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Gene expression profile of androgen modulated genes in the murine fetal developing lung

机译:雄性胎调节肺中雄激素调节基因的基因表达谱

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Background Accumulating evidences suggest that sex affects lung development. Indeed, a higher incidence of respiratory distress syndrome is observed in male compared to female preterm neonates at comparable developmental stage and experimental studies demonstrated an androgen-related delay in male lung maturation. However, the precise mechanisms underlying these deleterious effects of androgens in lung maturation are only partially understood. Methods To build up a better understanding of the effect of androgens on lung development, we analyzed by microarrays the expression of genes showing a sexual difference and those modulated by androgens. Lungs of murine fetuses resulting from a timely mating window of 1 hour were studied at gestational day 17 (GD17) and GD18, corresponding to the period of surge of surfactant production. Using injections of the antiandrogen flutamide to pregnant mice, we hunted for genes in fetal lungs which are transcriptionally modulated by androgens. Results Results revealed that 1844 genes were expressed with a sexual difference at GD17 and 833 at GD18. Many genes were significantly modulated by flutamide: 1597 at GD17 and 1775 at GD18. Datasets were analyzed by using in silico tools for reconstruction of cellular pathways. Between GD17 and GD18, male lungs showed an intensive transcriptional activity of proliferative pathways along with the onset of lung differentiation. Among the genes showing a sex difference or an antiandrogen modulation of their expression, we specifically identified androgen receptor interacting genes, surfactant related genes in particularly those involved in the pathway leading to phospholipid synthesis, and several genes of lung development regulator pathways. Among these latter, some genes related to Shh, FGF, TGF-beta, BMP, and Wnt signaling are modulated by sex and/or antiandrogen treatment. Conclusion Our results show clearly that there is a real delay in lung maturation between male and female in this period, the latter pursuing already lung maturation while the proper is not yet fully engaged in the differentiation processes at GD17. In addition, this study provides a list of genes which are under the control of androgens within the lung at the moment of surge of surfactant production in murine fetal lung.
机译:背景越来越多的证据表明,性会影响肺部发育。确实,在相当的发育阶段,与女性早产儿相比,男性呼吸窘迫综合征的发病率更高,实验研究表明,雄激素相关的延迟男性肺成熟。但是,仅部分了解雄激素在肺成熟中具有这些有害作用的确切机制。方法为了更好地了解雄激素对肺部发育的影响,我们通过微阵列分析了具有性别差异的基因和受雄激素调节的基因的表达。在第17天(GD17)和GD18对应于表面活性剂生产激增的时期,研究了因及时交配1小时而导致的鼠胎儿肺。通过向怀孕小鼠注射抗雄激素氟他胺,我们在胎儿肺中寻找受雄激素转录调节的基因。结果结果显示,在GD17处表达了1844个基因,在GD18处表达了性别差异,在833处表达了性别差异。氟他胺可显着调节许多基因:在GD17中为1597,在GD18中为1775。通过使用计算机工具重建细胞途径来分析数据集。在GD17和GD18之间,雄性肺显示出增殖途径的强烈转录活性以及肺分化的开始。在表现出性别差异或抗雄激素调节其表达的基因中,我们专门鉴定了雄激素受体相互作用基因,与表面活性剂相关的基因,尤其是那些参与导致磷脂合成的途径中涉及的基因,以及肺发育调节剂途径的几个基因。在这些后者中,与Shh,FGF,TGF-β,BMP和Wnt信号转导相关的一些基因是通过性别和/或抗雄激素治疗来调节的。结论我们的结果清楚地表明,在此期间,男性和女性之间的肺成熟确实存在延迟,后者已经在进行肺成熟,而GD17的正常分化尚未完全参与。另外,这项研究提供了在鼠胎肺表面活性剂产生激增时处于肺内雄激素控制下的基因清单。

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