Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 675

The DOI matches its Crossref record; 13 of the 13 references it cites were found in a registry or an index.

Neuronal Voltage-Gated Calcium Channels: Structure, Function, and Dysfunction

Open access
Simms, Brett A., Zamponi, Gerald W.·2014·Neuron

Abstract

Voltage-gated calcium channels are the primary mediators of depolarization-induced calcium entry into neurons. There is great diversity of calcium channel subtypes due to multiple genes that encode calcium channel α1 subunits, coassembly with a variety of ancillary calcium channel subunits, and alternative splicing. This allows these channels to fulfill highly specialized roles in specific neuronal subtypes and at particular subcellular loci. While calcium channels are of critical importance to brain function, their inappropriate expression or dysfunction gives rise to a variety of neurological disorders, including, pain, epilepsy, migraine, and ataxia. This Review discusses salient aspects of voltage-gated calcium channel function, physiology, and pathophysiology.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1016/j.neuron.2014.03.016

Cites

13 of 13 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 13 references

Research works printed but not linked: 324

  1. Adams, 1993, Toxityping rat brain calcium channels with omega-toxins from spider and cone snail venoms, Biochemistry, 32, 12566, 10.1021/bi00210a003 · DOI
  2. Adams, 2009, Ca(V)2.1 P/Q-type calcium channel alternative splicing affects the functional impact of familial hemiplegic migraine mutations: implications for calcium channelopathies, Channels (Austin), 3, 110, 10.4161/chan.3.2.7932 · DOI
  3. Altier, 2011, The Cavβ subunit prevents RFP2-mediated ubiquitination and proteasomal degradation of L-type channels, Nat. Neurosci., 14, 173, 10.1038/nn.2712 · DOI
  4. Alviña, 2009, T-type calcium channels mediate rebound firing in intact deep cerebellar neurons, Neuroscience, 158, 635, 10.1016/j.neuroscience.2008.09.052 · DOI
  5. Anderson, 2005, Thalamic Cav3.1 T-type Ca2+ channel plays a crucial role in stabilizing sleep, Proc. Natl. Acad. Sci. USA, 102, 1743, 10.1073/pnas.0409644102 · DOI
  6. Anderson, 2010, Regulation of neuronal activity by Cav3-Kv4 channel signaling complexes, Nat. Neurosci., 13, 333, 10.1038/nn.2493 · DOI
  7. Anderson, 2010, Regulation of the KV4.2 complex by CaV3.1 calcium channels, Channels (Austin), 4, 163, 10.4161/chan.4.3.11955 · DOI
  8. Anderson, 2013, The Cav3-Kv4 complex acts as a calcium sensor to maintain inhibitory charge transfer during extracellular calcium fluctuations, J. Neurosci., 33, 7811, 10.1523/JNEUROSCI.5384-12.2013 · DOI
  9. Arikkath, 2003, Auxiliary subunits: essential components of the voltage-gated calcium channel complex, Curr. Opin. Neurobiol., 13, 298, 10.1016/S0959-4388(03)00066-7 · DOI
  10. Armstrong, 1985, Two distinct populations of calcium channels in a clonal line of pituitary cells, Science, 227, 65, 10.1126/science.2578071 · DOI · Paper page
  11. Bader, 2011, Mouse model of Timothy syndrome recapitulates triad of autistic traits, Proc. Natl. Acad. Sci. USA, 108, 15432, 10.1073/pnas.1112667108 · DOI
  12. Baig, 2011, Loss of Ca(v)1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness, Nat. Neurosci., 14, 77, 10.1038/nn.2694 · DOI
  13. Ball, 2002, Role of the beta(2) subunit of voltage-dependent calcium channels in the retinal outer plexiform layer, Invest. Ophthalmol. Vis. Sci., 43, 1595
  14. Bazzazi, 2013, Continuously tunable Ca(2+) regulation of RNA-edited CaV1.3 channels, Cell Rep., 5, 367, 10.1016/j.celrep.2013.09.006 · DOI
  15. Bean, 1985, Two kinds of calcium channels in canine atrial cells. Differences in kinetics, selectivity, and pharmacology, J. Gen. Physiol., 86, 1, 10.1085/jgp.86.1.1 · DOI · Paper page
  16. Bech-Hansen, 1998, Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness, Nat. Genet., 19, 264, 10.1038/947 · DOI · Paper page
  17. Belardetti, 2012, Calcium channels as therapeutic targets, Wiley Interdiscip. Rev. Membr. Transp. Signal., 1, 433, 10.1002/wmts.38 · DOI
  18. Ben Johny, 2013, Dynamic switching of calmodulin interactions underlies Ca2+ regulation of CaV1.3 channels, Nat. Commun., 4, 1717, 10.1038/ncomms2727 · DOI
  19. Berggren, 2004, Removal of Ca2+ channel beta3 subunit enhances Ca2+ oscillation frequency and insulin exocytosis, Cell, 119, 273, 10.1016/j.cell.2004.09.033 · DOI · Paper page
  20. Berjukow, 2000, Molecular mechanism of calcium channel block by isradipine. Role of a drug-induced inactivated channel conformation, J. Biol. Chem., 275, 22114, 10.1074/jbc.M908836199 · DOI
  21. Berkefeld, 2008, Repolarizing responses of BKCa-Cav complexes are distinctly shaped by their Cav subunits, J. Neurosci., 28, 8238, 10.1523/JNEUROSCI.2274-08.2008 · DOI
