RESUMEN

Cardiac hypertrophy leads to contractile dysfunction and altered hormone responsiveness through incompletely understood mechanisms. Atrial tumor (AT-1) myocytes (AT-1 cells) are a cardiomyocyte lineage that proliferates but hypertrophies when proliferation is prevented with mitomycin C. Because both states maintain a highly differentiated phenotype, AT-1 cells were used to explore the signaling pathways that accompany and/or contribute to hypertrophic cardiomyocyte growth. Mitomycin C-induced AT-1 cell enlargement is associated with a pronounced increase in the amplitude and the duration of both electrically stimulated calcium transients and endothelin receptor-dependent calcium responses. Studies with caffeine indicate that the intracellular pool of releasable calcium is similar in control and hypertrophied AT-1 cells. This agrees with the results of Northern analyses that show similar steady-state levels of transcripts encoding the sarcoplasmic reticulum Ca-ATPase (and higher levels of transcripts encoding the Na+/Ca2+ exchanger) in hypertrophied AT-1 cells, relative to proliferating control cultures. However, immunoblot analyses reveal a marked increase in the expression of protein kinase C (PKC)-epsilon (a critical intermediate in the signaling pathway for endothelin receptor-dependent modulation of intracellular calcium) during AT-1 cell hypertrophy; the abundance of other PKC isoforms is not changed. Collectively, these results identify reciprocal regulation between calcium/PKC signaling and hypertrophic growth. The evidence that AT-1 cell hypertrophy leads to abnormalities in calcium regulation and specific changes in PKC-epsilon expression that alter endothelin receptor responsiveness supports the notion that pathophysiological changes in PKC-epsilon abundance lead to functionally important changes in hormonal modulation of cardiomyocyte function.

Asunto(s)

Señalización del Calcio/fisiología , Atrios Cardíacos/metabolismo , Neoplasias Cardíacas/metabolismo , Isoenzimas/metabolismo , Miocardio/metabolismo , Proteína Quinasa C/metabolismo , Animales , Cafeína/farmacología , Señalización del Calcio/efectos de los fármacos , ATPasas Transportadoras de Calcio/genética , ATPasas Transportadoras de Calcio/metabolismo , Cardiomegalia/metabolismo , Cardiomegalia/patología , Diferenciación Celular/efectos de los fármacos , División Celular/efectos de los fármacos , Tamaño de la Célula/efectos de los fármacos , Endotelinas/farmacología , Femenino , Atrios Cardíacos/efectos de los fármacos , Atrios Cardíacos/patología , Neoplasias Cardíacas/patología , Ratones , Mitomicina/farmacología , Modelos Cardiovasculares , Miocardio/patología , Inhibidores de la Síntesis del Ácido Nucleico/farmacología , Proteína Quinasa C-epsilon , Transporte de Proteínas/efectos de los fármacos , ARN Mensajero/metabolismo , ATPasas Transportadoras de Calcio del Retículo Sarcoplásmico , Transducción de Señal/efectos de los fármacos , Transducción de Señal/fisiología , Células Tumorales Cultivadas

RESUMEN

Differential modes for beta(1)- and beta(2)-adrenergic receptor (AR) regulation of adenylyl cyclase in cardiomyocytes is most consistent with spatial regulation in microdomains of the plasma membrane. This study examines whether caveolae represent specialized subdomains that concentrate and organize these moieties in cardiomyocytes. Caveolae from quiescent rat ventricular cardiomyocytes are highly enriched in beta(2)-ARs, Galpha(i), protein kinase A RIIalpha subunits, caveolin-3, and flotillins (caveolin functional homologues); beta(1)-ARs, m(2)-muscarinic cholinergic receptors, Galpha(s), and cardiac types V/VI adenylyl cyclase distribute between caveolae and other cell fractions, whereas protein kinase A RIalpha subunits, G protein-coupled receptor kinase-2, and clathrin are largely excluded from caveolae. Cell surface beta(2)-ARs localize to caveolae in cardiomyocytes and cardiac fibroblasts (with markedly different beta(2)-AR expression levels), indicating that the fidelity of beta(2)-AR targeting to caveolae is maintained over a physiologic range of beta(2)-AR expression. In cardiomyocytes, agonist stimulation leads to a marked decline in the abundance of beta(2)-ARs (but not beta(1)-ARs) in caveolae. Other studies show co-immunoprecipitation of cardiomyocytes adenylyl cyclase V/VI and caveolin-3, suggesting their in vivo association. However, caveolin is not required for adenylyl cyclase targeting to low density membranes, since adenylyl cyclase targets to low buoyant density membrane fractions of HEK cells that lack prototypical caveolins. Nevertheless, cholesterol depletion with cyclodextrin augments agonist-stimulated cAMP accumulation, indicating that caveolae function as negative regulators of cAMP accumulation. The inhibitory interaction between caveolae and the cAMP signaling pathway as well as domain-specific differences in the stoichiometry of individual elements in the beta-AR signaling cascade represent important modifiers of cAMP-dependent signaling in the heart.

