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Hashimoto’s thyroiditis impairs embryo implantation by compromising endometrial morphology and receptivity markers in euthyroid mice

机译:Hashimoto的甲状腺炎通过损害Euthyroid小鼠中的子宫内膜形态和接受标记来损害胚胎植入

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Although thyroid dysfunction caused by Hashimoto’s thyroiditis (HT) is believed to be related to implantation failure due to the underdevelopment of the receptive uterus, it is unknown whether HT itself, even in the euthyroid state, impairs embryo implantation associated with endometrial receptivity defects. To address whether HT itself can affect endometrial receptivity accompanied by implantation alterations, a euthyroid HT model was established in mice. Female NOD mice were immunized twice with thyroglobulin and adjuvant to induce the experimental HT model. Four weeks after the second treatment, the mice were normally mated, and pregnant ones were sacrificed in implantation window for thyroid-related parameter and steroid hormones measurements by electrochemiluminescence immunoassay and enzyme-linked immunosorbent assay and implantation site number calculation by uptake of Chicago Blue dye. In addition, certain morphological features of endometrial receptivity were observed by hematoxylin-eosin staining and scanning electron microscopy, and the expression of other receptivity markers were analyzed by immunohistochemistry, RT-qPCR or Western Blot. HT mice displayed intrathyroidal monocyte infiltration and elevated serum thyroid autoantibody levels without thyroid dysfunction, defined as euthyroid HT in humans. Euthyroid HT resulted in implantation failure, fewer pinopodes, retarded pinopode maturation, and inhibited expression of receptivity markers: estrogen receptor α (ERα), integrin β3, leukemia inhibitory factor (LIF), and cell adhesion molecule-1 (ICAM-1). Interestingly, despite this compromised endometrial receptivity response, no statistical differences in serum estradiol or progesterone level between groups were found. These findings are the first to indicate that HT induces a nonreceptive endometrial milieu in the euthyroid state, which may underlie the detrimental effects of HT itself on embryo implantation.
机译:虽然由于接受子宫的开发不发现,但由于接受子宫的不开发而被认为是与植入失败引起的甲状腺功能障碍,但是HT本身是否本身即使在Euthyroid状态下,否则损害与子宫内膜接受缺陷相关的胚胎植入。为了解决HT本身是否可以影响子宫内膜接受,在小鼠中建立了Euthyroid HT模型。将雌性NOD小鼠用甲状腺蛋白和佐剂免疫两次,以诱导实验HT模型。第二个治疗后四周,小鼠通常被混合,并在植入窗口中处死甲状腺相关参数的植入窗口和用电化学发光免疫测定和酶联免疫吸附测定和植入部位数计算通过摄取芝加哥蓝染料。 。此外,通过苏木精化染色和扫描电子显微镜观察了子宫内膜接受性的某些形态特征,并通过免疫组织化学,RT-QPCR或Western印迹分析了其他接受标记的表达。 HT小鼠显示抗酸血清单核细胞浸润和升高的血清甲状腺自身抗体水平,没有甲状腺功能障碍,定义为人类的Euthyroid HT。 Euthyroid HT导致植入失败,较少的波波,延迟探针成熟,并抑制接受标记的表达:雌激素受体α(ERα),整联蛋白β3,白血病抑制因子(LIF)和细胞粘附分子-1(ICAM-1)。有趣的是,尽管这种受损的子宫内膜接受应对反应,但发现血清雌二醇或基团之间的孕酮水平没有统计学差异。这些发现是第一个表明HT诱导肠道内膜中的非疫苗子宫内膜Milieu,这可能使HT本身对胚胎植入的不利影响。

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