Abstract
Adrenal chromaffin cells (CCs) are the main source of circulating catecholamines (CAs) that regulate the body response to stress. Release of CAs is controlled neurogenically by the activity of preganglionic sympathetic neurons through trains of action potentials (APs). APs in CCs are generated by robust depolarization following the activation of nicotinic and muscarinic receptors that are highly expressed in CCs. Bovine, rat, mouse, and human CCs also express a composite array of Na+, K+, and Ca2+ channels that regulate the resting potential, shape the APs, and set the frequency of AP trains. AP trains of increasing frequency induce enhanced release of CAs. If the primary role of CCs is simply to relay preganglionic nerve commands to CA secretion, why should they express such a diverse set of ion channels? An answer to this comes from recent observations that, like in neurons, CCs undergo complex firing patterns of APs suggesting the existence of an intrinsic CC excitability (non-neurogenically controlled). Recent work has shown that CCs undergo occasional or persistent burst firing elicited by altered physiological conditions or deletion of pore-regulating auxiliary subunits. In this review, we aim to give a rationale to the role of the many ion channel types regulating CC excitability. We will first describe their functional properties and then analyze how they contribute to pacemaking, AP shape, and burst waveforms. We will also furnish clear indications on missing ion conductances that may be involved in pacemaking and highlight the contribution of the crucial channels involved in burst firing.



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References
Albillos A, Artalejo AR, Lopez MG, Gandia L, Garcia AG, Carbone E (1994) Calcium channel subtypes in cat chromaffin cells. J Physiol 477:197–213
Albillos A, Carbone E, Gandia L, Garcia AG, Pollo A (1996) Opioid inhibition of Ca2+ channel subtypes in bovine chromaffin cells: selectivity of action and voltage dependence. Eur J Neurosci 8:1561–1570
Albillos A, Gandia L, Michelena P, Gilabert JA, del Valle M, Carbone E, Garcia AG (1996) The mechanism of calcium channel facilitation in bovine chromaffin cells. J Physiol 494:687–695
Albillos A, Neher E, Moser T (2000) R-type Ca2+ channels are coupled to the rapid component of secretion in mouse adrenal slice chromaffin cells. J Neurosci 20:8323–8330
Albinana E, Segura-Chama P, Baraibar AM, Hernandez-Cruz A, Hernandez-Guijo JM (2015) Different contributions of calcium channel subtypes to electrical excitability of chromaffin cells in rat adrenal slices. J Neurochem 133:511–521
Alvarez YD, Belingheri AV, Perez Bay AE, Javis SE, Tedford HW, Zamponi G, Marengo FD (2013) The immediately releasable pool of mouse chromaffin cell vesicles is coupled to P/Q-type calcium channels via the synaptic protein interaction site. PLoS One 8:e54846
Alvarez YD, Ibanez LI, Uchitel OD, Marengo FD (2008) P/Q Ca2+ channels are functionally coupled to exocytosis of the immediately releasable pool in mouse chromaffin cells. Cell Calcium 43:155–164
Artalejo AR, Garcia AG, Neher E (1993) Small-conductance Ca2+-activated K+ channels in bovine chromaffin cells. Pflügers Arch Eur J Physiol 423:97–103
Artalejo CR, Adams ME, Fox AP (1994) Three types of Ca2+ channel trigger secretion with different efficacies in chromaffin cells. Nature 367:72–76
Artalejo CR, Dahmer MK, Perlman RL, Fox AP (1991) Two types of Ca2+ currents are found in bovine chromaffin cells: facilitation is due to the recruitment of one type. J Physiol 432:681–707