Asunto(s)

Adenilil Ciclasas/metabolismo , Caveolas/química , AMP Cíclico/fisiología , Miocardio/química , Receptores Adrenérgicos beta/fisiología , Animales , Caveolina 3 , Caveolinas/fisiología , Proteínas Quinasas Dependientes de AMP Cíclico/fisiología , Quinasa 2 del Receptor Acoplado a Proteína-G , Peso Molecular , Miocardio/citología , Ratas , Ratas Wistar , Receptores Adrenérgicos beta/clasificación , Quinasas de Receptores Adrenérgicos beta

RESUMEN

Protein kinase C (PKC) isoforms constitute an important component of the signal transduction pathway used by cardiomyocytes to respond to a variety of extracellular stimuli. Translocation to distinct intracellular sites represents an essential step in the activation of PKC isoforms, presumably as a prerequisite for stable access to substrate. Caveolae are specialized subdomains of the plasma membrane that are reported to concentrate key signaling proteins and may represent a locus for PKC action, given that PKC activators have been reported to dramatically alter caveolae morphology. Accordingly, this study examines whether PKC isoforms initiate signaling in cardiomyocyte caveolae. Phorbol ester-sensitive PKC isoforms were detected at very low levels in caveolae fractions prepared from unstimulated cardiomyocytes; phorbol 12-myristate 13-acetate (PMA) (but not 4alpha-PMA, which does not activate PKC) recruited calcium-sensitive PKCalpha and novel PKCdelta and PKCepsilon to this compartment. The subcellular localization of the phorbol ester-insensitive PKClambda isoform was not influenced by PMA. Endothelin also induced the selective translocation of PKCalpha and PKCepsilon (but not PKCdelta or PKClambda) to caveolae. Multiple components of the extracellular signal-regulated protein kinase (ERK) cascade, including A-Raf, c-Raf-1, mitogen-activated protein kinase kinase, and ERK, were detected in caveolae under resting conditions. Although levels of these proteins were not altered by PMA, translocation of phorbol ester-sensitive PKC isoforms to caveolae was associated with the activation of a local ERK cascade as well as the phosphorylation of a approximately 36-kDa substrate protein in this fraction. Finally, a minor fraction of a protein that has been designated as a receptor for activated protein kinase C resides in caveolae and (along with caveolin-3) could represent a mechanism to target PKC isoforms to cardiomyocyte caveolae. These studies identify cardiomyocyte caveolae as a meeting place for activated PKC isoforms and their downstream target substrates.

Asunto(s)

Isoenzimas/metabolismo , Miocardio/enzimología , Proteína Quinasa C/metabolismo , Animales , Transporte Biológico/efectos de los fármacos , Proteínas Quinasas Dependientes de Calcio-Calmodulina/metabolismo , Membrana Celular/efectos de los fármacos , Membrana Celular/metabolismo , Membrana Celular/ultraestructura , Endotelinas/farmacología , Activación Enzimática/fisiología , Proteínas de la Membrana/metabolismo , Quinasas de Proteína Quinasa Activadas por Mitógenos , Miocardio/citología , Fosforilación , Proteínas Quinasas/metabolismo , Ratas , Ratas Wistar , Transducción de Señal/fisiología , Acetato de Tetradecanoilforbol/farmacología

RESUMEN

The cardiac alpha1-adrenergic chronotropic response changes from stimulatory to inhibitory post-natally. The mature inhibitory response is mediated by the alpha1B-adrenoceptor and a pertussis toxin sensitive G protein. In vivo and in vitro studies identify sympathetic innervation as critical for the maturation of this inhibitory response. Additional experiments in a culture model indicate the effect of innervation is dependent on neurally released neuropeptide Y. The present study establishes that the individual signaling elements in the neuropeptide Y induced alpha1-adrenergic cascade are the same as those appearing during normal in vivo development. In addition, the data demonstrate that the effect of neuropeptide Y does not result from activation of the putative cardiac Y3 neuropeptide Y receptor subtype, since it is reproduced by the peptide fragment neuropeptide Y-(13-36) but not by [Leu31, Pro34]neuropeptide Y.

