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Benzyl butyl phthalate decreases myogenic differentiation of endometrial mesenchymal stem/stromal cells through miR-137-mediated regulation of PITX2

机译:邻苯二甲酸苄基丁酯通过miR-137介导的PITX2调节减少子宫内膜间充质干/基质细胞的成肌分化

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摘要

Phthalate, an environmental toxin, has been considered as an endocrine-disrupting chemical. Growing evidence has demonstrated links between endocrine-disrupting chemicals, tissue development, and reproductive physiology, but the mechanisms of gene expression regulation by environmental factors that affect cell differentiation are unclear. Herein, we investigated the effects of butyl benzyl phthalate (BBP) on human endometrial mesenchymal stem/stromal cell (EN-MSC) differentiation and identified a novel signaling pathway. Differentiation of endometrial mesenchymal stem/stromal cells decreased after administration of BBP. We analyzed BBP regulation of gene expression in EN-MSC using cDNA microarrays and Ingenuity Pathway Analysis software to identify affected target genes and their biological functions. PITX2 emerged as a common gene hit from separate screens targeting skeletal and muscular disorders, cell morphology, and tissue development. BBP decreased transcription of PITX2 and elevated expression of the microRNA miR-137, the predicted upstream negative regulator of PITX2. These data indicated that BBP affects PITX2 expression through miR-137 targeting of the 3′ untranslated region of PITX2 mRNA. PITX2 down-regulation also decreased MyoD transcript levels in EN-MSC. Our results demonstrate that BBP decreases EN-MSC myogenic differentiation through up-regulation of miR-137, contribute to our understanding of EN-MSC differentiation, and underline the hazardous potential of environmental hormones.
机译:邻苯二甲酸盐是一种环境毒素,被认为是破坏内分泌的化学物质。越来越多的证据表明破坏内分泌的化学物质,组织发育和生殖生理之间存在联系,但是目前尚不清楚环境因素影响细胞分化的基因表达调控机制。在本文中,我们研究了邻苯二甲酸丁苄酯(BBP)对人子宫内膜间充质干/基质细胞(EN-MSC)分化的影响,并确定了一条新的信号通路。给予BBP后,子宫内膜间充质干/基质细胞的分化降低。我们使用cDNA微阵列和Ingenuity Pathway分析软件分析了EN-MSC中BBP对基因表达的调控,以鉴定受影响的靶基因及其生物学功能。 PITX2作为常见基因出现在针对骨骼和肌肉疾病,细胞形态和组织发育的单独筛选中。 BBP降低了PITX2的转录并提高了microRNA miR-137(PITX2的预期上游负调控子)的表达。这些数据表明BBP通过miR-137靶向PITX2 mRNA的3'非翻译区影响PITX2表达。 PITX2下调也降低了EN-MSC中的MyoD转录水平。我们的结果表明,BBP通过上调miR-137减少EN-MSC的肌源性分化,有助于我们对EN-MSC的理解,并强调环境激素的潜在危险。

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