PMID- 10559401 OWN - NLM STAT- MEDLINE DCOM- 19991202 LR - 20220310 IS - 1529-2401 (Electronic) IS - 0270-6474 (Print) IS - 0270-6474 (Linking) VI - 19 IP - 22 DP - 1999 Nov 15 TI - Brain-derived neurotrophic factor differentially regulates retinal ganglion cell dendritic and axonal arborization in vivo. PG - 9928-38 AB - Expression of the neurotrophin brain-derived neurotrophic factor (BDNF) and its receptor trkB in the ganglion cell layer of the Xenopus retina during retinal ganglion cell (RGC) dendritic arborization indicates that BDNF is spatially and temporally available to influence RGC morphological differentiation (; ). BDNF promotes RGC axon arborization in vivo by acting as a target-derived trophic factor (). To determine whether BDNF also acts locally to regulate RGC dendritic development in vivo, we altered retinal neurotrophin levels at the onset of dendritic arborization and assessed the resulting arbor morphologies of RGCs retrogradely labeled with fluorescent dextrans. Injecting neurotrophins or BDNF function-blocking antibodies coupled to microspheres provided local alterations of retinal neurotrophin levels. BDNF significantly decreased RGC dendritic arbor complexity, whereas neutralizing endogenous BDNF levels with function-blocking antibodies significantly increased dendritic arbor complexity. RGCs exposed to other neurotrophins, as well as RGCs in retinae treated with BDNF but in areas not directly exposed to the neurotrophin, developed dendritic arbors that were indistinguishable from controls, indicating that exogenous BDNF acts specifically and locally. In the tectum, where RGC axons arborize, BDNF had opposite effects. BDNF significantly increased RGC axon arbor complexity and anti-BDNF reduced RGC arborization. Thus, BDNF reduces RGC dendritic arborization within the retina and increases axon arborization in the tectum. These results indicate that BDNF can differentially modulate axonal and dendritic arborization within a single neuronal population in opposing manners and raise the possibility that differential modulation by a neurotrophic factor finely tunes the morphological differentiation program of a neuron. FAU - Lom, B AU - Lom B AD - Mental Retardation Research Center, Departments of Psychiatry and Neurobiology, University of California, Los Angeles, Los Angeles, California 90025, USA. FAU - Cohen-Cory, S AU - Cohen-Cory S LA - eng GR - R01 EY011912/EY/NEI NIH HHS/United States PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, P.H.S. PL - United States TA - J Neurosci JT - The Journal of neuroscience : the official journal of the Society for Neuroscience JID - 8102140 RN - 0 (Antibodies) RN - 0 (Brain-Derived Neurotrophic Factor) RN - 0 (Nerve Growth Factors) RN - 0 (Neurotrophin 3) RN - P658DCA9XD (neurotrophin 4) SB - IM MH - Animals MH - Antibodies/pharmacology MH - Axons/drug effects/physiology/*ultrastructure MH - Brain-Derived Neurotrophic Factor/immunology/*pharmacology/physiology MH - Cell Differentiation MH - Dendrites/drug effects/physiology/*ultrastructure MH - Embryo, Nonmammalian/physiology MH - Female MH - Nerve Growth Factors/*pharmacology MH - Neurotrophin 3/pharmacology MH - Retinal Ganglion Cells/drug effects/physiology/*ultrastructure MH - Xenopus laevis/embryology PMC - PMC6782992 EDAT- 1999/11/13 00:00 MHDA- 1999/11/13 00:01 PMCR- 2000/05/15 CRDT- 1999/11/13 00:00 PHST- 1999/11/13 00:00 [pubmed] PHST- 1999/11/13 00:01 [medline] PHST- 1999/11/13 00:00 [entrez] PHST- 2000/05/15 00:00 [pmc-release] AID - 3625 [pii] AID - 10.1523/JNEUROSCI.19-22-09928.1999 [doi] PST - ppublish SO - J Neurosci. 1999 Nov 15;19(22):9928-38. doi: 10.1523/JNEUROSCI.19-22-09928.1999.