RESUMO
During fasting, increased sympathoadrenal activity leads to epinephrine release and multiple forms of plasticity within the adrenal medulla including an increase in the strength of the preganglionic â chromaffin cell synapse and elevated levels of agouti-related peptide (AgRP), a peptidergic cotransmitter in chromaffin cells. Although these changes contribute to the sympathetic response, how fasting evokes this plasticity is not known. Here we report these effects involve activation of GPR109A (HCAR2). The endogenous agonist of this G protein-coupled receptor is ß-hydroxybutyrate, a ketone body whose levels rise during fasting. In wild-type animals, 24-hour fasting increased AgRP-ir in adrenal chromaffin cells but this effect was absent in GPR109A knockout mice. GPR109A agonists increased AgRP-ir in isolated chromaffin cells through a GPR109A- and pertussis toxin-sensitive pathway. Incubation of adrenal slices in nicotinic acid, a GPR109A agonist, mimicked the fasting-induced increase in the strength of the preganglionic â chromaffin cell synapse. Finally, reverse transcription polymerase chain reaction experiments confirmed the mouse adrenal medulla contains GPR109A messenger RNA. These results are consistent with the activation of a GPR109A signaling pathway located within the adrenal gland. Because fasting evokes epinephrine release, which stimulates lipolysis and the production of ß-hydroxybutyrate, our results indicate that chromaffin cells are components of an autonomic-adipose-hepatic feedback circuit. Coupling a change in adrenal physiology to a metabolite whose levels rise during fasting is presumably an efficient way to coordinate the homeostatic response to food deprivation.
Assuntos
Ácido 3-Hidroxibutírico , Medula Suprarrenal , Células Cromafins , Jejum , Receptores Acoplados a Proteínas G , Ácido 3-Hidroxibutírico/metabolismo , Ácido 3-Hidroxibutírico/farmacologia , Medula Suprarrenal/citologia , Medula Suprarrenal/metabolismo , Proteína Relacionada com Agouti/metabolismo , Animais , Plasticidade Celular , Células Cromafins/metabolismo , Epinefrina/metabolismo , Jejum/metabolismo , Camundongos , Receptores Acoplados a Proteínas G/agonistas , Receptores Acoplados a Proteínas G/metabolismoRESUMO
γ-Aminobutyric acid (GABA) is thought to play a paracrine role in adrenal medullary chromaffin (AMC) cells. Comparative physiological and immunocytochemical approaches were used to address the issue of how the paracrine function of GABA in AMC cells is established. GABAA receptor Cl- channel activities in AMC cells of rats and mice, where corticosterone is the major glucocorticoid, were much smaller than those in AMC cells of guinea-pigs and cattle, where cortisol is the major. The extent of enhancement of GABAA receptor α3 subunit expression in rat pheochromocytoma (PC12) cells by cortisol was larger than that by corticosterone in parallel with their glucocorticoid activities. Thus, the species difference in GABAA receptor expression may be ascribed to a difference in glucocorticoid activity between corticosterone and cortisol. GABAA receptor Cl- channel activity in mouse AMC cells was enhanced by allopregnanolone, as noted with that in guinea-pig AMC cells, and the enzymes involved in allopregnanolone production were immunohistochemically detected in the zona fasciculata in both mice and guinea pigs. The expression of glutamic acid decarboxylase 67 (GAD67), one of the GABA synthesizing enzymes, increased after birth, whereas GABAA receptors already developed at birth. Stimulation of pituitary adenylate cyclase-activating polypeptide (PACAP) receptors, but not nicotinic or muscarinic receptors, in PC12 cells, resulted in an increase in GAD67 expression in a protein-kinase A-dependent manner. The results indicate that glucocorticoid and PACAP are mainly responsible for the expressions of GABAA receptors and GAD67 involved in GABA signaling in AMC cells, respectively.
