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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...

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Autores principales: Geisler, Stefanie M., Benedetti, Ariane, Schöpf, Clemens L., Schwarzer, Christoph, Stefanova, Nadia, Schwartz, Arnold, Obermair, Gerald J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
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.
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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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