Artalejo CR, Garcia AG, Aunis D (1987) Chromaffin cell calcium channel kinetics measured isotopically through fast calcium, strontium, and barium fluxes. J Biol Chem 262:915–926
Artalejo CR, Mogul DJ, Perlman RL, Fox AP (1991) Three types of bovine chromaffin cell Ca2+ channels: facilitation increases the opening probability of a 27 pS channel. J Physiol 444:213–240
Artalejo CR, Perlman RL, Fox AP (1992) Omega-conotoxin GVIA blocks a Ca2+ current in bovine chromaffin cells that is not of the “classic” N type. Neuron 8:85–95
Barbara JG, Poncer JC, McKinney RA, Takeda K (1998) An adrenal slice preparation for the study of chromaffin cells and their cholinergic innervation. J Neurosci Methods 80:181–189
Bean BP, Nowycky MC, Tsien RW (1984) β-adrenergic modulation of calcium channels in frog ventricular heart cells. Nature 307:371–375
Biales B, Dichter M, Tischler A (1976) Electrical excitability of cultured adrenal chromaffin cells. J Physiol 262:743–753
Bond CT, Maylie J, Adelman JP (2005) SK channels in excitability, pacemaking and synaptic integration. Curr Opin Neurobiol 15:305–311
Bournaud R, Hidalgo J, Yu H, Jaimovich E, Shimahara T (2001) Low threshold T-type calcium current in rat embryonic chromaffin cells. J Physiol 537:35–44
Brandt BL, Hagiwara S, Kidokoro Y, Miyazaki S (1976) Action potentials in the rat chromaffin cell and effects of acetylcholine. J Physiol 263:417–439
Brown DA (2013) The other (muscarinic) acetylcholine receptors in sympathetic ganglia: actions and mechanisms. Neurophysiology 45:60–66
Carabelli V, Carra I, Carbone E (1998) Localized secretion of ATP and opioids revealed through single Ca2+ channel modulation in bovine chromaffin cells. Neuron 20:1255–1268
Carabelli V, Giancippoli A, Baldelli P, Carbone E, Artalejo AR (2003) Distinct potentiation of L-type currents and secretion by cAMP in rat chromaffin cells. Biophys J 85:1326–1337
Carabelli V, Hernandez-Guijo JM, Baldelli P, Carbone E (2001) Direct autocrine inhibition and cAMP-dependent potentiation of single L-type Ca2+ channels in bovine chromaffin cells. J Physiol 532:73–90
Carabelli V, Marcantoni A, Comunanza V, Carbone E (2007) Fast exocytosis mediated by T- and L-type channels in chromaffin cells: distinct voltage-dependence but similar Ca2+-dependence. Eur Biophys J 36:753–762
Carabelli V, Marcantoni A, Comunanza V, de Luca A, Diaz J, Borges R, Carbone E (2007) Chronic hypoxia up-regulates α1H T-type channels and low-threshold catecholamine secretion in rat chromaffin cells. J Physiol 584:149–165
Carbone E, Calorio C, Vandael DH (2014) T-type channel-mediated neurotransmitter release. Pflügers Arch Eur J Physiol 466:677–687
Carbone E, Carabelli V (2009) O2 sensing in chromaffin cells: new duties for T-type channels. J Physiol 587:1859–1860
Cesetti T, Hernandez-Guijo JM, Baldelli P, Carabelli V, Carbone E (2003) Opposite action of β1- and β2-adrenergic receptors on Cav1 L-channel current in rat adrenal chromaffin cells. J Neurosci 23:73–83
Chan SA, Hill J, Smith C (2012) Reduced calcium current density in female versus male mouse adrenal chromaffin cells in situ. Cell Calcium 52:313–320
Chan SA, Polo-Parada L, Smith C (2005) Action potential stimulation reveals an increased role for P/Q-calcium channel-dependent exocytosis in mouse adrenal tissue slices. Arch Biochem Biophys 435:65–73
Chatterjee O, Taylor LA, Ahmed S, Nagaraj S, Hall JJ, Finckbeiner SM, Chan PS, Suda N, King JT, Zeeman ML, McCobb DP (2009) Social stress alters expression of large conductance calcium-activated potassium channel subunits in mouse adrenal medulla and pituitary glands. J Neuroendocrinol 21:167–176
Comunanza V, Marcantoni A, Vandael DH, Mahapatra S, Gavello D, Carabelli V, Carbone E (2010) Cav1.3 as pacemaker channels in adrenal chromaffin cells: specific role on exo- and endocytosis? Channels 4:440–446
