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Functional Interactions between Newborn and Mature Neurons Leading to Integration into Established Neuronal Circuits
From development up to adulthood, the vertebrate brain is continuously supplied with newborn neurons that integrate into established mature circuits. However, how this process is coordinated during development remains unclear. Using two-photon imaging, GCaMP5 transgenic zebrafish larvae, and sparse...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5483231/ https://www.ncbi.nlm.nih.gov/pubmed/28578928 http://dx.doi.org/10.1016/j.cub.2017.05.029 |
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author | Boulanger-Weill, Jonathan Candat, Virginie Jouary, Adrien Romano, Sebastián A. Pérez-Schuster, Verónica Sumbre, Germán |
author_facet | Boulanger-Weill, Jonathan Candat, Virginie Jouary, Adrien Romano, Sebastián A. Pérez-Schuster, Verónica Sumbre, Germán |
author_sort | Boulanger-Weill, Jonathan |
collection | PubMed |
description | From development up to adulthood, the vertebrate brain is continuously supplied with newborn neurons that integrate into established mature circuits. However, how this process is coordinated during development remains unclear. Using two-photon imaging, GCaMP5 transgenic zebrafish larvae, and sparse electroporation in the larva’s optic tectum, we monitored spontaneous and induced activity of large neuronal populations containing newborn and functionally mature neurons. We observed that the maturation of newborn neurons is a 4-day process. Initially, newborn neurons showed undeveloped dendritic arbors, no neurotransmitter identity, and were unresponsive to visual stimulation, although they displayed spontaneous calcium transients. Later on, newborn-labeled neurons began to respond to visual stimuli but in a very variable manner. At the end of the maturation period, newborn-labeled neurons exhibited visual tuning curves (spatial receptive fields and direction selectivity) and spontaneous correlated activity with neighboring functionally mature neurons. At this developmental stage, newborn-labeled neurons presented complex dendritic arbors and neurotransmitter identity (excitatory or inhibitory). Removal of retinal inputs significantly perturbed the integration of newborn neurons into the functionally mature tectal network. Our results provide a comprehensive description of the maturation of newborn neurons during development and shed light on potential mechanisms underlying their integration into a functionally mature neuronal circuit. |
format | Online Article Text |
id | pubmed-5483231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54832312017-06-29 Functional Interactions between Newborn and Mature Neurons Leading to Integration into Established Neuronal Circuits Boulanger-Weill, Jonathan Candat, Virginie Jouary, Adrien Romano, Sebastián A. Pérez-Schuster, Verónica Sumbre, Germán Curr Biol Article From development up to adulthood, the vertebrate brain is continuously supplied with newborn neurons that integrate into established mature circuits. However, how this process is coordinated during development remains unclear. Using two-photon imaging, GCaMP5 transgenic zebrafish larvae, and sparse electroporation in the larva’s optic tectum, we monitored spontaneous and induced activity of large neuronal populations containing newborn and functionally mature neurons. We observed that the maturation of newborn neurons is a 4-day process. Initially, newborn neurons showed undeveloped dendritic arbors, no neurotransmitter identity, and were unresponsive to visual stimulation, although they displayed spontaneous calcium transients. Later on, newborn-labeled neurons began to respond to visual stimuli but in a very variable manner. At the end of the maturation period, newborn-labeled neurons exhibited visual tuning curves (spatial receptive fields and direction selectivity) and spontaneous correlated activity with neighboring functionally mature neurons. At this developmental stage, newborn-labeled neurons presented complex dendritic arbors and neurotransmitter identity (excitatory or inhibitory). Removal of retinal inputs significantly perturbed the integration of newborn neurons into the functionally mature tectal network. Our results provide a comprehensive description of the maturation of newborn neurons during development and shed light on potential mechanisms underlying their integration into a functionally mature neuronal circuit. Cell Press 2017-06-19 /pmc/articles/PMC5483231/ /pubmed/28578928 http://dx.doi.org/10.1016/j.cub.2017.05.029 Text en © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Boulanger-Weill, Jonathan Candat, Virginie Jouary, Adrien Romano, Sebastián A. Pérez-Schuster, Verónica Sumbre, Germán Functional Interactions between Newborn and Mature Neurons Leading to Integration into Established Neuronal Circuits |
title | Functional Interactions between Newborn and Mature Neurons Leading to Integration into Established Neuronal Circuits |
title_full | Functional Interactions between Newborn and Mature Neurons Leading to Integration into Established Neuronal Circuits |
title_fullStr | Functional Interactions between Newborn and Mature Neurons Leading to Integration into Established Neuronal Circuits |
title_full_unstemmed | Functional Interactions between Newborn and Mature Neurons Leading to Integration into Established Neuronal Circuits |
title_short | Functional Interactions between Newborn and Mature Neurons Leading to Integration into Established Neuronal Circuits |
title_sort | functional interactions between newborn and mature neurons leading to integration into established neuronal circuits |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5483231/ https://www.ncbi.nlm.nih.gov/pubmed/28578928 http://dx.doi.org/10.1016/j.cub.2017.05.029 |
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