摘要
子宫内膜异位症是引起不孕和盆腔疼痛的主要原因,影响10%以上的育龄妇女。孕激素抗体已被检测到在患有此病的妇女的子宫内膜中,以孕激素应答基因和蛋白表达的改变为依据。cAMPResponse元件结合蛋白样蛋白1(Creb3l1)通过高密度DNA微阵列分析已被确定为一种在小鼠子宫内的孕激素受体(PR)目标基因。然而,CREB3L1的功能还没有研究到子宫内膜异位症、子宫生物学的内容里。在这项研究中,我们证实了孕酮(P4)在野生型和孕激素受体(PRKO)的小鼠子宫内对creb3l1的调节。此外,我们观察到,CREB3L1分泌期子宫内膜的表达明显高于增殖期,CREB3L1在子宫内膜异位症患者的子宫内膜的表达明显下降。最后,通过在激素体外诱导蜕膜化之前将CREB3L1 siRNA转换成到人子宫内膜间质细胞(hESCs),我们发现,CREB3L1是蜕膜化过程所必需的。有趣的是,ERK1 / 2的磷酸化是蜕膜化的关键因素,也明显减少了CREB3L1沉默胚胎干细胞。众所周知,患者的子宫内膜异位症中人类胚胎干细胞显示蜕膜化的修复,P4-PR信号轴的失调与多种疾病如不孕、子宫内膜异位症内膜受损有联系。因此,这些结果表明,CREB3L1在人和小鼠蜕膜化中必不可少,可能会与P4依赖性子宫内膜异位症的发病机制有关联。
关键词: CREB3L1,蜕膜,子宫内膜,子宫内膜异位症,孕激素,子宫。
Current Molecular Medicine
Title:cAMP-Response Element-Binding 3-Like Protein 1 (CREB3L1) is Required for Decidualization and its Expression is Decreased in Women with Endometriosis
Volume: 16 Issue: 3
Author(s): J.I. Ahn, J.-Y. Yoo, T.H. Kim, Y.I. Kim, S.D. Ferguson, A.T. Fazleabas, S.L. Young and B.A. Lessey, J.Y. Ahn, J.M. Lim, J.-W. Jeong
Affiliation:
关键词: CREB3L1,蜕膜,子宫内膜,子宫内膜异位症,孕激素,子宫。
摘要: Endometriosis is a major cause of infertility and pelvic pain, affecting more than 10% of reproductive-aged women. Progesterone resistance has been observed in the endometrium of women with this disease, as evidenced by alterations in progesterone-responsive gene and protein expression. cAMPResponse Element-Binding 3-like protein 1 (Creb3l1) has previously been identified as a progesterone receptor (PR) target gene in mouse uterus via high density DNA microarray analysis. However, CREB3L1 function has not been studied in the context of endometriosis and uterine biology. In this study, we validated progesterone (P4) regulation of Creb3l1 in the uteri of wild-type and progesterone receptor knockout (PRKO) mice. Furthermore, we observed that CREB3L1 expression was significantly higher in secretory phase human endometrium compared to proliferative phase and that CREB3L1 expression was significantly decreased in the endometrium of women with endometriosis. Lastly, by transfecting CREB3L1 siRNA into cultured human endometrial stromal cells (hESCs) prior to hormonal induction of in vitro decidualization, we showed that CREB3L1 is required for the decidualization process. Interestingly, phosphorylation of ERK1/2, critical factor for decidualization, was also significantly reduced in CREB3L1-silenced hESCs. It is known that hESCs from patients with endometriosis show impaired decidualization and that dysregulation of the P4-PR signaling axis is linked to a variety of endometrial diseases including infertility and endometriosis. Therefore, these results suggest that CREB3L1 is required for decidualization in mice and humans and may be linked to the pathogenesis of endometriosis in a P4-dependent manner.
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J.I. Ahn, J.-Y. Yoo, T.H. Kim, Y.I. Kim, S.D. Ferguson, A.T. Fazleabas, S.L. Young and B.A. Lessey, J.Y. Ahn, J.M. Lim, J.-W. Jeong , cAMP-Response Element-Binding 3-Like Protein 1 (CREB3L1) is Required for Decidualization and its Expression is Decreased in Women with Endometriosis, Current Molecular Medicine 2016; 16 (3) . https://dx.doi.org/10.2174/1566524016666160225153659
DOI https://dx.doi.org/10.2174/1566524016666160225153659 |
Print ISSN 1566-5240 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5666 |
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