Protein Phosphatase 5 Contributes to the Overexpression of Epigenetically Regulated T-Lymphocyte Genes in Patients with Lupus.

Lupus (Los Angeles) Pub Date : 2016-12-01 Epub Date: 2016-12-30
D Patel, G Gorelik, B Richardson
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Abstract

Objective: Lupus develops when genetically predisposed people encounter certain drugs or environmental agents causing oxidative stress such as infections and sun exposure, and then typically follows a chronic relapsing course with flares triggered by the exogenous stressors. Current evidence indicates that these environmental agents can trigger lupus flares by inhibiting the replication of DNA methylation patterns during mitosis in CD4+ T cells, altering the expression of genes suppressed by this mechanism that convert normal "helper" cells into auto reactive cells which promote lupus flares. How environmental stressors inhibit T cell DNA methylation though is incompletely understood. Protein phosphatase 5 (PP5) is a stress induced inhibitor of T cell ERK and JNK signaling in "senescent" CD4+CD28- T cells, also characterized by DNA demethylation and altered expression of genes that promote atherosclerosis. We tested if PP5 is increased in CD4+CD28+ T cells by oxidative stress, if PP5 transfection causes overexpression of methylation sensitive genes in T cells, and if PP5 is overexpressed in lupus T cells.

Results: PP5 was found to be overexpressed in CD4+CD28+ T cells treated with H2O2 and ONOO- and in T cells from lupus patients.

Conclusion: The results indicate that PP5 increases expression of methylation sensitive T cell genes, and may contribute to the aberrant gene expression in CD4+CD28+ T cells that characterize lupus flares as well as the aberrant gene expression in CD4+CD28- T cells that promote atherosclerosis.

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蛋白磷酸酶5参与狼疮患者表观遗传调控t淋巴细胞基因的过度表达
目的:当遗传易感性的人遇到某些药物或环境因素引起氧化应激(如感染和阳光照射)时,狼疮就会发展,然后通常会经历一个慢性复发过程,并由外源性应激源引发耀斑。目前的证据表明,这些环境因子可以通过抑制CD4+ T细胞有丝分裂过程中DNA甲基化模式的复制来触发狼疮耀斑,改变被这种机制抑制的基因的表达,这些基因将正常的“辅助”细胞转化为促进狼疮耀斑的自身反应性细胞。环境应激因子如何抑制T细胞DNA甲基化尚不完全清楚。蛋白磷酸酶5 (PP5)是“衰老”CD4+CD28- T细胞中应激诱导的T细胞ERK和JNK信号抑制剂,也以DNA去甲基化和促进动脉粥样硬化的基因表达改变为特征。我们测试了PP5是否在CD4+CD28+ T细胞中因氧化应激而增加,PP5转染是否导致T细胞中甲基化敏感基因的过度表达,以及PP5是否在狼疮T细胞中过度表达。结果:PP5在H2O2和ONOO-处理的CD4+CD28+ T细胞和狼疮患者的T细胞中均过表达。结论:PP5增加了甲基化敏感T细胞基因的表达,并可能参与红斑狼疮斑块特征的CD4+CD28+ T细胞基因的异常表达以及促进动脉粥样硬化的CD4+CD28- T细胞基因的异常表达。
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