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在反复种植失败的女性中,Krüppel样因子12增加通过下调白血病抑制因子而损害胚胎着床。

Increased Krüppel-like factor 12 impairs embryo attachment via downregulation of leukemia inhibitory factor in women with recurrent implantation failure.

作者信息

Huang Chenyang, Sun Haixiang, Wang Zhilong, Liu Yang, Cheng Xi, Liu Jingyu, Jiang Ruiwei, Zhang Xindong, Zhen Xin, Zhou Jidong, Chen Linjun, Ding Lijun, Yan Guijun, Jiang Yue

机构信息

Reproductive Medicine Center, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, 210008 China.

出版信息

Cell Death Discov. 2018 Aug 6;4:23. doi: 10.1038/s41420-018-0088-8. eCollection 2018.

Abstract

Recurrent implantation failure (RIF) caused by various etiological factors remains a challenge for fertility clinicians using assisted reproductive technology (ART) worldwide. Dysregulation of leukemia inhibitory factor (LIF) in the endometria of women with RIF is involved in impaired endometrial receptivity and embryo adhesion. However, the mechanism through which LIF expression is regulated in women with RIF is still poorly understood. Our previous study noted that the abnormally increased endometrial Krüppel-like factor 12 (KLF12) in RIF women led to impaired decidualization and embryo implantation. Here, we further found that KLF12 inhibited embryo adhesion in vivo and in vitro by repressing LIF expression. Mechanistically, KLF12 bound to conserved sites (CAGTGGG, -6771 to -6765 and -7115 to -7109) within the LIF promoter region and repressed LIF transcription directly. Exogenous LIF significantly reversed the KLF12-mediated repression of BeWo spheroid adhesion. KLF12 expression was reduced significantly in Ishikawa cells treated with progestogen, which was due to the activation of Akt signaling. These findings may provide novel potential therapeutic regimens for patients with RIF and disrupted endometrial receptivity.

摘要

由各种病因引起的反复种植失败(RIF),对于全球使用辅助生殖技术(ART)的生育临床医生来说仍然是一个挑战。RIF女性子宫内膜中白血病抑制因子(LIF)的失调与子宫内膜容受性受损和胚胎黏附有关。然而,RIF女性中LIF表达的调控机制仍知之甚少。我们之前的研究指出,RIF女性子宫内膜中Krüppel样因子12(KLF12)异常增加会导致蜕膜化和胚胎着床受损。在此,我们进一步发现,KLF12通过抑制LIF表达在体内和体外抑制胚胎黏附。机制上,KLF12与LIF启动子区域内的保守位点(CAGTGGG,-6771至-6765和-7115至-7109)结合并直接抑制LIF转录。外源性LIF显著逆转了KLF12介导的BeWo球状体黏附抑制。用孕激素处理的 Ishikawa细胞中KLF12表达显著降低,这是由于Akt信号通路的激活。这些发现可能为RIF和子宫内膜容受性受损的患者提供新的潜在治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7e9/6079092/642fced49f53/41420_2018_88_Fig1_HTML.jpg

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