RESUMEN
Investigation of foodborne diseases requires the capture and analysis of time-sensitive information on microbial pathogens that is derived from multiple analytical methods and sources. The web-based Pathogen-annotated Tracking Resource Network (PATRN) system (www.patrn.net) was developed to address the data aggregation, analysis, and communication needs important to the global food safety community for the investigation of foodborne disease. PATRN incorporates a standard vocabulary for describing isolate metadata and provides a representational schema for a prototypic data exchange standard using a novel data loading wizard for aggregation of assay and attribution information. PATRN currently houses expert-curated, high-quality "foundational datasets" consisting of published experimental results from conventional assays and next generation analysis platforms for isolates of Escherichia coli, Listeria monocytogenes, and Salmonella, Shigella, Vibrio and Cronobacter species. A suite of computational tools for data mining, clustering, and graphical representation is available. Within PATRN, the public curated data repository is complemented by a secure private workspace for user-driven analyses, and for sharing data among collaborators. To demonstrate the data curation, loading wizard features, and analytical capabilities of PATRN, three use-case scenarios are presented. Use-case scenario one is a comparison of the distribution and prevalence of plasmid-encoded virulence factor genes among 249 Cronobacter strains with similar attributes to that of nine Cronobacter isolates from recent cases obtained between March and October, 2010-2011. To highlight PATRN's data management and trend finding tools, analysis of datasets, stored in PATRN as part of an ongoing surveillance project to identify the predominant molecular serogroups among Cronobacter sakazakii isolates observed in the USA is shown. Use-case scenario two demonstrates the secure workspace available for private users to upload and analyze sensitive data, and for collating cross-platform datasets to identify and validate congruent datapoints. SNP datasets from WGS assemblies and pan-genome microarrays are analyzed in a combinatorial fashion to determine relatedness of 33 Salmonella enterica strains to six strains collected as part of an outbreak investigation. Use-case scenario three utilizes published surveillance results that describe the incidence and sources of O157:H7 E. coli isolates associated with a produce pre-harvest surveillance study that occurred during 2002-2006. In summary, PATRN is a web-based integrated platform containing tools for the management, analysis and visualization of data about foodborne pathogens.
Asunto(s)
Bacterias/genética , Sistemas de Administración de Bases de Datos/instrumentación , Inocuidad de los Alimentos/métodos , Enfermedades Transmitidas por los Alimentos/microbiología , Servicios de Información/instrumentación , Internet , Bacterias/clasificación , Bacterias/aislamiento & purificación , Minería de Datos , Microbiología de Alimentos , Enfermedades Transmitidas por los Alimentos/prevención & control , Humanos , Difusión de la InformaciónRESUMEN
Fourteen profiles of electron density in the ionosphere of Venus were obtainecd by the dual-frequency radio occulation method with the Pioneer Venus orbiter between 5 and 30 December 1978. The solar zenith angles for these measurements were between about 85 degrees and 92 degrees , and the latitudes ranged from about 81 degrees to 88 degrees (ecliptic north). In addition to the expected decreasein peak electron density from about 1.5 x 10(3) to 0.5 x 10(3) per cubic centimeter with increasing solar zenith angle, a region of almost constant electron density above about 250 kilometers was observed. The ionopause height varies from about 300 to 700 kilometers and seems to be influenced by diurnal changes in solar wind conditions. The structures of the profiles are consistent with models in which O(2)(+) dominates near the ionization peak and is replaced by O(+) at higher altitudes.
RESUMEN
Pioneer Venus orbiter dual-frequency radio occultation measurements have produced many electron density profiles of the nightside ionosphere of Venus. Thirty-six of these profiles, measured at solar zenith angles (chi) from 90.60 degrees to 163.5 degrees , are discussed here. In the "deep" nightside ionosphere (chi > 110 degrees ), the structure and magnitude of the ionization peak are highly variable; the mean peak electron density is 16,700 +/- 7,200 (standard deviation) per cubic centimeter. In contrast, the altitude of the peak remains fairly constant with a mean of 142.2 +/- 4.1 kilometers, virtually identical to the altitude of the main peak of the dayside terminator ionosphere. The variations in the peak ionization are not directly related to contemporal variations in the solar wind speed. It is shown that electron density distributions similar to those observed in both magnitude and structure can be produced by the precipitation on the nightside of Venus of electron fluxes of about 108 per square centimeter per second with energies less than 100 electron volts. This mechanism could very likely be responsible for the maintenance of the persistent nightside ionosphere of Venus, although transport processes may also be important.
