Mujahid Sana, Logvinenko Tanya, Volpe Maryann V, Nielsen Heber C
Program in Cell, Molecular and Developmental Biology, Sackler School of Graduate Biomedical Sciences, Tufts University School of Medicine, Boston, MA, USA.
BMC Dev Biol. 2013 Apr 24;13:13. doi: 10.1186/1471-213X-13-13.
MicroRNAs play important roles in regulating biological processes, including organ morphogenesis and maturation. However, little is known about specific pathways regulated by miRNA during lung development. Between the canalicular and saccular stages of the developing lung several important cellular events occur, including the onset of surfactant synthesis, microvascular remodeling and structural preparation for subsequent alveolarization. The miRNAs that are actively regulated, and the identity of their targets during this important developmental interval in the lung remain elusive.
Using TLDA low density real-time PCR arrays, the expression of 376 miRNAs in male and female fetal mouse lungs of gestational days E15 - E18 were profiled. Statistical analyses identified 25 and 37 miRNAs that changed significantly between sexes and with gestation, respectively. In silico analysis using Ingenuity Pathway Analysis (IPA) identified specific pathways and networks known to be targets of these miRNAs which are important to lung development. Pathways that are targeted by sex regulated miRNAs include retinoin, IGFR1, Tp53 and Akt. Pathways targeted by gestation-regulated miRNAs include VEGFA and mediators of glucose metabolism.
MiRNAs are differentially regulated across time and between sexes during the canalicular and saccular stages of lung development. Sex-associated differential miRNA expression may regulate the differences in structural and functional male and female lung development, as shown by networks generated using in silico analysis. These data provide a valuable resource to further enhance the understanding of miRNA control of lung development and maturation.
微小RNA在调节包括器官形态发生和成熟在内的生物学过程中发挥着重要作用。然而,关于微小RNA在肺发育过程中调控的特定途径却知之甚少。在发育中的肺的小管期和囊泡期之间会发生几个重要的细胞事件,包括表面活性剂合成的开始、微血管重塑以及为随后的肺泡化进行的结构准备。在肺这个重要的发育间隔期内,被积极调控的微小RNA及其靶标的身份仍然难以捉摸。
使用TLDA低密度实时PCR阵列,对妊娠第E15 - E18天的雄性和雌性胎鼠肺中376种微小RNA的表达进行了分析。统计分析分别确定了25种和37种在性别之间以及随妊娠发生显著变化的微小RNA。使用 Ingenuity Pathway Analysis(IPA)进行的计算机分析确定了已知是这些微小RNA靶标的特定途径和网络,这些途径和网络对肺发育很重要。受性别调控的微小RNA靶向的途径包括视黄酸、IGFR1、Tp53和Akt。受妊娠调控的微小RNA靶向的途径包括VEGFA和葡萄糖代谢的介质。
在肺发育的小管期和囊泡期,微小RNA在不同时间和性别之间存在差异调控。如通过计算机分析生成的网络所示,与性别相关的微小RNA差异表达可能调节雄性和雌性肺在结构和功能发育上存在的差异。这些数据为进一步加深对微小RNA控制肺发育和成熟的理解提供了宝贵资源。