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Different functions of two putative Drosophila α(2)δ subunits in the same identified motoneurons
Voltage gated calcium channels (VGCCs) regulate neuronal excitability and translate activity into calcium dependent signaling. The α(1) subunit of high voltage activated (HVA) VGCCs associates with α(2)δ accessory subunits, which may affect calcium channel biophysical properties, cell surface expres...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426832/ https://www.ncbi.nlm.nih.gov/pubmed/32792569 http://dx.doi.org/10.1038/s41598-020-69748-8 |
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author | Heinrich, Laurin Ryglewski, Stefanie |
author_facet | Heinrich, Laurin Ryglewski, Stefanie |
author_sort | Heinrich, Laurin |
collection | PubMed |
description | Voltage gated calcium channels (VGCCs) regulate neuronal excitability and translate activity into calcium dependent signaling. The α(1) subunit of high voltage activated (HVA) VGCCs associates with α(2)δ accessory subunits, which may affect calcium channel biophysical properties, cell surface expression, localization and transport and are thus important players in calcium-dependent signaling. In vertebrates, the functions of the different combinations of the four α(2)δ and the seven HVA α(1) subunits are incompletely understood, in particular with respect to partially redundant or separate functions in neurons. This study capitalizes on the relatively simpler situation in the Drosophila genetic model containing two neuronal putative α(2)δ subunits, straightjacket and CG4587, and one Ca(v)1 and Ca(v)2 homolog each, both with well-described functions in different compartments of identified motoneurons. Straightjacket is required for normal Ca(v)1 and Ca(v)2 current amplitudes and correct Ca(v)2 channel function in all neuronal compartments. By contrast, CG4587 does not affect Ca(v)1 or Ca(v)2 current amplitudes or presynaptic function, but is required for correct Ca(v)2 channel allocation to the axonal versus the dendritic domain. We suggest that the two different putative α(2)δ subunits are required in the same neurons to regulate different functions of VGCCs. |
format | Online Article Text |
id | pubmed-7426832 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74268322020-08-14 Different functions of two putative Drosophila α(2)δ subunits in the same identified motoneurons Heinrich, Laurin Ryglewski, Stefanie Sci Rep Article Voltage gated calcium channels (VGCCs) regulate neuronal excitability and translate activity into calcium dependent signaling. The α(1) subunit of high voltage activated (HVA) VGCCs associates with α(2)δ accessory subunits, which may affect calcium channel biophysical properties, cell surface expression, localization and transport and are thus important players in calcium-dependent signaling. In vertebrates, the functions of the different combinations of the four α(2)δ and the seven HVA α(1) subunits are incompletely understood, in particular with respect to partially redundant or separate functions in neurons. This study capitalizes on the relatively simpler situation in the Drosophila genetic model containing two neuronal putative α(2)δ subunits, straightjacket and CG4587, and one Ca(v)1 and Ca(v)2 homolog each, both with well-described functions in different compartments of identified motoneurons. Straightjacket is required for normal Ca(v)1 and Ca(v)2 current amplitudes and correct Ca(v)2 channel function in all neuronal compartments. By contrast, CG4587 does not affect Ca(v)1 or Ca(v)2 current amplitudes or presynaptic function, but is required for correct Ca(v)2 channel allocation to the axonal versus the dendritic domain. We suggest that the two different putative α(2)δ subunits are required in the same neurons to regulate different functions of VGCCs. Nature Publishing Group UK 2020-08-13 /pmc/articles/PMC7426832/ /pubmed/32792569 http://dx.doi.org/10.1038/s41598-020-69748-8 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Heinrich, Laurin Ryglewski, Stefanie Different functions of two putative Drosophila α(2)δ subunits in the same identified motoneurons |
title | Different functions of two putative Drosophila α(2)δ subunits in the same identified motoneurons |
title_full | Different functions of two putative Drosophila α(2)δ subunits in the same identified motoneurons |
title_fullStr | Different functions of two putative Drosophila α(2)δ subunits in the same identified motoneurons |
title_full_unstemmed | Different functions of two putative Drosophila α(2)δ subunits in the same identified motoneurons |
title_short | Different functions of two putative Drosophila α(2)δ subunits in the same identified motoneurons |
title_sort | different functions of two putative drosophila α(2)δ subunits in the same identified motoneurons |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426832/ https://www.ncbi.nlm.nih.gov/pubmed/32792569 http://dx.doi.org/10.1038/s41598-020-69748-8 |
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