Search results for "Fluorescence"

showing 10 items of 2463 documents

Light-induced charge separation in a donor–chromophore–acceptor nanocomposite poly[TPA-Ru(tpy)2]@ZnO

2013

The synthesis and characterisation of a new donor–chromophore–acceptor system based on poly(vinyltriphenylamine) as the electron donor and a glycine-functionalised bis(2,2′;6′,2′′-terpyridine)ruthenium(II) complex acting both as a chromophore and as an anchor group attached to ZnO nanorods as the electron acceptor are described. The TPA-containing block copolymer was synthesised by Reversible Addition Fragmentation Chain Transfer (RAFT) polymerisation and the ruthenium complex glycine conjugates prepared by Solid Phase Peptide Synthesis (SPPS) were attached via post-polymerisation esterification. GPC, NMR, IR and UV-Visible spectroscopy were used to characterise the multifunctional chromoph…

Kelvin probe force microscopechemistry.chemical_classificationQuenching (fluorescence)Materials sciencechemistry.chemical_elementElectron donorGeneral ChemistryChromophoreElectron acceptorPhotochemistryAcceptorRutheniumchemistry.chemical_compoundchemistryPolymerizationPolymer chemistryMaterials ChemistryJ. Mater. Chem. C
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Unsaturated Fatty Acids Drive Disintegrin and Metalloproteinase (ADAM)-dependent Cell Adhesion, Proliferation, and Migration by Modulating Membrane F…

2011

The disintegrin-metalloproteinases ADAM10 and ADAM17 mediate the release of several cell signaling molecules and cell adhesion molecules such as vascular endothelial cadherin or L-selectin affecting endothelial permeability and leukocyte transmigration. Dysregulation of ADAM activity may contribute to the pathogenesis of vascular diseases, but the mechanisms underlying the control of ADAM functions are still incompletely understood. Atherosclerosis is characterized by lipid plaque formation and local accumulation of unsaturated free fatty acids (FFA). Here, we show that unsaturated FFA increase ADAM-mediated substrate cleavage. We demonstrate that these alterations are not due to genuine ch…

KeratinocytesMembrane FluidityADAM10Lipid BilayersVascular permeabilityBiologyADAM17 ProteinBiochemistryCapillary PermeabilityADAM10 ProteinCell MovementMembrane fluidityCell AdhesionAnimalsHumansCell adhesionMolecular BiologyCell ProliferationCell adhesion moleculeCell growthFluorescence recovery after photobleachingEndothelial CellsMembrane ProteinsCell BiologyAtherosclerosisADAM ProteinsCell biologyLipoproteins LDLADAM ProteinsHEK293 CellsFatty Acids UnsaturatedCholesterol EstersRabbitsAmyloid Precursor Protein SecretasesGranulocytes
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Induction of Cell Differentiation in Transformed Keratinocytes by Synthetic (Glyco)peptides from the Homophilic Recognition Domain of E-Cadherin

2002

KeratinocytesProtein ConformationCadherinChemistryStereochemistryCellular differentiationMolecular Sequence DataGlycopeptidesCell DifferentiationGeneral ChemistryCadherinsPeptide FragmentsCatalysisGlycopeptideProtein Structure TertiaryDomain (software engineering)Cell biologySolid-phase synthesisMicroscopy FluorescenceHumansAmino Acid SequenceNuclear Magnetic Resonance BiomolecularCell Line TransformedAngewandte Chemie International Edition
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Exosomes released by keratinocytes modulate melanocyte pigmentation

2015

Cells secrete extracellular vesicles (EVs), exosomes and microvesicles, which transfer proteins, lipids and RNAs to regulate recipient cell functions. Skin pigmentation relies on a tight dialogue between keratinocytes and melanocytes in the epidermis. Here we report that exosomes secreted by keratinocytes enhance melanin synthesis by increasing both the expression and activity of melanosomal proteins. Furthermore, we show that the function of keratinocyte-derived exosomes is phototype-dependent and is modulated by ultraviolet B. In sum, this study uncovers an important physiological function for exosomes in human pigmentation and opens new avenues in our understanding of how pigmentation is…

