| Literature DB >> 29233477 |
Akina Hoshino1, Rinki Ratnapriya2, Matthew J Brooks2, Vijender Chaitankar2, Matthew S Wilken1, Chi Zhang1, Margaret R Starostik2, Linn Gieser2, Anna La Torre3, Mario Nishio1, Olivia Bates1, Ashley Walton2, Olivia Bermingham-McDonogh1, Ian A Glass4, Rachel O L Wong1, Anand Swaroop5, Thomas A Reh6.
Abstract
Clinical and genetic heterogeneity associated with retinal diseases makes stem-cell-based therapies an attractive strategy for personalized medicine. However, we have limited understanding of the timing of key events in the developing human retina, and in particular the factors critical for generating the unique architecture of the fovea and surrounding macula. Here we define three key epochs in the transcriptome dynamics of human retina from fetal day (D) 52 to 136. Coincident histological analyses confirmed the cellular basis of transcriptional changes and highlighted the dramatic acceleration of development in the fovea compared with peripheral retina. Human and mouse retinal transcriptomes show remarkable similarity in developmental stages, although morphogenesis was greatly expanded in humans. Integration of DNA accessibility data allowed us to reconstruct transcriptional networks controlling photoreceptor differentiation. Our studies provide insights into human retinal development and serve as a resource for molecular staging of human stem-cell-derived retinal organoids.Entities:
Keywords: development; fetal; fovea; gene network; human; macula; organoids; photoreceptor; retina; transcriptome
Mesh:
Substances:
Year: 2017 PMID: 29233477 PMCID: PMC5776731 DOI: 10.1016/j.devcel.2017.10.029
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270