Search results for "labeling"

showing 10 items of 372 documents

In BCR-ABL-positive cells, STAT-5 tyrosine-phosphorylation integrates signals induced by imatinib mesylate and Ara-C.

2003

In BCR-ABL-positive cells, the transcription factor STAT-5 is constitutively activated by tyrosine phosphorylation. STAT-5 activation results in upregulation of bcl-X(L) and increased resistance to induction of apoptosis. Here, we investigated the effects of imatinib mesylate and cytosine arabinoside (Ara-C) on STAT-5 tyrosine-phosphorylation, cellular proliferation and induction of apoptosis in cell lines and primary hematopoietic cells. Imatinib mesylate treatment strongly suppressed STAT-5 tyrosine-phosphorylation in K562 and primary CML blasts. In contrast to JAK-2 and PI-3-kinase inhibition, exposure of K562 cells to imatinib mesylate resulted in obvious suppression of proliferation. R…

Cancer ResearchProgrammed cell deathBlotting WesternFusion Proteins bcr-ablDown-RegulationAntineoplastic AgentsApoptosisBiologyPiperazineschemistry.chemical_compoundDownregulation and upregulationhemic and lymphatic diseasesLeukemia Myelogenous Chronic BCR-ABL PositivemedicineIn Situ Nick-End LabelingSTAT5 Transcription FactorHumansEnzyme InhibitorsPhosphorylationCell growthCytarabineImatinibTyrosine phosphorylationDrug SynergismHematologyDNAU937 CellsProtein-Tyrosine KinasesMilk ProteinsPrecipitin TestsDNA-Binding ProteinsImatinib mesylatePyrimidinesOncologychemistryApoptosisCaspasesBenzamidesCancer researchImatinib MesylateTrans-ActivatorsTyrosinePoly(ADP-ribose) PolymerasesK562 CellsCell Divisionmedicine.drugK562 cellsSignal TransductionLeukemia
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Cell Harvesting Methods Affect Cellular Integrity of Adherent Cells During Apoptosis Detection.

2018

Background/aim Annexin V and propidium iodide (PI) dual staining is commonly applied in bioscience as a method to detect apoptosis. However, excessive handling of adherent cells may interfere with the integrity of plasma membrane and hence impede the accuracy of this method. Here, we exploited PI uptake as an indicator of cell integrity and investigated how cell harvesting methods and solutions involved in common apoptosis detection techniques affected measurement results. Materials and methods Different cell harvesting techniques, staining with PI and flow cytometry were performed. Results Non-fixed scrapped cells revealed significantly higher fractions of PI-positive staining compared to …

Cancer ResearchProgrammed cell deathCellCell Culture TechniquesApoptosis02 engineering and technologyCell Separation010402 general chemistry01 natural sciencesFlow cytometrychemistry.chemical_compoundAnnexinCell Line TumormedicineCell AdhesionHumansTrypsinPropidium iodideAnnexin A5medicine.diagnostic_testStaining and LabelingChemistryGeneral Medicine021001 nanoscience & nanotechnologyFlow Cytometry0104 chemical sciencesStainingCell biologyTrypsinizationmedicine.anatomical_structureOncologyApoptosisBiological Assay0210 nano-technologyPropidiumAnticancer research
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Desferrioxamine as an appropriate chelator for 90Nb: Comparison of its complexation properties for M-Df-Octreotide (M=Nb, Fe, Ga, Zr)

2014

The niobium-90 radioisotope ((90)Nb) holds considerable promise for use in immuno-PET, due to its decay parameters (t½ = 14.6h, positron yield=53%, Eß(+)(mean) = 0.35 MeV and Eß(+)(max) = 1.5 MeV). In particular, (90)Nb appears well suited to detect in vivo the pharmacokinetics of large targeting vectors (50-150 kDa). In order to be useful for immuno-PET chelators are required to both stabilize the radionuclide in terms of coordination chemistry and to facilitate the covalent attachment to the targeting vector. Different chelators were evaluated for this purpose in terms of radiolabelling efficiency and stability of the radiolabelled Nb(V) complex and in order to determine the most suitable…

Cancer ResearchStereochemistryNiobiumMetal ions in aqueous solutionKineticsOctreotideRadiation DosageCoordination complexTransmetalationDrug StabilityMaterials TestingMoleculeRadiology Nuclear Medicine and imagingChelationChelating AgentsIonsRadioisotopeschemistry.chemical_classificationChemistryMetalsCovalent bondIsotope LabelingMolecular MedicineRadiopharmaceuticalsNuclear chemistryConjugateNuclear Medicine and Biology
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Synthesis and PET studies of [11C-cyano]letrozole (Femara®), an aromatase inhibitor drug