Asunto(s)

Proteínas de Unión al GTP/fisiología , Frecuencia Cardíaca/fisiología , Corazón/efectos de los fármacos , Neuropéptido Y/farmacología , Receptores Adrenérgicos alfa 1/fisiología , Receptores de Neuropéptido Y/fisiología , Animales , Animales Lactantes , Células Cultivadas , Proteínas de Unión al GTP/efectos de los fármacos , Corazón/fisiología , Frecuencia Cardíaca/efectos de los fármacos , Toxina del Pertussis , Fenilefrina/farmacología , Ratas , Receptores Adrenérgicos alfa 1/efectos de los fármacos , Receptores de Neuropéptido Y/efectos de los fármacos , Factores de Virulencia de Bordetella/farmacología

RESUMEN

Neonatal rat ventricular myocytes express both beta 1-and beta 2-adrenergic receptors linked to enhanced intracellular adenosine 3',5'-cyclic monophosphate (cAMP) accumulation and the modulation of contractile function. This study tests the hypothesis that muscarinic agonists act via distinct mechanisms to interfere with beta 1-and beta 2-adrenergic receptor actions. The beta 2-selective agonist zinterol (10(-7) M) elicits approximately a fourfold increase in cAMP accumulation, which is mimicked, both in magnitude and kinetics, by 10(-9) M of the mixed beta 1-receptor agonist/beta 2-receptor agonist isoproterenol. At these concentrations, isoproterenol and zinterol elicit equivalent inotropic and lusitropic (i.e., enhanced relaxation) responses. Carbachol inhibits all three responses (cAMP, inotropic, and lusitropic) elicited by isoproterenol. In contrast, carbachol does not interfere with the effect of zinterol to augment cAMP accumulation or to induce a positive inotropic response. However, carbachol inhibits the lusitropic response to zinterol via an action at an M2-muscarinic receptor linked to a pertussis toxin-sensitive pathway. Additional studies indicate that beta 2-receptor-dependent phosphorylation of troponin I and phospholamban is substantially attenuated by carbachol. We conclude that carbachol interferes with beta 1-receptor actions by reducing cAMP accumulation. In contrast, the anti-beta 2-receptor actions of carbachol are mediated by a mechanism that is distinct from inhibition of cAMP accumulation, involving an M2-muscarinic receptor coupled to a pertussis toxin-sensitive G protein, which leads to inhibition of troponin I and phospholamban phosphorylation and inhibition of the beta 2-receptor-dependent lusitropic response.

Asunto(s)

Antagonistas Adrenérgicos beta/farmacología , Carbacol/farmacología , Colinérgicos/farmacología , Receptores Adrenérgicos beta/fisiología , Agonistas Adrenérgicos beta/farmacología , Animales , Proteínas de Unión al Calcio/metabolismo , Células Cultivadas , AMP Cíclico/metabolismo , Resistencia a Medicamentos , Etanolaminas/farmacología , Ventrículos Cardíacos , Isoproterenol/farmacología , Contracción Miocárdica/efectos de los fármacos , Miocardio/citología , Miocardio/metabolismo , Fosforilación , Ratas , Ratas Wistar , Troponina I/metabolismo

RESUMEN

We recently identified a developmental decline in protein kinase C (PKC) isoform expression, at the level of the protein, in rat ventricular myocardium. To investigate mechanisms regulating PKC isoform expression in cardiac tissue, this study uses Northern blot analysis to compare the abundance of PKC isoform mRNAs in neonatal and adult rat ventricular myocardium. PKC-epsilon protein and mRNA were detected in both neonatal and adult rat ventricular myocardial preparations. In contrast, coordinate postnatal declines in the abundance of PKC-alpha and PKC-delta proteins and transcripts were identified. An antiserum raised against the COOH-terminal sequence of PKC-zeta detected abundant immunoreactivity in neonatal, but not adult, ventricular myocytes. However, PKC-zeta transcripts were not detectable in the heart either by Northern blot analysis or a reverse transcriptase-polymerase chain reaction approach, indicating that neither the myocytes nor the contaminating cellular elements in the heart express PKC-zeta. Rather, PKC-lambda, another atypical PKC isoform that is structurally highly homologous to PKC-zeta, was detected at the protein and mRNA level in neonatal, but not adult, ventricular myocardium. Taken together, these results establish that developmental declines in calcium-sensitive, novel, and atypical PKC isoforms are paralleled by changes in the levels of the mRNAs encoding these proteins, suggesting transcriptional regulation of PKC during normal cardiac development. The results of this study further identify PKC-lambda as the atypical PKC isoform expressed by the immature ventricle.