  22. Berkefeld, 2006, BKCa-Cav channel complexes mediate rapid and localized Ca2+-activated K+ signaling, Science, 314, 615, 10.1126/science.1132915 · DOI · Paper page
  23. Berrou, 2001, Molecular determinants of inactivation within the I-II linker of alpha1E (CaV2.3) calcium channels, Biophys. J., 80, 215, 10.1016/S0006-3495(01)76008-0 · DOI
  24. Beuckmann, 2003, N-type calcium channel alpha1B subunit (Cav2.2) knock-out mice display hyperactivity and vigilance state differences, J. Neurosci., 23, 6793, 10.1523/JNEUROSCI.23-17-06793.2003 · DOI
  25. Bezprozvanny, 1995, Functional impact of syntaxin on gating of N-type and Q-type calcium channels, Nature, 378, 623, 10.1038/378623a0 · DOI · Paper page
  26. Bichet, 2000, The I-II loop of the Ca2+ channel alpha1 subunit contains an endoplasmic reticulum retention signal antagonized by the beta subunit, Neuron, 25, 177, 10.1016/S0896-6273(00)80881-8 · DOI · Paper page
  27. Bourinet, 1996, The alpha 1E calcium channel exhibits permeation properties similar to low-voltage-activated calcium channels, J. Neurosci., 16, 4983, 10.1523/JNEUROSCI.16-16-04983.1996 · DOI
  28. Bourinet, 1999, Splicing of alpha 1A subunit gene generates phenotypic variants of P- and Q-type calcium channels, Nat. Neurosci., 2, 407, 10.1038/8070 · DOI · Paper page
  29. Bourinet, 2001, Interaction of SNX482 with domains III and IV inhibits activation gating of alpha(1E) (Ca(V)2.3) calcium channels, Biophys. J., 81, 79, 10.1016/S0006-3495(01)75681-0 · DOI
  30. Brice, 1999, Differential plasma membrane targeting of voltage-dependent calcium channel subunits expressed in a polarized epithelial cell line, J. Physiol., 515, 685, 10.1111/j.1469-7793.1999.685ab.x · DOI
  31. Brodbeck, 2002, The ducky mutation in Cacna2d2 results in altered Purkinje cell morphology and is associated with the expression of a truncated alpha 2 delta-2 protein with abnormal function, J. Biol. Chem., 277, 7684, 10.1074/jbc.M109404200 · DOI
  32. Buraei, 2010, The ß subunit of voltage-gated Ca2+ channels, Physiol. Rev., 90, 1461, 10.1152/physrev.00057.2009 · DOI
  33. Burgess, 1997, Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse, Cell, 88, 385, 10.1016/S0092-8674(00)81877-2 · DOI
  34. Burgess, 1999, beta subunit reshuffling modifies N- and P/Q-type Ca2+ channel subunit compositions in lethargic mouse brain, Mol. Cell. Neurosci., 13, 293, 10.1006/mcne.1999.0748 · DOI
  35. Busquet, 2010, CaV1.3 L-type Ca2+ channels modulate depression-like behaviour in mice independent of deaf phenotype, Int. J. Neuropsychopharmacol., 13, 499, 10.1017/S1461145709990368 · DOI
  36. Cain, 2011, Voltage-gated calcium channels and disease, Biofactors, 37, 197, 10.1002/biof.158 · DOI
  37. Cantí, 2005, The metal-ion-dependent adhesion site in the Von Willebrand factor-A domain of alpha2delta subunits is key to trafficking voltage-gated Ca2+ channels, Proc. Natl. Acad. Sci. USA, 102, 11230, 10.1073/pnas.0504183102 · DOI
  38. Carabelli, 2007, Fast exocytosis mediated by T- and L-type channels in chromaffin cells: distinct voltage-dependence but similar Ca2+ -dependence, Eur. Biophys. J., 36, 753, 10.1007/s00249-007-0138-2 · DOI
  39. Carbone, 2006, T-type channels-secretion coupling: evidence for a fast low-threshold exocytosis, Pflugers Arch., 453, 373, 10.1007/s00424-006-0100-7 · DOI
  40. Catterall, 2010, Ion channel voltage sensors: structure, function, and pathophysiology, Neuron, 67, 915, 10.1016/j.neuron.2010.08.021 · DOI
  41. Catterall, 2005, International Union of Pharmacology. XLVIII. Nomenclature and structure-function relationships of voltage-gated calcium channels, Pharmacol. Rev., 57, 411, 10.1124/pr.57.4.5 · DOI · Paper page
  42. Chan, 2007, ‘Rejuvenation’ protects neurons in mouse models of Parkinson’s disease, Nature, 447, 1081, 10.1038/nature05865 · DOI · Paper page
  43. Chang, 2001, Voltage-gated channels block nicotinic regulation of CREB phosphorylation and gene expression in neurons, Neuron, 32, 855, 10.1016/S0896-6273(01)00516-5 · DOI
  44. Chang, 2006, The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses, Vis. Neurosci., 23, 11, 10.1017/S095252380623102X · DOI
  45. Chaudhuri, 2004, Alternative splicing as a molecular switch for Ca2+/calmodulin-dependent facilitation of P/Q-type Ca2+ channels, J. Neurosci., 24, 6334, 10.1523/JNEUROSCI.1712-04.2004 · DOI
  46. Chaudhuri, 2007, Elementary mechanisms producing facilitation of Cav2.1 (P/Q-type) channels, J. Gen. Physiol., 129, 385, 10.1085/jgp.200709749 · DOI
  47. Chen, 2003, Abnormal coronary function in mice deficient in alpha1H T-type Ca2+ channels, Science, 302, 1416, 10.1126/science.1089268 · DOI
