Search results for "Agglutinins"

showing 10 items of 62 documents

Proliferative response of synovial fluid and peripheral blood mononuclear cells to arthritogenic and non-arthritogenic microbial antigens and to the …

1990

Cellular immune responses to microbial antigens have been implicated in the pathogenesis of some forms of arthritis including reactive arthritis, Reiter's syndrome, ankylosing spondylitis and rheumatoid arthritis. We investigated the proliferative T cell responses of paired peripheral blood (PB) and synovial fluid (SF) mononuclear cells (MC) to so-called arthritogenic bacteria (Yersinia enterocolitica and Salmonella typhimurium), to control antigens, such as Candida albicans, mumps virus and purified protein derivative, to the recombinant mycobacterial 65-kDa heat-shock protein (hsp 65) and the mitogen phytohemagglutinin (PHA) in 16 patients with different inflammatory rheumatic diseases. T…

Salmonella typhimuriumMicrobiology (medical)Antigens FungalT cellImmunologyArthritisInflammationBiologyLymphocyte ActivationPeripheral blood mononuclear cellEpitopeImmune systemEnterobacteriaceaeAntigenCandida albicansSynovial FluidmedicineHumansImmunology and AllergySynovial fluidPhytohemagglutininsHeat-Shock ProteinsYersinia enterocoliticaAntigens BacterialArthritisGeneral Medicinemedicine.diseasemedicine.anatomical_structureImmunologyLeukocytes Mononuclearmedicine.symptomMedical Microbiology and Immunology
researchProduct

Inhibition of the pro-inflammatory mediators' production and anti-inflammatory effect of the iridoid scrovalentinoside.

2007

We have studied scrovalentinoside, an iridoid with anti-inflammatory properties isolated from Scrophularia auriculata ssp. pseudoauriculata, as an anti-inflammatory agent in different experimental models of delayed-type hypersensitivity. We found that scrovalentinoside reduced the edema induced by oxazolone at 0.5 mg/ear and sheep red blood cells at 10 mg/kg. The observed effect occurred during the last phase or inflammatory response; during the earlier phase or induction of the delayed-type hypersensitivity reaction, no significant activity was noted. Thus, scrovalentinoside reduced both the edema and cell infiltration in vivo and reduced lymphocyte proliferation in vitro, affecting the cy…

ScrophulariaLeukotriene B4medicine.medical_treatmentT-LymphocytesBlotting WesternAnti-Inflammatory AgentsInflammationLymphocyte proliferationPharmacologyOxazolonechemistry.chemical_compoundMiceReceptors GlucocorticoidEdemaDrug DiscoverymedicineAnimalsEdemaHumansHypersensitivity DelayedIridoidsGlycosidesPhytohemagglutininsUnsaturated fatty acidCell ProliferationPharmacologyPlants MedicinalChemistryMacrophagesCell CycleOxazoloneRatsDisease Models AnimalCytokineEicosanoidImmunologyIridoid GlycosidesFemalePlant Preparationsmedicine.symptomInflammation MediatorsJournal of ethnopharmacology
researchProduct

Surface and virulence properties of environmental Vibrio cholerae non-O1 from Albufera Lake (Valencia, Spain).

1990

A total of 140 environmental Vibrio cholerae non-O1 isolates, together with several culture collection strains from both environmental and clinical sources, were studied in relation to hemagglutination, surface hydrophobicity, and the enzymatic, hemolytic, cytotoxic, and enterotoxic activities of their extracellular products. A total of 78 and 62% of the strains produced hemagglutinins and exohemagglutinins, respectively. Four different hemagglutinating and two exohemagglutinating activities were found by using eight sugars in the inhibition assays. Cell-bound mannose-sensitive hemagglutination was detected mainly in chicken blood, whereas fucose-sensitive hemagglutination was recorded only…

SerotypeHemagglutinationVirulenceFresh WaterEnterotoxinBiologymedicine.disease_causeApplied Microbiology and BiotechnologyMicrobiologyHemolysin ProteinsVibrio cholerae non-O1VibrionaceaemedicineVibrio choleraeAntigens BacterialEcologyVirulenceCytotoxinsO AntigensHemagglutininbiology.organism_classificationEnzymesHemagglutininsVibrio choleraeSpainWater MicrobiologyFood ScienceBiotechnologyPlasmidsResearch ArticleApplied and environmental microbiology
researchProduct

Isolation and characterization of a fish F-type lectin from gilt head bream (Sparus aurata) serum.

