RESUMEN
A large body of evidence supports the concept that calcium (Ca2+) plays a pivotal role in the control of exocytosis. However, recent experiments suggest that a rise in intracellular Ca2+ does not necessarily trigger secretion, and also that secretion can occur independently of cytosolic free calcium levels. This article briefly summarizes the early evidence that has formulated the role of Ca2+ in secretion, and then examines some of the recent evidence suggesting a Ca2+-independent mechanism of exocytosis.
Asunto(s)
Calcio/fisiología , Exocitosis/fisiología , Animales , Proteínas de Unión al GTP/fisiología , HumanosRESUMEN
Enzyme digestion of rat pancreatic tissue yielded a preparation of isolated acinar cells, over 90% of which excluded trypan blue. These isolated cells responded to a variety of secretagogues, the responses being sensitive to the removal of extracellular calcium, increasing extracellular magnesium, and by trifluoperazine, an antagonist of Ca-dependent processes. When exposed to intense electric fields, isolated acinar cells became permeable to CaEGTA and MgATP, these markers gaining access to over 60% of the intracellular milieu within minutes. The accessibility to these markers seemed independent of the ionised Ca2+ level. Less than 0.5% of the cellular amylase was released when cells were rendered leaky in a medium containing about 10(-9) M Ca2+, but typically 4% was released when the Ca2+ level was subsequently raised to 10(-5)M levels, the EC50 for Ca2+ being 2 microM. This amount of amylase released was comparable to the amounts secreted from intact cells in response to a variety of agonists. The cytosolic marker lactate dehydrogenase was also released from leaky cells, but the extent was independent of Ca2+ concentration. No amylase was released at 10(-7)M Ca2+ when permeable cells were exposed to cyclic 3',5'-AMP or cyclic 3',5'-GMP. The calcium activation curve for amylase release seemed to be independent of cyclic nucleotides, but was markedly increased in both the extent of release and apparent affinity for Ca2+ in the presence of the phorbol ester 12-0-tetradecanoyl phorbol 13 acetate. These results suggest that when "functionally normal" isolated acinar cells are rendered permeable, Ca2+-but not cyclic nucleotides-acts as a second messenger for amylase secretion, and furthermore that protein kinase C may be involved in the secretory process.
Asunto(s)
Amilasas/metabolismo , Calcio/metabolismo , AMP Cíclico/metabolismo , GMP Cíclico/metabolismo , Páncreas/enzimología , Animales , Estimulación Eléctrica , L-Lactato Deshidrogenasa/metabolismo , Magnesio/metabolismo , PermeabilidadRESUMEN
Quantitative analysis of the effects of calcium on cell function requires methods for altering intracellular free Ca in a precise and reproducible manner. Microinjection of Ca is very unreliable largely because of the powerful Ca-binding properties of cytoplasm. Much more satisfactory are microinjection of Ca-buffers - provided enough buffer is introduced - and various forms of intracellular dialysis and perfusion which permit full equilibration of the cell interior with a defined artificial intracellular environment.
Asunto(s)
Calcio/análisis , Médula Suprarrenal/metabolismo , Aequorina , Animales , Tampones (Química) , Calcio/administración & dosificación , Permeabilidad de la Membrana Celular , Quelantes , Chironomidae , Decapodiformes , Detergentes , Diálisis , Ácido Egtácico , Macrófagos/análisis , Microinyecciones , Perfusión , Conejos , Glándulas Salivales/análisisRESUMEN
Evoked catecholamine secretion from cultured bovine adrenal medullary cells is inhibited by commercially available botulinum toxins - types A, B and D (10(4)-10(6) MLD/ml of culture medium). Basal secretion is also inhibited. The catecholamine content of such toxin-treated cells is larger than that of control cells and may in part be a result of the inhibition of basal release. The onset of action of botulinum toxin types A and D can be neutralised by their respective antisera. Concentrations of botulinum toxins A, B or D that inhibit secretion leave unaffected the 45Ca2+ influxes normally associated with secretion. These data provide further evidence to support the idea [(1985) Nature 317, 719-721] that botulinum toxins block secretion by acting downstream of the Ca2+ transient at or near the site of exocytosis.