Asunto(s)

Regulación del Desarrollo de la Expresión Génica , Isoenzimas/biosíntesis , Miocardio/enzimología , Proteína Quinasa C/biosíntesis , Animales , Animales Recién Nacidos , Feto , Regulación Enzimológica de la Expresión Génica , Corazón/crecimiento & desarrollo , Ventrículos Cardíacos , Reacción en Cadena de la Polimerasa , Proteína Quinasa C-alfa , Proteína Quinasa C-delta , Proteína Quinasa C-epsilon , ARN Mensajero/biosíntesis , Ratas , Ratas Wistar , Transcripción Genética

Asunto(s)

Expresión Génica , Isoenzimas/metabolismo , Contracción Miocárdica , Miocardio/enzimología , Proteína Quinasa C/metabolismo , Envejecimiento/metabolismo , Animales , Cardiomegalia/fisiopatología , Corazón/crecimiento & desarrollo , Humanos , Isoenzimas/biosíntesis , Mamíferos , Proteína Quinasa C/biosíntesis , Secuencias Reguladoras de Ácidos Nucleicos

RESUMEN

To determine whether age-dependent differences in cardiac responses to autonomic agonists could result from developmental changes in protein kinase C (PKC) isoform expression, we probed extracts from the fetal, neonatal, and adult heart as well as cultured neonatal and isolated adult ventricular myocytes with specific antisera to calcium-dependent (alpha and beta) and calcium-independent (delta, epsilon and zeta) isoforms of the enzyme. Although PKC-beta immunoreactivity could not be detected in cultured neonatal or isolated adult ventricular myocytes, adult and neonatal myocytes expressed multiple other isoforms of PKC. Our studies revealed an age-dependent decline in the immunoreactivity for three PKC isoforms. PKC-alpha was detected in extracts from the fetal and 2-day-old neonatal heart as well as cultured neonatal rat ventricular myocytes. Only faint PKC-alpha immunoreactivity was detected in extracts from the adult heart, and PKC-alpha was not detected in extracts from isolated adult ventricular myocytes, suggesting that PKC-alpha resides in nonmyocyte elements in the adult heart. PKC-delta also was detected in greater abundance in fetal and neonatal than in adult myocardial extracts. The decline in PKC-alpha and PKC-delta expression occurred during the first 2 postnatal weeks. PKC-zeta was detected in greatest abundance in extracts from the fetal heart. PKC-zeta expression declined markedly by the second postnatal day, and only faint PKC-zeta immunoreactivity was detected in extracts from adult myocardium. Failure to detect PKC-zeta in extracts from isolated adult ventricular myocytes suggests that PKC-zeta resides primarily in nonmyocyte elements in the adult heart. PKC-epsilon was detected in all preparations, but it was detected in greatest abundance in extracts from neonatal hearts. In vitro sympathetic innervation of previously noninnervated neonatal ventricular myocytes or in vivo chemical sympathectomy of the neonatal heart did not modulate PKC isoform expression, suggesting that sympathetic innervation does not significantly regulate PKC isoform expression. PKC-alpha partitioned to the soluble fraction of unstimulated myocytes and was selectively translocated to the particulate fraction by Ca2+. In contrast, a major portion of the novel PKC isoforms partitioned to the particulate fraction of unstimulated myocytes. The subcellular distribution of novel PKC isoforms was not influenced by Ca2+. 12-O-Tetradecanoylphorbol 13-acetate (TPA, 300 nmol/L) induced translocation of soluble PKC-alpha, PKC-delta, and PKC-epsilon to the particulate fraction at 30 minutes and complete (PKC-alpha and PKC-delta) or 80% (PKC-epsilon) downregulation at 24 hours. PKC-zeta was not affected by TPA.(ABSTRACT TRUNCATED AT 400 WORDS)

Asunto(s)

Corazón/crecimiento & desarrollo , Isoenzimas/metabolismo , Miocardio/metabolismo , Proteína Quinasa C/metabolismo , Envejecimiento/metabolismo , Animales , Animales Recién Nacidos , Calcio/farmacología , Sistema de Conducción Cardíaco/fisiología , Ventrículos Cardíacos , Immunoblotting , Ratas , Ratas Wistar , Fracciones Subcelulares/metabolismo , Sistema Nervioso Simpático/fisiología , Acetato de Tetradecanoilforbol/farmacología

