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1.
Neurobiol Aging ; 125: 98-108, 2023 05.
Artículo en Inglés | MEDLINE | ID: mdl-36889122

RESUMEN

Hyperphosphorylated tau in the locus coeruleus (LC) is ubiquitous in prodromal Alzheimer's disease (AD), and LC neurons degenerate as AD progresses. Hyperphosphorylated tau alters firing rates in other brain regions, but its effects on LC neurons are unknown. We assessed single unit LC activity in anesthetized wild-type (WT) and TgF344-AD rats at 6 months, which represents a prodromal stage when LC neurons are the only cells containing hyperphosphorylated tau in TgF344-AD animals, and at 15 months when amyloid-ß (Aß) and tau pathology are both abundant in the forebrain. At baseline, LC neurons from TgF344-AD rats were hypoactive at both ages compared to WT littermates but showed elevated spontaneous bursting properties. Differences in footshock-evoked LC firing depended on age, with 6-month TgF344-AD rats demonstrating aspects of hyperactivity, and 15-month transgenic rats showing hypoactivity. Early LC hyperactivity is consistent with appearance of prodromal neuropsychiatric symptoms and is followed by LC hypoactivity which contributes to cognitive impairment. These results support further investigation into disease stage-dependent noradrenergic interventions for AD.


Asunto(s)
Enfermedad de Alzheimer , Ratas , Animales , Enfermedad de Alzheimer/genética , Enfermedad de Alzheimer/patología , Locus Coeruleus/patología , Ratas Transgénicas , Péptidos beta-Amiloides , Prosencéfalo/metabolismo , Modelos Animales de Enfermedad , Proteínas tau/metabolismo
2.
Am J Physiol Regul Integr Comp Physiol ; 305(3): R187-204, 2013 Aug 01.
Artículo en Inglés | MEDLINE | ID: mdl-23697799

RESUMEN

The C1 neurons reside in the rostral and intermediate portions of the ventrolateral medulla (RVLM, IVLM). They use glutamate as a fast transmitter and synthesize catecholamines plus various neuropeptides. These neurons regulate the hypothalamic pituitary axis via direct projections to the paraventricular nucleus and regulate the autonomic nervous system via projections to sympathetic and parasympathetic preganglionic neurons. The presympathetic C1 cells, located in the RVLM, are probably organized in a roughly viscerotopic manner and most of them regulate the circulation. C1 cells are variously activated by hypoglycemia, infection or inflammation, hypoxia, nociception, and hypotension and contribute to most glucoprivic responses. C1 cells also stimulate breathing and activate brain stem noradrenergic neurons including the locus coeruleus. Based on the various effects attributed to the C1 cells, their axonal projections and what is currently known of their synaptic inputs, subsets of C1 cells appear to be differentially recruited by pain, hypoxia, infection/inflammation, hemorrhage, and hypoglycemia to produce a repertoire of stereotyped autonomic, metabolic, and neuroendocrine responses that help the organism survive physical injury and its associated cohort of acute infection, hypoxia, hypotension, and blood loss. C1 cells may also contribute to glucose and cardiovascular homeostasis in the absence of such physical stresses, and C1 cell hyperactivity may contribute to the increase in sympathetic nerve activity associated with diseases such as hypertension.


Asunto(s)
Bulbo Raquídeo/fisiología , Neuronas/fisiología , Animales , Barorreflejo/fisiología , Corticosterona/fisiología , Femenino , Glucosa/deficiencia , Humanos , Hipoxia/fisiopatología , Masculino , Bulbo Raquídeo/citología , Enfermedades del Sistema Nervioso/genética , Enfermedades del Sistema Nervioso/fisiopatología , Feniletanolamina N-Metiltransferasa/metabolismo , Reproducción/fisiología , Transducción de Señal/fisiología , Terminología como Asunto
3.
J Neurosci ; 33(7): 3164-77, 2013 Feb 13.
Artículo en Inglés | MEDLINE | ID: mdl-23407970

