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Protein Inhibitor of Activated STAT3 (PIAS3) Is Down-Regulated in Eutopic Endometrium of Women with Endometriosis

机译:激活的STAT3(PIAS3)的蛋白抑制剂在子宫内膜异位症妇女的异位内膜中被下调

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摘要

Endometriosis is a major cause of chronic pelvic pain and infertility. Activation of STAT3 appears central to the inflammatory phenotype of eutopic endometrium in women with endometriosis. However, the molecular mechanism by which this occurs remains unknown. Our objective is to determine how STAT3 activity is regulated in endometriosis. Protein inhibitor of activated STAT3 (PIAS3) is a negative regulator of STAT3 activity. We examined the levels of PIAS3 in endometrium from women with and without endometriosis using Western blot analysis and immunohistochemistry. Levels of PIAS3 are significantly lower, in contrast with phosphorylation of STAT3, in women with endometriosis compared to women without endometriosis. Furthermore, induction of endometriosis in the baboon showed a significant reduction of PIAS3 expression during the progression of the disease. Interferon-γ (INFγ) reduces PIAS3 protein levels and increases phospho-STAT3 levels through CXCL10 in endometrial cells, Ishikawa, and 12Z cells. These results suggest that attenuation of PIAS3 causes aberrant activation of STAT3 in endometriosis, leading to inflammatory changes that may impair fertility or cause pain.
机译:子宫内膜异位症是慢性盆腔疼痛和不育的主要原因。在患有子宫内膜异位症的妇女中,STAT3的激活似乎是对位子宫内膜炎性表型的关键。但是,发生这种情况的分子机理仍然未知。我们的目标是确定子宫内膜异位症中STAT3活性的调控方式。激活的STAT3的蛋白抑制剂(PIAS3)是STAT3活性的负调节剂。我们使用蛋白质印迹分析和免疫组化方法检查了有和没有子宫内膜异位症的妇女子宫内膜中PIAS3的水平。与没有子宫内膜异位的女性相比,患有子宫内膜异位的女性与STAT3的磷酸化相比,PIAS3的水平明显较低。此外,狒狒子宫内膜异位症的诱导显示出在疾病进展期间PIAS3表达的显着降低。干扰素-γ(INFγ)通过子宫内膜细胞,石川和12Z细胞中的CXCL10降低PIAS3蛋白水平并增加磷酸STAT3水平。这些结果表明,PIAS3的减弱会导致子宫内膜异位症中STAT3的异常激活,从而导致炎症变化,从而可能损害生育能力或引起疼痛。

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