2009

Abstract Introduction Aromatase, a member of the cytochrome P 450 family, converts androgens such as androstenedione and testosterone into estrone and estradiol, respectively. Letrozole (1-[bis-(4-cyanophenyl)methyl]-1 H -1,2,4-triazole; Femara) is a high-affinity aromatase inhibitor ( K i =11.5 nM) that has Food and Drug Administration approval for breast cancer treatment. Here we report the synthesis of carbon-11-labeled letrozole and its assessment as a radiotracer for brain aromatase in the baboon. Methods Letrozole and its precursor (4-[(4-bromophenyl)-1 H -1,2,4-triazol-1-ylmethyl]benzonitrile) were prepared in a two-step synthesis from 4-cyanobenzyl bromide and 4-bromobenzyl bromide,…

Cancer Researchmedicine.medical_specialtymedicine.drug_classEstronePharmacologyArticlechemistry.chemical_compoundAromatasePharmacokineticsInternal medicineNitrilesmedicineAnimalsRadiology Nuclear Medicine and imagingAndrostenedioneCarbon RadioisotopesAromataseTestosteroneAromatase inhibitorbiologyChemistryAromatase InhibitorsLetrozoleBrainTriazolesEndocrinologyFree fractionIsotope LabelingPositron-Emission TomographyLetrozolebiology.proteinMolecular MedicineFemaleRadiopharmaceuticalsmedicine.drugPapio
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Assessment of Escherichia coli B with enhanced permeability to fluorochromes for flow cytometric assays of bacterial cell function.

2002

Background Flow cytometry has become a choice methodology for microbiological research. However, functional cytometric assays in live bacteria are still limited. This is due, in part, to the cell wall impairing penetration of vital dyes in bacteria, thus imposing permeabilization procedures. These manipulations may affect cell physiology, provoke cell aggregation or lysis, and they are time-consuming. Escherichia coli B strains have been used for mutagenic assays because of an altered lipopolysaccharide that provokes increased membrane permeability. We assessed the use of these strains as possible alternatives for flow cytometric assays to avoid the permeabilization steps. Methods Suspensio…

Cell Membrane PermeabilityMembrane permeabilityBiophysicsBiologymedicine.disease_causePathology and Forensic MedicineFlow cytometrychemistry.chemical_compoundEndocrinologymedicineEscherichia coliPropidium iodideFluorescein isothiocyanateEscherichia coliFluorescent Dyesmedicine.diagnostic_testStaining and LabelingCell BiologyHematologyFlow CytometryMolecular biologyCell aggregationStainingOxidative StresschemistryBiochemistryCytometryCytometry
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Geographical mapping of metabolites in biological tissue with quantitative bioluminescence and single photon imaging

1993

This article features a novel technique for measuring the spatial distribution of metabolites, such as ATP, glucose, and lactate, in rapidly frozen tissue. Concentration values are obtained in absolute terms and with a spatial resolution of single-cell dimension. The method is based on enzymatic reactions that link the metabolite of interest to luciferase with subsequent light emission. Using a specific array, cryosections are brought into contact with the enzymes in a well-defined, reproducible way inducing a distribution of light across the section with an intensity that is proportional to the metabolite concentration. The emitted light can be visualized through a microscope and an imagin…

Cell SurvivalMetaboliteUterine Cervical NeoplasmsCarbohydrate metabolismBiologyMiceStructure-Activity Relationshipchemistry.chemical_compoundAdenosine TriphosphateNeoplasmsTumor Cells CulturedAnimalsFrozen SectionsHumansBioluminescenceTissue DistributionLuciferaseLactic AcidMelanomaCells Culturedchemistry.chemical_classificationMice Inbred BALB CStaining and LabelingHistocytochemistryMyocardiumCell BiologyPhoton countingRatsLactic acidGlucoseEnzymechemistryBiochemistryLuminescent MeasurementsLactatesBiophysicsFemaleLight emissionAnatomyThe Histochemical Journal
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Anti-inflammatory effects of chemically modified tetracyclines by the inhibition of nitric oxide and interleukin-12 synthesis in J774 cell line

2001

We investigated the effects of chemically modified tetracyclines (CMTs) on the production of nitric oxide (NO) and on the synthesis of some cytokines: tumour necrosis factor alpha (TNF-alpha), interleukin(IL)-10 and IL-12 in lipopolysaccharide (LPS)-treated J774 cell line. Furthermore, we studied the ability of these drugs to modify the viability in LPS-stimulated J774 macrophages. CMTs decreased, in a dose-dependent manner, inducible NO synthase (iNOS) activity and, consequently, nitrite formation in J774 cultures. The CMT-induced decrease in NO production is due to the inhibition of enzyme activity rather than to a direct effect on enzyme expression. The absence of the inhibition in mRNA …

Cell Survivalmedicine.medical_treatmentImmunologyNitric Oxide Synthase Type IIApoptosisEnzyme-Linked Immunosorbent AssayNitric OxideCell LineNitric oxideMicechemistry.chemical_compoundEthidiumIn Situ Nick-End LabelingmedicineAnimalsImmunology and AllergyRNA MessengerViability assayEnzyme InhibitorsFluorescent DyesPharmacologybiologyReverse Transcriptase Polymerase Chain ReactionAnti-Inflammatory Agents Non-SteroidalInterleukinBiological activityInterleukin-12Acridine OrangeCell biologyNitric oxide synthaseInterleukin 10CytokinechemistryBiochemistryTetracyclinesApoptosisbiology.proteinCytokinesElectrophoresis Polyacrylamide GelIndicators and ReagentsNitric Oxide SynthaseInternational Immunopharmacology
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A Safe and Effective Magnetic Labeling Protocol for MRI-Based Tracking of Human Adult Neural Stem Cells

