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表皮生长因子受体在妊娠早期对子宫内膜功能起着关键调节作用。

The epidermal growth factor receptor critically regulates endometrial function during early pregnancy.

作者信息

Large Michael J, Wetendorf Margeaux, Lanz Rainer B, Hartig Sean M, Creighton Chad J, Mancini Michael A, Kovanci Ertug, Lee Kuo-Fen, Threadgill David W, Lydon John P, Jeong Jae-Wook, DeMayo Francesco J

机构信息

Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas, United States of America.

Dan L. Duncan Cancer Center Division of Biostatistics, Department of Medicine, Baylor College of Medicine, Houston, Texas, United States of America.

出版信息

PLoS Genet. 2014 Jun 19;10(6):e1004451. doi: 10.1371/journal.pgen.1004451. eCollection 2014 Jun.

Abstract

Infertility and adverse gynecological outcomes such as preeclampsia and miscarriage represent significant female reproductive health concerns. The spatiotemporal expression of growth factors indicates that they play an important role in pregnancy. The goal of this study is to define the role of the ERBB family of growth factor receptors in endometrial function. Using conditional ablation in mice and siRNA in primary human endometrial stromal cells, we identified the epidermal growth factor receptor (Egfr) to be critical for endometrial function during early pregnancy. While ablation of Her2 or Erbb3 led to only a modest reduction in litter size, mice lacking Egfr expression are severely subfertile. Pregnancy demise occurred shortly after blastocyst implantation due to defects in decidualization including decreased proliferation, cell survival, differentiation and target gene expression. To place Egfr in a genetic regulatory hierarchy, transcriptome analyses was used to compare the gene signatures from mice with conditional ablation of Egfr, wingless-related MMTV integration site 4 (Wnt4) or boneless morphogenic protein 2 (Bmp2); revealing that not only are Bmp2 and Wnt4 key downstream effectors of Egfr, but they also regulate distinct physiological functions. In primary human endometrial stromal cells, marker gene expression, a novel high content image-based approach and phosphokinase array analysis were used to demonstrate that EGFR is a critical regulator of human decidualization. Furthermore, inhibition of EGFR signaling intermediaries WNK1 and AKT1S1, members identified in the kinase array and previously unreported to play a role in the endometrium, also attenuate decidualization. These results demonstrate that EGFR plays an integral role in establishing the cellular context necessary for successful pregnancy via the activation of intricate signaling and transcriptional networks, thereby providing valuable insight into potential therapeutic targets.

摘要

不孕症以及子痫前期和流产等不良妇科结局是女性生殖健康的重大问题。生长因子的时空表达表明它们在妊娠中发挥着重要作用。本研究的目的是确定生长因子受体ERBB家族在子宫内膜功能中的作用。通过对小鼠进行条件性基因敲除以及对原代人子宫内膜基质细胞使用小干扰RNA(siRNA),我们确定表皮生长因子受体(Egfr)在妊娠早期对子宫内膜功能至关重要。虽然敲除Her2或Erbb3仅导致窝仔数略有减少,但缺乏Egfr表达的小鼠严重不育。由于蜕膜化缺陷,包括增殖减少、细胞存活、分化和靶基因表达降低,妊娠在胚泡着床后不久就终止了。为了将Egfr置于基因调控层次结构中,我们使用转录组分析来比较来自条件性敲除Egfr、无翅相关MMTV整合位点4(Wnt4)或骨形态发生蛋白2(Bmp2)的小鼠的基因特征;结果表明,Bmp2和Wnt4不仅是Egfr的关键下游效应器,而且它们还调节不同的生理功能。在原代人子宫内膜基质细胞中,我们使用标记基因表达、一种基于高内涵图像的新方法和磷酸激酶阵列分析来证明EGFR是人类蜕膜化的关键调节因子。此外,抑制EGFR信号中介物WNK1和AKT1S1(这两个成员在激酶阵列中被鉴定出来,之前未报道它们在子宫内膜中发挥作用)也会减弱蜕膜化。这些结果表明,EGFR通过激活复杂的信号和转录网络,在建立成功妊娠所需的细胞环境中发挥不可或缺的作用,从而为潜在治疗靶点提供了有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90b3/4063709/1a9fa60e904b/pgen.1004451.g001.jpg

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