Coupland RE (1965) Electronic microscopic observations on the structure of the rat adrenal medulla. I. The ultrastructure and organization of chromaffin cells in normal adrenal medulla. J Anat 99:231–254
Cummins TR, Aglieco F, Renganathan M, Herzog RI, Dib-Hajj SD, Waxman SG (2001) Nav1.3 sodium channels: rapid repriming and slow closed-state inactivation display quantitative differences after expression in a mammalian cell line and in spinal sensory neurons. J Neurosci 21:5952–5961
Currie KP, Fox AP (1996) ATP serves as a negative feedback inhibitor of voltage-gated Ca2+ channel currents in cultured bovine adrenal chromaffin cells. Neuron 16:1027–1036
Currie KP, Fox AP (2002) Differential facilitation of N- and P/Q-type calcium channels during trains of action potential-like waveforms. J Physiol 539:419–431
Currie KP, Fox AP (2000) Voltage-dependent, pertussis toxin insensitive inhibition of calcium currents by histamine in bovine adrenal chromaffin cells. J Neurophysiol 83:1435–1442
de Diego AM, Gandia L, Garcia AG (2008) A physiological view of the central and peripheral mechanisms that regulate the release of catecholamines at the adrenal medulla. Acta Physiol 192:287–301
Delmas P, Brown DA (2005) Pathways modulating neural KCNQ/M (Kv7) potassium channels. Nat Rev Neurosci 6:850–862
Ding JP, Li ZW, Lingle CJ (1998) Inactivating BK channels in rat chromaffin cells may arise from heteromultimeric assembly of distinct inactivation-competent and noninactivating subunits. Biophys J 74:268–289
Dorval AD (2006) The rhythmic consequences of ion channel stochasticity. Neuroscientist 12:442–448
Duan K, Yu X, Zhang C, Zhou Z (2003) Control of secretion by temporal patterns of action potentials in adrenal chromaffin cells. J Neurosci 23:11235–11243
Engisch KL, Nowycky MC (1996) Calcium dependence of large dense-cored vesicle exocytosis evoked by calcium influx in bovine adrenal chromaffin cells. J Neurosci 16:1359–1369
Faber ES (2009) Functions and modulation of neuronal SK channels. Cell Biochem Biophys 55:127–139
Faber ES, Sah P (2007) Functions of SK channels in central neurons. Clin Exp Pharmacol Physiol 34:1077–1083
Fakler B, Adelman JP (2008) Control of K-Ca channels by calcium nano/microdomains. Neuron 59:873–881
Fenwick EM, Marty A, Neher E (1982) A patch-clamp study of bovine chromaffin cells and of their sensitivity to acetylcholine. J Physiol 331:577–597
Fenwick EM, Marty A, Neher E (1982) Sodium and calcium channels in bovine chromaffin cells. J Physiol 331:599–635
Gandia L, Garcia AG, Morad M (1993) ATP modulation of calcium channels in chromaffin cells. J Physiol 470:55–72
Gandia L, Mayorgas I, Michelena P, Cuchillo I, de Pascual R, Abad F, Novalbos JM, Larranaga E, Garcia AG (1998) Human adrenal chromaffin cell calcium channels: drastic current facilitation in cell clusters, but not in isolated cells. Pflügers Arch Eur J Physiol 436:696–704
Garcia AG, Garcia-De-Diego AM, Gandia L, Borges R, Garcia-Sancho J (2006) Calcium signaling and exocytosis in adrenal chromaffin cells. Physiol Rev 86:1093–1131
Gavello D, Rojo-Ruiz J, Marcantoni A, Franchino C, Carbone E, Carabelli V (2012) Leptin Counteracts the hypoxia-induced inhibition of spontaneously firing hippocampal neurons: a microelectrode array study. Plos One 7:e41530
Gavello D, Vandael D, Gosso S, Carbone E, Carabelli V (2015) Dual action of leptin on rest-firing and stimulated catecholamine release via phosphoinositide 3-kinase-driven BK channel up-regulation in mouse chromaffin cells. J Physiol 593:4835–4853