  48. Chen, 2004, Structural basis of the alpha1-beta subunit interaction of voltage-gated Ca2+ channels, Nature, 429, 675, 10.1038/nature02641 · DOI
  49. Chen, 2007, Calcium channel gamma subunits: a functionally diverse protein family, Cell Biochem. Biophys., 47, 178, 10.1007/s12013-007-0002-0 · DOI
  50. Choi, 2007, Attenuated pain responses in mice lacking Ca(V)3.2 T-type channels, Genes Brain Behav., 6, 425, 10.1111/j.1601-183X.2006.00268.x · DOI
  51. Chu, 2001, Calcium channel gamma subunits provide insights into the evolution of this gene family, Gene, 280, 37, 10.1016/S0378-1119(01)00738-7 · DOI
  52. Coulter, 1989, Characterization of ethosuximide reduction of low-threshold calcium current in thalamic neurons, Ann. Neurol., 25, 582, 10.1002/ana.410250610 · DOI
  53. Cribbs, 1998, Cloning and characterization of alpha1H from human heart, a member of the T-type Ca2+ channel gene family, Circ. Res., 83, 103, 10.1161/01.RES.83.1.103 · DOI
  54. Cueni, 2008, T-type Ca2+ channels, SK2 channels and SERCAs gate sleep-related oscillations in thalamic dendrites, Nat. Neurosci., 11, 683, 10.1038/nn.2124 · DOI
  55. Curtis, 1984, Purification of the calcium antagonist receptor of the voltage-sensitive calcium channel from skeletal muscle transverse tubules, Biochemistry, 23, 2113, 10.1021/bi00305a001 · DOI · Paper page
  56. Dai, 2009, Supramolecular assemblies and localized regulation of voltage-gated ion channels, Physiol. Rev., 89, 411, 10.1152/physrev.00029.2007 · DOI · Paper page
  57. Dao, 2010, Mood disorder susceptibility gene CACNA1C modifies mood-related behaviors in mice and interacts with sex to influence behavior in mice and diagnosis in humans, Biol. Psychiatry, 68, 801, 10.1016/j.biopsych.2010.06.019 · DOI
  58. Davies, 2010, The alpha2delta subunits of voltage-gated calcium channels form GPI-anchored proteins, a posttranslational modification essential for function, Proc. Natl. Acad. Sci. USA, 107, 1654, 10.1073/pnas.0908735107 · DOI
  59. Davies, 2011, Bipartite syntaxin 1A interactions mediate CaV2.2 calcium channel regulation, Biochem. Biophys. Res. Commun., 411, 562, 10.1016/j.bbrc.2011.06.185 · DOI
  60. Deisseroth, 1998, Translocation of calmodulin to the nucleus supports CREB phosphorylation in hippocampal neurons, Nature, 392, 198, 10.1038/32448 · DOI
  61. DeMaria, 2001, Calmodulin bifurcates the local Ca2+ signal that modulates P/Q-type Ca2+ channels, Nature, 411, 484, 10.1038/35078091 · DOI · Paper page
  62. Depil, 2011, Timothy mutation disrupts the link between activation and inactivation in Ca(V)1.2 protein, J. Biol. Chem., 286, 31557, 10.1074/jbc.M111.255273 · DOI
  63. Destexhe, 1998, Dendritic low-threshold calcium currents in thalamic relay cells, J. Neurosci., 18, 3574, 10.1523/JNEUROSCI.18-10-03574.1998 · DOI
  64. Dick, 2008, A modular switch for spatial Ca2+ selectivity in the calmodulin regulation of CaV channels, Nature, 451, 830, 10.1038/nature06529 · DOI · Paper page
  65. Doering, 2005, Molecular pharmacology of non-L-type calcium channels, Curr. Pharm. Des., 11, 1887, 10.2174/1381612054021042 · DOI
  66. Doering, 2005, Cav1.4 encodes a calcium channel with low open probability and unitary conductance, Biophys. J., 89, 3042, 10.1529/biophysj.105.067124 · DOI
  67. Dolmetsch, 2001, Signaling to the nucleus by an L-type calcium channel-calmodulin complex through the MAP kinase pathway, Science, 294, 333, 10.1126/science.1063395 · DOI · Paper page
  68. Dolphin, 2013, The α2δ subunits of voltage-gated calcium channels, Biochim. Biophys. Acta, 1828, 1541, 10.1016/j.bbamem.2012.11.019 · DOI
  69. Dubel, 1992, Molecular cloning of the alpha-1 subunit of an omega-conotoxin-sensitive calcium channel, Proc. Natl. Acad. Sci. USA, 89, 5058, 10.1073/pnas.89.11.5058 · DOI · Paper page
  70. Eckle, 2014, Mechanisms by which a CACNA1H mutation in epilepsy patients increases seizure susceptibility, J. Physiol., 592, 795, 10.1113/jphysiol.2013.264176 · DOI
  71. Egger, 2003, Mechanisms of lateral inhibition in the olfactory bulb: efficiency and modulation of spike-evoked calcium influx into granule cells, J. Neurosci., 23, 7551, 10.1523/JNEUROSCI.23-20-07551.2003 · DOI
  72. Eickelberg, 1999, Calcium channel blockers activate the interleukin-6 gene via the transcription factors NF-IL6 and NF-kappaB in primary human vascular smooth muscle cells, Circulation, 99, 2276, 10.1161/01.CIR.99.17.2276 · DOI
  73. Ellinor, 1995, Ca2+ channel selectivity at a single locus for high-affinity Ca2+ interactions, Neuron, 15, 1121, 10.1016/0896-6273(95)90100-0 · DOI · Paper page
  74. Engbers, 2012, Intermediate conductance calcium-activated potassium channels modulate summation of parallel fiber input in cerebellar Purkinje cells, Proc. Natl. Acad. Sci. USA, 109, 2601, 10.1073/pnas.1115024109 · DOI