RESUMEN
Radio occultation measurements at S band (2.293 gigahertz) of the ionosphere and upper neutral atmosphere of Saturn were obtained during the flyby of the Pioneer 11 Saturn spacecraft on 5 September 1979. Preliminary analysis of the occultation exit data taken at a latitude of 9.5 degrees S and a solar zenith angle of 90.6 degrees revealed the presence of a rather thin ionosphere, having a main peak electron density of about 9.4 x 10/(3) per cubic centimeter at an altitude of about 2800 above the level of a neutral number density of 10(19) per cubic centimeter and a lower peak of about 7 x 10(3) per cubic centimeter at 2200 kilometers. Data in the neutral atmosphere were obtained to a pressure level of about 120 millibars. The temperature structure derived from these data is consistent with the results of the Pioneer 11 Saturn infrared radiometer experiment (for a helium fraction of 15 percent) and with models derived from Earth-based observations for a helium fraction by number of about 4 to 10 percent. The helium fraction will be further defined by mutual iteration with the infrared radiometer team.
RESUMEN
Cartilage specimens from osteoarthritis (OA)-affected patients spontaneously released PGE2 at 48 h in ex vivo culture at levels at least 50-fold higher than in normal cartilage and 18-fold higher than in normal cartilage + cytokines + endotoxin. The superinduction of PGE2 production coincides with the upregulation of cyclooxygenase-2 (COX-2) in OA-affected cartilage. Production of both nitric oxide (NO) and PGE2 by OA cartilage explants is regulated at the level of transcription and translation. Dexamethasone inhibited only the spontaneously released PGE2 production, and not NO, in OA-affected cartilage. The NO synthase inhibitor HN(G)-monomethyl-L-arginine monoacetate inhibited OA cartilage NO production by > 90%, but augmented significantly (twofold) the spontaneous production of PGE2 in the same explants. Similarly, addition of exogenous NO donors to OA cartilage significantly inhibited PGE2 production. Cytokine + endotoxin stimulation of OA explants increased PGE2 production above the spontaneous release. Addition of L-NMMA further augmented cytokine-induced PGE2 production by at least fourfold. Inhibition of PGE2 by COX-2 inhibitors (dexamethasone or indomethacin) or addition of exogenous PGE2 did not significantly affect the spontaneous NO production. These data indicate that human OA-affected cartilage in ex vivo conditions shows (a) superinduction of PGE2 due to upregulation of COX-2, and (b) spontaneous release of NO that acts as an autacoid to attenuate the production of the COX-2 products such as PGE2. These studies, together with others, also suggest that PGE2 may be differentially regulated in normal and OA-affected chondrocytes.
Asunto(s)
Cartílago Articular/enzimología , Isoenzimas/biosíntesis , Óxido Nítrico/fisiología , Osteoartritis/enzimología , Prostaglandina-Endoperóxido Sintasas/biosíntesis , Adulto , Anciano , Secuencia de Bases , Ciclooxigenasa 2 , Dinoprostona/antagonistas & inhibidores , Dinoprostona/biosíntesis , Dinoprostona/metabolismo , Inducción Enzimática/efectos de los fármacos , Humanos , Isoenzimas/genética , Proteínas de la Membrana , Persona de Mediana Edad , Datos de Secuencia Molecular , Óxido Nítrico/metabolismo , Prostaglandina-Endoperóxido Sintasas/genética , ARN Mensajero/biosíntesisRESUMEN
Transfection of U937 and THP-1 cells with a recombinant plasmid, pIL1(4.0kb)-CAT, containing 4 kb of the interleukin 1 beta (IL-1 beta) gene upstream regulatory sequence resulted in inducer-dependent expression of chloramphenicol acetyltransferase activity. Treatment of the transfected cells with various combinations of the inducers lipopolysaccharide, phorbol myristate acetate, and dibutyryl cyclic AMP upregulated the IL-1 beta promoter. In U937 and THP-1 cells, maximum stimulation of both the endogenous IL-1 beta gene and pIL1(4.0kb)-CAT transfectants was observed following treatment with the combination of inducing agents lipopolysaccharide-phorbol myristate acetate-dibutyryl cyclic AMP. This combination of inducing agents was used to identify and study, at the molecular level, some of the regulatory elements necessary for induction of the IL-1 beta gene. A series of 5' deletion derivatives of the upstream regulatory sequence were used in transient transfection assays to identify an 80-bp fragment located between -2720 and -2800 bp upstream of the mRNA start site that was required for induction. Exonuclease III mapping, electrophoretic mobility shift assays (EMSA), and DNA sequence analysis of this region were used to identify a transcription factor binding sequence which contained a potential cyclic AMP response element (CRE/ATF)- and NF-kappa B-like binding site. Site-directed mutagenesis of the CRE/ATF-like site resulted in the loss of binding of a specific factor or factors as determined by EMSA. The loss of binding activity directly correlated with a loss of approximately 75% of promoter activity as determined in transient transfection assays. As determined by EMSA, the factor binding to the CRE/ATF-like site was present in nuclear extracts prepared from both uninduced and induced THP-1 and U937 cells. However, the intensity of the band appeared to be increased when nuclear extracts from induced cells were used. In contrast to the CRE/ATF mutation, which resulted in the loss of promoter activity, mutation of the NF-kappa B-like site resulted in a moderate increase in activity in U937 cells. A similar increase in promoter activity was not observed in THP-1 cells. From these studies, we conclude that a CRE/ATF-like site and a factor or factors interacting with this site are essential for the maximum induction of the IL-1 beta gene in stimulated U937 and THP-1 cells.