Asunto(s)

Proteínas de Unión al GTP/metabolismo , Hormonas Esteroides Gonadales/metabolismo , Hormonas Hipotalámicas/metabolismo , Hormonas Hipofisarias/metabolismo , Receptores de Catecolaminas/metabolismo , Hormonas Tiroideas/metabolismo , Adenosina Difosfato/metabolismo , Animales , Riñón/metabolismo , Pulmón/metabolismo , Peso Molecular , Miocardio/metabolismo , Unión Proteica , Ratas

RESUMEN

We studied the mechanisms underlying the increase in automaticity induced by alpha 1-adrenergic stimulation of normal and "ischemic" canine Purkinje fibers. Fibers were superfused with a control Tyrode's solution, followed by an ischemic superfusate that included 10 mM KCl, 5 mM NaHCO3, Po2 of 10-25 mm Hg, and pH 6.7. To exclude beta-adrenergic actions, propranolol was added to all solutions. In the presence of phenylephrine, normal automaticity at high membrane potentials usually decreased, whereas the incidence of abnormal automaticity during ischemia was increased from a control value of 10% to 30%. Block of an alpha 1-receptor subtype with chloroethylclonidine in the presence of phenylephrine caused normal automaticity to increase in all fibers studied and significantly increased abnormal automaticity to 70%. The alpha-adrenergic-induced increase in automaticity did not occur in ischemic fibers from animals pretreated with pertussis toxin (PTX), which ADP-ribosylated and functionally inactivated the 41-kd family of GTP regulatory proteins. In contrast, the use of PTX enhanced the increase in automaticity induced by phenylephrine in normally polarized Purkinje fibers. Ryanodine, which blocks sarcoplasmic reticulum Ca2+ release, attenuated the increase in normal automaticity in nonischemic fibers but had no effect on abnormal automaticity in ischemic fibers. The increase in abnormal automaticity was, however, blocked by the alpha 1 subtype blocker WB 4101, which also blocks the increase in automaticity in normal fibers. In conclusion, the increase in abnormal automaticity in ischemic Purkinje fibers depends on a WB 4101-sensitive alpha 1-adrenergic receptor subtype whose actions are transduced by a PTX-sensitive 41-kd G protein and are not blocked by ryanodine.(ABSTRACT TRUNCATED AT 250 WORDS)

Asunto(s)

Calcio/metabolismo , Enfermedad Coronaria/fisiopatología , Dioxanos/farmacología , Fenilefrina/farmacología , Ramos Subendocárdicos/efectos de los fármacos , Receptores Adrenérgicos alfa/efectos de los fármacos , Rianodina/farmacología , Retículo Sarcoplasmático/efectos de los fármacos , Potenciales de Acción , Animales , Perros , Proteínas de Unión al GTP/análisis , Homeostasis , Toxina del Pertussis , Ramos Subendocárdicos/fisiopatología , Verapamilo , Factores de Virulencia de Bordetella

RESUMEN

In the pig heart sarcolemma, a 65 kDa protein is found to be ADP-ribosylated by Clostridium botulinum ADP-ribosyltransferase (exoenzyme C3). ADP-ribosylation of this protein is regulated by guanyl nucleotides and cytosol factor in a fashion similar to that for other C3 substrates. The new exoenzyme C3 substrate was partially purified. This protein is supposed to be a GTP-binding one.

Asunto(s)

ADP Ribosa Transferasas/metabolismo , Proteínas Bacterianas/química , Toxinas Botulínicas , Clostridium botulinum/enzimología , Ventrículos Cardíacos/química , Sarcolema/química , ADP Ribosa Transferasas/aislamiento & purificación , Animales , Proteínas Bacterianas/aislamiento & purificación , Clostridium botulinum/química , Proteínas de Unión al GTP/análisis , Hidrólisis , Peso Molecular , Especificidad por Sustrato , Porcinos

