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Fast Retrograde Access to Projection Neuron Circuits Underlying Vocal Learning in Songbirds
Understanding the structure and function of neural circuits underlying speech and language is a vital step toward better treatments for diseases of these systems. Songbirds, among the few animal orders that share with humans the ability to learn vocalizations from a conspecific, have provided many i...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8236207/ https://www.ncbi.nlm.nih.gov/pubmed/33176132 http://dx.doi.org/10.1016/j.celrep.2020.108364 |
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author | Düring, Daniel N. Dittrich, Falk Rocha, Mariana D. Tachibana, Ryosuke O. Mori, Chihiro Okanoya, Kazuo Boehringer, Roman Ehret, Benjamin Grewe, Benjamin F. Gerber, Stefan Ma, Shouwen Rauch, Melanie Paterna, Jean-Charles Kasper, Robert Gahr, Manfred Hahnloser, Richard H.R. |
author_facet | Düring, Daniel N. Dittrich, Falk Rocha, Mariana D. Tachibana, Ryosuke O. Mori, Chihiro Okanoya, Kazuo Boehringer, Roman Ehret, Benjamin Grewe, Benjamin F. Gerber, Stefan Ma, Shouwen Rauch, Melanie Paterna, Jean-Charles Kasper, Robert Gahr, Manfred Hahnloser, Richard H.R. |
author_sort | Düring, Daniel N. |
collection | PubMed |
description | Understanding the structure and function of neural circuits underlying speech and language is a vital step toward better treatments for diseases of these systems. Songbirds, among the few animal orders that share with humans the ability to learn vocalizations from a conspecific, have provided many insights into the neural mechanisms of vocal development. However, research into vocal learning circuits has been hindered by a lack of tools for rapid genetic targeting of specific neuron populations to meet the quick pace of developmental learning. Here, we present a viral tool that enables fast and efficient retrograde access to projection neuron populations. In zebra finches, Bengalese finches, canaries, and mice, we demonstrate fast retrograde labeling of cortical or dopaminergic neurons. We further demonstrate the suitability of our construct for detailed morphological analysis, for in vivo imaging of calcium activity, and for multi-color brainbow labeling. |
format | Online Article Text |
id | pubmed-8236207 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
spelling | pubmed-82362072021-06-27 Fast Retrograde Access to Projection Neuron Circuits Underlying Vocal Learning in Songbirds Düring, Daniel N. Dittrich, Falk Rocha, Mariana D. Tachibana, Ryosuke O. Mori, Chihiro Okanoya, Kazuo Boehringer, Roman Ehret, Benjamin Grewe, Benjamin F. Gerber, Stefan Ma, Shouwen Rauch, Melanie Paterna, Jean-Charles Kasper, Robert Gahr, Manfred Hahnloser, Richard H.R. Cell Rep Article Understanding the structure and function of neural circuits underlying speech and language is a vital step toward better treatments for diseases of these systems. Songbirds, among the few animal orders that share with humans the ability to learn vocalizations from a conspecific, have provided many insights into the neural mechanisms of vocal development. However, research into vocal learning circuits has been hindered by a lack of tools for rapid genetic targeting of specific neuron populations to meet the quick pace of developmental learning. Here, we present a viral tool that enables fast and efficient retrograde access to projection neuron populations. In zebra finches, Bengalese finches, canaries, and mice, we demonstrate fast retrograde labeling of cortical or dopaminergic neurons. We further demonstrate the suitability of our construct for detailed morphological analysis, for in vivo imaging of calcium activity, and for multi-color brainbow labeling. 2020-11-10 /pmc/articles/PMC8236207/ /pubmed/33176132 http://dx.doi.org/10.1016/j.celrep.2020.108364 Text en https://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/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Article Düring, Daniel N. Dittrich, Falk Rocha, Mariana D. Tachibana, Ryosuke O. Mori, Chihiro Okanoya, Kazuo Boehringer, Roman Ehret, Benjamin Grewe, Benjamin F. Gerber, Stefan Ma, Shouwen Rauch, Melanie Paterna, Jean-Charles Kasper, Robert Gahr, Manfred Hahnloser, Richard H.R. Fast Retrograde Access to Projection Neuron Circuits Underlying Vocal Learning in Songbirds |
title | Fast Retrograde Access to Projection Neuron Circuits Underlying Vocal Learning in Songbirds |
title_full | Fast Retrograde Access to Projection Neuron Circuits Underlying Vocal Learning in Songbirds |
title_fullStr | Fast Retrograde Access to Projection Neuron Circuits Underlying Vocal Learning in Songbirds |
title_full_unstemmed | Fast Retrograde Access to Projection Neuron Circuits Underlying Vocal Learning in Songbirds |
title_short | Fast Retrograde Access to Projection Neuron Circuits Underlying Vocal Learning in Songbirds |
title_sort | fast retrograde access to projection neuron circuits underlying vocal learning in songbirds |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8236207/ https://www.ncbi.nlm.nih.gov/pubmed/33176132 http://dx.doi.org/10.1016/j.celrep.2020.108364 |
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