Assuntos
Medula Suprarrenal/fisiologia , Células Cromafins/fisiologia , Comunicação Parácrina/fisiologia , Ácido gama-Aminobutírico/fisiologia , Medula Suprarrenal/citologia , Animais , Bovinos , Canais de Cloreto/metabolismo , Cricetinae , Glutamato Descarboxilase/metabolismo , Cobaias , Hidrocortisona/metabolismo , Imuno-Histoquímica , Masculino , Mesocricetus , Camundongos , Camundongos Endogâmicos C57BL , Células PC12 , Pregnanolona/farmacologia , Ratos , Receptores de GABA-A/metabolismo , Receptores de Polipeptídeo Hipofisário Ativador de Adenilato Ciclase/efeitos dos fármacos , Receptores de Polipeptídeo Hipofisário Ativador de Adenilato Ciclase/metabolismoRESUMO
Pituitary adenylate cyclase-activating polypeptide (PACAP) acts on adrenal medullary (AM) cells as a neurotransmitter of the sympathetic preganglionic nerve. In guinea-pig AM cells, PACAP induces little catecholamine secretion, but enhances secretion evoked by stimulants, whereas in other animals, such as mouse, PACAP itself induces depolarization and/or catecholamine secretion. The present studies aim to explore the physiological implication of these species differences in PACAP actions, the ion channel mechanism for PACAP-induced depolarization, and the mechanism for facilitation of muscarinic receptor-mediated cation currents in mouse and guinea-pig AM cells. The perforated patch clamp technique was used to record the whole-cell current in isolated AM cells. The amplitudes of 3 nM PACAP-induced inward currents were significantly larger in mouse AM cells than guinea-pig, whereas 1 µM muscarine-induced currents were larger in guinea-pig AM cells than mouse. Exposure to PACAP consistently resulted in enhancement of muscarine-induced currents in guinea-pig AM cells and facilitation of cell membrane insertion of heteromeric TRPC1-TRPC4 channels in response to muscarine in PC12 cells. The PACAP-induced current was inhibited by 30 µM 9-phenanthrol, a specific TRPM4 channel inhibitor, and abolished by replacement of external Na+ with N-methyl D-glucamine. TRPM4-like immunoreactivity was located at the cell periphery in AM cells. The present results indicate that PACAP and muscarinic receptors are major metabotropic receptors mediating generation of depolarizing inward currents in mouse and guinea-pig AM cells, respectively. We conclude that PACAP activates TRPM4-like channels and enhance the muscarinic current through facilitating the membrane insertion of TRPC1-TRPC4 channels in AM cells.
Assuntos
Medula Suprarrenal/efeitos dos fármacos , Células Cromafins/efeitos dos fármacos , Potenciais da Membrana/efeitos dos fármacos , Polipeptídeo Hipofisário Ativador de Adenilato Ciclase/farmacologia , Receptores Muscarínicos/metabolismo , Medula Suprarrenal/citologia , Medula Suprarrenal/metabolismo , Animais , Linhagem Celular Tumoral , Células Cromafins/metabolismo , Cobaias , Células HEK293 , Humanos , Masculino , Camundongos , Muscarina/farmacologia , Técnicas de Patch-Clamp , Ratos , Canais de Cátion TRPC , Canais de Cátion TRPMRESUMO
REIC (reduced expression in immortalized cells) has been identified as a gene whose expression was reduced in immortalized cultured cells. The REIC gene is identical to Dickkopf-3 (Dkk3), which encodes a secreted glycoprotein belonging to the Dkk family. Previously, we showed that Dkk3 protein is present in the mouse adrenal medulla. However, its role in this tissue has not been elucidated. To explore it, we performed electron microscopic (EM) studies and RNA-sequencing (RNA-seq) analysis on Dkk3-null adrenal glands. EM studies showed that the number of dense core secretory vesicles were significantly reduced and empty vesicles were increased in the medulla endocrine cells. Quantitative PCR (qPCR) analysis showed relative expression levels of chromogranin A (Chga) and neuropeptide Y (Npy) were slightly but significantly reduced in the Dkk3-null adrenal glands. From the result of RNA-seq analysis as a parallel study, we selected three of the downregulated genes, uncoupled protein-1 (Ucp1), growth arrest and DNA-damage-inducible 45 gamma (Gadd45g), and Junb with regard to the estimated expression levels. In situ hybridization confirmed that these genes were regionally expressed in the adrenal gland. However, expression levels of these three genes were not consistent as revealed by qPCR. Thus, Dkk3 maintains the integrity of secreting vesicles in mouse adrenal medulla by regulating the expression of Chga and Npy.
