Department of Cell and Developmental Biology, Vanderbilt University Medical Center, Vanderbilt University, 1125 Light Hall/MRB IV Bldg., 2215 B Garland Ave., Nashville, TN 37232.
Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, 46202.
Semin Perinatol. 2018 Jun;42(4):212-220. doi: 10.1053/j.semperi.2018.05.003. Epub 2018 May 10.
DA closure is crucial for the transition from fetal to neonatal life. This closure is supported by changes to the DA's signaling and structural properties that distinguish it from neighboring vessels. Examining transcriptional differences between these vessels is key to identifying genes or pathways responsible for DA closure. Several microarray studies have explored the DA transcriptome in animal models but varied experimental designs have led to conflicting results. Thorough transcriptomic analysis of the human DA has yet to be performed. A clear picture of the DA transcriptome is key to guiding future research endeavors, both to allow more targeted treatments in the clinical setting, and to understand the basic biology of DA function. In this review, we use a cross-species cross-platform analysis to consider all available published rodent microarray data and novel human RNAseq data in order to provide high priority candidate genes for consideration in future DA studies.
动静脉(DA)的关闭对于胎儿到新生儿生命的过渡至关重要。这种关闭得到了 DA 信号和结构特性变化的支持,这些变化使其与邻近的血管区分开来。检查这些血管之间的转录差异是确定负责 DA 关闭的基因或途径的关键。几项微阵列研究已经在动物模型中探索了 DA 的转录组,但不同的实验设计导致了相互矛盾的结果。对人类 DA 的全面转录组分析尚未进行。DA 转录组的清晰图像是指导未来研究工作的关键,不仅可以在临床环境中提供更有针对性的治疗方法,还可以帮助理解 DA 功能的基本生物学。在这篇综述中,我们使用跨物种跨平台分析来考虑所有可用的发表的啮齿动物微阵列数据和新的人类 RNAseq 数据,以便为未来的 DA 研究提供高优先级候选基因。