RESUMEN

Activation of rostral ventrolateral medullary catecholaminergic (RVLM-CA) neurons e.g., by hypoxia is thought to increase sympathetic outflow thereby raising blood pressure (BP). Here we test whether these neurons also regulate breathing and cardiovascular variables other than BP. Selective expression of ChR2-mCherry by RVLM-CA neurons was achieved by injecting Cre-dependent vector AAV2-EF1α-DIO-ChR2-mCherry unilaterally into the brainstem of dopamine-ß-hydroxylase(Cre/0) mice. Photostimulation of RVLM-CA neurons increased breathing in anesthetized and conscious mice. In conscious mice, photostimulation primarily increased breathing frequency and this effect was fully occluded by hypoxia (10% O(2)). In contrast, the effects of photostimulation were largely unaffected by hypercapnia (3 and 6% CO(2)). The associated cardiovascular effects were complex (slight bradycardia and hypotension) and, using selective autonomic blockers, could be explained by coactivation of the sympathetic and cardiovagal outflows. ChR2-positive RVLM-CA neurons expressed VGLUT2 and their projections were mapped. Their complex cardiorespiratory effects are presumably mediated by their extensive projections to supraspinal sites such as the ventrolateral medulla, the dorsal vagal complex, the dorsolateral pons, and selected hypothalamic nuclei (dorsomedial, lateral, and paraventricular nuclei). In sum, selective optogenetic activation of RVLM-CA neurons in conscious mice revealed two important novel functions of these neurons, namely breathing stimulation and cardiovagal outflow control, effects that are attenuated or absent under anesthesia and are presumably mediated by the numerous supraspinal projections of these neurons. The results also suggest that RVLM-CA neurons may underlie some of the acute respiratory response elicited by carotid body stimulation but contribute little to the central respiratory chemoreflex.


Asunto(s)
Fenómenos Fisiológicos Cardiovasculares , Catecolaminas/fisiología , Bulbo Raquídeo/fisiología , Neuronas/fisiología , Fenómenos Fisiológicos Respiratorios , Animales , Circulación Cerebrovascular/fisiología , Channelrhodopsins , Estado de Conciencia , Dependovirus/genética , Dopamina beta-Hidroxilasa/genética , Dopamina beta-Hidroxilasa/fisiología , Femenino , Vectores Genéticos , Hipercapnia/fisiopatología , Hiperoxia/fisiopatología , Inmunohistoquímica , Proteínas Luminiscentes , Masculino , Ratones , Microinyecciones , Estimulación Luminosa , Proteína Fluorescente Roja
4.
J Neurosci ; 33(4): 1486-97, 2013 Jan 23.
Artículo en Inglés | MEDLINE | ID: mdl-23345223

RESUMEN

The C1 neurons are a nodal point for blood pressure control and other autonomic responses. Here we test whether these rostral ventrolateral medullary catecholaminergic (RVLM-CA) neurons use glutamate as a transmitter in the dorsal motor nucleus of the vagus (DMV). After injecting Cre-dependent adeno-associated virus (AAV2) DIO-Ef1α-channelrhodopsin2(ChR2)-mCherry (AAV2) into the RVLM of dopamine-ß-hydroxylase Cre transgenic mice (DßH(Cre/0)), mCherry was detected exclusively in RVLM-CA neurons. Within the DMV >95% mCherry-immunoreactive(ir) axonal varicosities were tyrosine hydroxylase (TH)-ir and the same proportion were vesicular glutamate transporter 2 (VGLUT2)-ir. VGLUT2-mCherry colocalization was virtually absent when AAV2 was injected into the RVLM of DßH(Cre/0);VGLUT2(flox/flox) mice, into the caudal VLM (A1 noradrenergic neuron-rich region) of DßH(Cre/0) mice or into the raphe of ePet(Cre/0) mice. Following injection of AAV2 into RVLM of TH-Cre rats, phenylethanolamine N-methyl transferase and VGLUT2 immunoreactivities were highly colocalized in DMV within EYFP-positive or EYFP-negative axonal varicosities. Ultrastructurally, mCherry terminals from RVLM-CA neurons in DßH(Cre/0) mice made predominantly asymmetric synapses with choline acetyl-transferase-ir DMV neurons. Photostimulation of ChR2-positive axons in DßH(Cre/0) mouse brain slices produced EPSCs in 71% of tested DMV preganglionic neurons (PGNs) but no IPSCs. Photostimulation (20 Hz) activated PGNs up to 8 spikes/s (current-clamp). EPSCs were eliminated by tetrodotoxin, reinstated by 4-aminopyridine, and blocked by ionotropic glutamate receptor blockers. In conclusion, VGLUT2 is expressed by RVLM-CA (C1) neurons in rats and mice regardless of the presence of AAV2, the C1 neurons activate DMV parasympathetic PGNs monosynaptically and this connection uses glutamate as an ionotropic transmitter.