Assuntos
Proteínas Adaptadoras de Transdução de Sinal/fisiologia , Medula Suprarrenal/fisiologia , Vesículas Secretórias/fisiologia , Proteínas Adaptadoras de Transdução de Sinal/genética , Medula Suprarrenal/citologia , Medula Suprarrenal/ultraestrutura , Animais , Cromogranina A/metabolismo , Regulação para Baixo , Feminino , Hibridização In Situ , Camundongos , Camundongos Knockout , Neuropeptídeo Y/metabolismo , RNA Mensageiro , RNA-Seq , Vesículas Secretórias/ultraestrutura , TranscriptomaRESUMO
Muscarinic receptor stimulation results in activation of nonselective cation (NSC) channels in guinea pig adrenal medullary (AM) cells. The biophysical and pharmacological properties of the NSC channel suggest the involvement of heteromeric channels of TRPC1 with TRPC4 or TRPC5. This possibility was explored in PC12 cells and guinea pig AM cells. Proximity ligation assay (PLA) revealed that when exogenously expressed in PC12 cells, TRPC1 forms a heteromeric channel with TRPC4, but not with TRPC5, in a STIM1-dependent manner. The heteromeric TRPC1-TRPC4 channel was also observed in AM cells and trafficked to the cell periphery in response to muscarine stimulation. To explore whether heteromeric channels are inserted into the cell membrane, tags were attached to the extracellular domains of TRPC1 and TRPC4. PLA products developed between the tags in cells stimulated by muscarine, but not in resting cells, indicating that muscarinic stimulation results in the membrane insertion of channels. This membrane insertion required expression of full-length STIM1. We conclude that muscarinic receptor stimulation results in the insertion of heteromeric TRPC1-TRPC4 channels into the cell membrane in PC12 cells and guinea pig AM cells.
Assuntos
Membrana Celular/metabolismo , Receptores Muscarínicos/metabolismo , Molécula 1 de Interação Estromal/metabolismo , Canais de Cátion TRPC/metabolismo , Medula Suprarrenal/citologia , Medula Suprarrenal/metabolismo , Animais , Linhagem Celular , Cobaias , Masculino , Células PC12 , Domínios Proteicos , RatosAssuntos
Medula Suprarrenal/metabolismo , Cálcio/metabolismo , Células Cromafins/metabolismo , Eletricidade , Retículo Endoplasmático/metabolismo , Potenciais de Ação , Medula Suprarrenal/citologia , Medula Suprarrenal/efeitos dos fármacos , Animais , Cafeína/farmacologia , Bovinos , Células Cultivadas , Células Cromafins/efeitos dos fármacos , Retículo Endoplasmático/efeitos dos fármacos , Receptores de Inositol 1,4,5-Trifosfato/metabolismo , Canal de Liberação de Cálcio do Receptor de Rianodina/metabolismoRESUMO
Adrenal chromaffin cells and sympathetic neurons synthesize and release catecholamines, and both cell types are derived from neural crest precursors. However, they have different developmental histories, with sympathetic neurons derived directly from neural crest precursors while adrenal chromaffin cells arise from neural crest-derived cells that express Schwann cell markers. We have sought to identify the genes, including imprinted genes, which regulate the development of the two cell types in mice. We developed a method of separating the two cell types as early as E12.5, using differences in expression of enhanced yellow fluorescent protein driven from the tyrosine hydroxylase gene, and then used RNA sequencing to confirm the characteristic molecular signatures of the two cell types. We identified genes differentially expressed by adrenal chromaffin cells and sympathetic neurons. Deletion of a gene highly expressed by adrenal chromaffin cells, NIK-related kinase, a gene on the X-chromosome, results in reduced expression of adrenaline-synthesizing enzyme, phenyl-N-methyl transferase, by adrenal chromaffin cells and changes in cell cycle dynamics. Finally, many imprinted genes are up-regulated in chromaffin cells and may play key roles in their development.