KeratinocytesProteomicsUltraviolet RaysGeneral Physics and AstronomyBiologyMelanocyteProteomicsExosomesReal-Time Polymerase Chain ReactionGeneral Biochemistry Genetics and Molecular BiologyArticleTandem Mass SpectrometrymedicineHumansSecretionRNA MessengerCells CulturedMelanosomeRegulation of gene expressionMelaninsMultidisciplinaryMelanosomesEpidermis (botany)PigmentationGeneral ChemistryMicrovesiclesCell biologyMicroscopy Electronmedicine.anatomical_structureGene Expression RegulationMicroscopy FluorescenceMelanocytesEpidermisIntracellularChromatography LiquidNature Communications
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Potential antipsoriatic effect of chondroitin sulfate through inhibition of NF-κB and STAT3 in human keratinocytes

2012

Abstract Chondroitin sulfate (CS) is a natural glycosaminoglycan, formed by the 1–3 linkage of d -glucuronic acid to N-acetylgalactosamine, present in the extracellular matrix. It is used as a slow acting disease modifying agent in the treatment of osteoarthritis, and part of its beneficial effects are due to its antiinflammatory properties that result from an inhibitory effect on NF-κB signaling pathway. This ability raises the hypothesis that CS might be effective in other chronic inflammatory processes such as psoriasis, in which a deregulation of NF-κB is a key feature. In addition, psoriasis is characterized by an upregulation of STAT3 signaling pathway that is related to the epidermal…

KeratinocytesSTAT3 Transcription FactorBlotting WesternPrimary Cell CultureAnti-Inflammatory AgentsDermoscopyElectrophoretic Mobility Shift AssayPharmacologyStat3 Signaling Pathwaychemistry.chemical_compoundDownregulation and upregulationPsoriasismedicineHumansPsoriasisChondroitin sulfateCells CulturedPharmacologyChemistryChondroitin SulfatesNF-kappa BNF-κBmedicine.diseaseMicroscopy FluorescenceImmunologyPhosphorylationTumor necrosis factor alphaSignal transductionProtein BindingPharmacological Research
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A region on human chromosome 4 (q35.1→qter) induces senescence in cell hybrids and is involved in cervical carcinogenesis

2005

Human papillomavirus (HPV) types 16 and 18 are known to play a major role in cervical carcinogenesis. Additional genetic alterations are required for the development and progression of cervical cancer. Previously, we showed that the introduction of an entire human chromosome 4 into HPV-immortalized cells by microcell-mediated chromosome transfer (MMCT) can induce senescence in cell hybrids. In the present study, we established eight new murine donor cell lines harboring different fragments of the human chromosome 4. These were tested for their ability to induce senescence by MMCT into HPV16-immortalized keratinocytes (HPK II) and cervical carcinoma cells (HeLa). By exclusion, we could ident…

KeratinocytesSenescenceCancer ResearchChromosome TransferUterine Cervical NeoplasmsLocus (genetics)Hybrid CellsBiologyPolymerase Chain ReactionLoss of heterozygosityGeneticsmedicineHumansAlleleCellular SenescenceIn Situ Hybridization FluorescenceSequence DeletionChromosome AberrationsCervical cancermedicine.diagnostic_testChromosome Mappingmedicine.diseaseMolecular biologyChromosome 4FemaleChromosomes Human Pair 4Microsatellite RepeatsFluorescence in situ hybridizationGenes, Chromosomes and Cancer
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Stereodifferentiation in the formation and decay of the encounter complex in bimolecular electron transfer with photoactivated acceptors.

