Search results for "Tissue distribution"

showing 10 items of 240 documents

Actin binding LIM protein 3 (abLIM3).

2005

LIM domain proteins were demonstrated to play key roles in various biological processes such as embryonic development, cell lineage determination, and cancer differentiation. Actin binding LIM protein 1 (abLIM1) was reported to be localized in a genomic region often deleted in human cancers and suggested to be involved in axon guidance. Recently, existence of a second family member was reported, actin binding LIM protein 2. By means of computational biology and comparative genomics, we now characterized an additional, third member of the actin binding LIM protein subgroup, actin binding LIM protein 3 (abLIM3). The human mRNA sequence was previously annotated as differentially regulated in h…

Homeodomain ProteinsMicrofilament ProteinsMolecular Sequence DataSequence alignmentGeneral MedicineGenomicsBiologyActin cytoskeletonMolecular biologyConserved sequenceGeneticsAnimalsHumansABLIM1Tissue DistributionAmino Acid SequenceABLIM3LHX3Databases Nucleic AcidSequence AlignmentActinLIM domainInternational journal of molecular medicine
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Magnetic Resonance Microscopy Contribution to Interpret High-Resolution Magic Angle Spinning Metabolomic Data of Human Tumor Tissue

2010

[EN] HRMAS NMR is considered a valuable technique to obtain detailed metabolic profile of unprocessed tissues. To properly interpret the HRMAS metabolomic results, detailed information of the actual state of the sample inside the rotor is needed. MRM (Magnetic Resonance Microscopy) was applied for obtaining structural and spatially localized metabolic information of the samples inside the HRMAS rotors. The tissue was observed stuck to the rotor wall under the effect of HRMAS spinning. MRM spectroscopy showed a transference of metabolites from the tissue to the medium. The sample shape and the metabolite transfer after HRMAS indicated that tissue had undergone alterations and it can not be s…

Hrmas nmrMagnetic Resonance SpectroscopyProteomelcsh:BiotechnologyHealth Toxicology and Mutagenesislcsh:MedicineHigh resolutionNuclear magnetic resonanceMetabolomicslcsh:TP248.13-248.65Tumor Cells CulturedGeneticsMagic angle spinningHumansTissue DistributionMolecular BiologyMethodology ReportBrain NeoplasmsMagnetic resonance microscopyChemistrylcsh:RGliomaGeneral MedicineNuclear magnetic resonance spectroscopyMagnetic Resonance ImagingHuman tumorBiochemistryMetabolomeMolecular MedicineSpin LabelsMetabolic profileBiotechnologyJournal of Biomedicine and Biotechnology
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RT-PCR and in situ hybridization analysis of apolipoprotein H expression in rat normal tissues

2006

In this study, by using different techniques (i.e. Northern blot hybridization, RT-PCR and Southern blot hybridization) on various normal rat tissues, we were able to identify liver, kidney, heart, small intestine, brain, spleen, stomach and prostate as tissues in which the ApoH gene is transcribed. Moreover, for some of these tissues, by in situ hybridization, we found a specific localization of apoH transcripts. For instance epithelial cells of the bile ducts in liver and of the proximal tubules in kidney are the major sites of apoH synthesis. Our data suggest that some of the different physiological roles proposed for apoH could correlate with its direct expression, while others could co…

In situ hybridizationBiologyß-2-glycoprotein I apoH antiphospholipid syndrome Fanconi syndromeKidneyGeneticsmedicineAnimalsHumansBeta 2-Glycoprotein ITissue DistributionRNA MessengerNorthern blotRats WistarCells CulturedIn Situ HybridizationGlycoproteinsSouthern blotReverse Transcriptase Polymerase Chain ReactionGene Expression ProfilingMyocardiumKidney metabolismGeneral MedicineMolecular biologySmall intestineRatsJejunumReal-time polymerase chain reactionmedicine.anatomical_structureLiverbeta 2-Glycoprotein IApolipoprotein H
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Age-Related Inflammation: the Contribution of Different Organs, Tissues and Systems. How to Face it for Therapeutic Approaches