Giancippoli A, Novara M, de Luca A, Baldelli P, Marcantoni A, Carbone E, Carabelli V (2006) Low-threshold exocytosis induced by cAMP-recruited Cav3.2 (α1H) channels in rat chromaffin cells. Biophys J 90:1830–1841
Goldfarb M (2005) Fibroblast growth factor homologous factors: evolution, structure, and function. Cytokine Growth Factor Rev 16:215–220
Guarina L, Vandael DH, Carabelli V, Carbone E (2017) Low pHo boosts burst firing and catecholamine release by blocking TASK-1 and BK channels while preserving Cav1 channels in mouse chromaffin cells. J Physiol 595:2587–2609
Guerineau NC, Desarmenien MG, Carabelli V, Carbone E (2012) Functional chromaffin cell plasticity in response to stress: focus on nicotinic, gap junction, and voltage-gated Ca2+ channels. J Mol Neurosci 48:368–386
Gullo F, Ales E, Rosati B, Lecchi M, Masi A, Guasti L, Cano-Abad MF, Arcangeli A, Lopez MG, Wanke E (2002) ERG K+ channel blockade enhances firing and epinephrine secretion in rat chromaffin cells: the missing link to LQT2-related sudden death? FASEB J 17:330–332
Guo X, Przywara DA, Wakade TD, Wakade AR (1996) Exocytosis coupled to mobilization of intracellular calcium by muscarine and caffeine in rat chromaffin cells. J Neurochem 67:155–162
Harada K, Matsuoka H, Miyata H, Matsui M, Inoue M (2015) Identification of muscarinic receptor subtypes involved in catecholamine secretion in adrenal medullary chromaffin cells by genetic deletion. Br J Pharmacol 172:1348–1359
Hernandez-Guijo JM, Carabelli V, Gandia L, Garcia AG, Carbone E (1999) Voltage-independent autocrine modulation of L-type channels mediated by ATP, opioids and catecholamines in rat chromaffin cells. Eur J Neurosci 11:3574–3584
Hernandez-Guijo JM, Gandia L, Lara B, Garcia AG (1998) Autocrine/paracrine modulation of calcium channels in bovine chromaffin cells. Pflügers Arch Eur J Physiol 437:104–113
Hernandez A, Segura-Chama P, Albinana E, Hernandez-Cruz A, Hernandez-Guijo JM (2010) Down-modulation of Ca2+ channels by endogenously released ATP and opioids: from the isolated chromaffin cell to the slice of adrenal medullae. Cell Mol Neurobiol 30:1209–1216
Herrington J, Solaro CR, Neely A, Lingle CJ (1995) The suppression of Ca2+- and voltage-dependent outward K+ current during mAChR activation in rat adrenal chromaffin cells. J Physiol 485:297–318
Herzog RI, Cummins TR, Ghassemi F, Dib-Hajj SD, Waxman SG (2003) Distinct repriming and closed-state inactivation kinetics of Nav1.6 and Nav1.7 sodium channels in mouse spinal sensory neurons. J Physiol 551:741–750
Hill J, Chan SA, Kuri B, Smith C (2011) Pituitary adenylate cyclase-activating peptide (PACAP) recruits low voltage-activated T-type calcium influx under acute sympathetic stimulation in mouse adrenal chromaffin cells. J Biol Chem 286:42459–42469
Ho C, Zhao J, Malinowski S, Chahine M, O’Leary ME (2012) Differential expression of sodium channel β subunits in dorsal root ganglion sensory neurons. J Biol Chem 287:15044–15053
Hoshi T, Rothlein J, Smith SJ (1984) Facilitation of Ca2+-channel currents in bovine adrenal chromaffin cells. Proc Natl Acad Sci U S A 81:5871–5875
Inoue M, Harada K, Matsuoka H, Sata T, Warashina A (2008) Inhibition of TASK1-like channels by muscarinic receptor stimulation in rat adrenal medullary cells. J Neurochem 106:1804–1814
Inoue M, Kuriyama H (1990) Muscarine induces two distinct current responses in adrenal chromaffin cells of the guinea-pig. Jpn J Physiol 40:679–691
Inoue M, Kuriyama H (1991) Muscarinic receptor is coupled with a cation channel through a GTP-binding protein in guinea-pig chromaffin cells. J Physiol 436:511–529
Kajiwara R, Sand O, Kidokoro Y, Barish ME, Iijima T (1997) Functional organization of chromaffin cells and cholinergic synaptic transmission in rat adrenal medulla. Jpn J Physiol 47:449–464
