Search results for "Isoform"

showing 10 items of 350 documents

NGF and TGF-beta mRNA expression during pregnancy in a rat corneal wound healing model.

2003

Background Growth factors seem to play a major role in corneal wound healing and TGF-beta seems to be associated with abnormal healing after corneal surgical procedures. Few studies have analysed the role of NGF and TGF-beta on corneal wound healing during pregnancy. The aim of the present study was to create an animal model to evaluate the expression of NGF and TGF-betas during corneal wound healing in two groups: control and pregnant rats. Methods Corneal mRNA for NGF and the three isoforms of TGF-beta were analysed by RT-PCR, in a time-course experiment on different days after epithelial wounding (2, 7, 14 days) in pregnant and control groups Results The results show high corneal mRNA ex…

Gene isoformPathologymedicine.medical_specialtyMrna expressionAndrologyCorneaRats Sprague-DawleyPregnancyTransforming Growth Factor betaCorneaNerve Growth FactormedicineAnimalsRNA MessengerMessenger RNAPregnancyWound Healingbusiness.industrymedicine.diseaseeye diseasesRatsOphthalmologymedicine.anatomical_structureCorneal woundPregnancy AnimalFemalesense organsWound healingbusinessOptometryTransforming growth factorCorneal InjuriesClinicalexperimental optometry
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Purification and Characterization of the Soluble Interleukin-6 Receptor from Human Plasma and Identification of An Isoform Generated through Alternat…

1996

The soluble human interleukin-6 receptor (shIL6R) was purified from human plasma. In a single immunoaffinity purification step a 140000-fold enrichment with a yield of 95% was achieved. A subsequent IL-6 affinity chromatography resulted in a homogeneous receptor preparation but only in a yield of less than 5%. The biological activity of the soluble receptor was clearly demonstrated by its ability to induce the synthesis of the acute-phase protein α1-antichymotrypsin in HepG2 cells stably transfected with IL-6. Upon gel filtration, the native shIL6R showed an apparent molecular mass of 93 kDa. Analysis by SDS/PAGE revealed an apparent molecular mass of 65 kDa for the soluble receptor. Deglyc…

Gene isoformPeptideBiologyTransfectionBiochemistryChromatography AffinityAmidohydrolasesCell LineAffinity chromatographyAntigens CDTumor Cells CulturedHumansPeptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine AmidaseRNA MessengerReceptorPeptide sequencechemistry.chemical_classificationMolecular massInterleukin-6Cell MembraneAlternative splicingReceptors InterleukinReceptors Interleukin-6Molecular biologyRecombinant ProteinsMolecular WeightAlternative SplicingBiochemistrychemistryInterleukin-6 receptorChromatography GelElectrophoresis Polyacrylamide GelEuropean Journal of Biochemistry
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Centrins, gatekeepers for the light-dependent translocation of transducin through the photoreceptor cell connecting cilium

2006

Centrins are members of a highly conserved subgroup of the EF-hand superfamily of Ca(2+)-binding proteins commonly associated with centrosome-related structures. In the retina, centrins are also prominent components of the photoreceptor cell ciliary apparatus. Centrin isoforms are differentially localized at the basal body and in the lumen of the connecting cilium. All molecular exchanges between the inner and outer segments occur through this narrow connecting cilium. Ca(2+)-activated centrin isoforms bind to the visual heterotrimeric G-protein transducin via an interaction with the betagamma-subunit. Ca(2+)-dependent assemblies of centrin/G-protein complexes may regulate the transducin mo…

Gene isoformPhotoreceptorsgenetic structuresPhotoreceptor cellHeterotrimeric G proteinConnecting ciliummedicineCentrinBasal bodyAnimalsPhotoreceptor CellsCiliaTransducinPhosphorylationVision OcularCentrosomeRetinaChemistryLight-dependent translocationCiliumCalcium-Binding ProteinsSensory SystemsCell biologyProtein TransportOphthalmologymedicine.anatomical_structureCentrinVertebratesTransducinsense organsPhotic StimulationVision Research
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Alternative Polyadenylation Events Contribute to the Induction of NF-ATc in Effector T Cells

1999

Abstract The transcription factor NF-ATc is synthesized in three prominent isoforms. These differ in the length of their C terminal peptides and mode of synthesis. Due to a switch from the use of a 3′ polyA site to a more proximal polyA site, NF-ATc expression switches from the synthesis of the two longer isoforms in naive T cells to that of short isoform A in T effector cells. The relative low binding affinity of cleavage stimulation factor CstF-64 to the proximal polyA site seems to contribute to its neglect in naive T cells. These alternative polyadenylation events ensure the rapid accumulation of high concentrations of NF-ATc necessary to exceed critical threshold levels of NF-ATc for g…