2007

A novel fucose-binding lectin, designated SauFBP32, was purified by affinity chromatography on fucose-agarose, from the serum of the gilt head bream Sparus aurata. Electrophoretic mobility of the subunit revealed apparent molecular weights of 35 and 30 kDa under reducing and non-reducing conditions, respectively. Size exclusion analysis suggests that the native lectin is a monomer under the selected experimental conditions. Agglutinating activity towards rabbit erythrocytes was not significantly modified by addition of calcium or EDTA; activity was optimal at 37 degrees C, retained partial activity by treatment at 70 degrees C, and was fully inactivated at 90 degrees C. On western blot anal…

Serum hemagglutininsTeleostMolecular Sequence DataBiophysicsBiochemistryAffinity chromatographyWestern blotSparus aurataLectinsmedicineAnimalsDicentrarchus labraxAmino Acid SequenceSea bassMolecular BiologyPeptide sequencePolyacrylamide gel electrophoresisbiologyMolecular massmedicine.diagnostic_testSequence Homology Amino AcidLectinF-type lectin; Sparus aurata; Dicentrarchus labrax; Teleost; Serum hemagglutininsbiology.organism_classificationSea BreamBiochemistrybiology.proteinChromatography GelDicentrarchusElectrophoresis Polyacrylamide GelF-type lectinBiochimica et biophysica acta
researchProduct

The hemagglutinin of Staphylococcus saprophyticus is a major adhesin for uroepithelial cells.

1996

The 160-kDa hemagglutinin of Staphylococcus saprophyticus also serves as a fibronectin-binding protein, and the two activities may be present on different parts of the molecule. Bacteria expressing the 160-kDa hemagglutinin bound in large numbers to histological sections of human ureters, whereas nonhemagglutinating bacteria did not bind. Binding was decreased by an antiserum to the 160-kDa protein and by a preparation of sheep erythrocyte membranes. Fibronectin had no effect. We therefore conclude that binding of S. saprophyticus to uroepithelial cells is mediated by the hemagglutinating activity of the 160-kDa surface protein.

StaphylococcusImmunologyBiologymedicine.disease_causeMicrobiologyBacterial AdhesionEpitheliumMicrobiologymedicineAnimalsHumansAntiserumchemistry.chemical_classificationStaphylococcus saprophyticusSheepBinding proteinErythrocyte MembraneHemagglutininbiology.organism_classificationFibronectinsBacterial adhesinInfectious DiseasesHemagglutininschemistryParasitologyUreterGlycoproteinStaphylococcusBacteriaResearch ArticleInfection and immunity
researchProduct

IMMUNOGENICITY OF AN ACELLULAR PERTUSSIS VACCINE COMPOSED OF GENETICALLY INACTIVATED PERTUSSIS TOXIN COMBINED WITH FILAMENTOUS HEMAGGLUTININ AND PERT…

1993

We studied the immunogenicity of an acellular pertussis vaccine composed of genetically detoxified pertussis toxin (PT-9K/129G), filamentous haemagglutinin, and a 69-kilodalton protein, pertactin, in 30 children aged 12 to 24 months and in 80 infants aged 2 to 4 months. A significant increase of the neutralizing titer and of the titers against pertussis toxin, filamentous hemagglutinin, and pertactin, as determined by enzyme-linked immunosorbent assay, was achieved after three doses of vaccine in all the children; a significant increase of these antibody titers was obtained in 100%, 96.1%, 93.5%, and 98.7% of the infants, respectively.

Time FactorsFilamentous haemagglutinin adhesinPertussis toxincomplex mixturesBordetella pertussisMicrobiologyNeutralization TestsHumansMedicineVirulence Factors BordetellaAdhesins BacterialImmunization ScheduleWhooping coughPertussis VaccineAntigens Bacterialbusiness.industryImmunogenicitypertussisAntibody titerInfantmedicine.diseaseAntibodies BacterialVirologyVaccinationTiterHemagglutininsPertussis ToxinVaccines InactivatedChild PreschoolImmunoglobulin GPediatrics Perinatology and Child HealthDrug EvaluationPertactinbusinessVaccinepertussis; VaccineBacterial Outer Membrane Proteins
researchProduct

The repair of oxidized purines in the DNA of human lymphocytes requires an activation involving NF-YA-mediated upregulation of OGG1.

2014

8-Oxoguanine DNA glycosylase (OGG1), which initiates the repair of DNA purine modifications such as 8-oxo-7,8-dihydroguanine (8-oxoG), is often regarded as a house keeping protein ubiquitously active in mammalian cells. We have analysed the repair rates of oxidized purines generated by photosensitization in peripheral human lymphocytes and observed that the cells were virtually unable to remove these lesions (less than 10% removal within 24h). However, stimulation of the lymphocytes with phytohemagglutinin (PHA) strongly accelerated the repair so that ∼30% of the lesions were repaired within 4h. Within 24h following PHA stimulation and preceding the induction of cell proliferation, Western …

Transcriptional ActivationDNA RepairBiologyBiochemistryDNA Glycosylaseschemistry.chemical_compoundDownregulation and upregulationHumansLymphocytesPhytohemagglutininsMolecular BiologyGeneTranscription factorCell Line TransformedCell growthCell BiologyBase excision repairDNAMolecular biologyUp-RegulationchemistryCCAAT-Binding FactorDNA glycosylasePurinesChromatin immunoprecipitationOxidation-ReductionDNADNA DamageDNA repair
researchProduct

