<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fligor CM</submitter><funding>National Center for Advancing Translational Sciences</funding><funding>NEI NIH HHS</funding><funding>NCATS NIH HHS</funding><funding>National Eye Institute</funding><funding>BrightFocus Foundation</funding><funding>Indiana State Department of Health</funding><pagination>2228-2241</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8452489</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(9)</volume><pubmed_abstract>The development of the visual system involves the coordination of spatial and temporal events to specify the organization of varied cell types, including the elongation of axons from retinal ganglion cells (RGCs) to post-synaptic targets in the brain. Retinal organoids recapitulate many features of retinal development, yet have lacked downstream targets into which RGC axons extend, limiting the ability to model projections of the human visual system. To address these issues, retinal organoids were generated and organized into an in vitro assembloid model of the visual system with cortical and thalamic organoids. RGCs responded to environmental cues and extended axons deep into assembloids, modeling the projections of the visual system. In addition, RGC survival was enhanced in long-term as</pubmed_abstract><journal>Stem cell reports</journal><pubmed_title>Extension of retinofugal projections in an assembled model of human pluripotent stem cell-derived organoids.</pubmed_title><pmcid>PMC8452489</pmcid><funding_grant_id>R01 EY024984</funding_grant_id><funding_grant_id>R21 EY031120</funding_grant_id><funding_grant_id>UL1 TR002529</funding_grant_id><pubmed_authors>Fligor CM</pubmed_authors><pubmed_authors>Lavekar SS</pubmed_authors><pubmed_authors>Gomes C</pubmed_authors><pubmed_authors>Meyer JS</pubmed_authors><pubmed_authors>VanderWall KB</pubmed_authors><pubmed_authors>Huang KC</pubmed_authors><pubmed_authors>Harkin J</pubmed_authors><pubmed_authors>Shields PK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Extension of retinofugal projections in an assembled model of human pluripotent stem cell-derived organoids.</name><description>The development of the visual system involves the coordination of spatial and temporal events to specify the organization of varied cell types, including the elongation of axons from retinal ganglion cells (RGCs) to post-synaptic targets in the brain. Retinal organoids recapitulate many features of retinal development, yet have lacked downstream targets into which RGC axons extend, limiting the ability to model projections of the human visual system. To address these issues, retinal organoids were generated and organized into an in vitro assembloid model of the visual system with cortical and thalamic organoids. RGCs responded to environmental cues and extended axons deep into assembloids, modeling the projections of the visual system. In addition, RGC survival was enhanced in long-term as</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Sep</publication><modification>2025-04-18T14:25:14.39Z</modification><creation>2025-04-07T00:33:06.697Z</creation></dates><accession>S-EPMC8452489</accession><cross_references><pubmed>34115986</pubmed><doi>10.1016/j.stemcr.2021.05.009</doi></cross_references></HashMap>