The Liggins Institute, The University of Auckland, Auckland 1142, New Zealand.
Mol Hum Reprod. 2010 May;16(5):297-310. doi: 10.1093/molehr/gaq010. Epub 2010 Feb 5.
The endometrium undergoes morphological and functional changes during the menstrual cycle which are essential for uterine receptivity. These changes are driven by estrogen and progesterone and involve the fine control of many different genes-several of which have been identified as being epigenetically regulated. Epigenetic modification may therefore influence the functional changes in the endometrium required for successful implantation. There is, however, only limited information on epigenetic regulation in endometrium. We review the potential role of epigenetic regulation of key processes during the menstrual cycle and present our own findings following a preliminary study into global acetylation levels in the human endometrium. A changing epigenetic state is associated with the differentiation of stem cells into different lineages and thus may be involved in endometrial regeneration. Histone acetylation is implicated in the vascular endothelial growth factor pathway during angiogenesis, and studies using histone deacetylase inhibitors suggest an involvement in endometrial proliferation and differentiation. The processes of decidualization and implantation are also associated with epigenetic change and epigenetic modulators show variable expression across the menstrual cycle. Our own studies found that endometrial global histone acetylation, as determined by western blotting, changed throughout the menstrual cycle and correlated well with expected transcription activity during the different phases. This suggests that epigenetics may be involved in the regulation of endometrial gene expression during the menstrual cycle and that abnormal epigenetic modifications may therefore be associated with implantation failure and early pregnancy loss as well as with other endometrial pathologies.
在月经周期中,子宫内膜经历形态和功能的变化,这对于子宫的接受性至关重要。这些变化由雌激素和孕激素驱动,涉及许多不同基因的精细调控,其中有几个基因已被确定为受表观遗传调控。因此,表观遗传修饰可能会影响子宫内膜成功着床所需的功能变化。然而,关于子宫内膜的表观遗传调控的信息非常有限。我们综述了在月经周期中关键过程的表观遗传调控的潜在作用,并介绍了我们在对人类子宫内膜进行全局乙酰化水平初步研究后的发现。表观遗传状态的变化与干细胞分化为不同谱系有关,因此可能与子宫内膜再生有关。组蛋白乙酰化参与血管内皮生长因子通路中的血管生成,使用组蛋白去乙酰化酶抑制剂的研究表明其参与子宫内膜的增殖和分化。蜕膜化和着床过程也与表观遗传变化有关,表观遗传调节剂在整个月经周期中的表达也存在差异。我们自己的研究发现,通过 Western blot 测定的子宫内膜全局组蛋白乙酰化在整个月经周期中发生变化,与不同阶段的预期转录活性密切相关。这表明表观遗传可能参与了月经周期中子宫内膜基因表达的调控,异常的表观遗传修饰可能与着床失败和早期妊娠丢失以及其他子宫内膜病变有关。