Asunto(s)
Médula Suprarrenal/metabolismo , Toxinas Botulínicas/farmacología , Catecolaminas/metabolismo , Animales , Toxinas Botulínicas/inmunología , Radioisótopos de Calcio/metabolismo , Bovinos , Células Cultivadas , Sueros Inmunes/farmacologíaRESUMEN
Parathyroid hormone-related peptide (PTHrP) and transforming growth factor-alpha (TGF-alpha) were found to stimulate proliferation of human lung cancer cells (BEN-57). TGF-alpha stimulated PTHrP secretion from these cells. The polyclonal antisera raised against PTHrP significantly inhibited the growth of BEN-57 cells, and also the proliferation induced by TGF-alpha. Treatment of cells for up to 10 days with either a PTHrP receptor antagonist (PTHrP(7-34)) or PTHrP antiserum significantly inhibited the subsequent growth of these cells. We suggest that PTHrP may be a component of a complex autocrine loop involving TGF-alpha.
Asunto(s)
Neoplasias Pulmonares/patología , Proteínas de Neoplasias/fisiología , Proteínas/fisiología , Factor de Crecimiento Transformador alfa/fisiología , División Celular/fisiología , Humanos , Neoplasias Pulmonares/metabolismo , Proteínas de Neoplasias/metabolismo , Proteína Relacionada con la Hormona Paratiroidea , Proteínas/metabolismo , Células Tumorales CultivadasRESUMEN
Exposure of 'leaky' adrenal medullary cells to GTP-y-S inhibits Ca-dependent exocytosis in bovine cells, but stimulates exocytosis in chicken cells. The inhibitory action on bovine cells persists in the presence of TPA suggesting that in this tissue an inhibitory GTP-binding protein may modulate the action of protein kinase C on exocytosis.
Asunto(s)
Glándulas Suprarrenales/citología , Calcio/metabolismo , Exocitosis , Nucleótidos de Guanina/metabolismo , Animales , Bovinos , Pollos , Diglicéridos/farmacología , Proteínas de Unión al GTP/metabolismo , Guanosina 5'-O-(3-Tiotrifosfato) , Guanosina Trifosfato/análogos & derivados , Guanosina Trifosfato/farmacología , Guanilil Imidodifosfato/farmacología , Acetato de Tetradecanoilforbol/farmacología , Tionucleótidos/farmacologíaRESUMEN
Addition of GTP markedly enhances the ability of thrombin to cause a leftward shift in the Ca2+ dose/response curve for 5-hydroxytryptamine secretion from permeabilised human platelets. Little effect is observed on addition of GTP in the absence of thrombin. Neither ADP nor adrenaline, in the presence or absence of GTP, causes such a shift, whereas 5-hydroxytryptamine does so to a small extent but only in the presence of GTP. The leftward shift in the Ca2+ dose/response curve induced by 12-O-tetradecanoyl-phorbol-13-acetate or 1-oleyl-2-acetylglycerol is not enhanced by addition of GTP. The thrombin concentration required for half-maximal enhancement of the response to Ca2+ is markedly reduced by addition of GTP. The results support the postulate that the effects of excitatory agonists in this system correlate with their ability to activate phospholipase C and provide further evidence for a role for GTP in signal transduction between the receptor and phospholipase C.
