Cargando…
An Evolutionarily Conserved Mechanism for Activity-Dependent Visual Circuit Development
Neural circuit development is an activity-dependent process. This activity can be spontaneous, such as the retinal waves that course across the mammalian embryonic retina, or it can be sensory-driven, such as the activation of retinal ganglion cells (RGCs) by visual stimuli. Whichever the source, ne...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073143/ https://www.ncbi.nlm.nih.gov/pubmed/27818623 http://dx.doi.org/10.3389/fncir.2016.00079 |
_version_ | 1782461515258920960 |
---|---|
author | Pratt, Kara G. Hiramoto, Masaki Cline, Hollis T. |
author_facet | Pratt, Kara G. Hiramoto, Masaki Cline, Hollis T. |
author_sort | Pratt, Kara G. |
collection | PubMed |
description | Neural circuit development is an activity-dependent process. This activity can be spontaneous, such as the retinal waves that course across the mammalian embryonic retina, or it can be sensory-driven, such as the activation of retinal ganglion cells (RGCs) by visual stimuli. Whichever the source, neural activity provides essential instruction to the developing circuit. Indeed, experimentally altering activity has been shown to impact circuit development and function in many different ways and in many different model systems. In this review, we contemplate the idea that retinal waves in amniotes, the animals that develop either in ovo or utero (namely reptiles, birds and mammals) could be an evolutionary adaptation to life on land, and that the anamniotes, animals whose development is entirely external (namely the aquatic amphibians and fish), do not display retinal waves, most likely because they simply don’t need them. We then review what is known about the function of both retinal waves and visual stimuli on their respective downstream targets, and predict that the experience-dependent development of the tadpole visual system is a blueprint of what will be found in future studies of the effects of spontaneous retinal waves on instructing development of retinorecipient targets such as the superior colliculus (SC) and the lateral geniculate nucleus. |
format | Online Article Text |
id | pubmed-5073143 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50731432016-11-04 An Evolutionarily Conserved Mechanism for Activity-Dependent Visual Circuit Development Pratt, Kara G. Hiramoto, Masaki Cline, Hollis T. Front Neural Circuits Neuroscience Neural circuit development is an activity-dependent process. This activity can be spontaneous, such as the retinal waves that course across the mammalian embryonic retina, or it can be sensory-driven, such as the activation of retinal ganglion cells (RGCs) by visual stimuli. Whichever the source, neural activity provides essential instruction to the developing circuit. Indeed, experimentally altering activity has been shown to impact circuit development and function in many different ways and in many different model systems. In this review, we contemplate the idea that retinal waves in amniotes, the animals that develop either in ovo or utero (namely reptiles, birds and mammals) could be an evolutionary adaptation to life on land, and that the anamniotes, animals whose development is entirely external (namely the aquatic amphibians and fish), do not display retinal waves, most likely because they simply don’t need them. We then review what is known about the function of both retinal waves and visual stimuli on their respective downstream targets, and predict that the experience-dependent development of the tadpole visual system is a blueprint of what will be found in future studies of the effects of spontaneous retinal waves on instructing development of retinorecipient targets such as the superior colliculus (SC) and the lateral geniculate nucleus. Frontiers Media S.A. 2016-10-21 /pmc/articles/PMC5073143/ /pubmed/27818623 http://dx.doi.org/10.3389/fncir.2016.00079 Text en Copyright © 2016 Pratt, Hiramoto and Cline. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Pratt, Kara G. Hiramoto, Masaki Cline, Hollis T. An Evolutionarily Conserved Mechanism for Activity-Dependent Visual Circuit Development |
title | An Evolutionarily Conserved Mechanism for Activity-Dependent Visual Circuit Development |
title_full | An Evolutionarily Conserved Mechanism for Activity-Dependent Visual Circuit Development |
title_fullStr | An Evolutionarily Conserved Mechanism for Activity-Dependent Visual Circuit Development |
title_full_unstemmed | An Evolutionarily Conserved Mechanism for Activity-Dependent Visual Circuit Development |
title_short | An Evolutionarily Conserved Mechanism for Activity-Dependent Visual Circuit Development |
title_sort | evolutionarily conserved mechanism for activity-dependent visual circuit development |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073143/ https://www.ncbi.nlm.nih.gov/pubmed/27818623 http://dx.doi.org/10.3389/fncir.2016.00079 |
work_keys_str_mv | AT prattkarag anevolutionarilyconservedmechanismforactivitydependentvisualcircuitdevelopment AT hiramotomasaki anevolutionarilyconservedmechanismforactivitydependentvisualcircuitdevelopment AT clinehollist anevolutionarilyconservedmechanismforactivitydependentvisualcircuitdevelopment AT prattkarag evolutionarilyconservedmechanismforactivitydependentvisualcircuitdevelopment AT hiramotomasaki evolutionarilyconservedmechanismforactivitydependentvisualcircuitdevelopment AT clinehollist evolutionarilyconservedmechanismforactivitydependentvisualcircuitdevelopment |