2005

Experimental evidence has been obtained for the involvement of encounter complexes between both enantiomers of a π,π* triplet excited ketone and a chiral phenol or indole. Determination of the pre-equilibrium constants (KEC) and the intrinsic decay rate constants (kd) indicates a significant stereodifferentiation in both steps of the quenching process. Perez Prieto, Julia, Julia.Perez@uv.es ; Galian, Raquel Eugenia, Raquel.Galian@uv.es ; Morant Miñana, Maria Carmen, Maica.Morant@uv.es

KetoneFormation and decayUNESCO::QUÍMICAPhotochemistry:QUÍMICA [UNESCO]Catalysischemistry.chemical_compoundElectron transferBimolecular electronReaction rate constantMaterials ChemistryPhenolUNESCO::QUÍMICA::Química orgánicaStereodifferentiatioPhotoactivated acceptorschemistry.chemical_classificationIndole testQuenching (fluorescence):QUÍMICA::Química orgánica [UNESCO]Metals and AlloysGeneral ChemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryExcited statePhotoactivated acceptors ; Bimolecular electron ; Stereodifferentiatio ; Formation and decayCeramics and CompositesEnantiomerChemical communications (Cambridge, England)
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Regio- and stereo-selectivity in the intramolecular quenching of the excited benzoylthiophene chromophore by tryptophan

2000

Laser flash photolysis studies on the photobehaviour of a series of bichromophoric derivatives bearing benzoylthiophene and tryptophan groups have shown that the efficiency of the intramolecular quenching process depends on both the stereochemistry of the chiral centers and the relative ketone versus tryptophan orientation. Perez Prieto, Julia, Julia.Perez@uv.es

KetoneUNESCO::QUÍMICAStereo-selectivityPhotochemistry:QUÍMICA [UNESCO]CatalysisTrytophanStereochemistryMaterials ChemistryRegio-selectivitychemistry.chemical_classificationQuenching (fluorescence)UNESCO::QUÍMICA::Química analíticaMetals and AlloysTryptophanGeneral ChemistryChromophoreRegio-selectivity ; Stereo-selectivity ; Benzoylthiophene chromophore ; Stereochemistry ; TrytophanSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBenzoylthiophene chromophorechemistryExcited stateIntramolecular force:QUÍMICA::Química analítica [UNESCO]Ceramics and CompositesFlash photolysisSelectivityChemical Communications
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Amyloid P component--a special type of collagen?

1978

The localization of amyloid P-components is demonstrated by immunofluorescence microscopy in normal human tissue (kidney, spleen, liver). The relation to collagen and to amyloidosis is discussed.

KidneyPathologymedicine.medical_specialtyAmyloidAmyloidChemistryAmyloidosisGoatsImmune SeraFluorescent Antibody TechniqueSpleenImmunofluorescence MicroscopyMiddle Agedmedicine.diseaseKidneyPathology and Forensic MedicineAmyloid P ComponentCollagen type I alpha 1medicine.anatomical_structureLivermedicineAnimalsHumansCollagenSpleenVirchows Archiv. B, Cell pathology
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Kininogen binding protein p33/gC1qR is localized in the vesicular fraction of endothelial cells

1996

AbstractThe endothelial protein p33/gC1qR is thought to mediate the assembly of components of the kinin-forming and complement-activating pathways on the surface of cardiovascular cells. FACS analysis of intact human umbilical vein endothelial cells using specific antibodies to p33 revealed a minor fluorescence on the cell surface whereas permeabilized cells showed a bright fluorescence indicative of an intracellular localization of p33. Immunostaining of fixed cells confirmed the predominant intracellular localization of p33. Fractionation studies demonstrated that the vesicular but not the membrane fraction of EA.hy926 cells is rich in p33. We conclude that externalization of p33 must pre…

Kininogen bindingp33Kininogen binding proteinCellBiophysicsComplementFluorescent Antibody TechniqueBiologyBiochemistryUmbilical veinMitochondrial ProteinsStructural BiologyGeneticsmedicineHumansMolecular BiologyCells CulturedMembrane GlycoproteinsImmune SeraCell BiologyKininFlow CytometryKininFluorescenceReceptors ComplementCell biologyEndothelial stem cellSpecific antibodyHyaluronan Receptorsmedicine.anatomical_structuregC1qREndothelium VascularCarrier ProteinsImmunostainingFEBS Letters
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