Gene isoformPolyadenylationImmunologyMolecular Sequence DataGene inductionBiologyLymphocyte ActivationTransfectionT-Lymphocytes RegulatoryJurkat CellsMiceGenes ReporterCritical thresholdTumor Cells CulturedImmunology and AllergyAnimalsHumansAmino Acid SequenceCloning MolecularLuciferasesTranscription factormRNA Cleavage and Polyadenylation FactorsCleavage stimulation factorBase SequenceNFATC Transcription FactorsEffectorNuclear ProteinsRNA-Binding ProteinsMolecular biologyDNA-Binding ProteinsInfectious DiseasesPoly ATranscription FactorsImmunity
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DNA Modification Induced After Metabolic Activation of the Potent Carcinogen Dibenzo[a, l]pyrene in V79 Chinese Hamster Cells Stably Expressing Singl…

2000

Abstract The polycyclic aromatic hydrocarbon (PAH) dibenzo[a, l]pyrene (DB[a, l]P) has been found to be an environmental pollutant and, considering the available data from rodent bioassays, it represents the most carcinogenic member compound of the class of PAH yet discovered. To sort out the contribution of individual cytochromes P450 (P450) in the metabolic activation of this PAH, V79 cells stably expressing a single P450 isoform were treated with DB[a, l]P or enantiomeric DB[a, l]P-11,12-dihydrodiols (diols). Subsequent analysis of the DNA adducts formed revealed substantial differences in the adduct pattern and the total DNA binding depending on the cell line used. Human P450 1B1 effect…

Gene isoformPolymers and PlasticsbiologyChemistryStereochemistryOrganic ChemistryCytochrome P450biology.organism_classificationChinese hamsterAdductchemistry.chemical_compoundCell cultureMaterials Chemistrybiology.proteinPyreneCarcinogenDNAPolycyclic Aromatic Compounds
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Species-dependent Metabolism of Benzo[c]phenanthrene and Dibenzo[a, l]pyrene by Various CYP450 Isoforms

2000

Abstract The metabolism of benzo[c]phenanthrene (B[c]Ph) and dibenzo[a, l]-pyrene (DB[a, l]P) with various CYP isoforms including rat 1A1, 1A2, 2B1, 2E1, human 1A1, 1A2, 1B1, 2A6, 3A4, 2E1 and fish 1A expressed in Chinese hamster V79 cells has been compared. Major differences in the catalytic activities and in the regioselectivity of the eleven CYP isoforms with B[c]Ph and DB[a, l]P as substrates have been observed. There have been found substantially species-specific differences between homologous CYP isoforms at least when human, rat and fish are compared, which have to be taken into account when animal experiments are extrapolated to human. In particular, complementary catalytic activiti…

Gene isoformPolymers and PlasticsbiologyStereochemistryMetaboliteOrganic ChemistryBenzo(c)phenanthreneMetabolismPhenanthrenebiology.organism_classificationChinese hamsterchemistry.chemical_compoundchemistryBiochemistryMaterials ChemistryPyreneheterocyclic compoundsCarcinogenPolycyclic Aromatic Compounds
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Kinetics of expression of prion protein in uninfected and scrapie-infected N2a mouse neuroblastoma cells.

1993

The scrapie prion protein, PrPSc, is formed from its isoform, the cellular PrPc. There is evidence available indicating that PrPSc is necessary component of the infectious prion particle to cause a series of transmissible spongiform encephalopathies. We have used immunocytochemistry and RNA blotting techniques to investigate if infection with prions results in an increased PrP gene expression. For the experiments we used N2a cells which had been infected with prions (ScN2a cells). We demonstrated by confocal laser scanning microscopy that PrP-protein was present in the nucleus (predominantly in the nucleoli) of ScN2a cells. Analysis of the PrP-mRNA levels both in N2a- and in ScN2a cells usi…

Gene isoformPrPSc ProteinsTranscription GeneticNucleolusPrionsanimal diseasesClinical BiochemistryCellImmunocytochemistryGene ExpressionScrapieNerve Tissue ProteinsBiologyBiochemistryMiceNeuroblastomaGene expressionmedicineTumor Cells CulturedAnimalsNorthern blotRNA MessengerCell NucleusMessenger RNACell BiologyGeneral MedicineMolecular biologynervous system diseasesKineticsmedicine.anatomical_structureCell NucleolusCell biochemistry and function
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SNAP-25a and -25b isoforms are both expressed in insulin-secreting cells and can function in insulin secretion