Asunto(s)
Proteínas Sanguíneas/metabolismo , Proteína de Unión a Elemento de Respuesta al AMP Cíclico/metabolismo , Proteínas de Unión al ADN/metabolismo , Expresión Génica , Interleucina-1/genética , Regiones Promotoras Genéticas , Secuencias Reguladoras de Ácidos Nucleicos , Factores de Transcripción/metabolismo , Factores de Transcripción Activadores , Secuencia de Bases , Sitios de Unión , Bucladesina/farmacología , Línea Celular , Cloranfenicol O-Acetiltransferasa/biosíntesis , Cloranfenicol O-Acetiltransferasa/metabolismo , Regulación Neoplásica de la Expresión Génica , Humanos , Lipopolisacáridos/farmacología , Datos de Secuencia Molecular , Monocitos/citología , Monocitos/efectos de los fármacos , Mutagénesis Sitio-Dirigida , FN-kappa B/metabolismo , Proteínas de Neoplasias/metabolismo , Sondas de Oligonucleótidos , Plásmidos , Regiones Promotoras Genéticas/efectos de los fármacos , ARN Mensajero/metabolismo , Proteínas Recombinantes/biosíntesis , Mapeo Restrictivo , Acetato de Tetradecanoilforbol/farmacología , Transfección , Células Tumorales CultivadasRESUMEN
We introduce draft genome sequences of strains CDC1121-73 (human bronchial wash isolate) and GK1025 (powdered infant formula manufacturing facility isolate), which are both malonate-positive Cronobacter sakazakii serogroup O:2, sequence type 64. Assemblies for these strains have sizes of 4,442,307 and 4,599,266 bp and % G+C contents of 56.9 and 56.7, respectively.
RESUMEN
Modern risk control and food safety practices involving food-borne bacterial pathogens are benefiting from new genomic technologies for rapid, yet highly specific, strain characterisations. Within the United States Food and Drug Administration (USFDA) Center for Food Safety and Applied Nutrition (CFSAN), optical genome mapping and DNA microarray genotyping have been used for several years to quickly assess genomic architecture and gene content, respectively, for outbreak strain subtyping and to enhance retrospective trace-back analyses. The application and relative utility of each method varies with outbreak scenario and the suspect pathogen, with comparative analytical power enhanced by database scale and depth. Integration of these two technologies allows high-resolution scrutiny of the genomic landscapes of enteric food-borne pathogens with notable examples including Shiga toxin-producing Escherichia coli (STEC) and Salmonella enterica serovars from a variety of food commodities. Moreover, the recent application of whole genome sequencing technologies to food-borne pathogen outbreaks and surveillance has enhanced resolution to the single nucleotide scale. This new wealth of sequence data will support more refined next-generation custom microarray designs, targeted re-sequencing and "genomic signature recognition" approaches involving a combination of genes and single nucleotide polymorphism detection to distil strain-specific fingerprinting to a minimised scale. This paper examines the utility of microarrays and optical mapping in analysing outbreaks, reviews best practices and the limits of these technologies for pathogen differentiation, and it considers future integration with whole genome sequencing efforts.
