Search results for "Protein Synthesis Inhibitors"

showing 10 items of 22 documents

ATP and endogenous agonists inhibit evoked [3H]-noradrenaline release in rat iris via A1 and P2y-like purinoceptors.

1993

Effects of ATP, adenosine and purinoceptor antagonists on field stimulation-evoked (3 Hz, 2 min) [3H]-noradrenaline overflow were investigated in the rat isolated iris. ATP and adenosine inhibited the evoked overflow of [3H]-noradrenaline. 1,3-Dipropyl-8-cyclopentylxanthine (DPCPX) shifted the concentration-response curve of ATP to the right in a concentration-dependent manner, but with a potency (-log KB = 7.88) much lower than expected for an A1 adenosine receptor. In the continuous presence of DPCPX, the ATP-induced prejunctional inhibition was unaffected by suramin (100 mumol/l) and DIDS (4,4'-diisothiocyanatostilbene-2,2'-disulfonic acid, 50 mumol/l) but was antagonized by the P2Y-rece…

Agonistmedicine.medical_specialtyAdenosinemedicine.drug_classSuraminIrisSuraminBiologyP2 receptor44'-Diisothiocyanostilbene-22'-Disulfonic AcidIn Vitro TechniquesSynaptic Transmissionchemistry.chemical_compoundNorepinephrineAdenosine TriphosphateInternal medicinemedicinePurinergic P2 Receptor AntagonistsAnimalsRats WistarPharmacologyProtein Synthesis InhibitorsReceptors Purinergic P2TriazinesPurinergic receptorReceptors Purinergic P1General MedicineAdenosine receptorAdenosineElectric StimulationRatsEndocrinologychemistryPurinergic P1 Receptor AntagonistsDIDSXanthinesAutoreceptormedicine.drugNaunyn-Schmiedeberg's archives of pharmacology
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Pharmacologic activation of p53 elicits Bax-dependent apoptosis in the absence of transcription

2003

AbstractRecent efforts to develop pharmacologic agents that restore function to mutant forms of p53 hold significant promise in cancer therapy. Here, we examine the effects of such pharmacologic activation of p53 function using a small molecule, PRIMA-1, and a model system employing a p53 protein fused to a mutant steroid binding domain of the murine estrogen receptor (p53ERtam) that renders it responsive only in the presence of 4-hydroxytamoxifen. In either case, p53 activation triggered apoptosis that was not inhibited by the presence of macromolecular synthesis inhibitors. This p53-induced, transcription-independent apoptosis is Bax dependent, proceeds in the absence of a nucleus, and in…

Cancer ResearchTranscription GeneticRecombinant Fusion ProteinsMutantEstrogen receptorApoptosis03 medical and health sciencesMice0302 clinical medicineBcl-2-associated X proteinProto-Oncogene ProteinsTumor Cells CulturedAnimalsHumansCloning MolecularReceptorCells Cultured030304 developmental biologybcl-2-Associated X ProteinCell NucleusProtein Synthesis Inhibitors0303 health sciencesAza CompoundsbiologyCytochrome cCytochromes cCell BiologyFibroblastsBridged Bicyclo Compounds Heterocyclic3. Good healthCell biologyTransport proteinMitochondriaProtein TransportTamoxifenProto-Oncogene Proteins c-bcl-2Receptors EstrogenOncologyApoptosis030220 oncology & carcinogenesisMutationbiology.proteinTumor Suppressor Protein p53Binding domainCancer Cell
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FAS(CD95) ligand expression by tumor cell variants can be unrelated to their capacity to induce tolerance or immune rejection.