Asunto(s)
Glutamina/metabolismo , Bulbo Raquídeo/metabolismo , Neuronas/metabolismo , Transmisión Sináptica/fisiología , Animales , Potenciales Postsinápticos Excitadores/fisiología , Inmunohistoquímica , Bulbo Raquídeo/citología , Ratones , Ratones Transgénicos , Neuronas/citología , Técnicas de Placa-Clamp , Nervio Vago/citología , Nervio Vago/metabolismo , Proteína 2 de Transporte Vesicular de Glutamato/metabolismo
5.
Adv Exp Med Biol ; 758: 115-22, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-23080151

RESUMEN

The retrotrapezoid nucleus (RTN) is located in the rostral medulla oblongata close to the ventral surface and consists of a bilateral cluster of glutamatergic neurons that are non-aminergic and express homeodomain transcription factor Phox2b throughout life. These neurons respond vigorously to increases in local pCO(2) via cell-autonomous and paracrine (glial) mechanisms and receive additional chemosensory information from the carotid bodies. RTN neurons exclusively innervate the regions of the brainstem that contain the respiratory pattern generator (RPG). Lesion or inhibition of RTN neurons largely attenuates the respiratory chemoreflex of adult rats whereas their activation increases respiratory rate, inspiratory amplitude and active expiration. Phox2b mutations that cause congenital central hypoventilation syndrome in humans prevent the development of RTN neurons in mice. Selective deletion of the RTN Phox2b-VGLUT2 neurons by genetic means in mice eliminates the respiratory chemoreflex in neonates.In short, RTN Phox2b-VGLUT2 neurons are a major nodal point of the CNS network that regulates pCO(2) via breathing and these cells are probable central chemoreceptors.


Asunto(s)
Células Quimiorreceptoras/fisiología , Bulbo Raquídeo/fisiología , Respiración , Animales , Dióxido de Carbono/metabolismo , Proteínas de Homeodominio/fisiología , Humanos , Reflejo , Factores de Transcripción/fisiología , Proteína 2 de Transporte Vesicular de Glutamato/fisiología
6.
J Neurosci ; 31(6): 1981-90, 2011 Feb 09.
Artículo en Inglés | MEDLINE | ID: mdl-21307236

RESUMEN

We used optogenetics to determine the global respiratory effects produced by selectively stimulating raphe obscurus (RO) serotonergic neurons in anesthetized mice and to test whether these neurons detect changes in the partial pressure of CO(2), and hence function as central respiratory chemoreceptors. Channelrhodopsin-2 (ChR2) was selectively (∼97%) incorporated into ∼50% of RO serotonergic neurons by injecting AAV2 DIO ChR2-mCherry (adeno-associated viral vector double-floxed inverse open reading frame of ChR2-mCherry) into the RO of ePet-Cre mice. The transfected neurons heavily innervated lower brainstem and spinal cord regions involved in autonomic and somatic motor control plus breathing but eschewed sensory related regions. Pulsed laser photostimulation of ChR2-transfected serotonergic neurons increased respiratory frequency (fR) and diaphragmatic EMG (dEMG) amplitude in relation to the duration and frequency of the light pulses (half saturation, 1 ms; 5-10 Hz). dEMG amplitude and fR increased slowly (half saturation after 10-15 s) and relaxed monoexponentially (tau, 13-15 s). The breathing stimulation was reduced ∼55% by methysergide (broad spectrum serotonin antagonist) and potentiated (∼16%) at elevated levels of inspired CO(2) (8%). RO serotonergic neurons, identified by their entrainment to short light pulses (threshold, 0.1-1 ms) were silent (nine cells) or had a low and regular level of activity (2.1 ± 0.4 Hz; 11 cells) that was not synchronized with respiration. These and nine surrounding neurons with similar characteristics were unaffected by adding up to 10% CO(2) to the breathing mixture. In conclusion, RO serotonergic neurons activate breathing frequency and amplitude and potentiate the central respiratory chemoreflex but do not appear to have a central respiratory chemoreceptor function.