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Enfermedades Transmitidas por los Alimentos/microbiología , Genoma Bacteriano , Genómica/métodos , Salmonella enterica/genética , Escherichia coli Shiga-Toxigénica/genética , Animales , ADN Bacteriano/genética , Brotes de Enfermedades , Enfermedades Transmitidas por los Alimentos/epidemiología , Genotipo , Humanos , Análisis de Secuencia por Matrices de Oligonucleótidos , Filogenia , Estados Unidos/epidemiología , United States Food and Drug AdministrationAsunto(s)
Carcinoma Hepatocelular/enzimología , Glutamato Deshidrogenasa/metabolismo , Neoplasias Hepáticas/enzimología , Hígado/enzimología , Adulto , Fosfatasa Alcalina/metabolismo , Aspartato Aminotransferasas/metabolismo , Biopsia , Carcinoma Hepatocelular/inmunología , Carcinoma Hepatocelular/patología , Colágeno , Femenino , Proteínas Fetales/análisis , Humanos , Hígado/patología , Cirrosis Hepática/enzimología , Neoplasias Hepáticas/inmunología , Neoplasias Hepáticas/patología , Masculino , Persona de Mediana Edad , Procolágeno-Prolina Dioxigenasa/metabolismoAsunto(s)
alfa-Globulinas/análisis , Carcinoma Hepatocelular/diagnóstico , Proteínas Fetales/análisis , Neoplasias Hepáticas/diagnóstico , Adolescente , Adulto , Factores de Edad , Transfusión Sanguínea , Carcinoma Hepatocelular/tratamiento farmacológico , Carcinoma Hepatocelular/inmunología , Femenino , Fluorouracilo/uso terapéutico , Hepatectomía , Humanos , Inmunodifusión , Neoplasias Hepáticas/tratamiento farmacológico , Neoplasias Hepáticas/inmunología , Masculino , Metotrexato/uso terapéutico , Persona de Mediana Edad , Compuestos de Nitrosourea/uso terapéutico , Factores Sexuales , Factores de TiempoRESUMEN
Mycoplasma gallisepticum (MG324), a tylosin resistant strain of low virulence, was compared with four other strains with respect to their survival at temperatures from 46.1 to 48.9 degrees C. MG324 was found to be more resistant than the other strains tested.
Asunto(s)
Pollos , Infecciones por Mycoplasma/veterinaria , Mycoplasma/crecimiento & desarrollo , Enfermedades de las Aves de Corral/prevención & control , Temperatura , Animales , Mycoplasma/aislamiento & purificaciónRESUMEN
A bacteriophage of Pseudomonas aeruginosa PAO1 was characterized. Bacteriophage PIK was found to adsorb on the cell wall of the host organism. Electron microscopy of the phage PIK revealed that it had a bipyramidal hexagonal prismatic head of 110 nm in diameter, a tail which was 158 nm long and a tail plate of 47 nm width. This paper describes its basic characters, and a quantitative study was made of its adsorption to exponential phase cells of two different strains of P. aeruginosa. PIK was found to contain double stranded DNA and it appears to be virulent towards its host, P. aeruginosa PAO1. It was classified into the group of phages possessing a contractile tail.
Asunto(s)
Bacteriófagos/ultraestructura , Pseudomonas aeruginosa , Naranja de Acridina , Bacteriófagos/clasificación , ADN Viral/análisis , ARN Viral/análisis , Coloración y EtiquetadoRESUMEN
Receptor for phage PIK specific for Pseudomonas aeruginosa strain PAO1 was studied. Phage PIK was strongly inactivated by lipopolysaccharide (LPS) in vitro, exhibiting a PhI50 of 4.8 micrograms/ml. Further it was noted that this inactivation by LPS was reduced to 50% by several mono- and disaccharides when tested in vitro. D-glucosamine, D-mannose and L-rhamnose were found to be most effective at the concentration of 0.045 M, 0.25 M and 0.35 M respectively. This suggests the possibility that phage PIK receptor in LPS contains D-mannose, L-rhamnose and D-glucosamine. Either one of the former two could be located at a terminal position alpha-linked to the adjacent residue or located internally in the polysaccharide chain linked through its C-4 position. A theoretical approach to the interpretation of phage cell interaction was also investigated.
