Division of Cell and Molecular Biology, Department of Biology, Boston University, Boston, MA 02215, USA.
Biol Reprod. 2013 Jul 18;89(1):13. doi: 10.1095/biolreprod.112.107334. Print 2013 Jul.
Changes in the CD-1 mouse uterine transcriptome during proestrus and estrus were investigated to help elucidate mechanisms of uterine tissue remodeling during the estrus cycle and their regulation by estrogen and progesterone in preparation of the uterus for pregnancy. Mice were staged beginning at 6 weeks of age, and uterine horns were harvested after monitoring two estrus cycles. Microarray analysis of whole uterine horn RNA identified 2428 genes differentially expressed in estrus compared to proestrus, indicating there is extensive remodeling of mouse uterus during the estrus cycle, affecting 10% of all protein-encoding genes. Many (50%) of these genes showed the same differential expression in independent analyses of isolated uterine lumenal epithelial cells. Changes in gene expression associated with structural alterations of the uterus included remodeling of the extracellular matrix, changes in cell keratins and adhesion molecules, activation of mitosis and changes in major histocompatibility complex class II (MHCII) presentation, complement and coagulation cascades, and cytochrome P450 expression. Signaling pathways regulated during the estrus cycle, involving ligand-gated channels, Wnt and hedgehog signaling, and transcription factors with poorly understood roles in reproductive tissues, included several genes and gene networks that have been implicated in pathological states. Many of the molecular pathways and biological functions represented by the genes differentially expressed from proestrus to estrus are also altered during the human menstrual cycle, although not necessarily at the corresponding phases of the cycle. These findings establish a baseline for further studies in the mouse model to dissect mechanisms involved in uterine tissue response to endocrine disruptors and the development of reproductive tract diseases.
研究了 CD-1 小鼠发情期和动情前期子宫转录组的变化,以帮助阐明发情周期中子宫组织重塑的机制及其受雌激素和孕激素的调节,为妊娠做准备。从 6 周龄开始对小鼠进行分期,在监测了两个发情周期后采集子宫角。对整个子宫角 RNA 的微阵列分析鉴定出 2428 个在发情期与发情前期相比差异表达的基因,表明发情周期中老鼠子宫有广泛的重塑,影响了约 10%的所有蛋白质编码基因。这些基因中有许多(约 50%)在对分离的子宫腔上皮细胞的独立分析中表现出相同的差异表达。与子宫结构改变相关的基因表达变化包括细胞外基质的重塑、细胞角蛋白和粘附分子的变化、有丝分裂的激活以及主要组织相容性复合体 II(MHCII)表达、补体和凝血级联以及细胞色素 P450 表达的改变。发情周期中调节的信号通路,涉及配体门控通道、Wnt 和 Hedgehog 信号通路以及在生殖组织中作用尚不清楚的转录因子,包括一些与病理状态有关的基因和基因网络。从发情前期到发情期差异表达的基因所代表的许多分子途径和生物学功能也在人类月经周期中发生改变,尽管不一定在周期的相应阶段。这些发现为在小鼠模型中进一步研究建立了一个基线,以剖析内分泌干扰物对子宫组织的反应和生殖道疾病发展所涉及的机制。