1999

According to the results of in vitro experiments, Fas(CD95) ligand expression by cancer cells might induce apoptosis of activated T cells and contribute to immune tolerance. However, Fas ligand expression had never been explored in vivo in tumor cell models yielding either immune response or tolerance. In the present study, we analyzed the expression and function of Fas ligand in 2 clones of tumor cells originating from the same rat colon carcinoma. REGb cells were immunogenic and yielded tumors that regressed in immune-competent syngeneic hosts, whereas PROb cells induced active tolerance and yielded progressive tumors. Fas ligand was expressed on the plasma membrane of both REGb and PROb …

Cancer Researchmedicine.medical_treatmentApoptosisBiologyLymphocyte ActivationFas ligandImmune toleranceImmune systemmedicineImmune ToleranceTumor Cells CulturedAnimalsfas ReceptorCycloheximideProtein Synthesis InhibitorsFas receptorClone CellsRatsCytokineOncologyApoptosisCancer cellImmunologyAntigens SurfaceCancer researchTumor necrosis factor alphaInternational journal of cancer
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Validation of the Tetracycline Regulatable Gene Expression System for the Study of the Pathogenesis of Infectious Disease

2011

Understanding the pathogenesis of infectious disease requires the examination and successful integration of parameters related to both microbial virulence and host responses. As a practical and powerful method to control microbial gene expression, including in vivo, the tetracycline-regulatable system has recently gained the favor of many investigative groups. However, some immunomodulatory effects of the tetracyclines, including doxycycline, could potentially limit its use to evaluate host responses during infection. Here we have used a well-established murine model of disseminated candidiasis, which is highly dependent on both the virulence displayed by the fungal cells and on the host im…

ChemokineScienceImmunologyVirulenceMycologyPathogenesisKidneyResponse ElementsMicrobiologyMicrobiologyPathogenesisMiceGene Expression Regulation FungalCandida albicansGene expressionmedicineAnimalsPromoter Regions GeneticCandida albicansBiologyImmunity to InfectionsProtein Synthesis InhibitorsDoxycyclineMultidisciplinaryVirulencebiologyQCandidiasisImmunityRTetracyclinebiology.organism_classificationDisseminated CandidiasisDisease Models AnimalInfectious DiseasesMedical MicrobiologyInfectious disease (medical specialty)DoxycyclineHost-Pathogen InteractionsMutationImmunologybiology.proteinCytokinesMedicineChemokinesSpleenResearch Articlemedicine.drug
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Pheromone-induced olfactory memory in newborn rabbits: Involvement of consolidation and reconsolidation processes.

2009

Mammary pheromone (MP)-induced odor memory is a new model of appetitive memory functioning early in a mammal, the newborn rabbit. Some properties of this associative memory are analyzed by the use of anisomycin as an amnesic agent. Long-term memory (LTM) was impaired by anisomycin delivered immediately, but not 4 h after either acquisition or reactivation. Thus, the results suggest that this form of neonatal memory requires both consolidation and reconsolidation. By extending these notions to appetitive memory, the results reveal that consolidation and reconsolidation processes are characteristics of associative memories of positive events not only in the adult, but also in the newborn.

Cognitive NeuroscienceConditioning ClassicalPheromones03 medical and health sciencesCellular and Molecular Neurosciencechemistry.chemical_compound0302 clinical medicineAnimals[SDV.NEU] Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]Olfactory memoryAnisomycinComputingMilieux_MISCELLANEOUS030304 developmental biologyProtein Synthesis Inhibitors0303 health sciencesAppetitive BehaviorChi-Square DistributionConsolidation (soil)Long-term memoryAssociation LearningBrainRecognition PsychologyContent-addressable memoryOlfactory PerceptionNeuropsychology and Physiological PsychologyMemory Short-TermOdorchemistryAnimals NewbornPheromoneMemory consolidation[SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]RabbitsPsychologyNeuroscience030217 neurology & neurosurgeryAnisomycinCognitive psychologyLearningmemory (Cold Spring Harbor, N.Y.)
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Cytochrome c is released in a single step during apoptosis

2005

Release of cytochrome c from mitochondria is a central event in apoptotic signaling. In this study, we utilized a cytochrome c fusion that binds fluorescent biarsenical ligands (cytochrome c-4CYS (cyt. c-4CYS)) as well as cytochrome c-green fluorescent protein (cyt. c-GFP) to measure its release from mitochondria in different cell types during apoptosis. In single cells, the kinetics of cyt. c-4CYS release was indistinguishable from that of cyt. c-GFP in apoptotic cells expressing both molecules. Lowering the temperature by 7 degrees C did not affect this corelease, but further separated cytochrome c release from the subsequent decrease in mitochondrial membrane potential (DeltaPsi(m)). Cyt…

