CAST/ELKS Proteins Control Voltage-Gated Ca2+ Channel Density and Synaptic Release Probability at a Mammalian Central Synapse
Summary: In the presynaptic terminal, the magnitude and location of Ca2+ entry through voltage-gated Ca2+ channels (VGCCs) regulate the efficacy of neurotransmitter release. However, how presynaptic active zone proteins control mammalian VGCC levels and organization is unclear. To address this, we d...
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doaj-d0af342b3d8e4174a4c8048e4caa66362020-11-24T21:21:54ZengElsevierCell Reports2211-12472018-07-01242284293.e6CAST/ELKS Proteins Control Voltage-Gated Ca2+ Channel Density and Synaptic Release Probability at a Mammalian Central SynapseWei Dong0Tamara Radulovic1R. Oliver Goral2Connon Thomas3Monica Suarez Montesinos4Debbie Guerrero-Given5Akari Hagiwara6Travis Putzke7Yamato Hida8Manabu Abe9Kenji Sakimura10Naomi Kamasawa11Toshihisa Ohtsuka12Samuel M. Young, Jr.13Research Group Molecular Mechanisms of Synaptic Function, Max Planck Florida Institute for Neuroscience, Jupiter, FL 33458, USA; Key Laboratory of Medical Electrophysiology, Ministry of Education, Collaborative Innovation Center for Prevention and Treatment of Cardiovascular Disease, Institute of Cardiovascular Research, Southwest Medical University, Luzhou 646000, ChinaDepartment of Anatomy and Cell Biology, University of Iowa, Iowa City, IA 52242, USADepartment of Anatomy and Cell Biology, University of Iowa, Iowa City, IA 52242, USAMax Planck Florida Institute for Neuroscience Electron Microscopy Facility, Max Planck Florida Institute for Neuroscience, Jupiter, FL 33458, USAResearch Group Molecular Mechanisms of Synaptic Function, Max Planck Florida Institute for Neuroscience, Jupiter, FL 33458, USAMax Planck Florida Institute for Neuroscience Electron Microscopy Facility, Max Planck Florida Institute for Neuroscience, Jupiter, FL 33458, USADepartment of Biochemistry, University of Yamanashi, Yamanashi 409-3898, JapanResearch Group Molecular Mechanisms of Synaptic Function, Max Planck Florida Institute for Neuroscience, Jupiter, FL 33458, USADepartment of Biochemistry, University of Yamanashi, Yamanashi 409-3898, JapanDepartment of Cellular Neurobiology, Brain Research Institute, Niigata University, Niigata 951-8585, JapanDepartment of Cellular Neurobiology, Brain Research Institute, Niigata University, Niigata 951-8585, JapanMax Planck Florida Institute for Neuroscience Electron Microscopy Facility, Max Planck Florida Institute for Neuroscience, Jupiter, FL 33458, USADepartment of Biochemistry, University of Yamanashi, Yamanashi 409-3898, Japan; Corresponding authorDepartment of Anatomy and Cell Biology, University of Iowa, Iowa City, IA 52242, USA; Department of Otolaryngology, University of Iowa, Iowa City, IA 52242, USA; Iowa Neuroscience Institute, University of Iowa, Iowa City, IA 52242, USA; Aging Mind Brain Initiative, University of Iowa, Iowa City, IA 52242, USA; Corresponding authorSummary: In the presynaptic terminal, the magnitude and location of Ca2+ entry through voltage-gated Ca2+ channels (VGCCs) regulate the efficacy of neurotransmitter release. However, how presynaptic active zone proteins control mammalian VGCC levels and organization is unclear. To address this, we deleted the CAST/ELKS protein family at the calyx of Held, a CaV2.1 channel-exclusive presynaptic terminal. We found that loss of CAST/ELKS reduces the CaV2.1 current density with concomitant reductions in CaV2.1 channel numbers and clusters. Surprisingly, deletion of CAST/ELKS increases release probability while decreasing the readily releasable pool, with no change in active zone ultrastructure. In addition, Ca2+ channel coupling is unchanged, but spontaneous release rates are elevated. Thus, our data identify distinct roles for CAST/ELKS as positive regulators of CaV2.1 channel density and suggest that they regulate release probability through a post-priming step that controls synaptic vesicle fusogenicity. : Dong et al. show that CAST/ELKS have multiple