RESUMEN

Secretion of pulmonary surfactant by type II pulmonary epithelial cells (T2P) is regulated by receptor-mediated mechanisms. In other systems, coupling of receptor-linked signals to intracellular events involves guanine nucleotide-binding proteins (G proteins), but the specific role of G proteins in T2P signaling pathways is poorly defined. The present studies begin to address the role of G proteins in transmembrane signaling in these pneumocytes. Membrane preparations from purified T2Ps demonstrated ADP ribosylation of specific substrates by pertussis, cholera, and botulinum toxins (PT, CT, and BT, respectively). Toxin-dependent T2P substrate labeling from 32P-labeled NAD was dependent on time and membrane protein concentration. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis and autoradiography showed ADP ribosylation of membrane substrates of the following molecular masses: PT, 40/41 kDa; CT, 47/51 kDa; BT, 22 kDa. BT-dependent ADP ribosylation of a 22-kDa cytosolic substrate was also observed. Pretreatment of cultured T2P with the individual toxins led to ADP ribosylation of their respective specific substrates in a time-dependent fashion. In cells pretreated with PT or CT, substrates for the complimentary toxins remained available for subsequent ADP ribosylation in vitro. This result supports the specificity of the toxin effects. Basal secretion of the major phospholipid of pulmonary surfactant, disaturated phosphatidylcholine (DSPC) was unaffected in T2P treated with PT, but was stimulated in cells exposed to CT or BT. Neither CT nor BT altered release of lactate dehydrogenase. In cells treated with AMP or with isoproterenol DSPC secretion was stimulated six- to eightfold; preexposure of the cells to CT reduced the response to either agonist by 70%.(ABSTRACT TRUNCATED AT 250 WORDS)

Asunto(s)

Proteínas de Unión al GTP/metabolismo , Pulmón/fisiología , NAD/metabolismo , Adenosina Difosfato Ribosa/metabolismo , Animales , Toxinas Botulínicas/farmacología , Membrana Celular/efectos de los fármacos , Membrana Celular/fisiología , Células Cultivadas , Toxina del Cólera/farmacología , AMP Cíclico/metabolismo , Citosol/metabolismo , Epitelio/efectos de los fármacos , Epitelio/fisiología , Proteínas de Unión al GTP/aislamiento & purificación , Guanilil Imidodifosfato/farmacología , Isoproterenol/farmacología , Cinética , Masculino , Proteínas de la Membrana/aislamiento & purificación , Proteínas de la Membrana/metabolismo , Toxina del Pertussis , Surfactantes Pulmonares/metabolismo , Ratas , Ratas Endogámicas , Transducción de Señal/efectos de los fármacos , Factores de Virulencia de Bordetella/farmacología

RESUMEN

The G-proteins which regulate hormonal turnover of phosphoinositide (PI) in human umbilical vein endothelial cells have been investigated. A 40-41 kDa doublet present in the membranes of these cells was selectively ADP ribosylated by pertussis toxin (PTx), and this doublet was Gi alpha 2 and Gi alpha 3 according to immunoblotting with specific antisera. By contrast, a doublet of 24-26 kDa proteins in the same membrane preparations was ADP ribosylated by the C3 component of botulinum toxin (BoTx). PTx-dependent ADP ribosylation blocked stimulation of PI turnover by histamine, but did not affect stimulation by bradykinin, whereas BoTx (C2 + C3 components) had the opposite effect. Thus two different groups of G-proteins may be involved in hormone-dependent stimulation of PI turnover in human umbilical vein endothelial cells.

Asunto(s)

Bradiquinina/farmacología , Endotelio Vascular/metabolismo , Proteínas de Unión al GTP/metabolismo , Histamina/farmacología , Fosfatidilinositoles/metabolismo , Adenosina Difosfato Ribosa/metabolismo , Toxinas Botulínicas/farmacología , Nucleótidos de Guanina/farmacología , Humanos , Técnicas In Vitro , Toxina del Pertussis , Factores de Virulencia de Bordetella/farmacología

RESUMEN

The effect of pertussis toxin on GTP-binding protein of bovine rod cell outer segments (transducin) was studied. Pertussis toxin was shown to ADP ribosylate either alpha subunit of free transducin or transducin-GDP complex, whereas GTP and its analogue Gpp(NH)p strongly inhibit ADP ribosylation of transducin. Pertussis toxin inhibits rod outer segment membrane GTPase and GTPase of homogeneous transducin by 40% and 70-80%, respectively. Activation of rod cell cyclic nucleotide phosphodiesterase by transducin is reduced after its preincubation with pertussis toxin. In transducin modified by pertussis toxin, 83% of GDP becomes tightly bound and cannot be exchanged with Gpp(NH)p. The stabilization of complex transducin-GDP after ADP ribosylation can explain the inhibitory effect of pertussis toxin on GTP hydrolysis by transducin, and on phosphodiesterase activation by guanyl nucleotides.