Kim SJ, Lim W, Kim J (1995) Contribution of L- and N-type calcium currents to exocytosis in rat adrenal medullary chromaffin cells. Brain Res 675:289–296
Klingauf J, Neher E (1997) Modeling buffered Ca2+ diffusion near the membrane: implications for secretion in neuroendocrine cells. Biophys J 72:674–690
Klugbauer N, Lacinova L, Flockerzi V, Hofmann F (1995) Structure and functional expression of a new member of the tetrodotoxin-sensitive voltage-activated sodium channel family from human neuroendocrine cells. EMBO J 14:1084–1090
Levitsky KL, Lopez-Barneo J (2009) Developmental change of T-type Ca2+ channel expression and its role in rat chromaffin cell responsiveness to acute hypoxia. J Physiol 587:1917–1929
Lingle CJ, Solaro CR, Prakriya M, Ding JP (1996) Calcium-activated potassium channels in adrenal chromaffin cells. Ion Channels 4:261–301
Liu C, Dib-Hajj SD, Waxman SG (2001) Fibroblast growth factor homologous factor 1B binds to the C terminus of the tetrodotoxin-resistant sodium channel rNav1.9a (NaN). J Biol Chem 276:18925–18933
Lopez MG, Albillos A, de la Fuente MT, Borges R, Gandia L, Carbone E, Garcia AG, Artalejo AR (1994) Localized L-type calcium channels control exocytosis in cat chromaffin cells. Pflügers Arch Eur J Physiol 427:348–354
Lopez MG, Villarroya M, Lara B, Martinez Sierra R, Albillos A, Garcia AG, Gandia L (1994) Q- and L-type Ca2+ channels dominate the control of secretion in bovine chromaffin cells. FEBS Lett 349:331–337
Lou XL, Yu X, Chen XK, Duan KL, He LM, Qu AL, Xu T, Zhou Z (2003) Na+ channel inactivation: a comparative study between pancreatic islet beta-cells and adrenal chromaffin cells in rat. J Physiol 548:191–202
Lovell PV, James DG, McCobb DP (2000) Bovine versus rat adrenal chromaffin cells: big differences in BK potassium channel properties. J Neurophysiol 83:3277–3286
Lovell PV, King JT, McCobb DP (2004) Acute modulation of adrenal chromaffin cell BK channel gating and cell excitability by glucocorticoids. J Neurophysiol 91:561–570
Lovell PV, McCobb DP (2001) Pituitary control of BK potassium channel function and intrinsic firing properties of adrenal chromaffin cells. J Neurosci 21:3429–3442
Lukyanetz EA, Neher E (1999) Different types of calcium channels and secretion from bovine chromaffin cells. Eur J Neurosci 11:2865–2873
Mahapatra S, Calorio C, Vandael DHF, Marcantoni A, Carabelli V, Carbone E (2012) Calcium channel types contributing to chromaffin cell excitability, exocytosis and endocytosis. Cell Calcium 51:321–330
Mahapatra S, Marcantoni A, Vandael DH, Striessnig J, Carbone E (2011) Are Cav1.3 pacemaker channels in chromaffin cells? Possible bias from resting cell conditions and DHP blockers usage. Channels 5:219–224
Mahapatra S, Marcantoni A, Zuccotti A, Carabelli V, Carbone E (2012) Equal sensitivity of Cav1.2 and Cav1.3 channels to the opposing modulations of PKA and PKG in mouse chromaffin cells. J Physiol 590:5053–5073
Maljevic S, Wuttke TV, Lerche H (2008) Nervous system Kv7 disorders: breakdown of a subthreshold brake. J Physiol 586:1791–1801
Marcantoni A, Baldelli P, Hernandez-Guijo JM, Comunanza V, Carabelli V, Carbone E (2007) L-type calcium channels in adrenal chromaffin cells: role in pace-making and secretion. Cell Calcium 42:397–408
Marcantoni A, Carabelli V, Comunanza V, Hoddah H, Carbone E (2008) Calcium channels in chromaffin cells: focus on L and T types. Acta Physiol 192:233–246
Marcantoni A, Vandael DHF, Mahapatra S, Carabelli V, Sinnegger-Brauns MJ, Striessnig J, Carbone E (2010) Loss of Cav1.3 channels reveals the critical role of L-type and BK channel coupling in pacemaking mouse adrenal chromaffin cells. J Neurosci 30:491–504