Assuntos
Medula Suprarrenal/embriologia , Medula Suprarrenal/metabolismo , Células Cromafins/metabolismo , Genes Ligados ao Cromossomo X , Impressão Genômica , Medula Suprarrenal/citologia , Animais , Proteínas de Bactérias/genética , Separação Celular , Células Cromafins/citologia , Feminino , Regulação da Expressão Gênica no Desenvolvimento , Ontologia Genética , Peptídeos e Proteínas de Sinalização Intracelular/deficiência , Peptídeos e Proteínas de Sinalização Intracelular/genética , Proteínas Luminescentes/genética , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Knockout , Camundongos Transgênicos , Células-Tronco Neurais/citologia , Células-Tronco Neurais/metabolismo , Gravidez , Proteínas Serina-Treonina Quinases/deficiência , Proteínas Serina-Treonina Quinases/genética , RNA-SeqRESUMO
The X-zone is a transient cortical region enriched in eosinophilic cells located in the cortical-medullary boundary of the mouse adrenal gland. Similar to the X-zone, the fetal zone in human adrenals is also a transient cortical compartment, comprising the majority of the human fetal adrenal gland. During adrenal development, fetal cortical cells are gradually replaced by newly formed adult cortical cells that develop into outer definitive zones. In mice, the regression of this fetal cell population is sexually dimorphic. Many mouse models with mutations associated with endocrine factors have been reported with X-zone phenotypes. Increasing findings indicate that the cell fate of this aged cell population of the adrenal cortex can be manipulated by many hormonal and nonhormonal factors. This review summarizes the current knowledge of this transient adrenocortical zone with an emphasis on genes and signaling pathways that affect X-zone cells.
Assuntos
Córtex Suprarrenal/metabolismo , Glândulas Suprarrenais/metabolismo , Medula Suprarrenal/metabolismo , Hormônio Adrenocorticotrópico/metabolismo , Córtex Suprarrenal/citologia , Córtex Suprarrenal/embriologia , Glândulas Suprarrenais/citologia , Glândulas Suprarrenais/embriologia , Medula Suprarrenal/citologia , Medula Suprarrenal/embriologia , Animais , Apoptose/genética , Desenvolvimento Fetal/genética , Regulação da Expressão Gênica no Desenvolvimento , Humanos , CamundongosRESUMO
Co-release of multiple neurotransmitters from secretory vesicles is common in neurons and neuroendocrine cells. However, whether and how the transmitters co-released from a single vesicle are differentially regulated remains unknown. In matrix-containing dense-core vesicles (DCVs) in chromaffin cells, there are two modes of catecholamine (CA) release from a single DCV: quantal and sub-quantal. By combining two microelectrodes to simultaneously record co-release of the native CA and ATP from a DCV, we report that (1) CA and ATP were co-released during a DCV fusion; (2) during kiss-and-run (KAR) fusion, the co-released CA was sub-quantal, whereas the co-released ATP was quantal; and (3) knockdown and knockout of the DCV matrix led to quantal co-release of both CA and ATP even in KAR mode. These findings strongly imply that, in contrast to sub-quantal CA release in chromaffin cells, fast synaptic transmission without transmitter-matrix binding is mediated exclusively via quantal release in neurons.
