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Combined 17β-Estradiol with TCDD Promotes M2 Polarization of Macrophages in the Endometriotic Milieu with Aid of the Interaction between Endometrial Stromal Cells and Macrophages

机译:17β-雌二醇与TCDD联合使用可促进子宫内膜间质细胞与巨噬细胞之间的相互作用促进子宫内膜异位环境中巨噬细胞的M2极化

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摘要

The goal of this study is to elucidate the effects of 17β-estradiol and TCDD (2,3,7,8-tetrachlorodibenzo-p-dioxin) on macrophage phenotypes in the endometriotic milieu. Co-culture of endometrial stromal cells (ESCs) and U937 cells (macrophage cell line) was performed to simulate the endometriotic milieu and to determine the effects of 17β-estradiol and/or TCDD on IL10, IL12 production and HLA-DR, CD86 expression by U937 macrophages. We found that combining 17β-estradiol with TCDD has a synergistic effect on inducing M2 activation when macrophages are co-cultured with ESCs. Moreover, the combination of 17β-estradiol and TCDD significantly enhanced STAT3 and P38 phosphorylation in macrophages. Differentiation of M2 macrophages induced by 17β-estradiol and TCDD were effectively abrogated by STAT3 and P38MAPK inhibitors, but not by ERK1/2 and JNK inhibitors. In conclusion, 17β-estradiol and TCDD in the ectopic milieu may lead to the development of endometriosis by inducing M2 polarization of macrophages through activation of the STAT3 and P38MAPK pathways.
机译:这项研究的目的是阐明17β-雌二醇和TCDD(2,3,7,8-四氯二苯并-p-二恶英)对子宫内膜异位症环境中巨​​噬细胞表型的影响。进行子宫内膜间质细胞(ESCs)和U937细胞(巨噬细胞系)的共培养,以模拟子宫内膜异位环境,并确定17β-雌二醇和/或TCDD对IL10,IL12产生以及HLA-DR,CD86表达的影响通过U937巨噬细胞。我们发现当巨噬细胞与ESCs共培养时,将17β-雌二醇与TCDD结合对诱导M2活化具有协同作用。此外,17β-雌二醇和TCDD的结合显着增强了巨噬细胞中STAT3和P38的磷酸化。 STAT3和P38MAPK抑制剂可以有效地消除17β-雌二醇和TCDD诱导的M2巨噬细胞的分化,而ERK1 / 2和JNK抑制剂则不能。总之,异位环境中的17β-雌二醇和TCDD可能通过激活STAT3和P38MAPK途径诱导巨噬细胞的M2极化而导致子宫内膜异位症的发展。

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