Marrion NV, Tavalin SJ (1998) Selective activation of Ca2+-activated K+ channels by co-localized Ca2+ channels in hippocampal neurons. Nature 395:900–905
Martinez-Espinosa PL, Yang C, Gonzalez-Perez V, Xia XM, Lingle CJ (2014) Knockout of the BK β2 subunit abolishes inactivation of BK currents in mouse adrenal chromaffin cells and results in slow-wave burst activity. J Gen Physiol 144:275–295
Marty A (1981) Ca-dependent K channels with large unitary conductance in chromaffin cell membranes. Nature 291:497–500
Marty A, Neher E (1985) Potassium channels in cultured bovine adrenal chromaffin cells. J Physiol 367:117–141
Neely A, Lingle CJ (1992) Effects of muscarine on single rat adrenal chromaffin cells. J Physiol 453:133–166
Neely A, Lingle CJ (1992) Two components of calcium-activated potassium current in rat adrenal chromaffin cells. J Physiol 453:97–131
Novara M, Baldelli P, Cavallari D, Carabelli V, Giancippoli A, Carbone E (2004) Exposure to cAMP and beta-adrenergic stimulation recruits Cav3 T-type channels in rat chromaffin cells through Epac cAMP-receptor proteins. J Physiol 558:433–449
O’Farrell M, Marley PD (1999) Different contributions of voltage-sensitive Ca2+ channels to histamine-induced catecholamine release and tyrosine hydroxylase activation in bovine adrenal chromaffin cells. Cell Calcium 25:209–217
Olivos L, Artalejo AR (2007) Muscarinic excitation-secretion coupling in chromaffin cells. Acta Physiol 192:213–220
Padin JF, Fernandez-Morales JC, de Diego AM, Garcia AG (2015) Calcium channel subtypes and exocytosis in chromaffin cells at early life. Curr Mol Pharmacol 8:81–86
Park YB (1994) Ion selectivity and gating of small conductance Ca2+-activated K+ channels in cultured rat adrenal chromaffin cells. J Physiol 481:555–570
Perez-Alvarez A, Hernandez-Vivanco A, Caba-Gonzalez JC, Albillos A (2011) Different roles attributed to Cav1 channel subtypes in spontaneous action potential firing and fine tuning of exocytosis in mouse chromaffin cells. J Neurochem 116:105–121
Perez-Alvarez A, Hernandez-Vivanco A, Cano-Abad M, Albillos A (2008) Pharmacological and biophysical properties of Ca2+ channels and subtype distributions in human adrenal chromaffin cells. Pflügers Arch Eur J Physiol 456:1149–1162
Platzer J, Engel J, Schrott-Fischer A, Stephan K, Bova S, Chen H, Zheng H, Striessnig J (2000) Congenital deafness and sinoatrial node dysfunction in mice lacking class D L-type Ca2+ channels. Cell 102:89–97
Prakriya M, Lingle CJ (1999) BK channel activation by brief depolarizations requires Ca2+ influx through L- and Q-type Ca2+ channels in rat chromaffin cells. J Neurophysiol 81:2267–2278
Role LW, Perlman RL (1983) Both nicotinic and muscarinic receptors mediate catecholamine secretion by isolated guinea-pig chromaffin cells. Neuroscience 10:979–985
Rosa JM, Gandia L, Garcia AG (2009) Inhibition of N and PQ calcium channels by calcium entry through L channels in chromaffin cells. Pflügers Arch Eur J Physiol 458:795–807
Rush AM, Wittmack EK, Tyrrell L, Black JA, Dib-Hajj SD, Waxman SG (2006) Differential modulation of sodium channel Nav1.6 by two members of the fibroblast growth factor homologous factor 2 subfamily. Eur J Neurosci 23:2551–2562
Scharinger A, Eckrich S, Vandael DH, Schonig K, Koschak A, Hecker D, Kaur G, Lee A, Sah A, Bartsch D, Benedetti B, Lieb A, Schick B, Singewald N, Sinnegger-Brauns MJ, Carbone E, Engel J, Striessnig J (2015) Cell-type-specific tuning of Cav1.3 Ca2+-channels by a C-terminal automodulatory domain. Front Cell Neurosci 9:18