Asunto(s)
Pseudomonas aeruginosa/análisis , Receptores Virales/análisis , Adsorción , Bacteriófagos/metabolismo , Glucosamina/análisis , Lipopolisacáridos/análisis , Lipopolisacáridos/farmacología , Manosa/análisis , Receptores Virales/metabolismo , Ramnosa/análisisRESUMEN
Microsomal metabolites of aflatoxin B1 (AFB1) causing induction of prophage in lysogenic strain of Pseudomonas aeruginosa SM was studied. Reduction of culture turbidity was determined at various concentrations of toxin. The effect of the toxin was also studied on deoxyribonucleic acid (DNA), ribonucleic acid (RNA) and protein synthesis. AFB1 at the concentration of 50 micrograms/ml reduced initial turbidity to approximately 90% in 4 h. DNA synthesis stopped completely in the first hour but reappeared due to induction of the temperate phage. Soon after induction both RNA and protein synthesis continued but later little or no net synthesis of these macromolecules occurred. Plaque forming units (pfu) were increased approximately 90 times at 2 h as compared to the control. Testing of the effect of AFB1 on the non-lysogenic, sensitive strain demonstrated that although there was no significant decrease in culture turbidity at 50 micrograms/ml concentration of AFB1, DNA synthesis stopped completely within 1 h, while RNA and protein synthesis were increasing throughout the test interval. It has been concluded that the liver microsomal fraction of AFB1 caused induction of prophage in lysogenic cells and inhibited DNA synthesis significantly in non-lysogenic cells.
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Aflatoxinas/farmacología , Lisogenia , Pseudomonas aeruginosa/efectos de los fármacos , Activación Viral/efectos de los fármacos , Aflatoxina B1 , Aflatoxinas/análisis , Aflatoxinas/metabolismo , Animales , Proteínas Bacterianas/biosíntesis , ADN Bacteriano/biosíntesis , Microsomas Hepáticos/metabolismo , Pseudomonas aeruginosa/metabolismo , ARN Bacteriano/biosíntesis , RatasRESUMEN
The CD4 molecule, a glycoprotein expressed primarily on the cell surface of specific T lymphocytes, is thought to function in T-cell antigen recognition and activation. In addition, CD4 serves as a receptor for human immunodeficiency virus type 1 (HIV-1) by a direct interaction with the HIV-1 surface glycoprotein (gp120). To further characterize the HIV-1-cell interaction, a HeLa cell line was established that expressed a chimeric molecule of CD4 and decay-accelerating factor (DAF). In the chimeric CD4-DAF molecule the transmembrane and cytoplasmic domains of CD4 were deleted and replaced with the carboxy-terminal 37 amino acids of DAF. This resulted in the anchoring of the extracellular domain of CD4 to the cell membrane via a glycophospholipid linkage. The glycophospholipid-anchored CD4 had a molecular size of approximately 56 to 62 kDa and was released following treatment of the cells with phosphatidylinositol-specific phospholipase C. HeLa cells expressing the CD4-DAF hybrid could be infected with HIV-1, as evidenced by reverse transcriptase activity, p24 core antigen content, and infectious virus production. In addition, transfection of the HeLa CD4-DAF cells with a plasmid that directs the synthesis of HIV-1 envelope glycoproteins or cocultivation with HeLa cells expressing the virus glycoproteins resulted in syncytium formation. These results indicate that the transmembrane and cytoplasmic domains of the CD4 molecule are dispensable for both HIV infection and syncytium formation.
