Wang Yun, Chen Hong, Wang NingLing, Guo HaiYan, Fu Yonglun, Xue Songguo, Ai Ai, Lyu Qifeng, Kuang Yanping
Department of Assisted Reproduction, Shanghai ninth people's hospital affiliated to JiaoTong University School of Medicine, Shanghai, China.
PLoS One. 2015 May 7;10(5):e0125559. doi: 10.1371/journal.pone.0125559. eCollection 2015.
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.
本研究的目的是阐明17β-雌二醇和2,3,7,8-四氯二苯并对二恶英(TCDD)对子宫内膜异位症环境中巨噬细胞表型的影响。进行子宫内膜基质细胞(ESC)与U937细胞(巨噬细胞系)的共培养,以模拟子宫内膜异位症环境,并确定17β-雌二醇和/或TCDD对U937巨噬细胞产生白细胞介素10(IL10)、白细胞介素12(IL12)以及HLA-DR、CD86表达的影响。我们发现,当巨噬细胞与ESC共培养时,17β-雌二醇与TCDD联合使用对诱导M2活化具有协同作用。此外,17β-雌二醇与TCDD的组合显著增强了巨噬细胞中信号转导和转录激活因子3(STAT3)和P38的磷酸化。STAT3和P38丝裂原活化蛋白激酶(P38MAPK)抑制剂可有效消除由17β-雌二醇和TCDD诱导的M2巨噬细胞分化,但细胞外信号调节激酶1/2(ERK1/2)和应激活化蛋白激酶(JNK)抑制剂则无此作用。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M2极化,从而导致子宫内膜异位症的发生。