Asunto(s)

Nucleótidos de Guanina/metabolismo , Toxina del Pertussis , Células Fotorreceptoras/metabolismo , Segmento Externo de la Célula en Bastón/metabolismo , Transducina/fisiología , Factores de Virulencia de Bordetella/farmacología , Adenosina Difosfato Ribosa/metabolismo , Animales , Bovinos , Membrana Celular/efectos de los fármacos , Membrana Celular/metabolismo , Activación Enzimática/efectos de los fármacos , GTP Fosfohidrolasas/antagonistas & inhibidores , GTP Fosfohidrolasas/metabolismo , Luz , Hidrolasas Diéster Fosfóricas/metabolismo , Segmento Externo de la Célula en Bastón/efectos de los fármacos , Transducina/efectos de los fármacos

RESUMEN

Transducin from bovine retinal rod outer segments possesses two sites responsible for the binding of guanyl nucleotides, one of which is specific only for GTP (GTP-site), while the other one may bind both GTP and GDP (GTP/GDP-site). Pertussis toxin covalently modifies the alpha-subunit of transducin as a result of which 83% of GDP bound at the GTP/GDP site of the protein remain tightly bound and are not displaced by Gpp(NH)p excess. The GTP-site in modified transducin binds Gpp(NH)p at the same rate and reveals the same sensitivity to rhodopsin as does native transducin. Presumably, the GTP/GDP site is localized in the alpha-subunit of transducin. The inhibiting effect of pertussis toxin on GTP hydrolysis by transducin and on stimulation of retinal rod outer segment phosphodiesterase by guanyl nucleotides is due to the tight binding of GDP in the active center of the protein after transducin ADP-ribosylation, which makes impossible the formation of a complex between GTP and the alpha-subunit of transducin.

Asunto(s)

Proteínas de Unión al GTP/metabolismo , Nucleótidos de Guanina/metabolismo , Proteínas de la Membrana/metabolismo , Toxina del Pertussis , Células Fotorreceptoras/metabolismo , Segmento Externo de la Célula en Bastón/metabolismo , Factores de Virulencia de Bordetella/farmacología , Animales , Sitios de Unión , Bovinos , Técnicas In Vitro , Cinética , Transducina

RESUMEN

The modified method for the isolation and purification of B. pertussis toxin has been proposed. Chromatography with the use of hydroxylapatite and lentil lectin--Sepharose 4B has permitted the isolation of the preparation purified 600 times. Its molecular weight is about 90,000. The preparation has been found to possess leukocytosis-stimulating, histamine-sensitising and hemagglutinating activity. Electrophoretic analysis has revealed that the isolated substance consists of four subunits with molecular weights 28,400, 24,300, 21,800 and 15,200. This substance has proved to be capable of hydrolyzing NAD+, as well as of suppressing the GTPase activity of transducin, which is indicative of the covalent modification (ADP-ribosylyzing) of GTP-binding protein under the action of B. pertussis toxin. Two methods for the isolation of B. pertussis toxin (from liquid and solid growth media), as well as the isolation of the toxin from different B. pertussis strains, are evaluated.

Asunto(s)

Toxina del Pertussis , Factores de Virulencia de Bordetella/aislamiento & purificación , Animales , Técnicas Bacteriológicas/instrumentación , Hemaglutinación/efectos de los fármacos , Histamina/inmunología , Hidrólisis , Leucocitosis/inducido químicamente , Ratones , Ratones Endogámicos CBA , Microscopía Electrónica , Peso Molecular , NAD/metabolismo , Temperatura , Factores de Virulencia de Bordetella/análisis , Factores de Virulencia de Bordetella/farmacología

RESUMEN

In the presence of guanyl nucleotides and rhodopsin-containing retinal rod outer segment membranes, transducin stimulates the light-sensitive cyclic nucleotide phosphodiesterase 5.5-7 times. The activation constant (Ka) for GTP and Gpp(NH)p is 0.25 microM, that for GDP and GDP beta S is 14 and 110 microM, respectively. GDP purified from other nucleotide contaminations at concentrations up to 1 mM does not stimulate phosphodiesterase but binds to transducin and inhibits the Gpp(NH)p-dependent activation of phosphodiesterase. The mode of transducin interaction with bleached rhodopsin also depends on the nature of the bound guanyl nucleotide: in the presence of GDP rhodopsin-containing membranes bind 70-100% of transducin, whereas in the presence of Gpp(NH)p the membranes bind only 13% of the protein. The experimental results suggest that GDP and GTP convert transducin into two different functional states, i.e., the transducin X GTP complex binds to phosphodiesterase causing its stimulation, while the transducin X GDP complex is predominantly bound to rhodopsin.