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Síndrome de Inmunodeficiencia Adquirida/microbiología , Antígenos CD4/metabolismo , Células Gigantes/fisiología , VIH-1 , Células HeLa/microbiología , Proteínas de la Membrana/inmunología , Síndrome de Inmunodeficiencia Adquirida/metabolismo , Secuencia de Aminoácidos , Linfocitos T CD4-Positivos/microbiología , Antígenos CD55 , Productos del Gen gag/inmunología , Células Gigantes/inmunología , Proteína p24 del Núcleo del VIH , Proteína gp120 de Envoltorio del VIH/inmunología , VIH-1/efectos de los fármacos , VIH-1/enzimología , VIH-1/inmunología , Células HeLa/inmunología , Células HeLa/metabolismo , Humanos , Datos de Secuencia Molecular , Peso Molecular , Fosfatidilinositol Diacilglicerol-Liasa , Fosfoinositido Fosfolipasa C , Hidrolasas Diéster Fosfóricas/farmacología , ADN Polimerasa Dirigida por ARN/metabolismo , Transfección , Proteínas del Núcleo Viral/inmunología , Cultivo de VirusRESUMEN
Interleukin-1 beta (IL-1 beta) plays a central role in the pathophysiology of cartilage damage and degradation in arthritis. In noninflammatory arthropathies such as osteoarthritis (OA), the synovial-derived IL-1 beta has been implicated in the disease process. In this study, we report that human OA-affected cartilage demonstrates upregulated IL-1 beta mRNA not seen in normal cartilage. The OA-affected cartilage in ex vivo conditions spontaneously releases detectable amounts of autocrine IL-1 beta, nitric oxide (NO), and prostaglandin E2 (PGE2), known to be involved in cartilage damage and inflammation, that cannot be detected in normal cartilage. The autocrine IL-1 beta released by the OA-affected cartilage (for at least 72 hr in ex vivo conditions) is present in sufficient quantities to modulate NO and PGE2 production because addition of recombinant soluble IL-1 beta receptor (but not soluble tumor necrosis factor-alpha receptor) and cytokine-suppressive antiinflammatory drugs (CSAIDs) significantly attenuates the spontaneous release of NO and PGE2. Furthermore, OA-affected cartilage releases significant amounts of IL-6 and IL-8 in ex vivo conditions. Addition of CSAIDs to OA-affected cartilage differentially regulates IL-6 and IL-8 production by inhibiting the spontaneous release of IL-6 but not IL-8 in ex vivo conditions. These experiments demonstrate that the human OA-affected cartilage itself releases sufficient amounts of functionally active autocrine IL-1 beta that can modulate endogenous NO, PGE2, and IL-6, but not IL-8, all of which are known to be stimulated by IL-1 beta in vitro. These IL-1 beta induced pleotropic inflammatory mediators in OA-affected cartilage may be sufficient to facilitate or augment cartilage degradation and inhibit cartilage repair, and therefore lead the cartilage into an autodestructive pathway in osteoarthritis.
Asunto(s)
Cartílago Articular/metabolismo , Dinoprostona/biosíntesis , Interleucina-1/metabolismo , Interleucina-6/biosíntesis , Interleucina-8/biosíntesis , Ácido Nítrico/metabolismo , Osteoartritis/metabolismo , Antiinflamatorios/farmacología , Cartílago Articular/efectos de los fármacos , Línea Celular , Humanos , Imidazoles/farmacología , Interleucina-1/biosíntesis , Interleucina-1/genética , Técnicas de Cultivo de Órganos , Osteoartritis/patología , Piridinas/farmacologíaRESUMEN
Osteoarthritis-affected cartilage exhibits enhanced expression of fibronectin (FN) and osteopontin (OPN) mRNA in differential display and bioinformatics screen. Functional genomic analysis shows that the engagement of the integrin receptors alpha 5 beta 1 and alpha v beta 3 of FN and OPN, respectively, have profound effects on chondrocyte functions. Ligation of alpha 5 beta 1 using activating mAb JBS5 (which acts as agonist similar to FN N-terminal fragment) up-regulates the inflammatory mediators such as NO and PGE2 as well as the cytokines, IL-6 and IL-8. Furthermore, up-regulation of these proinflammatory mediators by alpha 5 beta1 integrin ligation is mediated via induction and autocrine production of IL-1 beta, because type II soluble IL-1 decoy receptor inhibits their production. In contrast, alpha v beta 3 complex-specific function-blocking mAb (LM609), which acts as an agonist similar to OPN, attenuates the production of IL-1 beta, NO, and PGE2 (triggered by alpha 5 beta 1, IL-1 beta, IL-18, or IL-1 beta, TNF-alpha, plus LPS) in a dominant negative fashion by osteoarthritis-affected cartilage and activated bovine chondrocytes. These data demonstrate a cross-talk in signaling mechanisms among integrins and show that integrin-mediated "outside in" and "inside out" signaling very likely influences cartilage homeostasis, and its deregulation may play a role in the pathogenesis of osteoarthritis.