Asunto(s)
Plaquetas/metabolismo , Calcio/farmacología , Guanosina Trifosfato/farmacología , Serotonina/metabolismo , Adenosina Difosfato/farmacología , Adenosina Trifosfato/metabolismo , Plaquetas/efectos de los fármacos , Permeabilidad de la Membrana Celular/efectos de los fármacos , Diglicéridos/farmacología , Relación Dosis-Respuesta a Droga , Epinefrina/farmacología , Humanos , Acetato de Tetradecanoilforbol/farmacología , Trombina/farmacologíaRESUMEN
Enhancement by thrombin of Ca2+-dependent 5HT secretion in the absence of added GTP decreases as the time between electropermeabilisation and addition of thrombin is increased. No decrease occurs if thrombin is added with GTP. Observation of apparent GTP-independent receptor/phospholipase C coupling may result from the presence of bound GTP in the preparation. Enhancement by GTP of Ca2+-dependent 5HT secretion occurs with a significant lag indicating an agonist-independent effect. Cyclic 3'5'-AMP inhibits enhancement by GTP of Ca2+-dependent 5HT secretion while having no effect on enhancement induced by GTP gamma S. Hence cyclic AMP may impair receptor/phospholipase C coupling by enhancing Np GTPase activity.
Asunto(s)
Plaquetas/metabolismo , AMP Cíclico/farmacología , Guanosina Trifosfato/farmacología , Serotonina/metabolismo , Calcio/fisiología , Permeabilidad de la Membrana Celular , Electricidad , Humanos , Técnicas In Vitro , Trombina/farmacología , Factores de Tiempo , Fosfolipasas de Tipo C/fisiologíaRESUMEN
Exposure of 'leaky' bovine adrenal medullary cells to the phorbol ester TPA causes a shift in the calcium-activation curve to lower calcium concentrations without altering the levels of secretion at the extremes of the activation curve. These results are consistent with a role for protein kinase C in exocytosis.
Asunto(s)
Médula Suprarrenal/metabolismo , Calcio/metabolismo , Exocitosis/efectos de los fármacos , Forboles/farmacología , Acetato de Tetradecanoilforbol/farmacología , Médula Suprarrenal/efectos de los fármacos , Animales , Calcio/farmacología , Bovinos , Membrana Celular/efectos de los fármacos , Membrana Celular/metabolismo , Electricidad , CinéticaRESUMEN
The extracellular fluid phase marker, horseradish peroxidase, enters chromaffin cells when triggered to secrete catecholamine. This triggered uptake, like secretion, is abolished in cells pre-incubated with botulinum toxin. Endocytosis of horseradish peroxidase into unstimulated cells is unaffected by botulinum toxin but is inhibited when the temperature is reduced. Once internalised by the unstimulated cells, horseradish peroxidase is released back into the extracellular fluid, the rate of release being temperature sensitive but unaffected by carbamylcholine or botulinum toxin. These results suggest that triggered exocytosis is a necessary event to precede triggered endocytosis, and that botulinum toxin may affect only the triggered exocytosis/endocytosis cycle and not the constitutive cycle.
Asunto(s)
Médula Suprarrenal/efectos de los fármacos , Toxinas Botulínicas/farmacología , Endocitosis/efectos de los fármacos , Exocitosis/efectos de los fármacos , Médula Suprarrenal/citología , Médula Suprarrenal/metabolismo , Animales , Catecolaminas/metabolismo , Bovinos , Células Cultivadas , Peroxidasa de Rábano Silvestre/metabolismo , CinéticaRESUMEN
The hypothesis that inhibition of secretion by botulinum neurotoxin type D occurs by an intracellular process involving ADP-ribosylation has been directly tested by measuring both the extent of inhibition of secretion and of ADP-ribosylation in the same cells. Although the inhibitory effect of unpurified toxin closely parallels intracellular ribosylation, the two events are clearly unrelated, as using purified D and C3 toxins together with their antibodies, each of these events can be either stimulated or inhibited independently of each other.