Asunto(s)

2',3'-Nucleótido Cíclico Fosfodiesterasas/metabolismo , Nucleótidos de Guanina/metabolismo , Guanosina Difosfato/metabolismo , Proteínas de la Membrana/metabolismo , Células Fotorreceptoras/metabolismo , Segmento Externo de la Célula en Bastón/metabolismo , Animales , Bovinos , Activación Enzimática , Técnicas In Vitro , Estimulación Luminosa , Segmento Externo de la Célula en Bastón/enzimología , Transducina

RESUMEN

Effect of B. pertussis lymphocytosis-promoting factor (LPF) on the lympho-hematopoietic system of mice was studied. The injection of LPF was shown to sharply enhance endogenous colony formation and to induce a severe depletion of thymus cells, reaching its maximum of day 4. Thymocytes obtained on day 2 or 3 after the injection of LPF produced a suppressive effect on endogenous colony formation. The proliferative activity of hematopoietic stem cells sharply increased under the influence of LPF, though it had no radioprotective action. On the following day after the injection of LPF a steep rise in the number of hematopoietic stem cells was observed in the blood of mice: their content increased 20-fold in comparison with the control level. These data may be important for the evaluation of the side effects of pertussis vaccine on the lympho-hematopoietic system.

Asunto(s)

Células Madre Hematopoyéticas/efectos de los fármacos , Linfocitos/efectos de los fármacos , Toxina del Pertussis , Factores de Virulencia de Bordetella/farmacología , Animales , Médula Ósea/efectos de los fármacos , Médula Ósea/efectos de la radiación , Trasplante de Médula Ósea , Recuento de Células/efectos de los fármacos , Recuento de Células/efectos de la radiación , Ensayo de Unidades Formadoras de Colonias , Células Madre Hematopoyéticas/efectos de la radiación , Interfase/efectos de los fármacos , Interfase/efectos de la radiación , Linfocitos/efectos de la radiación , Ratones , Ratones Endogámicos C57BL , Ratones Endogámicos CBA , Bazo/efectos de los fármacos , Bazo/efectos de la radiación , Bazo/trasplante , Timo/efectos de los fármacos , Timo/efectos de la radiación , Factores de Tiempo , Factores de Virulencia de Bordetella/aislamiento & purificación

RESUMEN

The effects of choleragen- and pertussis toxin (PT)-induced ADP-ribosylation on the GTP-binding protein transducin (TD) from retinal rod outer segments (ROS) have been studied. It has been shown that both toxins cause inhibition of the TD GTPase activity. PT inhibited the GTPase by 30-40% in "native" ROS and by 70-80% in homogeneous TD. Choleragen, in contrast with PT, had no effect on the GTPase activity of homogeneous TD, but was as effective as PT in membrane preparations. The effects of both toxins on the GTPase activity of TD were found to be dependent on the chemical structure of the guanyl nucleotide present in the vehicle. The data obtained suggest that PT and choleragen differ in their specificity for the TD-guanyl nucleotide complex. The former can interact with free TD as well as with the TD-GDP complex, while the latter affects only the TD-GTP complex.

Asunto(s)

Toxinas Bacterianas/farmacología , GTP Fosfohidrolasas/antagonistas & inhibidores , Proteínas de Unión al GTP/antagonistas & inhibidores , Proteínas de la Membrana/antagonistas & inhibidores , Monoéster Fosfórico Hidrolasas/antagonistas & inhibidores , Células Fotorreceptoras/enzimología , Segmento Externo de la Célula en Bastón/enzimología , Animales , Bovinos , Toxina del Cólera/farmacología , Nucleótidos de Guanina/metabolismo , Técnicas In Vitro , NAD/metabolismo , Toxina del Pertussis , Segmento Externo de la Célula en Bastón/metabolismo , Especificidad por Sustrato , Transducina , Factores de Virulencia de Bordetella/farmacología

RESUMEN

The action of calmodulin (CM) given in doses of 10(-5)-10(-8) M on lymphocyte proliferation in healthy subjects was studied. All the test doses of CM produced a stimulant effect 72 h after the lymphocyte incubation was commenced. The rate of 3H-thymidine incorporation experimentally was 1.5-3 times higher than in the control. It is assumed that the release of CM in the foci of tissue injury or inflammation may serve one of the factors stimulating lymphocyte proliferation in an individual focus.

Asunto(s)

Proteínas de Unión al Calcio/fisiología , Calmodulina/fisiología , Linfocitos/citología , Animales , Calmodulina/farmacología , Bovinos , División Celular , Células Cultivadas , Relación Dosis-Respuesta a Droga , Humanos , Activación de Linfocitos