CytochromeUltraviolet RaysGreen Fluorescent ProteinsApoptosisLigandsMembrane PotentialsJurkat CellsCytochrome C1HumansCytochrome c oxidaseEnzyme InhibitorsMolecular BiologyProtein Synthesis InhibitorsMicroscopy VideobiologyTumor Necrosis Factor-alphaCytochrome bCytochrome cTemperatureCytochromes cCytochrome P450 reductaseCell BiologyStaurosporineMitochondriaCell biologyKineticsenzymes and coenzymes (carbohydrates)Coenzyme Q – cytochrome c reductaseDactinomycinbiology.proteinApoptosomeBiomarkersHeLa CellsCell Death & Differentiation
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Selective targeting of avidin/mannose 6-phosphate receptor chimeras to early or late endosomes

2000

Summary In this study we have used the Semliki forest virus expression system to transiently express chimeric proteins that contain transmembrane and cytoplasmic domains of the cation-independent mannose 6-phosphate receptor (CI-MPR) fused to chicken avidin. Immunofluorescence and electron microscopy studies showed that the chimeric protein with the entire cytoplasmic domain of CI-MPR was transported to late endosomes, where it accumulated. We made use of the biotin-binding capacity of lumenal avidin, and found that, in agreement with this distribution, the chimeric protein could be labelled with biotinylated HRP endocytosed for a long, but not a brief, period of time. However, truncation o…

CytoplasmTime FactorsHistologyEndosomeRecombinant Fusion ProteinsAmino Acid MotifsGreen Fluorescent ProteinsEndosomesEndocytosisReceptor IGF Type 2Pathology and Forensic Medicine03 medical and health sciencesCationsCricetinaeAnimalsBiotinylation030304 developmental biologyProtein Synthesis Inhibitors0303 health sciencesBrefeldin AMannose 6-phosphate receptorbiologyCell Membrane030302 biochemistry & molecular biologyPovidoneBiological TransportCell BiologyGeneral MedicineAvidinSilicon DioxideSemliki forest virusFusion proteinMolecular biologyEndocytosisTransmembrane proteinProtein Structure TertiaryLuminescent ProteinsMicroscopy ElectronTransmembrane domainCross-Linking ReagentsMicroscopy FluorescenceBiotinylationbiology.proteinCattleChickensDimerizationAvidinEuropean Journal of Cell Biology
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Trafficking of the human transferrin receptor in plant cells: effects of tyrphostin A23 and brefeldin A.

2006

Plant cells possess much of the molecular machinery necessary for receptor-mediated endocytosis (RME), but this process still awaits detailed characterization. In order to identify a reliable and well-characterized marker to investigate RME in plant cells, we have expressed the human transferrin receptor (hTfR) in Arabidopsis protoplasts. We have found that hTfR is mainly found in endosomal (Ara7- and FM4-64-positive) compartments, but also at the plasma membrane, where it mediates binding and internalization of its natural ligand transferrin (Tfn). Cell surface expression of hTfR increases upon treatment with tyrphostin A23, which inhibits the interaction between the YTRF endocytosis signa…

Endosomemedia_common.quotation_subjectArabidopsisTransferrin receptorPlant ScienceBiologyEndocytosischemistry.chemical_compoundReceptors TransferrinGeneticsHumansEnzyme InhibitorsInternalizationmedia_commonchemistry.chemical_classificationProtein Synthesis InhibitorsBrefeldin AProtoplastsCell BiologyReceptor-mediated endocytosisBrefeldin ATyrphostinsPlants Genetically ModifiedCell biologyAdaptor Protein Complex mu SubunitsCytosolProtein TransportchemistryGene Expression RegulationTransferrinThe Plant journal : for cell and molecular biology
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A novel putative insect chitinase with multiple catalytic domains: hormonal regulation during metamorphosis

