PMID- 19350645 OWN - NLM STAT- MEDLINE DCOM- 20090529 LR - 20211020 IS - 1096-9861 (Electronic) IS - 0021-9967 (Print) IS - 0021-9967 (Linking) VI - 514 IP - 5 DP - 2009 Jun 10 TI - Regulation of neonatal development of retinal ganglion cell dendrites by neurotrophin-3 overexpression. PG - 449-58 LID - 10.1002/cne.22016 [doi] AB - The morphology of dendrites constrains and reflects the nature of synaptic inputs to neurons. The visual system has served as a useful model to show how visual function is determined by the arborization patterns of neuronal processes. In retina, light ON and light OFF responding ganglion cells selectively elaborate their dendritic arbors in distinct sublamina, where they receive, respectively, inputs from ON and OFF bipolar cells. During neonatal maturation, the bilaminarly distributed dendritic arbors of ON-OFF retinal ganglion cells (RGCs) are refined to more narrowly localized monolaminar structures characteristic of ON or OFF RGCs. Recently, brain-derived neurotrophic factor (BDNF) has been shown to regulate this laminar refinement, and to enhance the development of dendritic branches selectively of ON RGCs. Although other related neurotrophins are known to regulate neuronal process formation in the central nervous system, little is known about their action in maturing retina. Here, we report that overexpression of neurotrophin-3 (NT-3) in the eye accelerates RGC laminar refinement before eye opening. Furthermore, NT-3 overexpression increases dendritic branch number but reduces dendritic elongation preferentially in ON-OFF RGCs, a process that also occurs before eye opening. NT-3 overexpression does affect dendritic maturation in ON RGCs, but to a much less degree. Taken together, our results suggest that NT-3 and BDNF exhibit overlapping effects in laminar refinement but distinct RGC-cell-type specific effects in shaping dendritic arborization during postnatal development. FAU - Liu, Xiaorong AU - Liu X AD - Department of Neurobiology and Physiology, Northwestern University, Evanston, Illinois 60208, USA. cope@phy.ucsf.edu FAU - Robinson, Michael L AU - Robinson ML FAU - Schreiber, Ann Marie AU - Schreiber AM FAU - Wu, Vincent AU - Wu V FAU - Lavail, Matthew M AU - Lavail MM FAU - Cang, Jianhua AU - Cang J FAU - Copenhagen, David R AU - Copenhagen DR LA - eng GR - R01 EY018621/EY/NEI NIH HHS/United States GR - R01 EY012995/EY/NEI NIH HHS/United States GR - R01 EY001919-32/EY/NEI NIH HHS/United States GR - R01 EY019034-01/EY/NEI NIH HHS/United States GR - R01 EY019034/EY/NEI NIH HHS/United States GR - R01EY012995/EY/NEI NIH HHS/United States GR - R01 EY001919/EY/NEI NIH HHS/United States GR - R01EY018621/EY/NEI NIH HHS/United States GR - R01EY019034/EY/NEI NIH HHS/United States GR - P30 EY002162-32/EY/NEI NIH HHS/United States GR - R01 EY001869/EY/NEI NIH HHS/United States GR - R01EY001869/EY/NEI NIH HHS/United States GR - P30 EY002162/EY/NEI NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Research Support, Non-U.S. Gov't PL - United States TA - J Comp Neurol JT - The Journal of comparative neurology JID - 0406041 RN - 0 (Brain-Derived Neurotrophic Factor) RN - 0 (Neurotrophin 3) SB - IM MH - Analysis of Variance MH - Animals MH - Blotting, Western MH - Brain-Derived Neurotrophic Factor/metabolism MH - Dendrites/*physiology/ultrastructure MH - Eye/cytology/*growth & development/metabolism MH - Immunohistochemistry MH - Mice MH - Mice, Transgenic MH - Microscopy, Confocal MH - Neurotrophin 3/genetics/*metabolism MH - Rats MH - Retinal Ganglion Cells/cytology/*physiology PMC - PMC2691146 MID - NIHMS114256 EDAT- 2009/04/08 09:00 MHDA- 2009/05/30 09:00 PMCR- 2010/06/10 CRDT- 2009/04/08 09:00 PHST- 2009/04/08 09:00 [entrez] PHST- 2009/04/08 09:00 [pubmed] PHST- 2009/05/30 09:00 [medline] PHST- 2010/06/10 00:00 [pmc-release] AID - 10.1002/cne.22016 [doi] PST - ppublish SO - J Comp Neurol. 2009 Jun 10;514(5):449-58. doi: 10.1002/cne.22016.