Yamagata Yoshiaki, Asada Hiromi, Tamura Isao, Lee Lifa, Maekawa Ryo, Taniguchi Ken, Taketani Toshiaki, Matsuoka Aki, Tamura Hiroshi, Sugino Norihiro
Department of Obstetrics and Gynecology, Yamaguchi University Graduate School of Medicine, Minamikogushi 1-1-1, Ube 755-8505, Japan.
Hum Reprod. 2009 May;24(5):1126-32. doi: 10.1093/humrep/dep015. Epub 2009 Feb 6.
Epigenetic regulation may be involved in modulation of gene expression during the normal cyclic changes of the human endometrium. We investigated expression of DNA methyltransferases (DNMTs) in endometrium during the menstrual cycle and the influence of sex steroid hormones on DNMT in endometrial stromal cells (ESC) in culture.
Expression of DNMT1, DNMT3a and DNMT3b was assessed by immunohistochemistry and real-time RT-PCR in endometrial tissue (n = 42 women). ESC (n = 3 women) were cultured with estradiol and medroxyprogesterone acetate (E + MPA) for 17 days, and DNMT mRNA levels were measured by real-time RT-PCR.
Nuclei of both epithelial and stromal cells immunostained for DNMT1, DNMT3a and DNMT3b during each phase of the menstrual cycle. Tissue levels of DNMT1 and DNMT3a mRNA were significantly lower in the mid-secretory phase than in the proliferative phase (P < 0.01). For DNMT3b, the change in mRNA levels showed a similar trend to that for DNMT3a. In ESC culture, DNMT3a and DNMT3b mRNA levels were significantly decreased by E + MPA treatment (P < 0.01 and P < 0.05, respectively) at Day 8 and Day 17.
DNMT mRNAs declined in the human endometrium during the secretory phase, and E + MPA down-regulated DNMT3a and DNMT3b mRNAs in ESC in culture. These results suggest that DNMTs have regulatory functions in gene expression that is associated with decidualization.
表观遗传调控可能参与人类子宫内膜正常周期性变化过程中的基因表达调节。我们研究了月经周期中子宫内膜中DNA甲基转移酶(DNMTs)的表达以及性激素对培养的子宫内膜基质细胞(ESC)中DNMT的影响。
通过免疫组织化学和实时逆转录聚合酶链反应(RT-PCR)评估42例女性子宫内膜组织中DNMT1、DNMT3a和DNMT3b的表达。3例女性的ESC用雌二醇和醋酸甲羟孕酮(E+MPA)培养17天,通过实时RT-PCR测量DNMT mRNA水平。
月经周期各阶段,上皮细胞和基质细胞的细胞核均对DNMT1、DNMT3a和DNMT3b进行免疫染色。分泌中期DNMT1和DNMT3a mRNA的组织水平显著低于增殖期(P<0.01)。对于DNMT3b,mRNA水平的变化与DNMT3a相似。在ESC培养中,E+MPA处理在第8天和第17天显著降低了DNMT3a和DNMT3b mRNA水平(分别为P<0.01和P<0.05)。
分泌期人类子宫内膜中DNMT mRNA下降,E+MPA下调培养的ESC中DNMT3a和DNMT3b mRNA。这些结果表明DNMTs在与蜕膜化相关的基因表达中具有调节功能。