2002

0264-6021 (Print) Journal Article Research Support, Non-U.S. Gov't; We have used differential display to identify genes that are regulated by juvenile hormone in the epidermis of the beetle Tenebrio molitor. One of the genes encodes T. molitor chitinase 5 (TmChit5), a chitinase possessing an unusual structure. Sequence analysis of TmChit5 identified five 'chitinase units' of approx. 480 amino acids with similarity to chitinase family 18. These units are separated by less conserved regions containing putative PEST (rich in proline, glutamic acid, serine and threonine) sequences, putative chitin-binding domains and mucin domains. Northern-blot analysis identified a single transcript of approx…

InsectaMessenger/metabolismBiochemistrychemistry.chemical_compoundCatalytic DomainHormone metabolismNorthernCloning MolecularCycloheximideTenebrioPeptide sequencePhylogenychemistry.chemical_classificationProtein Synthesis InhibitorsDifferential displayBlottingChitinasesMetamorphosis BiologicalAmino acidInsectsBiochemistryProtein Synthesis Inhibitors/pharmacologyInsect ProteinsResearch ArticleProtein StructureDNA ComplementarySequence analysisChitinase/*chemistry/genetics/*metabolismMolecular Sequence DataTenebrio/metabolismMethopreneBiologyComplementary/metabolismAnimalsHormones/*metabolismRNA MessengerAmino Acid SequenceMolecular BiologyGene LibraryInsect Proteins/*chemistry/genetics/*metabolismMetamorphosisGene Expression ProfilingMolecularCell BiologyDNAMethoprene/pharmacologyBlotting NorthernMethopreneBiologicalHormonesProtein Structure TertiarychemistryChitinaseJuvenile hormonebiology.proteinRNACycloheximide/pharmacologyEpidermisTertiaryCloningEpidermis/metabolism
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Independence of first- and second-order memories in newborn rabbits

2011

WOS:000291649400006; International audience; The mammary pheromone promotes the acquisition of novel odorants (CS1) in newborn rabbits. Here, experiments pinpoint that CS1 becomes able to support neonatal learning of other odorants (CS2). We therefore evaluated whether these first- and second-order memories remained dependent after reactivation. Amnesia induced after CS2 recall selectively blocked this memory, when recall and amnesia of CS1 left the souvenir of CS2 safe; this finding partially differed from results obtained in adult mammals. Thus, in this model of neonatal appetitive odor learning, second-order memory seems to depend on first-order memory for its formation but not for its m…

MaleAging[SDV]Life Sciences [q-bio]MESH: Mental RecallMESH: RabbitsMESH: Conditioning OperantPheromonesMESH : PheromonesMESH: Animals NewbornDevelopmental psychologyMESH : Learning0302 clinical medicineMESH: SmellComputingMilieux_COMPUTERSANDEDUCATIONMESH : FemaleMESH: AgingMESH: AnimalsMESH: MemoryMESH : AnisomycinProtein Synthesis InhibitorsMESH: Pheromones0303 health sciencesMESH : Animals NewbornMESH : MemoryMESH : OdorsSmellNeuropsychology and Physiological PsychologyMESH : MotivationFemaleMemory consolidationRabbitsmedicine.symptomMESH: AmnesiaPsychologyAnisomycinpsychological phenomena and processesOlfactory perceptionMESH : MaleCognitive NeuroscienceMESH: MotivationAmnesiaMESH: AnisomycinMESH : Conditioning Operant03 medical and health sciencesCellular and Molecular NeuroscienceMESH : AmnesiaMemoryparasitic diseasesmedicineAnimalsLearningMESH : RabbitsMESH : Protein Synthesis Inhibitors030304 developmental biologyMotivationMESH: Odors[ SDV ] Life Sciences [q-bio]MESH: Protein Synthesis InhibitorsRecallMESH : Mental RecallMESH : AgingMESH: MaleAnimals NewbornOdorMental RecallOdorantsConditioning OperantMESH : Smell MESH: LearningAmnesiaMESH : AnimalsMESH: FemaleNeuroscience030217 neurology & neurosurgeryLearning & Memory
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