Safir Nadia, Wendel Albrecht, Saile Rachid, Chabraoui Layachi
Laboratory of Biochemistry, Faculté de Sciences Ben Msik, Casablanca, Morocco.
Clin Chem Lab Med. 2003 Aug;41(8):1005-11. doi: 10.1515/CCLM.2003.154.
The J774.1 macrophage cell line was used as a tool to investigate the influence of selenium on macrophage function. In vitro selenium supplementation enhanced phagocytosis, degranulation by the release of beta-glucuronidase after N-formyl-methionyl-leucyl-phenylalanine (FMLP) or cytochalasin B, and the production of superoxide anion after phorbol myristate acetate stimulation of these cells, while the release of nitric oxide was not affected by the selenium status. Selenium supplementation enhanced significantly (p < 0.05) the release of tumor necrosis factor (5-fold), interleukin-1 (3-fold) and interleukin-6 (2.5-fold) after 10 microg/ml lipopolysaccharide stimulation compared to selenium-deficient cells.
J774.1巨噬细胞系被用作研究硒对巨噬细胞功能影响的工具。体外补充硒可增强吞噬作用、在N-甲酰甲硫氨酰亮氨酰苯丙氨酸(FMLP)或细胞松弛素B刺激后通过β-葡萄糖醛酸酶释放实现的脱颗粒作用,以及佛波酯刺激这些细胞后超氧阴离子的产生,而一氧化氮的释放不受硒状态的影响。与缺硒细胞相比,在10微克/毫升脂多糖刺激后,补充硒显著(p < 0.05)增强了肿瘤坏死因子(5倍)、白细胞介素-1(3倍)和白细胞介素-6(2.5倍)的释放。