自身免疫性疾病的性别差异:雌激素增加系统性红斑狼疮钙调磷酸酶的表达

Virginia Rider , Raymond T. Foster , Marilyn Evans , Ronsuke Suenaga , Nabih I. Abdou
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引用次数: 77

摘要

系统性红斑狼疮(SLE)主要影响育龄妇女(与男性的比例为9:1),绝经后妇女的发病强度通常会降低,这表明性激素在其发病机制中起作用。使用RNase保护实验比较稳态水平的钙调磷酸酶mRNA显示,在9名女性狼疮患者培养的T细胞中,雌二醇反应增加了钙调磷酸酶的表达。在8名年龄匹配的正常对照女性志愿者的T细胞中,钙调磷酸酶mRNA水平没有显著增加。雌激素依赖性钙调磷酸酶mRNA呈剂量依赖性增加,而黄体酮和地塞米松不增加患者细胞中的钙调磷酸酶mRNA。狼疮T细胞钙调磷酸酶mRNA对雌二醇的反应在6 h升高,而在3 h没有。与雌二醇孵育后狼疮T细胞提取物中钙调磷酸酶活性升高,而正常T细胞的磷酸酶活性不受雌激素的影响。血管炎和类风湿关节炎患者服用与狼疮患者相似的药物后,其T细胞中钙调磷酸酶的表达不受雌二醇的影响。这项研究为狼疮患者雌激素作用的分子标记提供了第一个证据,并表明狼疮T细胞钙调磷酸酶中雌激素依赖性的变化可能改变促炎细胞因子基因调控和T - b细胞相互作用。
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Gender Differences in Autoimmune Diseases: Estrogen Increases Calcineurin Expression in Systemic Lupus Erythematosus

Systemic lupus erythematosus (SLE) predominantly affects women (9:1 compared to men) of childbearing age and often decreases its intensity in postmenopausal women, suggesting that sex hormones play a role in its pathogenesis. Comparison of steady-state levels of calcineurin mRNA using RNase protection assays revealed increased calcineurin expression in response to estradiol in cultured T cells from nine female lupus patients. Calcineurin mRNA levels did not increase significantly in T cells from eight age-matched normal control female volunteers. Estrogen-dependent calcineurin mRNA increased in a dose-dependent fashion, while progesterone and dexamethasone did not increase calcineurin mRNA in patient cells. Lupus T cell calcineurin mRNA increased in response to estradiol at 6 h but not at 3 h. Calcineurin phosphatase activity increased in lupus T cell extracts after incubation of cells with estradiol, while phosphatase activity in normal T cells was unaffected by estrogen. Calcineurin expression in T cells from patients with vasculitis and rheumatoid arthritis taking medications similar to those taken by the lupus patients was unaffected by estradiol. This study provides the first evidence for a molecular marker of estrogen action in lupus patients and suggests that estrogen-dependent changes in lupus T cell calcineurin could alter proinflammatory cytokine gene regulation and T–B cell interactions.

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