Assuntos
Trifosfato de Adenosina/metabolismo , Catecolaminas/metabolismo , Células Cromafins/metabolismo , Exocitose/fisiologia , Vesículas Secretórias/metabolismo , Transmissão Sináptica/fisiologia , Medula Suprarrenal/citologia , Animais , Cálcio/metabolismo , Sinalização do Cálcio , Células HEK293 , Humanos , Fusão de Membrana , Camundongos , Camundongos Knockout , Neurotransmissores/metabolismo , Técnicas de Patch-Clamp , Sinaptotagminas/genéticaRESUMO
The observation of two precursor groups of the early stem cells (Groups I and II) leads to the realization that a first amount of fetal stem cells (Group I) migrate from the AMG (Aortal-Mesonephric-Gonadal)-region into the aorta and its branching vessels. A second group (Group II) gains quite a new significance during human development. This group presents a specific developmental step which is found only in the human. This continuation of the early development along a different way indicates a general alteration of the stem cell biology. This changed process in the stem cell scene dominates the further development of the human stem cells. It remains unclear where this phylogenetic step first appears. By far not all advanced mammals show this second group of stem cells and their axonal migration. Essentially only primates seem to be involved in this special development.
Assuntos
Células-Tronco Embrionárias/citologia , Células-Tronco Embrionárias/ultraestrutura , Gônadas/citologia , Gônadas/embriologia , Células APUD/citologia , Córtex Suprarrenal/citologia , Córtex Suprarrenal/embriologia , Córtex Suprarrenal/fisiologia , Córtex Suprarrenal/ultraestrutura , Medula Suprarrenal/citologia , Medula Suprarrenal/embriologia , Medula Suprarrenal/fisiologia , Aorta/citologia , Aorta/embriologia , Aorta/ultraestrutura , Sistema Nervoso Autônomo/citologia , Sistema Nervoso Autônomo/embriologia , Sistema Nervoso Autônomo/fisiologia , Orientação de Axônios/fisiologia , Movimento Celular/fisiologia , Células-Tronco Embrionárias/fisiologia , Gônadas/fisiologia , Gônadas/ultraestrutura , Desenvolvimento Humano/fisiologia , Humanos , Microscopia Eletrônica , Crista Neural/citologia , Crista Neural/embriologia , Crista Neural/fisiologia , Pâncreas/citologia , Pâncreas/crescimento & desenvolvimento , Pâncreas/ultraestrutura , Paragânglios Cromafins/citologia , Paragânglios Cromafins/fisiologia , Paragânglios Cromafins/ultraestrutura , Teratoma/embriologia , Teratoma/fisiopatologiaRESUMO
Muscarinic receptor stimulation induces depolarizing inward currents and catecholamine secretion in adrenal medullary (AM) cells from various mammals. In guinea-pig AM cells muscarine and oxotremorine at concentrations ≤â¯1⯵M produce activation of nonselective cation channels with a similar potency and efficacy, whereas muscarine at higher concentrations produces not only nonselective cation channel activation, but also TASK1 channel inhibition. In rat AM cells, the muscarinic M1 receptor is involved in TASK1 channel inhibition in response to muscarinic agonists, and the efficacy of oxotremorine is half that of muscarine. These pharmacological findings might indicate that different muscarinic receptor subtypes are responsible for the regulation of nonselective cation and TASK1 channel activities. The present study aimed to determine the muscarinic receptor subtypes involved in nonselective cation channel activation in guinea-pig and mouse AM cells. The inward current evoked by 1⯵M muscarine was completely suppressed by 100⯵M quinine, whereas 30⯵M muscarine-induced inward currents were comprised of quinine-sensitive and -insensitive components. The electrophysiological and pharmacological properties of the muscarine-induced currents indicated that the quinine-sensitive and insensitive components are due to nonselective cation channel activation and TASK1 channel inhibition, respectively. Muscarine at 30⯵M failed to induce any current in AM cells treated with muscarinic toxin 7 or genetically deleted of the M1 receptor. The KD value of VU0255035 against the muscarinic receptor mediating nonselective cation channel activation was 17.5â¯nM. These results indicate that the M1 receptor mediates nonselective cation channel activation as well as TASK1 channel inhibition.