Asunto(s)
Adenosina Difosfato Ribosa/metabolismo , Médula Suprarrenal/metabolismo , Toxinas Botulínicas/farmacología , Catecolaminas/metabolismo , Sistema Cromafín/metabolismo , Exocitosis , Animales , Anticuerpos/fisiología , Calcio/farmacología , Bovinos , Células Cultivadas , Poli(ADP-Ribosa) Polimerasas/metabolismoRESUMEN
Parathyroid hormone-related peptide (PTHrP) has been detected in fetal serum and amniotic fluid. Using a combination of immunocytochemistry and molecular biology we have detected the peptide and its mRNA in a variety of fetal tissues throughout gestation. Tissue-specific mRNA isoforms were observed, the pattern of hybridization of which changed throughout gestation. In addition, the intensity and pattern of immunocytochemical localization of the peptide was found to vary over the time-period studied (8-30 weeks). PTHrP is expressed by a variety of tumours associated with the syndrome of humoral hypercalcaemia of malignancy and probably accounts for the hypercalcaemia by virtue of its limited amino acid homology with parathyroid hormone. These data demonstrate for the first time that PTHrP, a tumour-related peptide, is expressed during normal human fetal development, and suggest the possibility that it may function to regulate fetal calcium balance and growth in utero.
Asunto(s)
Líquido Amniótico/química , Desarrollo Embrionario y Fetal , Sangre Fetal/química , Proteínas/análisis , Bioensayo , Calcio/metabolismo , Sondas de ADN , Feto/química , Edad Gestacional , Humanos , Hipercalcemia/metabolismo , Técnicas para Inmunoenzimas , Hormona Paratiroidea/biosíntesis , Proteína Relacionada con la Hormona Paratiroidea , Placenta/química , Proteínas/genética , Proteínas/fisiología , ARN Mensajero/análisis , Células Tumorales Cultivadas/químicaRESUMEN
Cells were isolated by collagenase digestion of chicken adrenal glands. Catecholamine secretion could be stimulated by acetylcholine, carbamylcholine, potassium or veratridine. Methacholine, muscarine and oxotremorine were also effective secretagogues whereas nicotine was not. Secretion evoked by acetylcholine was blocked by low concentrations of atropine but was relatively insensitive to hexamethonium. Atropine-sensitive secretion required both external sodium and calcium, was unaffected by tetrodotoxin, blocked by methoxy verapamil and nifedipine, and potentiated by BAY-K-8644. These data suggest that muscarinic activation of these cells facilitates tetrodotoxin insensitive depolarization, thereby opening conventional voltage-sensitive calcium channels. The mechanism by which calcium activates catecholamine secretion was investigated in cells that had been made permeable by exposure to brief intense electric fields. Catecholamine release required Mg-adenosine 5' triphosphate, was half-maximally activated by 1 microM Ca2+ and could be inhibited by high concentrations of Mg2+. At low Ca2+ concentrations, release was potentiated by 12-O-tetradecanoylphorbol 13-acetate, dioctanoylglycerol, guanosine 5'-O-(3-thiotriphosphate) and 5'-guanylylimidodiphosphate, all of which increased the apparent affinity of exocytosis for Ca2+.
Asunto(s)
Médula Suprarrenal/metabolismo , Catecolaminas/metabolismo , Parasimpaticomiméticos/fisiología , Receptores Muscarínicos/efectos de los fármacos , Acetilcolina/farmacología , Acetilcolina/fisiología , Médula Suprarrenal/efectos de los fármacos , Animales , Calcio/metabolismo , Calcio/farmacología , Permeabilidad de la Membrana Celular , Pollos , Exocitosis/efectos de los fármacos , Nucleótidos de Guanina/farmacología , Canales Iónicos/efectos de los fármacos , Canales Iónicos/metabolismo , Ésteres del Forbol/farmacología , Receptores Muscarínicos/fisiologíaRESUMEN
Using a polyclonal antiserum raised against the first 34 amino acids of human parathyroid hormone-related peptide (PTHrP), we have localized PTHrP throughout the uro-genital tract of the human fetus aged between 8 and 40 weeks. Staining was present in the developing mesonephros, metanephros, gonads and in both the adrenal cortex and medulla. In particular, the developing mesonephric and metanephric renal tubules were intensely positive. Using Northern hybridization analysis we have detected a complex pattern of PTHrP mRNA transcripts ranging in size from 1.4 to 4.5 kb in early second trimester human fetal kidney. The presence of PTHrP in the mesonephros and metanephros provides evidence for a role for PTHrP in the regulation of fetal calcium metabolism. However, its presence in the gonad and adrenal gland invites the possibility of a wider role for PTHrP.