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Cartílago Articular/inmunología , Mediadores de Inflamación/metabolismo , Osteoartritis/genética , Osteoartritis/inmunología , Receptores de Fibronectina/fisiología , Receptores de Vitronectina/fisiología , Adulto , Anciano , Animales , Anticuerpos Monoclonales/farmacología , Cartílago Articular/metabolismo , Cartílago Articular/patología , Bovinos , Condrocitos/metabolismo , Dinoprostona/antagonistas & inhibidores , Dinoprostona/biosíntesis , Humanos , Interleucina-1/antagonistas & inhibidores , Interleucina-1/biosíntesis , Interleucina-1/genética , Interleucina-18/fisiología , Interleucina-6/biosíntesis , Interleucina-8/biosíntesis , Ligandos , Lipopolisacáridos/antagonistas & inhibidores , Lipopolisacáridos/farmacología , Persona de Mediana Edad , Óxido Nítrico/antagonistas & inhibidores , Óxido Nítrico/biosíntesis , Osteoartritis/metabolismo , ARN Mensajero/metabolismo , Receptores de Fibronectina/antagonistas & inhibidores , Receptores de Fibronectina/inmunología , Receptores de Fibronectina/metabolismo , Receptores de Vitronectina/inmunología , Receptores de Vitronectina/metabolismo , Transducción de Señal/inmunología , Factor de Necrosis Tumoral alfa/antagonistas & inhibidores , Regulación hacia Arriba/inmunologíaRESUMEN
Nitric oxide synthesized by inducible nitric oxide synthase (iNOS) has been implicated as a mediator of inflammation in rheumatic and autoimmune diseases. We report that exposure of lipopolysaccharide-stimulated murine macrophages to therapeutic concentrations of aspirin (IC50 = 3 mM) and hydrocortisone (IC50 = 5 microM) inhibited the expression of iNOS and production of nitrite. In contrast, sodium salicylate (1-3 mM), indomethacin (5-20 microM), and acetaminophen (60-120 microM) had no significant effect on the production of nitrite at pharmacological concentrations. At suprapharmacological concentrations, sodium salicylate (IC50 = 20 mM) significantly inhibited nitrite production. Immunoblot analysis of iNOS expression in the presence of aspirin showed inhibition of iNOS expression (IC50 = 3 mM). Sodium salicylate variably inhibited iNOS expression (0-35%), whereas indomethacin had no effect. Furthermore, there was no significant effect of these nonsteroidal anti-inflammatory drugs on iNOS mRNA expression at pharmacological concentrations. The effect of aspirin was not due to inhibition of cyclooxygenase 2 because both aspirin and indomethacin inhibited prostaglandin E2 synthesis by > 75%. Aspirin and N-acetylimidazole (an effective acetylating agent), but not sodium salicylate or indomethacin, also directly interfered with the catalytic activity of iNOS in cell-free extracts. These studies indicate that the inhibition of iNOS expression and function represents another mechanism of action for aspirin, if not for all aspirin-like drugs. The effects are exerted at the level of translational/posttranslational modification and directly on the catalytic activity of iNOS.
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Aminoácido Oxidorreductasas/biosíntesis , Antiinflamatorios no Esteroideos/farmacología , Aspirina/farmacología , Expresión Génica/efectos de los fármacos , Indometacina/farmacología , Salicilato de Sodio/farmacología , Acetaminofén/farmacología , Aminoácido Oxidorreductasas/antagonistas & inhibidores , Aminoácido Oxidorreductasas/metabolismo , Animales , Línea Celular , Sistema Libre de Células , Dinoprostona/biosíntesis , Relación Dosis-Respuesta a Droga , Complejo IV de Transporte de Electrones/biosíntesis , Complejo IV de Transporte de Electrones/metabolismo , Inducción Enzimática , Hidrocortisona/farmacología , Cinética , Lipopolisacáridos/farmacología , Macrófagos , Ratones , Óxido Nítrico SintasaRESUMEN
The genetic loci agouti and extension control the relative amounts of eumelanin (brown-black) and phaeomelanin (yellow-red) pigments in mammals: extension encodes the receptor for melanocyte-stimulating hormone (MSH) and agouti encodes a novel 131-amino-acid protein containing a signal sequence. Agouti, which is produced in the hair follicle, acts on follicular melanocytes to inhibit alpha-MSH-induced eumelanin production, resulting in the subterminal band of phaeomelanin often visible in mammalian fur. Here we use partially purified agouti protein to demonstrate that agouti is a high-affinity antagonist of the MSH receptor and blocks alpha-MSH stimulation of adenylyl cyclase, the effector through which alpha-MSH induces eumelanin synthesis. Agouti was also found to be an antagonist of the melanocortin-4 receptor, a related MSH-binding receptor. Consequently, the obesity caused by ectopic expression of agouti in the lethal yellow (Ay) mouse may be due to the inhibition of melanocortin receptor(s) outside the hair follicle.