Department of Human Molecular Genetics and Biochemistry, Sackler Faculty of Medicine, Sagol School of Neurosciences, Tel Aviv University, Tel Aviv 69978, Israel.
Department of Particle Physics, Raymond and Beverly Sackler School of Physics and Astronomy, Tel-Aviv University, Tel Aviv 69978, Israel.
Development. 2018 Aug 9;145(15):dev163691. doi: 10.1242/dev.163691.
The synchronized differentiation of neuronal and vascular tissues is crucial for normal organ development and function, although there is limited information about the mechanisms regulating the coordinated development of these tissues. The choroid vasculature of the eye serves as the main blood supply to the metabolically active photoreceptors, and develops together with the retinal pigmented epithelium (RPE). Here, we describe a novel regulatory relationship between the RPE transcription factors Pax6 and Sox9 that controls the timing of RPE differentiation and the adjacent choroid maturation. We used a novel machine learning algorithm tool to analyze high resolution imaging of the choroid in and conditional mutant mice. Additional unbiased transcriptomic analyses in mutant mice and RPE cells generated from human embryonic stem cells, as well as chromatin immunoprecipitation and high-throughput analyses, revealed secreted factors that are regulated by Pax6 and Sox9. These factors might be involved in choroid development and in the pathogenesis of the common blinding disease: age-related macular degeneration (AMD).
神经组织和血管组织的同步分化对于正常器官的发育和功能至关重要,但关于调节这些组织协调发育的机制的信息有限。眼睛的脉络膜血管为代谢活跃的光感受器提供主要的血液供应,并与视网膜色素上皮 (RPE) 一起发育。在这里,我们描述了 RPE 转录因子 Pax6 和 Sox9 之间的一种新的调控关系,它控制着 RPE 分化和相邻脉络膜成熟的时间。我们使用一种新的机器学习算法工具来分析 和 条件性突变小鼠的脉络膜高分辨率成像。在突变小鼠和源自人类胚胎干细胞的 RPE 细胞中的额外无偏转录组学分析,以及染色质免疫沉淀和高通量分析,揭示了受 Pax6 和 Sox9 调控的分泌因子。这些因子可能参与脉络膜发育和常见致盲疾病:年龄相关性黄斑变性 (AMD) 的发病机制。