Li Zhijian, Li Youji, Huang Linghong, Xu Hanshi, Yu Xueqing, Ye Rengao
Department of Nephrology, Institute of Nephrology, the First Affiliated Hospital, Sun Yat-Sen University of Medical Sciences, Guangzhou 510080, China.
Chin Med J (Engl). 2002 Jun;115(6):846-50.
To determine the in vitro expression of interleukin-12 (IL-12) and its effect on signal transducers and activators of transcription (STAT) signaling molecules in peripheral blood mononuclear cells (PBMCs) in patients with systemic lupus erythematosus (SLE).
Peripheral blood mononuclear cells in 39 patients with definite systemic lupus erythematosus and 11 healthy volunteers were collected. Expression of IL-12 P40mRNA in PBMCs was determined with reverse transcription-polymerase chain reaction (RT-PCR). Quantity of IL-12 protein supernatant was measured by enzyme-linked immunosorbent assay (ELISA). The levels of phosphorylated STAT3 and STAT4 signaling molecules in PBMCs were detected by immunoblot.
Levels of IL-12 protein and mRNA expression in patients with active or inactive SLE were significantly higher than those in controls. Phytohemagglutinin (PHA ) may promote the expression of IL-12. IL-12 alone induced the phosphorylation of STAT3 and STAT4 in PBMCs from patients with SLE, especially in active SLE. However it had no obvious effect on normal PBMCs. Phosphorylated STAT3 and STAT4 might be observed in normal PBMCs treated with IL-12 plus PHA.
IL-12 is produced aberrantly in patients with SLE. IL-12 might exert its biological role in SLE via the aberrantly phosphorylated STAT3 and STAT4 signaling molecules.
测定系统性红斑狼疮(SLE)患者外周血单个核细胞(PBMC)中白细胞介素12(IL-12)的体外表达及其对信号转导子和转录激活子(STAT)信号分子的影响。
收集39例确诊的系统性红斑狼疮患者和11名健康志愿者的外周血单个核细胞。采用逆转录-聚合酶链反应(RT-PCR)测定PBMC中IL-12 P40mRNA的表达。用酶联免疫吸附测定法(ELISA)检测IL-12蛋白上清液的量。通过免疫印迹法检测PBMC中磷酸化STAT3和STAT4信号分子的水平。
活动期或非活动期SLE患者的IL-12蛋白和mRNA表达水平显著高于对照组。植物血凝素(PHA)可促进IL-12的表达。单独的IL-12可诱导SLE患者PBMC中STAT3和STAT4的磷酸化,尤其是在活动期SLE患者中。然而,它对正常PBMC没有明显影响。在用IL-12加PHA处理的正常PBMC中可观察到磷酸化的STAT3和STAT4。
SLE患者IL-12产生异常。IL-12可能通过异常磷酸化的STAT3和STAT4信号分子在SLE中发挥其生物学作用。