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BDNF signaling in correlation-dependent structural plasticity in the developing visual system

During development, patterned neural activity instructs topographic map refinement. Axons with similar patterns of neural activity converge onto target neurons and stabilize their synapses with these postsynaptic partners, restricting exploratory branch elaboration (Hebbian structural plasticity). O...

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Autores principales: Kutsarova, Elena, Schohl, Anne, Munz, Martin, Wang, Alex, Zhang, Yuan Yuan, Bilash, Olesia M., Ruthazer, Edward S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10101647/
https://www.ncbi.nlm.nih.gov/pubmed/37011100
http://dx.doi.org/10.1371/journal.pbio.3002070
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author Kutsarova, Elena
Schohl, Anne
Munz, Martin
Wang, Alex
Zhang, Yuan Yuan
Bilash, Olesia M.
Ruthazer, Edward S.
author_facet Kutsarova, Elena
Schohl, Anne
Munz, Martin
Wang, Alex
Zhang, Yuan Yuan
Bilash, Olesia M.
Ruthazer, Edward S.
author_sort Kutsarova, Elena
collection PubMed
description During development, patterned neural activity instructs topographic map refinement. Axons with similar patterns of neural activity converge onto target neurons and stabilize their synapses with these postsynaptic partners, restricting exploratory branch elaboration (Hebbian structural plasticity). On the other hand, non-correlated firing in inputs leads to synapse weakening and increased exploratory growth of axons (Stentian structural plasticity). We used visual stimulation to control the correlation structure of neural activity in a few ipsilaterally projecting (ipsi) retinal ganglion cell (RGC) axons with respect to the majority contralateral eye inputs in the optic tectum of albino Xenopus laevis tadpoles. Multiphoton live imaging of ipsi axons, combined with specific targeted disruptions of brain-derived neurotrophic factor (BDNF) signaling, revealed that both presynaptic p75(NTR) and TrkB are required for Stentian axonal branch addition, whereas presumptive postsynaptic BDNF signaling is necessary for Hebbian axon stabilization. Additionally, we found that BDNF signaling mediates local suppression of branch elimination in response to correlated firing of inputs. Daily in vivo imaging of contralateral RGC axons demonstrated that p75(NTR) knockdown reduces axon branch elongation and arbor spanning field volume.
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spelling pubmed-101016472023-04-14 BDNF signaling in correlation-dependent structural plasticity in the developing visual system Kutsarova, Elena Schohl, Anne Munz, Martin Wang, Alex Zhang, Yuan Yuan Bilash, Olesia M. Ruthazer, Edward S. PLoS Biol Research Article During development, patterned neural activity instructs topographic map refinement. Axons with similar patterns of neural activity converge onto target neurons and stabilize their synapses with these postsynaptic partners, restricting exploratory branch elaboration (Hebbian structural plasticity). On the other hand, non-correlated firing in inputs leads to synapse weakening and increased exploratory growth of axons (Stentian structural plasticity). We used visual stimulation to control the correlation structure of neural activity in a few ipsilaterally projecting (ipsi) retinal ganglion cell (RGC) axons with respect to the majority contralateral eye inputs in the optic tectum of albino Xenopus laevis tadpoles. Multiphoton live imaging of ipsi axons, combined with specific targeted disruptions of brain-derived neurotrophic factor (BDNF) signaling, revealed that both presynaptic p75(NTR) and TrkB are required for Stentian axonal branch addition, whereas presumptive postsynaptic BDNF signaling is necessary for Hebbian axon stabilization. Additionally, we found that BDNF signaling mediates local suppression of branch elimination in response to correlated firing of inputs. Daily in vivo imaging of contralateral RGC axons demonstrated that p75(NTR) knockdown reduces axon branch elongation and arbor spanning field volume. Public Library of Science 2023-04-03 /pmc/articles/PMC10101647/ /pubmed/37011100 http://dx.doi.org/10.1371/journal.pbio.3002070 Text en © 2023 Kutsarova et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kutsarova, Elena
Schohl, Anne
Munz, Martin
Wang, Alex
Zhang, Yuan Yuan
Bilash, Olesia M.
Ruthazer, Edward S.
BDNF signaling in correlation-dependent structural plasticity in the developing visual system
title BDNF signaling in correlation-dependent structural plasticity in the developing visual system
title_full BDNF signaling in correlation-dependent structural plasticity in the developing visual system
title_fullStr BDNF signaling in correlation-dependent structural plasticity in the developing visual system
title_full_unstemmed BDNF signaling in correlation-dependent structural plasticity in the developing visual system
title_short BDNF signaling in correlation-dependent structural plasticity in the developing visual system
title_sort bdnf signaling in correlation-dependent structural plasticity in the developing visual system
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10101647/
https://www.ncbi.nlm.nih.gov/pubmed/37011100
http://dx.doi.org/10.1371/journal.pbio.3002070
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