Asunto(s)
Neuronas Motoras/fisiología , Núcleos del Rafe/citología , Respiración , Serotonina/metabolismo , Animales , Vías Autónomas/fisiología , Biofisica , Carbocianinas/metabolismo , Carbonatos/farmacología , Channelrhodopsins , Colina O-Acetiltransferasa/metabolismo , Diafragma/efectos de los fármacos , Diafragma/fisiología , Relación Dosis-Respuesta a Droga , Estimulación Eléctrica/métodos , Electromiografía/métodos , Femenino , Hipercapnia/fisiopatología , Masculino , Metisergida/farmacología , Ratones , Estimulación Luminosa/métodos , Respiración/efectos de los fármacos , Respiración/genética , Antagonistas de la Serotonina/farmacología , Estadísticas no Paramétricas , Transfección/métodos , Triptófano Hidroxilasa/metabolismo
7.
J Physiol ; 589(Pt 4): 903-17, 2011 Feb 15.
Artículo en Inglés | MEDLINE | ID: mdl-21173073

RESUMEN

The ventrolateral pons contains the A5 group of noradrenergic neurons which regulate the circulation and probably breathing. The present experiments were designed to identify these neurons definitively in vivo, to examine their response to chemoreceptor stimuli (carotid body stimulation and changes in brain pH) and to determine their effects on sympathetic outflow. Bulbospinal A5 neurons, identified by juxtacellular labelling in anaesthetized rats, had a slow regular discharge, were vigorously activated by peripheral chemoreceptor stimulation with cyanide, but only mildly activated by hyperoxic hypercapnia (central chemoreceptor stimulation). The caudal end of the A5 region also contained neurons with properties reminiscent of retrotrapezoid neurons. These cells lacked a spinal axon and were characterized by a robust response to CO2. The pH sensitivity of A5 neurons, examined in brain slices from neonatal (postnatal days 6­10) tyrosine hydroxylase (TH)-GFP transgenic mice, was about 10 times smaller than that of similarly recorded retrotrapezoid neurons. Selective stimulation of the A5 neurons in rats using channelrhodopsin optogenetics (A5 TH neurons represented 66% of transfected cells) produced fivefold greater activation of the renal nerve than the lumbar sympathetic chain. In summary, adult A5 noradrenergic neurons are vigorously activated by carotid body stimulation. This effect presumably contributes to the increase in visceral sympathetic nerve activity elicited by acute hypoxia. A5 neurons respond weakly to hypercapnia in vivo or to changes in pH in slices suggesting that their ability to sense local variations in brain pH or Pco2 is limited.


Asunto(s)
Cuerpo Carotídeo/fisiología , Células Quimiorreceptoras/fisiología , Neuronas/fisiología , Norepinefrina/fisiología , Puente/fisiología , Fibras Simpáticas Posganglionares/fisiología , Animales , Masculino , Ratones , Ratones Transgénicos , Ratas , Ratas Sprague-Dawley , Vísceras/inervación , Vísceras/fisiología
8.
J Appl Physiol (1985) ; 108(4): 995-1002, 2010 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-20075262

RESUMEN

In this review, we examine why blood pressure (BP) and sympathetic nerve activity (SNA) increase during a rise in central nervous system (CNS) P(CO(2)) (central chemoreceptor stimulation). CNS acidification modifies SNA by two classes of mechanisms. The first one depends on the activation of the central respiratory controller (CRG) and causes the much-emphasized respiratory modulation of the SNA. The CRG probably modulates SNA at several brain stem or spinal locations, but the most important site of interaction seems to be the caudal ventrolateral medulla (CVLM), where unidentified components of the CRG periodically gate the baroreflex. CNS P(CO(2)) also influences sympathetic tone in a CRG-independent manner, and we propose that this process operates differently according to the level of CNS P(CO(2)). In normocapnia and indeed even below the ventilatory recruitment threshold, CNS P(CO(2)) exerts a tonic concentration-dependent excitatory effect on SNA that is plausibly mediated by specialized brain stem chemoreceptors such as the retrotrapezoid nucleus. Abnormally high levels of P(CO(2)) cause an aversive interoceptive awareness in awake individuals and trigger arousal from sleep. These alerting responses presumably activate wake-promoting and/or stress-related pathways such as the orexinergic, noradrenergic, and serotonergic neurons. These neuronal groups, which may also be directly activated by brain acidification, have brainwide projections that contribute to the CO(2)-induced rise in breathing and SNA by facilitating neuronal activity at innumerable CNS locations. In the case of SNA, these sites include the nucleus of the solitary tract, the ventrolateral medulla, and the preganglionic neurons.