Asunto(s)
Proteínas de Neoplasias/análisis , Proteína Relacionada con la Hormona Paratiroidea , Fragmentos de Péptidos/análisis , Proteínas , Sistema Urogenital/embriología , Glándulas Suprarrenales/análisis , Glándulas Suprarrenales/embriología , Edad Gestacional , Gónadas/análisis , Gónadas/embriología , Humanos , Técnicas para Inmunoenzimas , Riñón/análisis , Riñón/embriología , Mesonefro/análisis , Proteínas de Neoplasias/genética , Hibridación de Ácido Nucleico , Fragmentos de Péptidos/genética , ARN Mensajero/análisis , Sistema Urogenital/análisisRESUMEN
The squid giant axon has proved a useful model in the study of ionic channel gating, intracellular homeostasis and receptor-mediated signal transduction leading to generation of intracellular second messengers. In the latter category, previous studies on activation of adenylate or guanylate cyclase have used intact and intracellularly perfused axons to investigate the effects of extra- and intracellular agents on the transduction processes. However, the perfusion of the axon interior washes out many factors which may be important in the processes under study. We introduce here the use of porous cellulose dialysis tubing as a means to circumvent these problems. We find that this dialysis technique is a simple procedure to set-up, and the serotonin/G-protein/adenylate cyclase system can readily be studied in the dialysed axon. This approach should allow investigation under conditions which retain asymmetric transmembrane conditions.
Asunto(s)
Axones/fisiología , Decapodiformes/fisiología , Diálisis/métodos , Transducción de Señal/fisiología , Adenilil Ciclasas/metabolismo , Animales , Axones/efectos de los fármacos , Axones/enzimología , Membrana Celular/efectos de los fármacos , AMP Cíclico/metabolismo , Electrofisiología , Proteínas de Unión al GTP/metabolismo , Potasio/farmacología , Serotonina/farmacología , Transducción de Señal/efectos de los fármacosRESUMEN
A procedure for fitting multi-exponential functions to experimental data is described. It is fast, requires no initial parameter estimates and is particularly suited to sums of several closely spaced exponentials. The method comprises the application of three well tried numerical techniques: (i) the signal is smoothed by representing it as an abbreviated Legendre series; (ii) the coefficients of a certain kind of differential equation are determined such that it's solution is the closest fit to the smoothed signal; and (iii) the amplitudes of the exponential components are determined, given the calculated values of the exponential rate constants. The method is computationally efficient, since determination of amplitudes and exponents involves the use of linear techniques, and therefore does not require multiple iterations, and the smoothed signal is contained in a handful of coefficients rather than as a lengthy time series. The severe ill-conditioning that is unavoidable in this problem is contained within the well-understood procedures of inverting a matrix and determining the roots of a polynomial. This method is particularly appropriate for analysis of data that may be modelled by a scheme of linked first-order reactions, describing for example the stochastic behaviour of ion channels, a chemical reaction, or the uptake and distribution of a drug within body compartments.
Asunto(s)
Interpretación Estadística de Datos , MatemáticaRESUMEN
Primary linitis plastica type carcinoma of the urinary bladder in a sixty-one-year-old man is described. Only 2 other cases have been reported in the English medical literature.
