Oróstica Lorena, García Paula, Vera Carolina, García Víctor, Romero Carmen, Vega Margarita
1 Laboratory of Endocrinology and Reproductive Biology, Clinical Hospital, University of Chile, Santiago, Chile.
2 Faculty of Health Sciences, University of Antofagasta, Antofagasta, Chile.
Reprod Sci. 2018 Jul;25(7):1000-1009. doi: 10.1177/1933719117732157. Epub 2017 Sep 25.
Polycystic ovary syndrome (PCOS) affects not only ovarian functions but is also able to affect endometrium metabolism. Around 80% of women with PCOS are obese. High tumor necrosis factor (TNF)-α production and low adiponectin levels are characteristics of obesity. Interestingly, endometrium from obese women with PCOS presents an insulin-resistance condition, high TNF-α levels, and low adiponectin levels. However, TNF-α effect on molecules associated with insulin action in endometrial cells remains unclear. Therefore, the objective of this work was to evaluate TNF-α effect on expression of molecules associated with adiponectin (insulin sensitizing) and TNF-α signaling pathways and on Glucose Transporter type 4 (GLUT-4) levels in human endometrial cells under the characteristic conditions of hyperandrogenic/hyperinsulinic (HA/HI) PCOS. Two human endometrial stromal cell lines (T-HESC/St-T1b) under HA/HI conditions were used to assay the effect of high TNF-α concentration (100 ng/mL) on adiponectin, AdipoR1-AdipoR2 receptors, Adaptor protein phosphotyrosine interacting with PH domain and leucine zipper 1 (APPL1), Phospho-AMP-activated protein kinase T172 (p-AMPKT172), GLUT-4, Tumor necrosis factor receptor 1 (TNFR1)-Tumor necrosis factor receptor 2 (TNFR2) receptors protein levels, and nuclear factor κB (NFκB) nuclear content, by Western blot or immunocytochemistry. The NFκB participation in TNF-α effect on adiponectin expression was assayed using an NFκB inhibitor (pyrrolidine dithiocarbamate). The TNF-α increases the expression of molecules associated with its own signaling pathway ( P < .05) and decreases the protein levels of adiponectin and its associated molecules ( P < .05). Moreover, TNF-α increases NFκB nuclear content ( P < .001), whereas with NFκB inhibition the decrease in adiponectin content induced by TNF-α was not observed. GLUT-4 levels were lower with TNF-α treatment ( P < .01). Thus, in human endometrial stromal cells, high TNF-α levels negatively affect the insulin action through decreased adiponectin signaling and GLUT-4 protein. This could explain the failures observed in endometrial function of obese women with PCOS.
多囊卵巢综合征(PCOS)不仅会影响卵巢功能,还会影响子宫内膜代谢。约80%的PCOS女性肥胖。肿瘤坏死因子(TNF)-α产生增加和脂联素水平降低是肥胖的特征。有趣的是,患有PCOS的肥胖女性的子宫内膜呈现胰岛素抵抗状态、TNF-α水平升高和脂联素水平降低。然而,TNF-α对子宫内膜细胞中与胰岛素作用相关分子的影响仍不清楚。因此,本研究的目的是评估在高雄激素/高胰岛素(HA/HI)PCOS特征条件下,TNF-α对与脂联素(胰岛素增敏)和TNF-α信号通路相关分子表达以及对人子宫内膜细胞中葡萄糖转运蛋白4(GLUT-4)水平的影响。使用处于HA/HI条件下的两个人子宫内膜基质细胞系(T-HESC/St-T1b)来检测高浓度TNF-α(100 ng/mL)对脂联素、脂联素受体1-脂联素受体2、与PH结构域和亮氨酸拉链1相互作用的衔接蛋白磷酸酪氨酸(APPL1)、磷酸化-AMP活化蛋白激酶T172(p-AMPKT172)、GLUT-4、肿瘤坏死因子受体1(TNFR1)-肿瘤坏死因子受体2(TNFR2)受体蛋白水平以及核因子κB(NFκB)核含量的影响,采用蛋白质印迹法或免疫细胞化学法。使用NFκB抑制剂(吡咯烷二硫代氨基甲酸盐)检测NFκB在TNF-α对脂联素表达影响中的作用。TNF-α增加与其自身信号通路相关分子的表达(P <.05),并降低脂联素及其相关分子的蛋白水平(P <.05)。此外,TNF-α增加NFκB核含量(P <.001),而在抑制NFκB时未观察到TNF-α诱导的脂联素含量降低。TNF-α处理后GLUT-4水平降低(P <.01)。因此,在人子宫内膜基质细胞中,高TNF-α水平通过降低脂联素信号传导和GLUT-4蛋白对胰岛素作用产生负面影响。这可以解释患有PCOS的肥胖女性在子宫内膜功能方面观察到的异常。