| Literature DB >> 30995485 |
Takae Kiyama1, Ye Long1, Ching-Kang Chen2, Christopher M Whitaker1, Allison Shay2, Hongyu Wu1, Tudor C Badea3, Amir Mohsenin4, Jan Parker-Thornburg5, William H Klein6, Stephen L Mills1, Stephen C Massey1, Chai-An Mao7.
Abstract
In the mouse retina, more than 30 retinal ganglion cell (RGC) subtypes have been classified based on a combined metric of morphological and functional characteristics. RGCs arise from a common pool of retinal progenitor cells during embryonic stages and differentiate into mature subtypes in adult retinas. However, the cellular and molecular mechanisms controlling formation and maturation of such remarkable cellular diversity remain unknown. Here, we demonstrate that T-box transcription factor T-brain 1 (Tbr1) is expressed in two groups of morphologically and functionally distinct RGCs: the orientation-selective J-RGCs and a group of OFF-sustained RGCs with symmetrical dendritic arbors. When Tbr1 is genetically ablated during retinal development, these two RGC groups cannot develop. Ectopically expressing Tbr1 in M4 ipRGCs during development alters dendritic branching and density but not the inner plexiform layer stratification level. Our data indicate that Tbr1 plays critical roles in regulating the formation and dendritic morphogenesis of specific RGC types.Entities:
Keywords: J-RGC; Jam2; OFF RGC; OFF-sustained RGC; RGC development; RGC subtype; Tbr1; dendritic branching; dendritic morphogenesis
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Year: 2019 PMID: 30995485 PMCID: PMC6542366 DOI: 10.1016/j.celrep.2019.03.077
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423