  75. Erickson, 2001, Preassociation of calmodulin with voltage-gated Ca(2+) channels revealed by FRET in single living cells, Neuron, 31, 973, 10.1016/S0896-6273(01)00438-X · DOI · Paper page
  76. Erickson, 2003, FRET two-hybrid mapping reveals function and location of L-type Ca2+ channel CaM preassociation, Neuron, 39, 97, 10.1016/S0896-6273(03)00395-7 · DOI
  77. Escayg, 2000, Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia, Am. J. Hum. Genet., 66, 1531, 10.1086/302909 · DOI
  78. Fallon, 2005, Structure of calmodulin bound to the hydrophobic IQ domain of the cardiac Ca(v)1.2 calcium channel, Structure, 13, 1881, 10.1016/j.str.2005.09.021 · DOI
  79. Fallon, 2009, Crystal structure of dimeric cardiac L-type calcium channel regulatory domains bridged by Ca2+∗ calmodulins, Proc. Natl. Acad. Sci. USA, 106, 5135, 10.1073/pnas.0807487106 · DOI
  80. Fang, 2011, Mechanism of auxiliary β-subunit-mediated membrane targeting of L-type (Ca(V)1.2) channels, J. Physiol., 589, 4437, 10.1113/jphysiol.2011.214247 · DOI
  81. Findeisen, 2013, Apo states of calmodulin and CaBP1 control CaV1 voltage-gated calcium channel function through direct competition for the IQ domain, J. Mol. Biol., 425, 3217, 10.1016/j.jmb.2013.06.024 · DOI
  82. Fouad, 1997, Genotype-phenotype correlations of DHP receptor alpha 1-subunit gene mutations causing hypokalemic periodic paralysis, Neuromuscul. Disord., 7, 33, 10.1016/S0960-8966(96)00401-4 · DOI
  83. Fox, 1987, Single-channel recordings of three types of calcium channels in chick sensory neurones, J. Physiol., 394, 173, 10.1113/jphysiol.1987.sp016865 · DOI · Paper page
  84. Frank, 2010, Bassoon and the synaptic ribbon organize Ca2+ channels and vesicles to add release sites and promote refilling, Neuron, 68, 724, 10.1016/j.neuron.2010.10.027 · DOI
  85. Fuller, 2010, Molecular mechanism of calcium channel regulation in the fight-or-flight response, Sci. Signal., 3, ra70, 10.1126/scisignal.2001152 · DOI
  86. Fuller-Bicer, 2009, Targeted disruption of the voltage-dependent calcium channel alpha2/delta-1-subunit, Am. J. Physiol. Heart Circ. Physiol., 297, H117, 10.1152/ajpheart.00122.2009 · DOI
  87. Giordano, 2010, Molecular switch from L-type Ca v 1.3 to Ca v 1.2 Ca2+ channel signaling underlies long-term psychostimulant-induced behavioral and molecular plasticity, J. Neurosci., 30, 17051, 10.1523/JNEUROSCI.2255-10.2010 · DOI
  88. Giusti-Rodríguez, 2013, The genomics of schizophrenia: update and implications, J. Clin. Invest., 123, 4557, 10.1172/JCI66031 · DOI
  89. Gomez-Ospina, 2006, The C terminus of the L-type voltage-gated calcium channel Ca(V)1.2 encodes a transcription factor, Cell, 127, 591, 10.1016/j.cell.2006.10.017 · DOI
  90. Gomez-Ospina, 2013, A promoter in the coding region of the calcium channel gene CACNA1C generates the transcription factor CCAT, PLoS ONE, 8, e60526, 10.1371/journal.pone.0060526 · DOI
  91. Gomora, 2001, Block of cloned human T-type calcium channels by succinimide antiepileptic drugs, Mol. Pharmacol., 60, 1121, 10.1124/mol.60.5.1121 · DOI
  92. Graef, 1999, L-type calcium channels and GSK-3 regulate the activity of NF-ATc4 in hippocampal neurons, Nature, 401, 703, 10.1038/44378 · DOI
  93. Graf, 2012, RIM promotes calcium channel accumulation at active zones of the Drosophila neuromuscular junction, J. Neurosci., 32, 16586, 10.1523/JNEUROSCI.0965-12.2012 · DOI
  94. Green, 2010, The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia, Mol. Psychiatry, 15, 1016, 10.1038/mp.2009.49 · DOI · Paper page
  95. Gregg, 1996, Absence of the beta subunit (cchb1) of the skeletal muscle dihydropyridine receptor alters expression of the alpha 1 subunit and eliminates excitation-contraction coupling, Proc. Natl. Acad. Sci. USA, 93, 13961, 10.1073/pnas.93.24.13961 · DOI
  96. Griessmeier, 2009, Calmodulin is a functional regulator of Cav1.4 L-type Ca2+ channels, J. Biol. Chem., 284, 29809, 10.1074/jbc.M109.048082 · DOI
  97. Haeseleer, 2004, Essential role of Ca2+-binding protein 4, a Cav1.4 channel regulator, in photoreceptor synaptic function, Nat. Neurosci., 7, 1079, 10.1038/nn1320 · DOI
  98. Hagalili, 2008, The voltage-gated Ca(2+) channel is the Ca(2+) sensor protein of secretion, Biochemistry, 47, 13822, 10.1021/bi801619f · DOI
  99. Hagiwara, 1966, Effects of the intracellular Ca ion concentration upon the excitability of the muscle fiber membrane of a barnacle, J. Gen. Physiol., 49, 807, 10.1085/jgp.49.4.807 · DOI
  100. Hall, 2013, Competition between α-actinin and Ca2+-calmodulin controls surface retention of the L-type Ca2+ channel Ca(V)1.2, Neuron, 78, 483, 10.1016/j.neuron.2013.02.032 · DOI