Asunto(s)
Adenocarcinoma Escirroso/diagnóstico , Linitis Plástica/diagnóstico , Neoplasias de la Vejiga Urinaria/diagnóstico , Humanos , Linitis Plástica/patología , Linitis Plástica/cirugía , Masculino , Persona de Mediana Edad , Vejiga Urinaria/patología , Neoplasias de la Vejiga Urinaria/patología , Neoplasias de la Vejiga Urinaria/cirugía , Derivación UrinariaRESUMEN
The effects of endothelin, a potent endogenous vasoconstrictor peptide, were examined in a range of vascular and non-vascular tissues. At concentrations that cause vasoconstriction in portal vein and aorta, the peptide strongly contracted rat uterus, trachea and vas deferens, but not guinea pig ileum. Nifedipine, a dihydropyridine calcium anatgonist, partially inhibited these contractions. Endothelin had no inotropic or chronotropic effect on the isolated rat heart. The peptide did not modulate secretion at the neuromuscular junction, from adrenal medullary cells or neutrophils, nor affect secretion or aggregation of platelets. The tissue responsiveness to endothelin was not the same as the tissue distribution of dihydropyridine receptors. This supports the idea that endothelin interacts with a specific receptor distinct from dihydropyridine sensitive calcium channels. The contractile effect of endothelin on non vascular smooth muscle suggests that the concept of endothelium dependent modulation of vascular smooth muscle tone may be extended to include epithelium dependent modulation of non vascular tissues.
Asunto(s)
Péptidos/farmacología , Animales , Canales de Calcio , Bovinos , Sistema Cromafín/efectos de los fármacos , Sistema Cromafín/metabolismo , Endotelinas , Femenino , Cobayas , Corazón/efectos de los fármacos , Humanos , Técnicas In Vitro , Masculino , Músculo Liso/efectos de los fármacos , Músculo Liso Vascular/efectos de los fármacos , Músculos/efectos de los fármacos , Unión Neuromuscular/efectos de los fármacos , Neutrófilos/efectos de los fármacos , Neutrófilos/metabolismo , Especificidad de Órganos , Agregación Plaquetaria/efectos de los fármacos , Ratas , Ratas Endogámicas , Receptores Nicotínicos/metabolismoRESUMEN
Measurements of intracellular Ca2+ in adrenal medullary cells suggest that a transient rise in Ca2+ leads to a transient secretory response, the rise in Ca2+ being brought about by an influx through voltage-sensitive Ca channels which subsequently inactivate. The level of Ca2+ observed is much smaller than the Ca2+ needed to trigger secretion when introduced directly into the cell. The discrepancy is removed by the presence of diacylglycerol, which increases the sensitivity of the secretory process to Ca2+. The site of action of Ca2+ and diacylglycerol is probably protein kinase C, and the different secretory responses to increases of Ca2+ and diacylglycerol can be modelled in terms of a preferential order of binding of these two substrates to the enzyme. ATP is needed for secretion: one role is possibly to confer stability to the secretory apparatus; another may involve phosphorylation of some key protein. The kinetics of secretion suggest that if Ca2+ regulates phosphorylation or dephosphorylation, then it is the rate of change of phosphorylation that controls secretion rather than the extent of phosphorylation or dephosphorylation. Guanine nucleotide-binding proteins may play a role not only at the level of signal transduction coupling, but also at or near the site of exocytosis, and the mechanism by which some Botulinum toxins inhibit secretion may be associated with these proteins.
Asunto(s)
Glándulas Suprarrenales/metabolismo , Calcio/fisiología , Diglicéridos/metabolismo , Glicéridos/metabolismo , Animales , BovinosRESUMEN
Studies were undertaken between the summers of 1970 and 1974 to determine the effects of swimming on the incidence of external otitis and on the isolation of Pseudomonas aeruginosa from infected outer ears. The frequency of "earaches" reported by swimmers during a telephone survey conducted during the summer of 1971 was 2.4 times the frequency reported by nonswimmers. Furthermore, the risk of a swimmer acquiring external otitis, determined from reports of outer-ear infections received from physicians during the same period, was approximately five times as great as the risk to nonswimmers. Swimming also increased the risk of P aeruginosa involvement in otitis externa, and reported infections among swimmers tended to be more severe than infections among nonswimmers.