Pax6 regulation of Sox9 in the mouse retinal pigmented epithelium controls its timely differentiation and choroid vasculature development.
Yamit Cohen-TayarHadar CohenYulia MitiaginZohar AbravanelCarmit LevyMasha IdelsonBenjamin ReubinoffShalev ItzkovitzShaul RavivKlaus H KaestnerPablo BlinderRan ElkonRuth Ashery-PadanPublished in: Development (Cambridge, England) (2018)
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 Pax6 and Sox9 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).
Keyphrases
- transcription factor
- machine learning
- high resolution
- stem cells
- age related macular degeneration
- high throughput
- gene expression
- embryonic stem cells
- single cell
- endothelial cells
- optical coherence tomography
- induced apoptosis
- type diabetes
- dna damage
- healthcare
- oxidative stress
- high fat diet induced
- dna binding
- artificial intelligence
- social media
- cell proliferation
- endoplasmic reticulum stress
- mass spectrometry
- rna seq
- cell cycle arrest
- big data
- liquid chromatography
- induced pluripotent stem cells
- basal cell carcinoma