roles in presynaptic function. These proteins positively regulate CaV2.1 channel abundance and negatively regulate release probability. The authors propose that CAST/ELKS regulate release probability at a step in synaptic vesicle release that regulates the energy barrier for synaptic vesicle fusion. Keywords: calyx of Held, release probability, calcium channels, active zone, synaptic transmission, CAST/ELKS, exocytosis, auditory signalinghttp://www.sciencedirect.com/science/article/pii/S2211124718309197 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Wei Dong Tamara Radulovic R. Oliver Goral Connon Thomas Monica Suarez Montesinos Debbie Guerrero-Given Akari Hagiwara Travis Putzke Yamato Hida Manabu Abe Kenji Sakimura Naomi Kamasawa Toshihisa Ohtsuka Samuel M. Young, Jr. |
spellingShingle |
Wei Dong Tamara Radulovic R. Oliver Goral Connon Thomas Monica Suarez Montesinos Debbie Guerrero-Given Akari Hagiwara Travis Putzke Yamato Hida Manabu Abe Kenji Sakimura Naomi Kamasawa Toshihisa Ohtsuka Samuel M. Young, Jr. CAST/ELKS Proteins Control Voltage-Gated Ca2+ Channel Density and Synaptic Release Probability at a Mammalian Central Synapse Cell Reports |
author_facet |
Wei Dong Tamara Radulovic R. Oliver Goral Connon Thomas Monica Suarez Montesinos Debbie Guerrero-Given Akari Hagiwara Travis Putzke Yamato Hida Manabu Abe Kenji Sakimura Naomi Kamasawa Toshihisa Ohtsuka Samuel M. Young, Jr. |
author_sort |
Wei Dong |
title |
CAST/ELKS Proteins Control Voltage-Gated Ca2+ Channel Density and Synaptic Release Probability at a Mammalian Central Synapse |
title_short |
CAST/ELKS Proteins Control Voltage-Gated Ca2+ Channel Density and Synaptic Release Probability at a Mammalian Central Synapse |
title_full |
CAST/ELKS Proteins Control Voltage-Gated Ca2+ Channel Density and Synaptic Release Probability at a Mammalian Central Synapse |
title_fullStr |
CAST/ELKS Proteins Control Voltage-Gated Ca2+ Channel Density and Synaptic Release Probability at a Mammalian Central Synapse |
title_full_unstemmed |
CAST/ELKS Proteins Control Voltage-Gated Ca2+ Channel Density and Synaptic Release Probability at a Mammalian Central Synapse |
title_sort |
cast/elks proteins control voltage-gated ca2+ channel density and synaptic release probability at a mammalian central synapse |
publisher |
Elsevier |
series |
Cell Reports |
issn |
2211-1247 |
publishDate |
2018-07-01 |
description |
Summary: In the presynaptic terminal, the magnitude and location of Ca2+ entry through voltage-gated Ca2+ channels (VGCCs) regulate the efficacy of neurotransmitter release. However, how presynaptic active zone proteins control mammalian VGCC levels and organization is unclear. To address this, we deleted the CAST/ELKS protein family at the calyx of Held, a CaV2.1 channel-exclusive presynaptic terminal. We found that loss of CAST/ELKS reduces the CaV2.1 current density with concomitant reductions in CaV2.1 channel numbers and clusters. Surprisingly, deletion of CAST/ELKS increases release probability while decreasing the readily releasable pool, with no change in active zone ultrastructure. In addition, Ca2+ channel coupling is unchanged, but spontaneous release rates are elevated. Thus, our data identify distinct roles for CAST/ELKS as positive regulators of CaV2.1 channel density and suggest that they regulate release probability through a post-priming step that controls synaptic vesicle fusogenicity. : Dong et al. show that CAST/ELKS have multiple roles in presynaptic function. These proteins positively regulate CaV2.1 channel abundance and negatively regulate release probability. The authors propose that CAST/ELKS regulate release probability at a step in synaptic vesicle release that regulates the energy barrier for synaptic vesicle fusion. Keywords: calyx of Held, release probability, calcium channels, active zone, synaptic transmission, CAST/ELKS, exocytosis, auditory signaling |
url |
http://www.sciencedirect.com/science/article/pii/S2211124718309197 |
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