度极高。因此,我们评估了生理浓度的PN如何影响LPS刺激的COX-2和iNOS基因表达。在补充有10%胎牛血清(DMEM(ΔPN+ FBS))的无PN的DMEM中培养小鼠巨噬细胞细胞RAW264.7 7天。尽管这些细胞中的吡ido醛5'-磷酸水平降低了65%,但在7 d内未观察到细胞增殖速率或天冬氨酸转氨酶活性的变化。在DMEM(+ FBS)和DMEM(ΔPN+ FBS)之间比较LPS诱导的COX-2 mRNA的表达。经过1或3 d处理后,COX-2表达分别提高了2.2或1.9倍;然而,在第7天没有观察到差异。将添加到DMEM(ΔPN+ FBS)中的PN(0.032-100μm)和RAW264.7细胞在含有每种PN浓度的培养基中培养1天。 PN的添加以浓度依赖的方式抑制了COX-2和iNOS基因表达的增强。 COX-2和iNOS mRNA在含有PN的4μm或更高的培养基中生长的细胞中类似表达。总体而言,当以生理PN浓度培养RAW264.7细胞时,LPS对COX-2和iNOS的诱导会暂时增强。

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