1999

The tSNARE (the target-membrane soluble NSF-attachment protein receptor, where NSF is N-ethylmaleimide-sensitive fusion protein) synaptosomal-associated protein of 25 kDa (SNAP-25) is expressed in pancreatic B-cells and its cleavage by botulinum neurotoxin E (BoNT/E) abolishes stimulated secretion of insulin. In the nervous system, two SNAP-25 isoforms (a and b) have been described that are produced by alternative splicing. Here it is shown, using reverse transcriptase PCR, that messages for both SNAP-25 isoforms are expressed in primary pancreatic B and non-B cells as well as in insulin-secreting cell lines. After transfection, both isoforms can be detected at the plasma membrane as well a…

Gene isoformProtein Isoforms/genetics/ metabolismBotulinum ToxinsSynaptosomal-Associated Protein 25RNA Messenger/genetics/metabolismmedicine.medical_treatmentMutantNerve Tissue ProteinsBiologyBiochemistryCell LineIslets of LangerhansInsulin SecretionmedicineBotulinum Toxins/pharmacologyInsulinProtein IsoformsAnimalsHumansSecretionRNA MessengerReceptorMolecular BiologyDNA Primersddc:616Base SequenceInsulinMembrane ProteinsCell BiologyTransfectionNerve Tissue Proteins/genetics/ metabolismFusion proteinMolecular biologyRatsCell cultureMutagenesis Site-DirectedIslets of Langerhans/cytology/drug effects/ secretionInsulin/ secretionResearch Article
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The Xenopus Oocyte as an Ectopic Expression System for the Selection of Protein Isoform-Specific Antibodies

1993

A panel of Xenopus oocytes, each injected with cRNA coding for one specific isoform of the rat brain RCK family of voltage gated potassium channel proteins, was employed to screen for isoform-specific monoclonal antibodies. Several days after injection, cryosections of embedded oocytes were produced and were employed in immunohistochemical analysis of antibody binding. Of the advantageous properties of the assay, it employs the native antigen, it can be applied to homooligomeric and heterooligomeric proteins, and cryosections of the same batch can be stored frozen for later tests. The method may be advantageous also for the selection of isoform-specific antibodies of other protein families.

Gene isoformProtein isoformPotassium ChannelsProtein familymedicine.drug_classRecombinant Fusion ProteinsXenopusNerve Tissue ProteinsBiologyMonoclonal antibodyEpitopeMiceXenopus laevisAntigenAntibody SpecificitymedicineAnimalsPharmacologyMice Inbred BALB CHybridomasAntibodies Monoclonalbiology.organism_classificationMolecular biologyOocytesFemaleEctopic expressionJournal of Receptor Research
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Application of an ectopic expression system for the selection of protein-isoform-specific antibodies. The monoclonal antibody K1 C3 is specific for t…

1993

Monoclonal antibodies were raised against a fusion protein consisting of a fragment of 141 amino acids of the C-terminal region of the rat brain voltage-gated K(+)-channel protein (RCK1) and the lambda N protein (fusion protein I). Selection of K(+)-channel-specific hybridoma cell lines was performed by means of an ELISA employing a fusion protein consisting of the K(+)-channel-specific peptide sequence and glutathione S-transferase (fusion protein II). For final selection of RCK1 isoform-specific antibodies, a panel of Xenopus oocytes was employed, each injected with cRNA coding for a specific RCK isoform (RCK 1, 2, 4 or 5). Several days after injection, cryosections of embedded oocytes we…

Gene isoformProtein isoformPotassium Channelsmedicine.drug_classBlotting WesternMolecular Sequence DataEnzyme-Linked Immunosorbent AssayMonoclonal antibodyBiochemistryMiceAntibody SpecificityProtein A/GTumor Cells CulturedmedicineAnimalsAmino Acid SequenceRats WistarPeptide sequenceBrain ChemistryMice Inbred BALB CHybridomasSequence Homology Amino AcidbiologyAntibodies MonoclonalFusion proteinMolecular biologyRatsBiochemistryPotassium Channels Voltage-Gatedbiology.proteinImmunohistochemistryAntibodyKv1.1 Potassium ChannelEuropean Journal of Biochemistry
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