Asunto(s)
Dióxido de Carbono/metabolismo , Sistema Nervioso Central/fisiología , Células Quimiorreceptoras/fisiología , Hemodinámica/fisiología , Receptores de Superficie Celular/fisiología , Mecánica Respiratoria/fisiología , Animales , Modelos Animales de Enfermedad , Humanos
9.
Respir Physiol Neurobiol ; 168(1-2): 59-68, 2009 Aug 31.
Artículo en Inglés | MEDLINE | ID: mdl-19712903

RESUMEN

Breathing automaticity and CO(2) regulation are inseparable neural processes. The retrotrapezoid nucleus (RTN), a group of glutamatergic neurons that express the transcription factor Phox2b, may be a crucial nodal point through which breathing automaticity is regulated to maintain CO(2) constant. This review updates the analysis presented in prior publications. Additional evidence that RTN neurons have central respiratory chemoreceptor properties is presented, but this is only one of many factors that determine their activity. The RTN is also regulated by powerful inputs from the carotid bodies and, at least in the adult, by many other synaptic inputs. We also analyze how RTN neurons may control the activity of the downstream central respiratory pattern generator. Specifically, we review the evidence which suggests that RTN neurons (a) innervate the entire ventral respiratory column and (b) control both inspiration and expiration. Finally, we argue that the RTN neurons are the adult form of the parafacial respiratory group in neonate rats.


Asunto(s)
Células Quimiorreceptoras/fisiología , Respiración , Centro Respiratorio/citología , Centro Respiratorio/fisiología , Animales , Dióxido de Carbono/metabolismo , Proteínas de Homeodominio/metabolismo , Concentración de Iones de Hidrógeno , Modelos Biológicos , Red Nerviosa , Nervio Frénico/fisiología , Factores de Transcripción/metabolismo
10.
J Comp Neurol ; 517(1): 69-86, 2009 Nov 01.
Artículo en Inglés | MEDLINE | ID: mdl-19711410

RESUMEN

The retrotrapezoid nucleus (RTN) contains noncholinergic noncatecholaminergic glutamatergic neurons that express the transcription factor Phox2b (chemically coded or "cc" RTN neurons). These cells regulate breathing and may be central chemoreceptors. Here we explore their ultrastructure and their acid sensitivity by using two novel BAC eGFP-Phox2b transgenic mice (B/G, GENSAT JX99) in which, respectively, 36% and 100% of the cc RTN neurons express the transgene in complete or partial anatomical isolation from other populations of eGFP neurons. All but one of the eGFP-labeled RTN neurons recorded in these mice were acid activated in slices. These cells contained VGLUT2 mRNA, and 50% contained preprogalanin mRNA (determined by single-cell PCR in the B/G mouse). Two neuronal subgroups were revealed, which differed in discharge rate at pH 7.3 (type I approximately 2; type II approximately 4 Hz) and the degree of alkalization that silenced the cells (type I 7.4-7.6, type II 7.8-8.0). Medial to the RTN, C1 neurons recorded in a tyrosine hydroxylase-GFP mouse were pH insensitive between pH 6.9 and pH 7.5. Ultrastructural studies demonstrated that eGFP-labeled RTN neurons were surrounded by numerous capillaries and were often in direct contact with glial cells, pericytes, and the basement membrane of capillaries. Terminals contacting large proximal eGFP dendrites formed mainly symmetric, likely inhibitory, synapses. Terminals on more distal eGFP dendrites formed preferentially asymmetric, presumably excitatory, synapses. In sum, C1 cells are pH insensitive, whereas cc RTN neurons are uniformly acid sensitive. The RTN neurons receive inhibitory and excitatory synaptic inputs and may have unfettered biochemical interactions with glial cells and the local microvasculature.