2010

A typical feature of ageing is a chronic, low-grade inflammation characterized by a general increase in the production of pro-inflammatory cytokines and inflammatory markers ("inflamm-ageing"). This status may slowly damage one or several organs, especially when unfavorable genetic polymorphisms and epigenetic alterations are concomitant, leading to an increased risk of frailty together with the onset of age-related chronic diseases. The contribution of different tissues (adipose tissue, muscle), organs (brain, liver), immune system and ecosystems (gut microbiota) to age-related inflammation ("inflamm-ageing") will be discussed in this review in the context of its onset/progression leading …

InflammationPharmacologySenescenceAgingbiologyLongevityAdipose tissueInflammationAgeing age-related diseases immunosenescence inflammationImmunosenescenceGut florabiology.organism_classificationPhenotypeImmune systemOrgan SpecificityDrug DiscoveryImmunologymedicineAnimalsHumansTissue DistributionEpigeneticsmedicine.symptomCurrent Pharmaceutical Design
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Sublethal bioconcentration of fenitrothion in the blood and brain of the european eel.

1998

InsecticidesHealth Toxicology and MutagenesisWater pollutantsZoologyBrainBioconcentrationGeneral MedicineEnvironmental exposureEnvironmental ExposureFenitrothionBiologyToxicologyAnguillaPollutionFenitrothionToxicologychemistry.chemical_compoundchemistryEcotoxicologyAnimalsTissue DistributionTissue distributionWater Pollutants ChemicalBulletin of environmental contamination and toxicology
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Pesticide toxicokinetics in fish: accumulation and elimination.

1998

Bioaccumulation of fenitrothion in the European eel (Anguilla anguilla) was studied using two sublethal concentrations of this pesticide in a flow-through test system. The pesticide concentrations used were one-tenth (0.002 ppm) and one-fifth (0.04 ppm) the 96-h LC50 of fenitrothion in this species. Steady state was reached early (2 h) when the animals were exposed to 0.02 ppm of toxicant, and after 48 h when the animals were exposed to 0.04 ppm. Toxicokinetic parameters for fenitrothion in eel muscle (K1, K2, and T1/2) were calculated for both experiments. The highest bioconcentration factor was calculated for animals exposed to 0.04 ppm of toxicant, indicating the relationship between the…

InsecticidesbiologyHealth Toxicology and MutagenesisMusclesPublic Health Environmental and Occupational HealthBioconcentrationGeneral MedicineFenitrothionPesticidebiology.organism_classificationAnguillaPollutionFenitrothionExcretionchemistry.chemical_compoundchemistryAnguillidaeBioaccumulationEnvironmental chemistryToxicokineticsAnimalsTissue DistributionWater Pollutants ChemicalToxicantHalf-LifeEcotoxicology and environmental safety
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Preliminary approach to elucidate the role of pigment as a binding site for drugs and chemicals in anagen hair: differential uptake of 3 H-haloperido…

2002

A striking difference was observed for cellular-bound drug in HaCaT and Sk-Mel-1 cells for a fixed drug exposure time of 72 h and varying 3H-haloperidol concentrations in the culture media. Drug uptake was dependent on drug concentration and linearly correlated for both the non-pigment- and the pigment-producing cells which however was different in magnitude. In an additional investigation the time course of drug uptake during 3H-haloperidol exposure (400 pmol/ml; 28 days) revealed increasing drug concentrations in the Sk-Mel-1 population, whereas drug concentrations in the keratinocytes reached a plateau within a short time period. In contrast to the HaCaT cells no tendency to saturation w…

KeratinocytesDrugmedia_common.quotation_subjectPopulationBiologyPharmacologyCell LinePathology and Forensic MedicineMelaninPigmentHaloperidolmedicineHumansTissue DistributionBinding siteeducationmedia_commonMelaninseducation.field_of_studyBinding SitesMelanosomesPigmentationHaCaTCell culturevisual_artvisual_art.visual_art_mediumHaloperidolHairmedicine.drugInternational Journal of Legal Medicine
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Preliminary approach to elucidate the role of pigment as a binding site for drugs and chemicals in anagen hairs: pigments as carriers for 3 H-haloper…

2002

In view of the melanin-binding characteristics of haloperidol and its differential uptake by pigment- and non-pigment-producing cells, a co-culture of HaCaT with Sk-Mel-1 cell lines was performed to investigate whether melanosomes act as carriers for drug molecules associated with the pigments. Initially, HaCaT and Sk-Mel-1 cells were separately cultivated in the presence of 3H-haloperidol (400 pmol/ml medium ) for 28 days followed by subsequent co-cultivation in the absence of 3H-haloperidol for 5 days. The transfer of pigments into the keratinocytes during co-culture was confirmed by transmission electron microscopy. After the co-culture experiments a striking increase (or = 50%) of 3H-ha…