Assuntos
Medula Suprarrenal/citologia , Canais Iônicos/fisiologia , Agonistas Muscarínicos/farmacologia , Receptor Muscarínico M1/fisiologia , Animais , Cobaias , Masculino , Camundongos Endogâmicos C57BL , Camundongos Knockout , Muscarina/farmacologia , Oxotremorina/farmacologia , Quinina/farmacologiaRESUMO
Cultured bovine chromaffin cells have been tested as a successful neuroendocrine model to study the secretory process. Changes in the dynamics of the secretory vesicles and the exocytotic machinery microdomains could be studied in control and stimulated conditions using appropriate molecular tools such as fluorescent SNARE protein expression or fluorochrome vesicular labeling in these neuroendocrine cells. Since most of these changes occur in or near the plasma membrane, the use of the total internal reflection fluorescent microscopy (TIRFM) and the implement of particle motion analysis could be essential tools to study the structural and dynamic changes of secretory machinery related with its function in this exocytotic cell model.
Assuntos
Células Cromafins/metabolismo , Vesículas Secretórias/metabolismo , Proteína 25 Associada a Sinaptossoma/metabolismo , Medula Suprarrenal/citologia , Animais , Bovinos , Exocitose , Corantes Fluorescentes/química , Fusão de Membrana , Microscopia de Fluorescência/instrumentação , Microscopia de Fluorescência/métodos , Cultura Primária de Células/instrumentação , Cultura Primária de Células/métodos , Proteínas Recombinantes/química , Proteínas Recombinantes/isolamento & purificação , Proteínas Recombinantes/metabolismo , Vesículas Secretórias/química , Proteína 25 Associada a Sinaptossoma/química , Proteína 25 Associada a Sinaptossoma/isolamento & purificaçãoRESUMO
In the present study, the relevance of EphB2 and EphB3 tyrosine kinase receptors for the maturation of medullary thymic epithelial cells (TECs) is analyzed. The absence of both molecules, but particularly that of EphB2, courses with altered maturation of medullary Cld3,4hiSSEA1+ epithelial progenitor cells, mature medulla epithelial cells, defined by the expression of specific cell markers, including UEA1, MHCII, CD40, CD80, and AIRE, and reduced expansion of medullary islets. In vivo assays demonstrate that these changes are a consequence of the absence of EphBs in both TECs and thymocytes. On the other hand, the changes, that remains in the adult thymus, correlated well with reduced proportions of E15.5 Vγ5+RANKL+ cells in EphB-deficient thymi that could result in decreased stimulation of RANK+ medullary TECs to mature, a fact that was confirmed by recovering of proportions of both CD40hiCD80+ and MHCIIhiUEA1+ mature medullary TECs of mutant E14.5 alymphoid thymic lobes by agonist anti-RANK antibody treatment. Accordingly, the effects of EphB deficiency on medullary TECs maturation are recovered by RANK stimulation.
Assuntos
Medula Suprarrenal/citologia , Células Epiteliais/imunologia , Receptor Ativador de Fator Nuclear kappa-B/metabolismo , Receptor EphB2/genética , Receptor EphB3/genética , Transdução de Sinais , Medula Suprarrenal/imunologia , Animais , Diferenciação Celular , Feminino , Camundongos , Receptor EphB2/imunologia , Receptor EphB3/imunologia , Timócitos/imunologiaRESUMO
Chromaffin cells of adrenal medulla have traditionally been considered as modified sympathetic neurons. However, the results of recent studies indicate the need to revise this concept. The article reviews recent findings in origin and ontogeny of adrenal chromaffin cells and transcriptional and posttranscriptional regulation of developmental processes. The article summarizes data on transcriptional control of chromaffin cells proliferation and maturation and participation of microRNA in regulation of chromaffin and sympathetic neuronal phenotype gene expression.