Asunto(s)
Proteínas de Homeodominio/metabolismo , Bulbo Raquídeo/fisiología , Bulbo Raquídeo/ultraestructura , Neuronas/fisiología , Neuronas/ultraestructura , Factores de Transcripción/metabolismo , Potenciales de Acción/fisiología , Animales , Membrana Basal/fisiología , Membrana Basal/ultraestructura , Tronco Encefálico/irrigación sanguínea , Tronco Encefálico/fisiología , Tronco Encefálico/ultraestructura , Cromosomas Artificiales Bacterianos , Dendritas/fisiología , Dendritas/ultraestructura , Galanina/metabolismo , Proteínas Fluorescentes Verdes/genética , Proteínas de Homeodominio/genética , Concentración de Iones de Hidrógeno , Técnicas In Vitro , Bulbo Raquídeo/irrigación sanguínea , Ratones , Ratones Transgénicos , Neuroglía/ultraestructura , Pericitos/ultraestructura , ARN Mensajero/metabolismo , Sinapsis/fisiología , Sinapsis/ultraestructura , Factores de Transcripción/genética , Tirosina 3-Monooxigenasa/genética , Tirosina 3-Monooxigenasa/metabolismo , Proteína 2 de Transporte Vesicular de Glutamato/metabolismo
11.
J Neurosci ; 29(18): 5806-19, 2009 May 06.
Artículo en Inglés | MEDLINE | ID: mdl-19420248

RESUMEN

The retrotrapezoid "nucleus" (RTN), located in the rostral ventrolateral medullary reticular formation, contains a bilateral cluster of approximately 1000 glutamatergic noncatecholaminergic Phox2b-expressing propriobulbar neurons that are activated by CO(2) in vivo and by acidification in vitro. These cells are thought to function as central respiratory chemoreceptors, but this theory still lacks a crucial piece of evidence, namely that stimulating these particular neurons selectively in vivo increases breathing. The present study performed in anesthetized rats seeks to test whether this expectation is correct. We injected into the left RTN a lentivirus that expresses the light-activated cationic channel ChR2 (channelrhodopsin-2) (H134R mutation; fused to the fluorescent protein mCherry) under the control of the Phox2-responsive promoter PRSx8. Transgene expression was restricted to 423 +/- 38 Phox2b-expressing neurons per rat consisting of noncatecholaminergic and C1 adrenergic neurons (3:2 ratio). Photostimulation delivered to the RTN region in vivo via a fiberoptic activated the CO(2)-sensitive neurons vigorously, produced a long-lasting (t(1/2) = 11 s) increase in phrenic nerve activity, and caused a small and short-lasting cardiovascular stimulation. Selective lesions of the C1 cells eliminated the cardiovascular response but left the respiratory stimulation intact. In rats with C1 cell lesions, the mCherry-labeled axon terminals originating from the transfected noncatecholaminergic neurons were present exclusively in the lower brainstem regions that contain the respiratory pattern generator. These results provide strong evidence that the Phox2b-expressing noncatecholaminergic neurons of the RTN region function as central respiratory chemoreceptors.


Asunto(s)
Proteínas de Homeodominio/metabolismo , Luz , Neuronas/metabolismo , Respiración , Centro Respiratorio/citología , Potenciales de Acción/efectos de los fármacos , Potenciales de Acción/fisiología , Análisis de Varianza , Animales , Presión Sanguínea/fisiología , Mapeo Encefálico , Dióxido de Carbono/farmacología , Colina O-Acetiltransferasa/metabolismo , Electromiografía/métodos , Lateralidad Funcional , Regulación de la Expresión Génica/genética , Proteínas Fluorescentes Verdes/biosíntesis , Proteínas Fluorescentes Verdes/genética , Proteínas de Homeodominio/genética , Masculino , Músculo Liso/efectos de los fármacos , Músculo Liso/fisiología , Mutación/fisiología , Neuronas/efectos de los fármacos , Nervio Frénico/fisiología , Ratas , Ratas Sprague-Dawley , Respiración/efectos de los fármacos , Respiración/genética , Centro Respiratorio/lesiones , Centro Respiratorio/fisiología , Rodopsina/genética , Rodopsina/metabolismo , Factores de Tiempo , Transducción Genética/métodos , Tirosina 3-Monooxigenasa/metabolismo
12.
J Biol Chem ; 284(12): 7465-73, 2009 Mar 20.
Artículo en Inglés | MEDLINE | ID: mdl-19131331