  101. Hamid, 2006, Determinants of the differential gating properties of Cav3.1 and Cav3.3 T-type channels: a role of domain IV?, Neuroscience, 143, 717, 10.1016/j.neuroscience.2006.08.023 · DOI
  102. Hatakeyama, 2001, Differential nociceptive responses in mice lacking the alpha(1B) subunit of N-type Ca(2+) channels, Neuroreport, 12, 2423, 10.1097/00001756-200108080-00027 · DOI
  103. He, 2014, CACNA1C, schizophrenia and major depressive disorder in the Han Chinese population, Br. J. Psychiatry, 204, 36, 10.1192/bjp.bp.113.126979 · DOI
  104. Hemara-Wahanui, 2005, A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation, Proc. Natl. Acad. Sci. USA, 102, 7553, 10.1073/pnas.0501907102 · DOI
  105. Herlitze, 1997, Molecular determinants of inactivation and G protein modulation in the intracellular loop connecting domains I and II of the calcium channel alpha1A subunit, Proc. Natl. Acad. Sci. USA, 94, 1512, 10.1073/pnas.94.4.1512 · DOI
  106. Hernández-Ochoa, 2007, Ca2+ signal summation and NFATc1 nuclear translocation in sympathetic ganglion neurons during repetitive action potentials, Cell Calcium, 41, 559, 10.1016/j.ceca.2006.10.006 · DOI
  107. Heron, 2004, Genetic variation of CACNA1H in idiopathic generalized epilepsy, Ann. Neurol., 55, 595, 10.1002/ana.20028 · DOI
  108. Heron, 2007, Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants, Ann. Neurol., 62, 560, 10.1002/ana.21169 · DOI
  109. Hibino, 2003, Direct interaction with a nuclear protein and regulation of gene silencing by a variant of the Ca2+-channel beta 4 subunit, Proc. Natl. Acad. Sci. USA, 100, 307, 10.1073/pnas.0136791100 · DOI
  110. Hirano, 2011, A novel mutation in the calcium channel gene in a family with hypokalemic periodic paralysis, J. Neurol. Sci., 309, 9, 10.1016/j.jns.2011.07.046 · DOI
  111. Hirtz, 2011, Cav1.3 calcium channels are required for normal development of the auditory brainstem, J. Neurosci., 31, 8280, 10.1523/JNEUROSCI.5098-10.2011 · DOI
  112. Hoppa, 2012, α2δ expression sets presynaptic calcium channel abundance and release probability, Nature, 486, 122, 10.1038/nature11033 · DOI · Paper page
  113. Hoshi, 1990, Biophysical and molecular mechanisms of Shaker potassium channel inactivation, Science, 250, 533, 10.1126/science.2122519 · DOI · Paper page
  114. Hu, 2010, Dual variation in SCN5A and CACNB2b underlies the development of cardiac conduction disease without Brugada syndrome, Pacing Clin. Electrophysiol., 33, 274, 10.1111/j.1540-8159.2009.02642.x · DOI
  115. Huang, 2012, RNA editing of the IQ domain in Ca(v)1.3 channels modulates their Ca2+-dependent inactivation, Neuron, 73, 304, 10.1016/j.neuron.2011.11.022 · DOI
  116. Huber, 2000, Conserved Ca2+-antagonist-binding properties and putative folding structure of a recombinant high-affinity dihydropyridine-binding domain, Biochem. J., 347, 829, 10.1042/bj3470829 · DOI
  117. Hudmon, 2005, CaMKII tethers to L-type Ca2+ channels, establishing a local and dedicated integrator of Ca2+ signals for facilitation, J. Cell Biol., 171, 537, 10.1083/jcb.200505155 · DOI · Paper page
  118. Huguenard, 1998, Anatomical and physiological considerations in thalamic rhythm generation, J. Sleep Res., 7, 24, 10.1046/j.1365-2869.7.s1.5.x · DOI
  119. Hulme, 2006, Autoinhibitory control of the CaV1.2 channel by its proteolytically processed distal C-terminal domain, J. Physiol., 576, 87, 10.1113/jphysiol.2006.111799 · DOI
  120. Hurley, 2013, Parkinson’s disease is associated with altered expression of CaV1 channels and calcium-binding proteins, Brain, 136, 2077, 10.1093/brain/awt134 · DOI
  121. Impey, 1996, Induction of CRE-mediated gene expression by stimuli that generate long-lasting LTP in area CA1 of the hippocampus, Neuron, 16, 973, 10.1016/S0896-6273(00)80120-8 · DOI · Paper page
  122. Imredy, 1994, Mechanism of Ca(2+)-sensitive inactivation of L-type Ca2+ channels, Neuron, 12, 1301, 10.1016/0896-6273(94)90446-4 · DOI
  123. Inagaki, 2014, Pharmacological correction of gating defects in the voltage-gated Ca(v)2.1 Ca2+ channel due to a familial hemiplegic migraine mutation, Neuron, 81, 91, 10.1016/j.neuron.2013.10.056 · DOI
  124. Jacus, 2012, Presynaptic Cav3.2 channels regulate excitatory neurotransmission in nociceptive dorsal horn neurons, J. Neurosci., 32, 9374, 10.1523/JNEUROSCI.0068-12.2012 · DOI
  125. Jagodic, 2007, Cell-specific alterations of T-type calcium current in painful diabetic neuropathy enhance excitability of sensory neurons, J. Neurosci., 27, 3305, 10.1523/JNEUROSCI.4866-06.2007 · DOI · Paper page
  126. Jagodic, 2008, Upregulation of the T-type calcium current in small rat sensory neurons after chronic constrictive injury of the sciatic nerve, J. Neurophysiol., 99, 3151, 10.1152/jn.01031.2007 · DOI
  127. Jalkanen, 2006, X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene, J. Med. Genet., 43, 699, 10.1136/jmg.2006.040741 · DOI
