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Altered brain-wide auditory networks in a zebrafish model of fragile X syndrome

BACKGROUND: Loss or disrupted expression of the FMR1 gene causes fragile X syndrome (FXS), the most common monogenetic form of autism in humans. Although disruptions in sensory processing are core traits of FXS and autism, the neural underpinnings of these phenotypes are poorly understood. Using cal...

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Autores principales: Constantin, Lena, Poulsen, Rebecca E., Scholz, Leandro A., Favre-Bulle, Itia A., Taylor, Michael A., Sun, Biao, Goodhill, Geoffrey J., Vanwalleghem, Gilles C., Scott, Ethan K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7493858/
https://www.ncbi.nlm.nih.gov/pubmed/32938458
http://dx.doi.org/10.1186/s12915-020-00857-6
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author Constantin, Lena
Poulsen, Rebecca E.
Scholz, Leandro A.
Favre-Bulle, Itia A.
Taylor, Michael A.
Sun, Biao
Goodhill, Geoffrey J.
Vanwalleghem, Gilles C.
Scott, Ethan K.
author_facet Constantin, Lena
Poulsen, Rebecca E.
Scholz, Leandro A.
Favre-Bulle, Itia A.
Taylor, Michael A.
Sun, Biao
Goodhill, Geoffrey J.
Vanwalleghem, Gilles C.
Scott, Ethan K.
author_sort Constantin, Lena
collection PubMed
description BACKGROUND: Loss or disrupted expression of the FMR1 gene causes fragile X syndrome (FXS), the most common monogenetic form of autism in humans. Although disruptions in sensory processing are core traits of FXS and autism, the neural underpinnings of these phenotypes are poorly understood. Using calcium imaging to record from the entire brain at cellular resolution, we investigated neuronal responses to visual and auditory stimuli in larval zebrafish, using fmr1 mutants to model FXS. The purpose of this study was to model the alterations of sensory networks, brain-wide and at cellular resolution, that underlie the sensory aspects of FXS and autism. RESULTS: Combining functional analyses with the neurons’ anatomical positions, we found that fmr1(−/−) animals have normal responses to visual motion. However, there were several alterations in the auditory processing of fmr1(−/−) animals. Auditory responses were more plentiful in hindbrain structures and in the thalamus. The thalamus, torus semicircularis, and tegmentum had clusters of neurons that responded more strongly to auditory stimuli in fmr1(−/−) animals. Functional connectivity networks showed more inter-regional connectivity at lower sound intensities (a − 3 to − 6 dB shift) in fmr1(−/−) larvae compared to wild type. Finally, the decoding capacities of specific components of the ascending auditory pathway were altered: the octavolateralis nucleus within the hindbrain had significantly stronger decoding of auditory amplitude while the telencephalon had weaker decoding in fmr1(−/−) mutants. CONCLUSIONS: We demonstrated that fmr1(−/−) larvae are hypersensitive to sound, with a 3–6 dB shift in sensitivity, and identified four sub-cortical brain regions with more plentiful responses and/or greater response strengths to auditory stimuli. We also constructed an experimentally supported model of how auditory information may be processed brain-wide in fmr1(−/−) larvae. Our model suggests that the early ascending auditory pathway transmits more auditory information, with less filtering and modulation, in this model of FXS.
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spelling pubmed-74938582020-09-23 Altered brain-wide auditory networks in a zebrafish model of fragile X syndrome Constantin, Lena Poulsen, Rebecca E. Scholz, Leandro A. Favre-Bulle, Itia A. Taylor, Michael A. Sun, Biao Goodhill, Geoffrey J. Vanwalleghem, Gilles C. Scott, Ethan K. BMC Biol Research Article BACKGROUND: Loss or disrupted expression of the FMR1 gene causes fragile X syndrome (FXS), the most common monogenetic form of autism in humans. Although disruptions in sensory processing are core traits of FXS and autism, the neural underpinnings of these phenotypes are poorly understood. Using calcium imaging to record from the entire brain at cellular resolution, we investigated neuronal responses to visual and auditory stimuli in larval zebrafish, using fmr1 mutants to model FXS. The purpose of this study was to model the alterations of sensory networks, brain-wide and at cellular resolution, that underlie the sensory aspects of FXS and autism. RESULTS: Combining functional analyses with the neurons’ anatomical positions, we found that fmr1(−/−) animals have normal responses to visual motion. However, there were several alterations in the auditory processing of fmr1(−/−) animals. Auditory responses were more plentiful in hindbrain structures and in the thalamus. The thalamus, torus semicircularis, and tegmentum had clusters of neurons that responded more strongly to auditory stimuli in fmr1(−/−) animals. Functional connectivity networks showed more inter-regional connectivity at lower sound intensities (a − 3 to − 6 dB shift) in fmr1(−/−) larvae compared to wild type. Finally, the decoding capacities of specific components of the ascending auditory pathway were altered: the octavolateralis nucleus within the hindbrain had significantly stronger decoding of auditory amplitude while the telencephalon had weaker decoding in fmr1(−/−) mutants. CONCLUSIONS: We demonstrated that fmr1(−/−) larvae are hypersensitive to sound, with a 3–6 dB shift in sensitivity, and identified four sub-cortical brain regions with more plentiful responses and/or greater response strengths to auditory stimuli. We also constructed an experimentally supported model of how auditory information may be processed brain-wide in fmr1(−/−) larvae. Our model suggests that the early ascending auditory pathway transmits more auditory information, with less filtering and modulation, in this model of FXS. BioMed Central 2020-09-16 /pmc/articles/PMC7493858/ /pubmed/32938458 http://dx.doi.org/10.1186/s12915-020-00857-6 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Constantin, Lena
Poulsen, Rebecca E.
Scholz, Leandro A.
Favre-Bulle, Itia A.
Taylor, Michael A.
Sun, Biao
Goodhill, Geoffrey J.
Vanwalleghem, Gilles C.
Scott, Ethan K.
Altered brain-wide auditory networks in a zebrafish model of fragile X syndrome
title Altered brain-wide auditory networks in a zebrafish model of fragile X syndrome
title_full Altered brain-wide auditory networks in a zebrafish model of fragile X syndrome
title_fullStr Altered brain-wide auditory networks in a zebrafish model of fragile X syndrome
title_full_unstemmed Altered brain-wide auditory networks in a zebrafish model of fragile X syndrome
title_short Altered brain-wide auditory networks in a zebrafish model of fragile X syndrome
title_sort altered brain-wide auditory networks in a zebrafish model of fragile x syndrome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7493858/
https://www.ncbi.nlm.nih.gov/pubmed/32938458
http://dx.doi.org/10.1186/s12915-020-00857-6
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