RESUMEN

Low voltage-activated (LVA), T-type, calcium channels mediate diverse biological functions and are inhibited by Gbetagamma dimers, yet the molecular events required for channel inhibition remain unknown. Here, we identify protein kinase A (PKA) as a molecular switch that allows Gbeta(2)gammax dimers to effect voltage-independent inhibition of Ca(v)3.2 channels. Inhibition requires phosphorylation of Ser(1107), a critical serine residue on the II-III loop of the channel pore protein. S1107A prevents inhibition of unitary currents by recombinant Gbeta(2)gamma(2) dimers but does not disrupt dimer binding nor change its specificity. Gbetagamma dimers released upon receptor activation also require PKA activity for their inhibitory actions. Hence, dopamine inhibition of Ca(v)3.2 whole cell current is precluded by Gbetagamma-scavenger proteins or a peptide that blocks PKA catalytic activity. Fittingly, when used alone at receptor-selective concentrations, D(1) or D(2) agonists do not elicit channel inhibition yet together synergize to inhibit Ca(v)3.2 channel currents. We propose that a dual-receptor regulatory mechanism is used by dopamine to control Ca(v)3.2 channel activity. This mechanism, for example, would be important in aldosterone producing adrenal glomerulosa cells where channel dysregulation would lead to overproduction of aldosterone and consequent cardiac, renal, and brain target organ damage.


Asunto(s)
Canales de Calcio Tipo T/metabolismo , Proteínas Quinasas Dependientes de AMP Cíclico/metabolismo , Subunidades beta de la Proteína de Unión al GTP/metabolismo , Subunidades gamma de la Proteína de Unión al GTP/metabolismo , Zona Glomerular/metabolismo , Aldosterona/biosíntesis , Aldosterona/genética , Sustitución de Aminoácidos , Canales de Calcio Tipo T/genética , Línea Celular Tumoral , Proteínas Quinasas Dependientes de AMP Cíclico/genética , Dimerización , Dopamina/genética , Dopamina/metabolismo , Agonistas de Dopamina/farmacología , Subunidades beta de la Proteína de Unión al GTP/genética , Subunidades gamma de la Proteína de Unión al GTP/genética , Humanos , Mutación Missense , Fosforilación/efectos de los fármacos , Fosforilación/genética
13.
Proc Natl Acad Sci U S A ; 103(39): 14590-5, 2006 Sep 26.
Artículo en Inglés | MEDLINE | ID: mdl-16973746

RESUMEN

Gbetagamma, a ubiquitous second messenger, relays external signals from G protein-coupled receptors to networks of intracellular effectors, including voltage-dependent calcium channels. Unlike high-voltage-activated Ca(2+) channels, the inhibition of low-voltage-activated Ca(2+) channels is subtype-dependent and mediated selectively by Gbeta(2)-containing dimers. Yet, the molecular basis for this exquisite selectivity remains unknown. Here, we used pure recombinant Gbetagamma subunits to establish that the Gbeta(2)gamma(2) dimer can selectively reconstitute the inhibition of alpha(1H) channels in isolated membrane patches. This inhibition is the result of a reduction in channel open probability that is not accompanied by a change in channel expression or an alteration in active-channel gating. By exchanging residues between the active Gbeta(2) subunit and the inactive Gbeta(1) subunit, we identified a cluster of amino acids that functionally distinguish Gbeta(2) from other Gbeta subunits. These amino acids on the beta-torus identify a region that is distinct from those regions that contact the Galpha subunit or other effectors.


Asunto(s)
Canales de Calcio Tipo T/metabolismo , Subunidades beta de la Proteína de Unión al GTP/metabolismo , Subunidades gamma de la Proteína de Unión al GTP/metabolismo , Subunidades de Proteína/metabolismo , Aminoácidos/metabolismo , Células Cultivadas , Humanos , Activación del Canal Iónico , Proteínas Recombinantes/metabolismo
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