  128. Jarvis, 2001, Distinct molecular determinants govern syntaxin 1A-mediated inactivation and G-protein inhibition of N-type calcium channels, J. Neurosci., 21, 2939, 10.1523/JNEUROSCI.21-09-02939.2001 · DOI
  129. Jeng, 2006, Dominant-negative effects of human P/Q-type Ca2+ channel mutations associated with episodic ataxia type 2, Am. J. Physiol. Cell Physiol., 290, C1209, 10.1152/ajpcell.00247.2005 · DOI
  130. Jeon, 2010, Observational fear learning involves affective pain system and Cav1.2 Ca2+ channels in ACC, Nat. Neurosci., 13, 482, 10.1038/nn.2504 · DOI · Paper page
  131. Jing, 2013, Disruption of the presynaptic cytomatrix protein bassoon degrades ribbon anchorage, multiquantal release, and sound encoding at the hair cell afferent synapse, J. Neurosci., 33, 4456, 10.1523/JNEUROSCI.3491-12.2013 · DOI
  132. Jodice, 1997, Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p, Hum. Mol. Genet., 6, 1973, 10.1093/hmg/6.11.1973 · DOI · Paper page
  133. Jouvenceau, 2001, Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel, Lancet, 358, 801, 10.1016/S0140-6736(01)05971-2 · DOI
  134. Jun, 1999, Ablation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunit, Proc. Natl. Acad. Sci. USA, 96, 15245, 10.1073/pnas.96.26.15245 · DOI
  135. Kadurin, 2012, Calcium currents are enhanced by α2δ-1 lacking its membrane anchor, J. Biol. Chem., 287, 33554, 10.1074/jbc.M112.378554 · DOI
  136. Kaeser, 2011, RIM proteins tether Ca2+ channels to presynaptic active zones via a direct PDZ-domain interaction, Cell, 144, 282, 10.1016/j.cell.2010.12.029 · DOI · Paper page
  137. Kaneko, 2002, Identification and characterization of novel human Ca(v)2.2 (alpha 1B) calcium channel variants lacking the synaptic protein interaction site, J. Neurosci., 22, 82, 10.1523/JNEUROSCI.22-01-00082.2002 · DOI
  138. Kang, 2012, CaV1.3-selective L-type calcium channel antagonists as potential new therapeutics for Parkinson’s disease, Nat. Commun., 3, 1146, 10.1038/ncomms2149 · DOI
  139. Katz, 1967, The timing of calcium action during neuromuscular transmission, J. Physiol., 189, 535, 10.1113/jphysiol.1967.sp008183 · DOI · Paper page
  140. Khosravani, 2004, Gating effects of mutations in the Cav3.2 T-type calcium channel associated with childhood absence epilepsy, J. Biol. Chem., 279, 9681, 10.1074/jbc.C400006200 · DOI
  141. Khosravani, 2005, Effects of Cav3.2 channel mutations linked to idiopathic generalized epilepsy, Ann. Neurol., 57, 745, 10.1002/ana.20458 · DOI
  142. Kim, 2001, Altered nociceptive response in mice deficient in the alpha(1B) subunit of the voltage-dependent calcium channel, Mol. Cell. Neurosci., 18, 235, 10.1006/mcne.2001.1013 · DOI
  143. Kim, 2001, Lack of the burst firing of thalamocortical relay neurons and resistance to absence seizures in mice lacking alpha(1G) T-type Ca(2+) channels, Neuron, 31, 35, 10.1016/S0896-6273(01)00343-9 · DOI · Paper page
  144. Kim, 2008, Structures of CaV2 Ca2+/CaM-IQ domain complexes reveal binding modes that underlie calcium-dependent inactivation and facilitation, Structure, 16, 1455, 10.1016/j.str.2008.07.010 · DOI
  145. Kim, 2010, Multiple C-terminal tail Ca(2+)/CaMs regulate Ca(V)1.2 function but do not mediate channel dimerization, EMBO J., 29, 3924, 10.1038/emboj.2010.260 · DOI
  146. Kipfer, 2013, Novel CACNA1A mutation(s) associated with slow saccade velocities, J. Neurol., 260, 3010
  147. Kiyonaka, 2007, RIM1 confers sustained activity and neurotransmitter vesicle anchoring to presynaptic Ca2+ channels, Nat. Neurosci., 10, 691, 10.1038/nn1904 · DOI
  148. Klassen, 2011, Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy, Cell, 145, 1036, 10.1016/j.cell.2011.05.025 · DOI
  149. Knoflach, 2013, Cav1.4 IT mouse as model for vision impairment in human congenital stationary night blindness type 2, Channels (Austin), 7, 7, 10.4161/chan.26368 · DOI
  150. Kraus, 1998, Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics, J. Biol. Chem., 273, 5586, 10.1074/jbc.273.10.5586 · DOI
  151. Krey, 2013, Timothy syndrome is associated with activity-dependent dendritic retraction in rodent and human neurons, Nat. Neurosci., 16, 201, 10.1038/nn.3307 · DOI · Paper page
  152. Langwieser, 2010, Homeostatic switch in hebbian plasticity and fear learning after sustained loss of Cav1.2 calcium channels, J. Neurosci., 30, 8367, 10.1523/JNEUROSCI.4164-08.2010 · DOI
  153. Lansman, 1986, Blockade of current through single calcium channels by Cd2+, Mg2+, and Ca2+. Voltage and concentration dependence of calcium entry into the pore, J. Gen. Physiol., 88, 321, 10.1085/jgp.88.3.321 · DOI · Paper page
  154. Lee, 1999, Ca2+/calmodulin binds to and modulates P/Q-type calcium channels, Nature, 399, 155, 10.1038/20194 · DOI · Paper page