Schmich RM, Miller MI (1997) Stochastic threshold characterization of the intensity of active channel dynamical action potential generation. J Neurophysiol 78:2616–2630
Schneidman E, Freedman B, Segev I (1998) Ion channel stochasticity may be critical in determining the reliability and precision of spike timing. Neural Comput 10:1679–1703
Scott RS, Bustillo D, Olivos-Oré LA, Cuchillo-Ibanez I, Barahona MV, Carbone E, Artalejo AR (2011) Contribution of BK channels to action potential repolarisation at minimal cytosolic Ca2+ concentration in chromaffin cells. Pflügers Arch Eur J Physiol 462:545–557
Shanley LJ, O’Malley D, Irving AJ, Ashford ML, Harvey J (2002) Leptin inhibits epileptiform-like activity in rat hippocampal neurones via PI3-kinase-driven activation of BK channels. J Physiol 545:933–944
Shukla R, Wakade AR (1991) Functional aspects of calcium channels of splanchnic neurons and chromaffin cells of the rat adrenal medulla. J Neurochem 56:753–758
Solaro CR, Lingle CJ (1992) Trypsin-sensitive, rapid inactivation of a calcium-activated potassium channel. Science 257:1694–1698
Solaro CR, Prakriya M, Ding JP, Lingle CJ (1995) Inactivating and noninactivating Ca2+- and voltage-dependent K+ current in rat adrenal chromaffin cells. J Neurosci 15:6110–6123
Sun L, Xiong Y, Zeng X, Wu Y, Pan N, Lingle CJ, Qu A, Ding J (2009) Differential regulation of action potentials by inactivating and noninactivating BK channels in rat adrenal chromaffin cells. Biophys J 97:1832–1842
Tamura R, Nemoto T, Maruta T, Onizuka S, Yanagita T, Wada A, Murakami M, Tsuneyoshi I (2014) Up-regulation of Nav1.7 sodium channels expression by tumor necrosis factor-α in cultured bovine adrenal chromaffin cells and rat dorsal root ganglion neurons. Anesth Analg 118:318–324
Thiagarajan R, Tewolde T, Li Y, Becker PL, Rich MM, Engisch KL (2003) Rab3A negatively regulates activity-dependent modulation of exocytosis in bovine adrenal chromaffin cells. J Physiol 555:439–457
Twitchell WA, Pena TL, Rane SG (1997) Ca2+-dependent K+ channels in bovine adrenal chromaffin cells are modulated by lipoxygenase metabolites of arachidonic acid. J Membr Biol 158:69–75
Twitchell WA, Rane SG (1994) Nucleotide-independent modulation of Ca2+-dependent K+ channel current by a μ-type opioid receptor. Mol Pharmacol 46:793–798
Twitchell WA, Rane SG (1993) Opioid peptide modulation of Ca2+-dependent K+ and voltage-activated Ca2+ currents in bovine adrenal chromaffin cells. Neuron 10:701–709
Van Goor F, Li YX, Stojilkovic SS (2001) Paradoxical role of large-conductance calcium-activated K+ (BK) channels in controlling action potential-driven Ca2+ entry in anterior pituitary cells. J Neurosci 21:5902–5915
Van Goor F, Zivadinovic D, Stojilkovic SS (2001) Differential expression of ionic channels in rat anterior pituitary cells. Mol Endocrinol 15:1222–1236
Vandael DH, Mahapatra S, Calorio C, Marcantoni A, Carbone E (2013) Cav1.3 and Cav1.2 channels of adrenal chromaffin cells: emerging views on cAMP/cGMP-mediated phosphorylation and role in pacemaking. Biochim Biophys Acta 1828:1608–1618
Vandael DH, Marcantoni A, Carbone E (2015) Cav1.3 channels as key regulators of neuron-like firings and catecholamine release in chromaffin cells. Curr Mol Pharmacol 8:149–161
Vandael DH, Marcantoni A, Mahapatra S, Caro A, Ruth P, Zuccotti A, Knipper M, Carbone E (2010) Cav1.3 and BK channels for timing and regulating cell firing. Mol Neurobiol 42:185–198
Vandael DH, Ottaviani MM, Legros C, Lefort C, Guerineau NC, Allio A, Carabelli V, Carbone E (2015) Reduced availability of voltage-gated sodium channels by depolarization or blockade by tetrodotoxin boosts burst firing and catecholamine release in mouse chromaffin cells. J Physiol 593:905–927
