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LY294002通过抑制核因子κB激活来抑制脂多糖诱导的一氧化氮生成:磷脂酰肌醇3激酶的独立机制

LY294002 inhibits LPS-induced NO production through a inhibition of NF-kappaB activation: independent mechanism of phosphatidylinositol 3-kinase.

作者信息

Kim Young Ho, Choi Kwang-Hae, Park Jong-Wook, Kwon Taeg Kyu

机构信息

Department of Immunology, School of Medicine, Keimyung University, 194 DongSan-Dong Jung-Gu, Taegu 700-712, South Korea.

出版信息

Immunol Lett. 2005 Jun 15;99(1):45-50. doi: 10.1016/j.imlet.2004.12.007. Epub 2005 Jan 6.

Abstract

Phosphatidylinositol 3-kinase (PI3K) is critical player in cell proliferation and survival. The effects of LY294002 and wortmannin, inhibitors of PI3K, on nitric oxide (NO) production and inducible nitric oxide synthase (iNOS) expression in lipoploysaccharide (LPS)-induced Raw 264.7 cells were investigated. Significant inhibition of LPS-induced protein kinase B (PKB, Akt) phosphorylation occurred at 25 microM LY294002 or 0.5 microM wortmannin. At the same concentrations, LY294002, but not wortmannin, significantly inhibited NO production and iNOS expression. LY303511, an inactive analogue of LY294002, also inhibited NO production and iNOS expression. In addition, LY294002 and LY303511 significantly inhibited the DNA binding activity of NF-kappaB and NF-kappaB dependent reporter gene expression. These results suggest that LY294002 inhibits iNOS expression at least in part via inhibition of NF-kappaB activation, independent of PI3K.

摘要

磷脂酰肌醇3激酶(PI3K)是细胞增殖和存活中的关键因子。研究了PI3K抑制剂LY294002和渥曼青霉素对脂多糖(LPS)诱导的Raw 264.7细胞中一氧化氮(NO)生成和诱导型一氧化氮合酶(iNOS)表达的影响。在25微摩尔LY294002或0.5微摩尔渥曼青霉素作用下,LPS诱导的蛋白激酶B(PKB,Akt)磷酸化受到显著抑制。在相同浓度下,LY294002能显著抑制NO生成和iNOS表达,而渥曼青霉素则无此作用。LY303511是LY294002的无活性类似物,也能抑制NO生成和iNOS表达。此外,LY294002和LY303511能显著抑制NF-κB的DNA结合活性以及NF-κB依赖性报告基因的表达。这些结果表明,LY294002至少部分通过抑制NF-κB激活来抑制iNOS表达,且这一作用与PI3K无关。

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