  155. Lee, 1999, Cloning and expression of a novel member of the low voltage-activated T-type calcium channel family, J. Neurosci., 19, 1912, 10.1523/JNEUROSCI.19-06-01912.1999 · DOI
  156. Lee, 2011, Genome-wide association study of bipolar I disorder in the Han Chinese population, Mol. Psychiatry, 16, 548, 10.1038/mp.2010.43 · DOI · Paper page
  157. Lee, 2012, Selective genetic deletion of cacna1c in the mouse prefrontal cortex, Mol. Psychiatry, 17, 1051, 10.1038/mp.2012.149 · DOI
  158. Letts, 1998, The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit, Nat. Genet., 19, 340, 10.1038/1228 · DOI · Paper page
  159. Li, 2012, Balanced interactions of calcineurin with AKAP79 regulate Ca2+-calcineurin-NFAT signaling, Nat. Struct. Mol. Biol., 19, 337, 10.1038/nsmb.2238 · DOI
  160. Liang, 2003, Unified mechanisms of Ca2+ regulation across the Ca2+ channel family, Neuron, 39, 951, 10.1016/S0896-6273(03)00560-9 · DOI · Paper page
  161. Liao, 2005, Splicing for alternative structures of Cav1.2 Ca2+ channels in cardiac and smooth muscles, Cardiovasc. Res., 68, 197, 10.1016/j.cardiores.2005.06.024 · DOI
  162. Lin, 2011, Genetic variations in CYP17A1, CACNB2 and PLEKHA7 are associated with blood pressure and/or hypertension in She ethnic minority of China, Atherosclerosis, 219, 709, 10.1016/j.atherosclerosis.2011.09.006 · DOI
  163. Lipkind, 2003, Molecular modeling of interactions of dihydropyridines and phenylalkylamines with the inner pore of the L-type Ca2+ channel, Mol. Pharmacol., 63, 499, 10.1124/mol.63.3.499 · DOI
  164. Lipscombe, 2005, Neuronal proteins custom designed by alternative splicing, Curr. Opin. Neurobiol., 15, 358, 10.1016/j.conb.2005.04.002 · DOI
  165. Lipscombe, 2013, Alternative splicing: functional diversity among voltage-gated calcium channels and behavioral consequences, Biochim. Biophys. Acta, 1828, 1522, 10.1016/j.bbamem.2012.09.018 · DOI
  166. Liu, 2012, Structural basis for the regulation of L-type voltage-gated calcium channels: interactions between the N-terminal cytoplasmic domain and Ca(2+)-calmodulin, Front. Mol. Neurosci., 5, 38, 10.3389/fnmol.2012.00038 · DOI
  167. Liu, 2010, Enzyme-inhibitor-like tuning of Ca(2+) channel connectivity with calmodulin, Nature, 463, 968, 10.1038/nature08766 · DOI
  168. Liu, 2013, Dysregulation of Cav 1.4 channels disrupts the maturation of photoreceptor synaptic ribbons in congenital stationary night blindness type 2, Channels (Austin), 7, 7, 10.4161/chan.26376 · DOI
  169. Lodha, 2010, Congenital stationary night blindness in mice - a tale of two Cacna1f mutants, Adv. Exp. Med. Biol., 664, 549, 10.1007/978-1-4419-1399-9_63 · DOI
  170. Lodha, 2012, Congenital stationary night blindness: mutation update and clinical variability, Adv. Exp. Med. Biol., 723, 371, 10.1007/978-1-4614-0631-0_48 · DOI
  171. Lu, 2012, Support for calcium channel gene defects in autism spectrum disorders, Mol. Autism, 3, 18, 10.1186/2040-2392-3-18 · DOI
  172. Mangoni, 2006, Bradycardia and slowing of the atrioventricular conduction in mice lacking CaV3.1/alpha1G T-type calcium channels, Circ. Res., 98, 1422, 10.1161/01.RES.0000225862.14314.49 · DOI
  173. Marger, 2011, T-type calcium channels contribute to colonic hypersensitivity in a rat model of irritable bowel syndrome, Proc. Natl. Acad. Sci. USA, 108, 11268, 10.1073/pnas.1100869108 · DOI
  174. Mark, 2011, Delayed postnatal loss of P/Q-type calcium channels recapitulates the absence epilepsy, dyskinesia, and ataxia phenotypes of genomic Cacna1a mutations, J. Neurosci., 31, 4311, 10.1523/JNEUROSCI.5342-10.2011 · DOI
  175. Marom, 2010, Conformational changes induced in voltage-gated calcium channel Cav1.2 by BayK 8644 or FPL64176 modify the kinetics of secretion independently of Ca2+ influx, J. Biol. Chem., 285, 6996, 10.1074/jbc.M109.059865 · DOI
  176. Marshall, 2003, Calcium channel and NMDA receptor activities differentially regulate nuclear C/EBPbeta levels to control neuronal survival, Neuron, 39, 625, 10.1016/S0896-6273(03)00496-3 · DOI
  177. Matsuda, 2013, Stargazin regulates AMPA receptor trafficking through adaptor protein complexes during long-term depression, Nat. Commun., 4, 2759, 10.1038/ncomms3759 · DOI
  178. Maximov, 2002, Synaptic targeting of N-type calcium channels in hippocampal neurons, J. Neurosci., 22, 6939, 10.1523/JNEUROSCI.22-16-06939.2002 · DOI
  179. McCleskey, 1987, Omega-conotoxin: direct and persistent blockade of specific types of calcium channels in neurons but not muscle, Proc. Natl. Acad. Sci. USA, 84, 4327, 10.1073/pnas.84.12.4327 · DOI
  180. McRory, 2004, The CACNA1F gene encodes an L-type calcium channel with unique biophysical properties and tissue distribution, J. Neurosci., 24, 1707, 10.1523/JNEUROSCI.4846-03.2004 · DOI
