Li H, Hu J, Xin W, Zhao B
Department of Molecular and Cell Biophysics, Institute of Biophysics, Academia Sinica, Beijing, People's Republic of China.
Redox Rep. 2000;5(6):353-8. doi: 10.1179/135100000101535915.
The activity of nitric oxide synthase (NOS) during the respiratory burst in phorbol-1,2-myristate-1,3-acetate (PMA) stimulated macrophages has been the topic of much debate in the literature. To help clarify the role of NOS, we have examined the chemiluminescence arising from peroxynitrite production, nitrite/nitrate and nitric oxide production, and oxygen consumption during the respiratory burst in PMA-stimulated macrophages. The Griess reaction was used to measure nitrite/nitrate, spin trapping with N-methyl D-glucamine dithiocarbamate (MGD)2-Fe2+ was used to quantify nitric oxide, and the spin probe 2,2,6,6-tetramethylpiperidine-N-oxyl-4-ol (TEMPOL) was used to measure oxygen consumption. Oxygen free radical production (hydroxyl and superoxide free radicals) was also investigated using the spin trap 5,5-dimethyl-1-pyroline-1-oxide (DMPO). The chemiluminescence emitted by the PMA-stimulated macrophages and nitrite/nitrate in the culture system were both found to increase. However, the rate of nitric oxide release remained constant, indicating that the activity of NOS is not enhanced during the respiratory burst in PMA stimulated macrophages.
在佛波醇-1,2-十四烷酸酯-1,3-乙酸酯(PMA)刺激的巨噬细胞呼吸爆发过程中,一氧化氮合酶(NOS)的活性一直是文献中诸多争论的主题。为了帮助阐明NOS的作用,我们研究了PMA刺激的巨噬细胞呼吸爆发过程中过氧亚硝酸盐产生、亚硝酸盐/硝酸盐和一氧化氮产生以及氧气消耗所产生的化学发光。采用格里斯反应测量亚硝酸盐/硝酸盐,用N-甲基-D-葡糖胺二硫代氨基甲酸盐(MGD)2-Fe2+进行自旋捕获来定量一氧化氮,并用自旋探针2,2,6,6-四甲基哌啶-N-氧基-4-醇(TEMPOL)测量氧气消耗。还使用自旋捕获剂5,5-二甲基-1-吡咯啉-N-氧化物(DMPO)研究了氧自由基的产生(羟基和超氧阴离子自由基)。发现PMA刺激的巨噬细胞发出的化学发光和培养系统中的亚硝酸盐/硝酸盐均增加。然而,一氧化氮释放速率保持恒定,这表明在PMA刺激的巨噬细胞呼吸爆发过程中NOS的活性并未增强。