Assuntos
Medula Suprarrenal/metabolismo , Células Cromafins/metabolismo , Epigênese Genética , Regulação da Expressão Gênica no Desenvolvimento , Medula Suprarrenal/citologia , Medula Suprarrenal/crescimento & desenvolvimento , Animais , Fatores de Transcrição Hélice-Alça-Hélice Básicos/genética , Fatores de Transcrição Hélice-Alça-Hélice Básicos/metabolismo , Diferenciação Celular , Proliferação de Células , Células Cromafins/citologia , Proteínas de Homeodomínio/genética , Proteínas de Homeodomínio/metabolismo , Humanos , MicroRNAs/genética , MicroRNAs/metabolismo , Neurônios/citologia , Neurônios/metabolismo , Proteínas Repressoras/genética , Proteínas Repressoras/metabolismo , Fatores de Transcrição/genética , Fatores de Transcrição/metabolismo , Transcrição GênicaRESUMO
OBJECTIVE: Prior to maturation of the human sympathetic nervous system, the neonatal adrenal medulla senses and responds to hypoxia. In addition to catecholamine release, the adrenal medulla synthesizes and stores opioid peptides, notably enkephalin (ENK). However, it is not known whether acute hypoxia evokes adrenal ENK production and release, as seen in the central nervous system (CNS). We hypothesize that acute hypoxia stimulates synthesis and release of ENK in chromaffin cells. STUDY DESIGN: Cultures of adrenergic mouse pheochromocytoma cells (MPC) 10/9/96CR were incubated in 10% oxygen (O2) at intervals of up to 60 minutes. ENK content and release were measured by Met-ENK enzyme-linked immunosorbent assay (ELISA). ENK messenger ribonucleic acid (mRNA) was analyzed by quantitative reverse-transcriptase polymerase chain reaction (PCR). RESULTS: Incubation of MPC 10/9 cells in 10% O2 evoked rapid release of epinephrine and of Met-ENK which increased approximately twofold in 15 minutes. Reduced [O2] also induced an overall increase (14%) in cellular ENK peptide content within 60 minutes. Acute hypoxia-stimulated release of Met-ENK was accompanied by increased mRNAENK expression in MPC 10/9s, a cell culture model of adrenergic chromaffin cells. CONCLUSION: We speculate that the ability of reduced [O2] to evoke ENK release from chromaffin cells may influence blood pressure regulation and heart contractility, thereby providing an adaptive survival advantage during neonatal asphyxia.
Assuntos
Medula Suprarrenal/metabolismo , Células Cromafins/metabolismo , Encefalinas/metabolismo , Hipóxia/metabolismo , Medula Suprarrenal/citologia , Animais , Pressão Sanguínea , Linhagem Celular , Encefalina Metionina/análise , Encefalinas/genética , Camundongos , Norepinefrina/metabolismoRESUMO
M-type K+ channels contribute to the resting membrane potential in the sympathetic ganglion neurons of various animals, whereas their expression in adrenal medullary (AM) cells has been controversial. The present experiment aims to explore the expression of M channels comprising the KCNQ2 subunit in the rat AM cell and its immortalized cell line PC12 cells at the protein level and how its expression in PC12 cells is regulated. The KCNQ2 isoform was recognized in homogenates of PC12 cells but not the rat adrenal medullae by immunoblotting and KCNQ2-like immunoreactivity (IR) was detected in PC12 cells but not in rat AM cells. When the PC12 cells were maintained in a dexamethasone-containing medium, KCNQ2-like IR in the cells was suppressed, whereas the removal of fetal bovine serum from the culture medium for 1 day resulted in an increase in KCNQ2-like IR. A similar enhancement occurred when PC12 cells were cultured under conditions where glucocorticoid receptor (GR) and/or mineralocorticoid receptor (MR) activities were suppressed. These morphological findings were confirmed in functional analysis. The cells cultured in the presence of an inhibitor of either GR or MR exhibited larger amplitudes of Ca2+ signal in response to an M channel inhibitor than did the cells in its absence, whereas the resting Ca2+ level in the former was lower than that in the latter. These results indicate that the M channel is not expressed in rat AM cells and this absence of expression may be ascribed to the suppression by glucocorticoid activity.
