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目的:探讨白细胞介素1β(IL1β)及其受体拮抗剂(IL1ra)对系膜细胞增殖及产生NO的影响。方法:培养的第10~12代SD大鼠肾小球系膜细胞(GMC)用于实验,分别加入IL1β或IL1β加IL1ra,12h后用化学方法测定培养上清中亚硝酸盐的含量,用3HTDR掺入率测定GMC的增殖,狭缝和Northern杂交测定细胞iNOSmRNA表达。结果:IL1β组GMC出现iNOSmRNA表达及亚硝酸盐增多(053±013vs018±007nmol/104细胞),但无明显细胞增殖(404606±19126vs39779±28041);IL1β加IL1ra组,无iNOSmRNA表达,上清亚硝酸盐含量更高(094±015nmol/104细胞),GMC增殖被抑制(31155±31398)。结论:IL1β能刺激GMC的iNOSmRNA表达和产生亚硝酸盐,IL1ra虽抑制GMC的iNOSmRNA表达,但没能减少其亚硝酸盐的产生。
Objective: To investigate the effects of interleukin-1β (IL1β) and its receptor antagonist (IL1ra) on the proliferation and NO production of mesangial cells. Methods: The cultured rat glomerular mesangial cells (GMC) from the 10th to the 12th generation were used in the experiment and were respectively added with IL1β or IL1β plus IL1ra. After 12 hours, the mesangial cells Nitrate content, 3H-TDR incorporation rate determination of GMC proliferation, slit and Northern hybridization determination of cell iNOSmRNA expression. Results: The expression of iNOS mRNA and nitrite increased in GMCs of IL1β group (053 ± 013vs018 ± 007nmol / 104cells), but no significant cell proliferation (404606 ± 19126vs39779 ± 280 41); IL 1 汕 plus IL 1ra group, no iNOS mRNA expression, the supernatant nitrite content was higher (0 94 ± 0 15nmol / 104 cells), GMC proliferation was inhibited (3115 5 313 98). Conclusion: IL1β can stimulate the expression of iNOS mRNA in GMC and produce nitrite. Although IL1ra inhibits the expression of iNOS mRNA in GMC, IL1ra failed to reduce nitrite production.