  181. Meissner, 2011, Moderate calcium channel dysfunction in adult mice with inducible cardiomyocyte-specific excision of the cacnb2 gene, J. Biol. Chem., 286, 15875, 10.1074/jbc.M111.227819 · DOI
  182. Mezghrani, 2008, A destructive interaction mechanism accounts for dominant-negative effects of misfolded mutants of voltage-gated calcium channels, J. Neurosci., 28, 4501, 10.1523/JNEUROSCI.2844-07.2008 · DOI
  183. Mich, 2008, Alternative splicing of the Ca2+ channel beta4 subunit confers specificity for gabapentin inhibition of Cav2.1 trafficking, Mol. Pharmacol., 74, 904, 10.1124/mol.108.045153 · DOI
  184. Mikami, 1989, Primary structure and functional expression of the cardiac dihydropyridine-sensitive calcium channel, Nature, 340, 230, 10.1038/340230a0 · DOI
  185. Minor, 2010, Progress in the structural understanding of voltage-gated calcium channel (CaV) function and modulation, Channels (Austin), 4, 459, 10.4161/chan.4.6.12867 · DOI
  186. Molineux, 2006, Specific T-type calcium channel isoforms are associated with distinct burst phenotypes in deep cerebellar nuclear neurons, Proc. Natl. Acad. Sci. USA, 103, 5555, 10.1073/pnas.0601261103 · DOI
  187. Moosmang, 2005, Role of hippocampal Cav1.2 Ca2+ channels in NMDA receptor-independent synaptic plasticity and spatial memory, J. Neurosci., 25, 9883, 10.1523/JNEUROSCI.1531-05.2005 · DOI · Paper page
  188. Morgans, 2000, Neurotransmitter release at ribbon synapses in the retina, Immunol. Cell Biol., 78, 442, 10.1046/j.1440-1711.2000.00923.x · DOI
  189. Mori, 2002, Ca(2+) channel alpha(1B) subunit (Ca(V) 2.2) knockout mouse reveals a predominant role of N-type channels in the sympathetic regulation of the circulatory system, Trends Cardiovasc. Med., 12, 270, 10.1016/S1050-1738(02)00173-1 · DOI
  190. Mori, 2008, Crystal structure of the CaV2 IQ domain in complex with Ca2+/calmodulin: high-resolution mechanistic implications for channel regulation by Ca2+, Structure, 16, 607, 10.1016/j.str.2008.01.011 · DOI
  191. Morrill, 1999, Effects of mutations causing hypokalaemic periodic paralysis on the skeletal muscle L-type Ca2+ channel expressed in Xenopus laevis oocytes, J. Physiol., 520, 321, 10.1111/j.1469-7793.1999.00321.x · DOI
  192. Morrill, 1998, Gating of the L-type Ca channel in human skeletal myotubes: an activation defect caused by the hypokalemic periodic paralysis mutation R528H, J. Neurosci., 18, 10320, 10.1523/JNEUROSCI.18-24-10320.1998 · DOI
  193. Müller, 2010, Quantitative proteomics of the Cav2 channel nano-environments in the mammalian brain, Proc. Natl. Acad. Sci. USA, 107, 14950, 10.1073/pnas.1005940107 · DOI
  194. Murphy, 1991, L-type voltage-sensitive calcium channels mediate synaptic activation of immediate early genes, Neuron, 7, 625, 10.1016/0896-6273(91)90375-A · DOI
  195. Namkung, 1998, Targeted disruption of the Ca2+ channel beta3 subunit reduces N- and L-type Ca2+ channel activity and alters the voltage-dependent activation of P/Q-type Ca2+ channels in neurons, Proc. Natl. Acad. Sci. USA, 95, 12010, 10.1073/pnas.95.20.12010 · DOI
  196. Newcomb, 1998, Selective peptide antagonist of the class E calcium channel from the venom of the tarantula Hysterocrates gigas, Biochemistry, 37, 15353, 10.1021/bi981255g · DOI · Paper page
  197. Newton, 2004, Deletion of N-type calcium channels alters ethanol reward and reduces ethanol consumption in mice, J. Neurosci., 24, 9862, 10.1523/JNEUROSCI.3446-04.2004 · DOI
  198. Nowycky, 1985, Three types of neuronal calcium channel with different calcium agonist sensitivity, Nature, 316, 440, 10.1038/316440a0 · DOI
  199. Obeid, 1996, Thyroxine exacerbates absence seizures in juvenile myoclonic epilepsy, Neurology, 47, 605, 10.1212/WNL.47.2.605-a · DOI
  200. Ohkubo, 2005, Identification and electrophysiological characteristics of isoforms of T-type calcium channel Ca(v)3.2 expressed in pregnant human uterus, Cell. Physiol. Biochem., 16, 245, 10.1159/000089850 · DOI

200 of 324 shown

Cited by

See all 675

Metadata

Authors
Simms, B. A., & Zamponi, G. W.
Venue
Neuron
Publisher
Elsevier BV
Published
2014-04
Volume
82
Issue
1
Pages
24-45
ISSN
0896-6273 (ISSN-L)
OpenAlex
W1977584840
Cited by
675
References
13
FWCI
20.93
Type
journal article
Language
en
Open access
bronze
Licence

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: Neuronal Voltage-Gated Calcium Channels: Structure, Function, and Dysfunction. https://app.cochat.ai/papers/10.1016/j.neuron.2014.03.016
The paper
Simms, B. A., & Zamponi, G. W. (2014). Neuronal Voltage-Gated Calcium Channels: Structure, Function, and Dysfunction. Neuron. https://doi.org/10.1016/j.neuron.2014.03.016

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.