Assuntos
Medula Suprarrenal/citologia , Medula Suprarrenal/metabolismo , Canal de Potássio KCNQ2/metabolismo , Animais , Glucocorticoides/sangue , Proteínas de Fluorescência Verde/metabolismo , Masculino , Antagonistas de Receptores de Mineralocorticoides/farmacologia , Células PC12 , Ratos , Ratos Wistar , Receptores de Glucocorticoides/antagonistas & inibidores , Receptores de Glucocorticoides/metabolismo , Receptores de Mineralocorticoides/metabolismoRESUMO
Monitoring responsiveness to acute hypoxia of whole animals and single cells is essential to investigate the nature of the mechanisms underlying oxygen (O2) sensing. Here we describe the protocols followed in our laboratory to evaluate the ventilatory response to hypoxia in normal and genetically modified animals. We also describe the amperometric technique used to monitor single-cell catecholamine release from chemoreceptor cells in carotid body and adrenal medulla slices.
Assuntos
Animais Geneticamente Modificados/metabolismo , Catecolaminas/metabolismo , Células Quimiorreceptoras/metabolismo , Oxigênio/metabolismo , Medula Suprarrenal/citologia , Medula Suprarrenal/metabolismo , Animais , Corpo Carotídeo/citologia , Corpo Carotídeo/metabolismo , Hipóxia Celular , Camundongos , Pletismografia , Análise de Célula ÚnicaRESUMO
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.
Assuntos
Potenciais de Ação , Medula Suprarrenal/citologia , Relógios Biológicos , Células Cromafins/metabolismo , Canais Iônicos/metabolismo , Medula Suprarrenal/metabolismo , Animais , Células Cromafins/fisiologia , HumanosRESUMO
Adrenal medullary chromaffin cells in mammals are innervated by sympathetic preganglionic nerve fibers, as are sympathetic ganglion neurons. Acetylcholine in the ganglion neurons is well established as mediating fast and slow excitatory postsynaptic potentials through nicotinic and muscarinic acetylcholine receptors (AChRs), respectively. The role of muscarinic AChRs during neuronal transmission in chromaffin cells varies among different mammals. Furthermore, the ion channel mechanisms associated with the muscarinic AChR-mediated increase in excitability of chromaffin cells are complicated and different from the excitation of ganglion neurons, which has been ascribed to the inhibition of M-type K+ channels. In this review, we focus on muscarinic receptor-mediated excitation in rodent and guinea pig chromaffin cells, in particular, on the role of muscarinic receptors in neuronal transmission, the muscarinic receptor subtypes involved in excitation and secretion, and the muscarinic regulation of ion channels including TWIK-related acid-sensitive K+ channels. Finally, we discuss prospectively the future of muscarinic receptor research in adrenal chromaffin cells.
Assuntos
Medula Suprarrenal/citologia , Células Cromafins/metabolismo , Canais de Potássio/metabolismo , Receptores Muscarínicos/metabolismo , Canais de Cátion TRPC/metabolismo , Potenciais de Ação , Medula Suprarrenal/metabolismo , Animais , Células Cromafins/fisiologia , Humanos , Receptores Muscarínicos/genéticaRESUMO
In our previous immuno-light microscopic study with an antibody for fatty acid binding protein of type 7 or brain type (FABP-7, B-FABP), the adrenomedullary sustentacular cells were revealed to have secondary processes that present faint immunostaining and an ill-defined sheet-like appearance, in addition to the well-recognized primary processes that present distinct immunostaining and a fibrous appearance. The secondary processes were regarded as corresponding to known ultrastructural profiles of sustentacular cells with a thickness of less than 0.2 µm (the resolution limit of light microscopy), and the processes were considered to be largely responsible for enveloping chromaffin cells. Due to those findings, the present immuno-electron microscopic study was performed to determine whether the secondary processes change the extent of their envelope for chromaffin cells under the intense secretion induced by water immersion-restraint stress. To achieve this, we focused on immunopositive ultrastructural profiles with a thickness of less than 0.2 µm. The measured lengths of the immunopositive profiles in the specimens from stressed mice were found to be significantly larger than those in specimens from normal mice, indicating an increase in the extent of the envelope of the sheet-like processes for the chromaffin cells. Thus, confining our measurements to the secondary process profiles, not the entire cell profiles, proved to be a key factor in the detection-for the first time-of the change in size of the sustentacular cell envelope upon changes in the secretory activity of enveloped chromaffin cells. The possible functional significance of this change in size is discussed here.