KeratinocytesStereochemistryCellBiologyPathology and Forensic MedicineMelaninPigmentmedicineHumansTissue DistributionMelanosomeMelaninsBinding SitesMelanosomesintegumentary systemPigmentationHair follicleMolecular biologyCoculture TechniquesIn vitroMicroscopy ElectronHaCaTmedicine.anatomical_structureCell culturevisual_artvisual_art.visual_art_mediumHaloperidolsense organsHairInternational Journal of Legal Medicine
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Rare earths, zirconium and hafnium distribution in coastal areas: The example of Sabella spallanzanii (Gmelin, 1791)

2016

The Zr, Hf, Y and lanthanide (REE) distribution in biological tissues of Sabella spallanzanii and Styela plicata species collected from two harbours from the northern Sicily is studied for providing information regarding the Zr, Hf and REE uptake from the environment. Previous studies determined the fractionation of dissolved REE scavenged on binding sites onto biological surfaces. By comparing the recognised shale-normalised REE patterns of studied samples with evidence from reference data, the observed behaviour of these elements in biological tissues of Sabella spallanzanii and Styela plicata is interpreted to result from the preferential uptake of intermediate REE onto carboxylic sites.…

LanthanideSabella spallanzaniiEnvironmental EngineeringHealth Toxicology and Mutagenesischemistry.chemical_elementMineralogyFractionation010501 environmental sciences010502 geochemistry & geophysics01 natural sciencesRare earths Sabella spallanzanii Styela plicataAnimalsEnvironmental ChemistryTissue DistributionSicilyDissolutionVehicle Emissions0105 earth and related environmental sciencesZirconiumbiologyPublic Health Environmental and Occupational HealthDustPolychaetaGeneral MedicineGeneral Chemistrybiology.organism_classificationPollutionHafniumStyela plicatachemistryEnvironmental chemistryBioaccumulationMetals Rare EarthZirconiumHafniumEnvironmental Monitoring
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Dual Labeling of Lipopolysaccharides for SPECT-CT Imaging and Fluorescence Microscopy.

2013

International audience; : Lipopolysaccharides (LPS) or endotoxins are amphipathic, pro-inflammatory components of the outer membrane of Gram-negative bacteria. In the host, LPS can trigger a systemic inflammatory response syndrome. To bring insight into in vivo tissue distribution and cellular uptake of LPS, dual labeling was performed with a bimodal molecular probe designed for fluorescence and nuclear imaging. LPS were labeled with DOTA-Bodipy-NCS, and pro-inflammatory properties were controlled after each labeling step. LPS were then radiolabeled with (111)In and subsequently injected intravenously into wild-type, C57B16 mice, and their in vivo behavior was followed by single photon emis…

LipopolysaccharidesBiodistribution[CHIM.THER]Chemical Sciences/Medicinal Chemistry[ SDV.BBM.BM ] Life Sciences [q-bio]/Biochemistry Molecular Biology/Molecular biology010402 general chemistry01 natural sciencesBiochemistryLipopolysaccharide transport03 medical and health sciencesMiceIn vivoCoordination ComplexesFluorescence microscope[INFO.INFO-IM]Computer Science [cs]/Medical ImagingAnimals[CHIM.COOR]Chemical Sciences/Coordination chemistryTissue Distribution030304 developmental biologyFluorescent DyesTomography Emission-Computed Single-Photon0303 health sciencesMolecular Structure[ INFO.INFO-IM ] Computer Science [cs]/Medical ImagingChemistryIndium Radioisotopes[ CHIM.COOR ] Chemical Sciences/Coordination chemistry[SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry Molecular Biology/Molecular biology[ CHIM.THER ] Chemical Sciences/Medicinal ChemistryGeneral MedicineFluorescence0104 chemical sciencesMice Inbred C57BLMicroscopy FluorescenceIsotope LabelingBiophysicsMolecular Medicinelipids (amino acids peptides and proteins)Bacterial outer membraneMolecular probe[CHIM.RADIO]Chemical Sciences/Radiochemistry[ CHIM.RADIO ] Chemical Sciences/RadiochemistryEx vivo
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