Direct Activation of Bax by p53 Mediates Mitochondrial Membrane Permeabilization and Apoptosis

2004

The tumor suppressor p53 exerts its anti-neoplastic activity primarily through the induction of apoptosis. We found that cytosolic localization of endogenous wild-type or trans-activation–deficient p53 was necessary and sufficient for apoptosis. p53 directly activated the proapoptotic Bcl-2protein Bax in the absence of other proteins to permeabilize mitochondria and engage the apoptotic program. p53 also released both proapoptotic multidomain proteins and BH3-only proteins [Proapoptotic Bcl-2family proteins that share only the third Bcl-2homology domain (BH3)] that were sequestered by Bcl-xL. The transcription-independent activation of Bax by p53 occurred with similar kinetics and concentra…

Tumor suppressor geneProtein ConformationUltraviolet RaysWheat Germ AgglutininsRecombinant Fusion Proteinsbcl-X ProteinApoptosisEndogenyMitochondrionBiologyPermeabilityHomology (biology)law.inventionMiceCytosollawProto-Oncogene ProteinsMitochondrial membrane permeabilizationAnimalsHumansCells CulturedCell Line Transformedbcl-2-Associated X ProteinCell NucleusMultidisciplinaryCytochromes cIntracellular MembranesGenes p53MitochondriaCell biologyCytosolGene Expression RegulationProto-Oncogene Proteins c-bcl-2ApoptosisLiposomesMutationSuppressorTumor Suppressor Protein p53biological phenomena cell phenomena and immunityCarrier ProteinsBH3 Interacting Domain Death Agonist ProteinHeLa CellsScience
researchProduct

Prenatal androgen exposure modulates cellular and humoral immune function of black-headed gull chicks

2005

Avian eggs contain considerable amounts of maternal yolk androgens, which have been shown to beneficially influence the physiology and behaviour of the chick. As androgens may suppress immune functions, they may also entail costs for the chick. This is particularly relevant for colonial species, such as the black-headed gull (Larus ridibundus), in which the aggregation of large numbers of birds during the breeding season enhances the risk of infectious diseases for the hatching chick.To test the effect of maternal yolk androgens on the chick's immune function, we experimentally manipulated, in a field study, yolk androgen levels within the physiological range by in ovo injection of either a…

WITHIN-CLUTCHCharadriiformesEVOLUTIONARY ECOLOGYantibodyhumoral immunityECOLOGICAL IMMUNOLOGYTestosteroneNetherlandsLIFE-SPANGeneral Environmental ScienceTRADE-OFFSGeneral MedicineEgg Yolkembryonic structuresAndrogensLARUS-RIDIBUNDUSGeneral Agricultural and Biological SciencesResearch ArticleYOLK TESTOSTERONEmedicine.medical_specialtyanimal structuresfood.ingredientmedicine.drug_classOffspringMATERNAL TESTOSTERONEEnzyme-Linked Immunosorbent AssayphytohemagglutininBiologyIn ovoAntibodiesGeneral Biochemistry Genetics and Molecular BiologyImmune systemfoodPASSER-DOMESTICUSImmunityYolkInternal medicinemedicineAnimalsEGGPhytohemagglutininsBiologyGeneral Immunology and MicrobiologyBody WeightImmunitylipopolysaccharidesAndrogenEndocrinologytestosteroneHumoral immunityProceedings of the Royal Society B: Biological Sciences
researchProduct

Regeneration of the cell wall in protoplasts of Candida albicans. A cytochemical study using wheat germ agglutinin and concanavalin A.

1988

To assess the dynamics of synthesis of the wall by regenerating Candida albicans protoplasts deposition of chitin and mannoproteins were investigated ultrastructurally using wheat germ agglutinin conjugated with either horseradish peroxidase or colloidal gold, and Concanavalin A coupled to ferritin respectively. Freshly prepared protoplasts lacked wheat germ agglutinin receptor sites but after 1-2 h of regeneration, they were detected. After 4-5 h of regeneration, the cell wall showed a discrete structure which was only labelled with wheat germ agglutinin in thin sections. At this stage of regeneration the outermost layer of the wall was labelled with clusters of Concanavalin A-ferritin par…

Wheat Germ AgglutininsChitinBiochemistryMicrobiologyHorseradish peroxidaseCell wallchemistry.chemical_compoundChitinCell WallCandida albicansGeneticsConcanavalin AColloidsCandida albicansMolecular BiologyGlucanGlycoproteinschemistry.chemical_classificationMembrane GlycoproteinsbiologyHistocytochemistryProtoplastsGeneral MedicineProtoplastbiology.organism_classificationWheat germ agglutininMicroscopy ElectronchemistryBiochemistryConcanavalin AFerritinsbiology.proteinGoldArchives of microbiology
researchProduct