2019

Magnetic resonance imaging (MRI) provides a unique tool for in vivo visualization and tracking of stem cells in the brain. This is of particular importance when assessing safety of experimental cell treatments in the preclinical or clinical setup. Yet, specific imaging requires an efficient and non-perturbing cellular magnetic labeling which precludes adverse effects of the tag, e.g., the impact of iron-oxide-nanoparticles on the critical differentiation and integration processes of the respective stem cell population investigated. In this study we investigated the effects of very small superparamagnetic iron oxide particle (VSOP) labeling on viability, stemness, and neuronal differentiatio…

Cell physiologyImmunocytochemistryImaging phantomlcsh:RC321-57103 medical and health sciences0302 clinical medicineMedizinische FakultätIn vivomedicinemagnetic resonance imagingddc:610lcsh:Neurosciences. Biological psychiatry. NeuropsychiatryCNS – disorderOriginal Research030304 developmental biology0303 health sciencesmedicine.diagnostic_testChemistryQHGeneral Neurosciencemagnetic labelingCNS-disorderMagnetic resonance imagingVSOPR1Neural stem cellQRddc:Human Adult Stem Cells ; Magnetic Labeling ; Mri ; Cell Tracking ; Cns - DisorderCell biologycell trackingCNS – disorder ; human adult stem cells ; magnetic labeling ; MRI ; cell trackingStem cell030217 neurology & neurosurgeryNeuroscienceRChuman adult stem cellsMRIFrontiers in Neuroscience
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Immunohistochemical location of HPL, SP1 and β-HCG in normal placentas of varying gestational age

1986

Sixty-four placentas at various gestational ages were examined by immunohistochemical stains for HPL, SP1 and beta-HCG according to a modified PAP method (Sternberger 1970). Syncytiotrophoblast cell layer was identified as the main site of synthesis. Extravillous immunohistochemical reactions for HPL and SP1 (but not for beta-HCG) were found in X-cells of the basal plate and in the intervillous trophoblast islands. These cell types would thus seem to be derived from trophoblast. Hofbauer-cells of villous connective tissue stained specifically for beta-HCG apparently because of HCG phagocytosis. The intensity of staining for HPL, SP1 and beta-HCG was evaluated semiquantitatively in the syncy…

Cell typeTime FactorsPlacentaBasal plate (neural tube)Connective tissuePregnancy ProteinsBiologyChorionic GonadotropinImmunoenzyme TechniquesAndrologySyncytiotrophoblastPregnancymedicineHumansreproductive and urinary physiologyStaining and LabelingHistocytochemistryPregnancy-Specific beta 1-GlycoproteinsObstetrics and GynecologyGestational ageTrophoblastGeneral MedicinePlacental Lactogenfemale genital diseases and pregnancy complicationsTrophoblastsStainingmedicine.anatomical_structureembryonic structuresImmunologyImmunohistochemistryFemaleChorionic VilliArchives of Gynecology
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Neurons of the dentate molecular layer in the rabbit hippocampus.

2012

The molecular layer of the dentate gyrus appears as the main entrance gate for information into the hippocampus, i.e., where the perforant path axons from the entorhinal cortex synapse onto the spines and dendrites of granule cells. A few dispersed neuronal somata appear intermingled in between and probably control the flow of information in this area. In rabbits, the number of neurons in the molecular layer increases in the first week of postnatal life and then stabilizes to appear permanent and heterogeneous over the individuals' life span, including old animals. By means of Golgi impregnations, NADPH histochemistry, immunocytochemical stainings and intracellular labelings (lucifer yellow…

Central Nervous SystemAnatomy and PhysiologyCell Countchemistry.chemical_compoundMolecular Cell BiologyComparative AnatomyNeuronsMultidisciplinaryNeuronal MorphologyPyramidal CellsQRAnimal ModelsAnatomyElectrophysiologymedicine.anatomical_structureNissl BodiesNissl bodysymbolsMedicineFemaleRabbitsCellular TypesResearch Articlemedicine.drugHistologyScienceNeurophysiologyBiologygamma-Aminobutyric acidsymbols.namesakeModel OrganismsDevelopmental NeuroscienceBiocytinmedicineAnimalsBiologyCell ShapeLucifer yellowStaining and LabelingDentate gyrusPerforant pathEntorhinal cortexElectrophysiological PhenomenaNeuroanatomyElectrophysiologychemistrynervous systemCellular NeuroscienceDentate GyrusBiophysicsNeural Circuit FormationNeurosciencePLoS ONE
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