中华风湿病学杂志
中華風濕病學雜誌
중화풍습병학잡지
CHINESE JOURNAL OF RHEUMATOLOGY
2008年
9期
629-631
,共3页
陈东育%宋兆峰%李芳%张德庆
陳東育%宋兆峰%李芳%張德慶
진동육%송조봉%리방%장덕경
红斑狼疮,系统性%转录因子%外周血单个核细胞%FOXO1%FOXO3a
紅斑狼瘡,繫統性%轉錄因子%外週血單箇覈細胞%FOXO1%FOXO3a
홍반랑창,계통성%전록인자%외주혈단개핵세포%FOXO1%FOXO3a
Lupus erythematosus,systemic%Transcription factor%Peripheral blood mononuclear cell%FOXO1%FOXO3a
目的 探讨转录因子FOXO1和FOXO3a在系统性红斑狼疮(SLE)患者外周血单个核细胞(PBMC)中的表达水平及其与SLE疾病活动性的关系.方法 选择SLE活动性、SLE非活动性患者和正常对照,运用反转录一聚合酶链反应(RT-PCR)和Western blot检测SLE患者和健康对照组PBMC中FOXO1和FOXO3a mRNA及蛋白的表达水平.结果 活动性SLE患者PBMC中FOXO1 mRNA和蛋白的表达水平明显低于SLE非活动性患者和正常对照(P<0.05),非活动性SLE患者FOXO1 mRNA和蛋白的表达水平明显低于正常对照(P<0.05).FOX03a mRNA和蛋白的表达水平在3组间差异无统计学意义.FOXO1 mRNA水平与狼疮活动指数(SLEDAI)呈显著负相关(r=-0.651,P<0.05).结论 SLE患者PBMC中FOXO1 mRNA和蛋白的表达水平显著低于健康对照,随着SLE患者病情的好转,FOXO1 mRNA和蛋白的表达水平逐渐增高.FOXO1与SLE疾病的活动性呈负相关.FOXO3a与SLE疾病的活动性无关.
目的 探討轉錄因子FOXO1和FOXO3a在繫統性紅斑狼瘡(SLE)患者外週血單箇覈細胞(PBMC)中的錶達水平及其與SLE疾病活動性的關繫.方法 選擇SLE活動性、SLE非活動性患者和正常對照,運用反轉錄一聚閤酶鏈反應(RT-PCR)和Western blot檢測SLE患者和健康對照組PBMC中FOXO1和FOXO3a mRNA及蛋白的錶達水平.結果 活動性SLE患者PBMC中FOXO1 mRNA和蛋白的錶達水平明顯低于SLE非活動性患者和正常對照(P<0.05),非活動性SLE患者FOXO1 mRNA和蛋白的錶達水平明顯低于正常對照(P<0.05).FOX03a mRNA和蛋白的錶達水平在3組間差異無統計學意義.FOXO1 mRNA水平與狼瘡活動指數(SLEDAI)呈顯著負相關(r=-0.651,P<0.05).結論 SLE患者PBMC中FOXO1 mRNA和蛋白的錶達水平顯著低于健康對照,隨著SLE患者病情的好轉,FOXO1 mRNA和蛋白的錶達水平逐漸增高.FOXO1與SLE疾病的活動性呈負相關.FOXO3a與SLE疾病的活動性無關.
목적 탐토전록인자FOXO1화FOXO3a재계통성홍반랑창(SLE)환자외주혈단개핵세포(PBMC)중적표체수평급기여SLE질병활동성적관계.방법 선택SLE활동성、SLE비활동성환자화정상대조,운용반전록일취합매련반응(RT-PCR)화Western blot검측SLE환자화건강대조조PBMC중FOXO1화FOXO3a mRNA급단백적표체수평.결과 활동성SLE환자PBMC중FOXO1 mRNA화단백적표체수평명현저우SLE비활동성환자화정상대조(P<0.05),비활동성SLE환자FOXO1 mRNA화단백적표체수평명현저우정상대조(P<0.05).FOX03a mRNA화단백적표체수평재3조간차이무통계학의의.FOXO1 mRNA수평여랑창활동지수(SLEDAI)정현저부상관(r=-0.651,P<0.05).결론 SLE환자PBMC중FOXO1 mRNA화단백적표체수평현저저우건강대조,수착SLE환자병정적호전,FOXO1 mRNA화단백적표체수평축점증고.FOXO1여SLE질병적활동성정부상관.FOXO3a여SLE질병적활동성무관.
Objective To study the expression of transcription factor FOXO1 and FOXO3a on peripheral blood mononuclear cells (PBMC) in patients with active or inactive systemic lupus erythematosus (SLE) and investigate the effect of FOXO1 and FOXO3a on the clinical features of SLE. Methods Thirty SLE patients and 10 healthy controls were enrolled. PBMC were separated from the peripheral blood. Reverse transcription-polymerase chain reaction (RT-PCR) and western blot were applied to analyze the expression of FOXOI and FOXO3a. Results The level of FOXO1 expression was significantly decreased in active SLE patients compared with controls and patients with inactive SLE (P<0.05). The level of FOXO1 expression in inactive SLE patients was lower than that of the controls (P<0.05). The expression of FOXO1 mRNA was negatively correlated to SLEDAI. However, the level of FOXO3a was similar among the three groups. Conclusion The result suggests that FOXO1 may be involved in the pathogenesis of SLE and the expression level of FOXOI may be a good indicator for the disease activity of SLE.