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Phenotypic Characterization and Brain Structure Analysis of Calcium Channel Subunit α(2)δ-2 Mutant (Ducky) and α(2)δ Double Knockout Mice
Auxiliary α(2)δ subunits of voltage-gated calcium channels modulate channel trafficking, current properties, and synapse formation. Three of the four isoforms (α(2)δ-1, α(2)δ-2, and α(2)δ-3) are abundantly expressed in the brain; however, of the available knockout models, only α(2)δ-2 knockout or mu...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933509/ https://www.ncbi.nlm.nih.gov/pubmed/33679366 http://dx.doi.org/10.3389/fnsyn.2021.634412 |
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author | Geisler, Stefanie M. Benedetti, Ariane Schöpf, Clemens L. Schwarzer, Christoph Stefanova, Nadia Schwartz, Arnold Obermair, Gerald J. |
author_facet | Geisler, Stefanie M. Benedetti, Ariane Schöpf, Clemens L. Schwarzer, Christoph Stefanova, Nadia Schwartz, Arnold Obermair, Gerald J. |
author_sort | Geisler, Stefanie M. |
collection | PubMed |
description | Auxiliary α(2)δ subunits of voltage-gated calcium channels modulate channel trafficking, current properties, and synapse formation. Three of the four isoforms (α(2)δ-1, α(2)δ-2, and α(2)δ-3) are abundantly expressed in the brain; however, of the available knockout models, only α(2)δ-2 knockout or mutant mice display an obvious abnormal neurological phenotype. Thus, we hypothesize that the neuronal α(2)δ isoforms may have partially specific as well as redundant functions. To address this, we generated three distinct α(2)δ double knockout mouse models by crossbreeding single knockout (α(2)δ-1 and -3) or mutant (α(2)δ-2/ducky) mice. Here, we provide a first phenotypic description and brain structure analysis. We found that genotypic distribution of neonatal litters in distinct α(2)δ-1/-2, α(2)δ-1/-3, and α(2)δ-2/-3 breeding combinations did not conform to Mendel’s law, suggesting premature lethality of single and double knockout mice. Notably, high occurrences of infant mortality correlated with the absence of specific α(2)δ isoforms (α(2)Δ-2 > α(2)δ-1 > α(2)δ-3), and was particularly observed in cages with behaviorally abnormal parenting animals of α(2)δ-2/-3 cross-breedings. Juvenile α(2)δ-1/-2 and α(2)δ-2/-3 double knockout mice displayed a waddling gate similar to ducky mice. However, in contrast to ducky and α(2)δ-1/-3 double knockout animals, α(2)δ-1/-2 and α(2)δ-2/-3 double knockout mice showed a more severe disease progression and highly impaired development. The observed phenotypes within the individual mouse lines may be linked to differences in the volume of specific brain regions. Reduced cortical volume in ducky mice, for example, was associated with a progressively decreased space between neurons, suggesting a reduction of total synaptic connections. Taken together, our findings show that α(2)δ subunits differentially regulate premature survival, postnatal growth, brain development, and behavior, suggesting specific neuronal functions in health and disease. |
format | Online Article Text |
id | pubmed-7933509 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79335092021-03-06 Phenotypic Characterization and Brain Structure Analysis of Calcium Channel Subunit α(2)δ-2 Mutant (Ducky) and α(2)δ Double Knockout Mice Geisler, Stefanie M. Benedetti, Ariane Schöpf, Clemens L. Schwarzer, Christoph Stefanova, Nadia Schwartz, Arnold Obermair, Gerald J. Front Synaptic Neurosci Neuroscience Auxiliary α(2)δ subunits of voltage-gated calcium channels modulate channel trafficking, current properties, and synapse formation. Three of the four isoforms (α(2)δ-1, α(2)δ-2, and α(2)δ-3) are abundantly expressed in the brain; however, of the available knockout models, only α(2)δ-2 knockout or mutant mice display an obvious abnormal neurological phenotype. Thus, we hypothesize that the neuronal α(2)δ isoforms may have partially specific as well as redundant functions. To address this, we generated three distinct α(2)δ double knockout mouse models by crossbreeding single knockout (α(2)δ-1 and -3) or mutant (α(2)δ-2/ducky) mice. Here, we provide a first phenotypic description and brain structure analysis. We found that genotypic distribution of neonatal litters in distinct α(2)δ-1/-2, α(2)δ-1/-3, and α(2)δ-2/-3 breeding combinations did not conform to Mendel’s law, suggesting premature lethality of single and double knockout mice. Notably, high occurrences of infant mortality correlated with the absence of specific α(2)δ isoforms (α(2)Δ-2 > α(2)δ-1 > α(2)δ-3), and was particularly observed in cages with behaviorally abnormal parenting animals of α(2)δ-2/-3 cross-breedings. Juvenile α(2)δ-1/-2 and α(2)δ-2/-3 double knockout mice displayed a waddling gate similar to ducky mice. However, in contrast to ducky and α(2)δ-1/-3 double knockout animals, α(2)δ-1/-2 and α(2)δ-2/-3 double knockout mice showed a more severe disease progression and highly impaired development. The observed phenotypes within the individual mouse lines may be linked to differences in the volume of specific brain regions. Reduced cortical volume in ducky mice, for example, was associated with a progressively decreased space between neurons, suggesting a reduction of total synaptic connections. Taken together, our findings show that α(2)δ subunits differentially regulate premature survival, postnatal growth, brain development, and behavior, suggesting specific neuronal functions in health and disease. Frontiers Media S.A. 2021-02-19 /pmc/articles/PMC7933509/ /pubmed/33679366 http://dx.doi.org/10.3389/fnsyn.2021.634412 Text en Copyright © 2021 Geisler, Benedetti, Schöpf, Schwarzer, Stefanova, Schwartz and Obermair. 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 or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) 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 Geisler, Stefanie M. Benedetti, Ariane Schöpf, Clemens L. Schwarzer, Christoph Stefanova, Nadia Schwartz, Arnold Obermair, Gerald J. Phenotypic Characterization and Brain Structure Analysis of Calcium Channel Subunit α(2)δ-2 Mutant (Ducky) and α(2)δ Double Knockout Mice |
title | Phenotypic Characterization and Brain Structure Analysis of Calcium Channel Subunit α(2)δ-2 Mutant (Ducky) and α(2)δ Double Knockout Mice |
title_full | Phenotypic Characterization and Brain Structure Analysis of Calcium Channel Subunit α(2)δ-2 Mutant (Ducky) and α(2)δ Double Knockout Mice |
title_fullStr | Phenotypic Characterization and Brain Structure Analysis of Calcium Channel Subunit α(2)δ-2 Mutant (Ducky) and α(2)δ Double Knockout Mice |
title_full_unstemmed | Phenotypic Characterization and Brain Structure Analysis of Calcium Channel Subunit α(2)δ-2 Mutant (Ducky) and α(2)δ Double Knockout Mice |
title_short | Phenotypic Characterization and Brain Structure Analysis of Calcium Channel Subunit α(2)δ-2 Mutant (Ducky) and α(2)δ Double Knockout Mice |
title_sort | phenotypic characterization and brain structure analysis of calcium channel subunit α(2)δ-2 mutant (ducky) and α(2)δ double knockout mice |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933509/ https://www.ncbi.nlm.nih.gov/pubmed/33679366 http://dx.doi.org/10.3389/fnsyn.2021.634412 |
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