Li R W S, Man Ricky Y K, Vanhoutte Paul M, Leung George P H
Department of Pharmacology, The University of Hong Kong, Pokfulam, Hong Kong.
Am J Physiol Heart Circ Physiol. 2008 Sep;295(3):H1177-H1181. doi: 10.1152/ajpheart.91513.2007. Epub 2008 Jul 18.
The involvement of ecto-5'-nucleotidase (E-5'Nu) in the elevation of extracellular adenosine during inflammation is unclear. In the present study, the effect of lipopolysaccharide (LPS), an inflammation inducer, was investigated on E-5'Nu in human umbilical vein endothelial cells (HUVECs). E-5'Nu activity was enhanced after a 24 h exposure to LPS. This effect was dose dependent, with an EC50 of 1.66 ng/ml. At 10 microM, the phosphatidylinositol 3-kinase (PI3K) inhibitor LY-294002 abolished the LPS-induced E-5'Nu activity. However, at 10 microM, the NF-kappaB inhibitor ammonium pyrrolidine dithiocarbamate had no effect. LPS upregulated the protein expression but not the messenger RNA expression of E-5'Nu. The inhibition of E-5'Nu by 100 microM alpha,beta-methylene adenosine-5'-diphosphate increased the LPS-induced inflammation, suggesting that E-5'Nu plays a significant role in reducing inflammation, probably through the generation of adenosine. In conclusion, the experiments indicate that LPS upregulates E-5'Nu activity in HUVECs through a PI3K-dependent increase in the abundance of E-5'Nu on cell membranes. Since adenosine is an anti-inflammatory molecule, E-5'Nu upregulation may be crucial in protecting endothelial cells against inflammatory damage.
胞外5'-核苷酸酶(E-5'Nu)在炎症过程中对细胞外腺苷升高的作用尚不清楚。在本研究中,我们研究了炎症诱导剂脂多糖(LPS)对人脐静脉内皮细胞(HUVECs)中E-5'Nu的影响。暴露于LPS 24小时后,E-5'Nu活性增强。这种作用呈剂量依赖性,半数有效浓度(EC50)为1.66 ng/ml。在10 microM时,磷脂酰肌醇3-激酶(PI3K)抑制剂LY-294002消除了LPS诱导的E-5'Nu活性。然而,在10 microM时,核因子κB(NF-κB)抑制剂吡咯烷二硫代氨基甲酸铵没有作用。LPS上调了E-5'Nu的蛋白表达,但未上调其信使核糖核酸(mRNA)表达。100 microM的α,β-亚甲基腺苷-5'-二磷酸对E-5'Nu的抑制增加了LPS诱导的炎症,这表明E-5'Nu可能通过生成腺苷在减轻炎症中发挥重要作用。总之,实验表明LPS通过PI3K依赖性增加细胞膜上E-5'Nu的丰度来上调HUVECs中的E-5'Nu活性。由于腺苷是一种抗炎分子,E-5'Nu的上调可能对保护内皮细胞免受炎症损伤至关重要。