Vandael DHF, Zuccotti A, Striessnig J, Carbone E (2012) Cav1.3-driven SK Channel activation regulates pacemaking and spike frequency adaptation in mouse chromaffin cells. J Neurosci 32:16345–16359
Vijayaragavan K, O’Leary ME, Chahine M (2001) Gating properties of Nav1.7 and Nav1.8 peripheral nerve sodium channels. J Neurosci 21:7909–7918
Wada A, Wanke E, Gullo F, Schiavon E (2008) Voltage-dependent Nav1.7 sodium channels: multiple roles in adrenal chromaffin cells and peripheral nervous system. Acta Physiol 192:221–231
Wada A, Yanagita T, Yokoo H, Kobayashi H (2004) Regulation of cell surface expression of voltage-dependent Nav1.7 sodium channels: mRNA stability and posttranscriptional control in adrenal chromaffin cells. Front Biosci 9:1954–1966
Wallace DJ, Chen C, Marley PD (2002) Histamine promotes excitability in bovine adrenal chromaffin cells by inhibiting an M-current. J Physiol 540:921–939
Wallner M, Meera P, Toro L (1999) Molecular basis of fast inactivation in voltage and Ca2+-activated K+ channels: a transmembrane beta-subunit homolog. Proc Natl Acad Sci U S A 96:4137–4142
Wang Y-W, Ding JP, Xia X-M, Lingle CJ (2002) Consequences of the stoichiometry of Slo1 α and auxiliary β subunits on functional properties of BK-type Ca2+-activated K+ channels. J Neurosci 22:1550–1561
Wittmack EK, Rush AM, Craner MJ, Goldfarb M, Waxman SG, Dib-Hajj SD (2004) Fibroblast growth factor homologous factor 2B: association with Nav1.6 and selective colocalization at nodes of Ranvier of dorsal root axons. J Neurosci 24:6765–6775
Womack MD, Chevez C, Khodakhah K (2004) Calcium-activated potassium channels are selectively coupled to P/Q-type calcium channels in cerebellar Purkinje neurons. J Neurosci 24:8818–8822
Xia X-M, Ding JP, Lingle CJ (1999) Molecular basis for the inactivation of Ca2+- and voltage-dependent BK channels in adrenal chromaffin cells and rat insulinoma tumor cells. J Neurosci 19:5255–5264
Xia XM, Ding JP, Lingle CJ (2003) Inactivation of BK channels by the NH2 terminus of the β2 auxiliary subunit: an essential role of a terminal peptide segment of three hydrophobic residues. J Gen Physiol 121:125–148
Zamponi GW, Currie KP (2013) Regulation of Cav2 calcium channels by G protein coupled receptors. Biochim Biophys Acta 1828:1629–1643
Zhang Q, Chibalina MV, Bengtsson M, Groschner LN, Ramracheya R, Rorsman NJ, Leiss V, Nassar MA, Welling A, Gribble FM, Reimann F, Hofmann F, Wood JN, Ashcroft FM, Rorsman P (2014) Na+ current properties in islet α- and β-cells reflect cell-specific Scn3a and Scn9a expression. J Physiol 592:4677–4696
Zhao J, O’Leary ME, Chahine M (2011) Regulation of Nav1.6 and Nav1.8 peripheral nerve Na+ channels by auxiliary beta-subunits. J Neurophysiol 106:608–619
Zhou Z, Misler S (1995) Action potential-induced quantal secretion of catecholamines from rat adrenal chromaffin cells. J Biol Chem 270:3498–3505
Zhou Z, Neher E (1993) Calcium permeability of nicotinic acetylcholine receptor channels in bovine adrenal chromaffin cells. Pflügers Arch Eur J Physiol 425:511–517
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This article is part of the special issue on Chromaffin Cells in Pflügers Archiv – European Journal of Physiology
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Lingle, C.J., Martinez-Espinosa, P.L., Guarina, L. et al. Roles of Na+, Ca2+, and K+ channels in the generation of repetitive firing and rhythmic bursting in adrenal chromaffin cells. Pflugers Arch - Eur J Physiol 470, 39–52 (2018). https://doi.org/10.1007/s00424-017-2048-1
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DOI: https://doi.org/10.1007/s00424-017-2048-1