Search results for "CYTOSKELETON"

showing 10 items of 272 documents

The Cannabinoid Receptor CB1 Interacts with the WAVE1 Complex and Plays a Role in Actin Dynamics and Structural Plasticity in Neurons.

2015

The molecular composition of the cannabinoid type 1 (CB1) receptor complex beyond the classical G-protein signaling components is not known. Using proteomics on mouse cortex in vivo, we pulled down proteins interacting with CB1 in neurons and show that the CB1 receptor assembles with multiple members of the WAVE1 complex and the RhoGTPase Rac1 and modulates their activity. Activation levels of CB1 receptor directly impacted on actin polymerization and stability via WAVE1 in growth cones of developing neurons, leading to their collapse, as well as in synaptic spines of mature neurons, leading to their retraction. In adult mice, CB1 receptor agonists attenuated activity-dependent remodeling o…

MaleReceptor complexCannabinoid receptorDendritic spineQH301-705.5medicine.medical_treatmentDendritic SpinesNeurogenesisRecombinant Fusion ProteinsGrowth ConesWiskott-Aldrich Syndrome Protein NeuronalNerve Tissue ProteinsBiologyCannabinoidergicGeneral Biochemistry Genetics and Molecular Biology03 medical and health sciencesActin remodeling of neurons0302 clinical medicineReceptor Cannabinoid CB1Parietal LobeChlorocebus aethiopsmedicineAnimalsBiology (General)Cells Cultured030304 developmental biologyMice KnockoutNeurons0303 health sciencesNeuronal PlasticityGeneral Immunology and MicrobiologyCannabinoidsGeneral NeuroscienceNeurogenesisActin cytoskeletonEmbryo MammalianCell biologyFrontal LobeMice Inbred C57BLActin CytoskeletonLuminescent Proteinsnervous systemCOS Cellslipids (amino acids peptides and proteins)CannabinoidGeneral Agricultural and Biological Sciences030217 neurology & neurosurgeryResearch ArticlePLoS Biology
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Proteomic Analysis of Protein Components in Periodontal Ligament Fibroblasts

2005

BACKGROUND: Characterization of periodontal ligament (PDL) fibroblast proteome is an important tool for understanding PDL physiology and regulation and for identifying disease-related protein markers. PDL fibroblast protein expression has been studied using immunological methods, although limited to previously identified proteins for which specific antibodies are available. METHODS: We applied proteomic analysis coupled with mass spectrometry and database knowledge to human PDL fibroblasts. RESULTS: We detected 900 spots and identified 117 protein spots originating in 74 different genes. In addition to scaffold cytoskeletal proteins, e.g., actin, tubulin, and vimentin, we identified protein…

MaleSpectrometry Mass Electrospray IonizationAdolescentProteomeFluorescent Antibody TechniqueVimentinProteomicsPeptide Mappingperidontal ligamentproteomicsstomatognathic systemmedicineMembrane activityHumansPeriodontal fiberElectrophoresis Gel Two-DimensionalSettore BIO/06 - Anatomia Comparata E CitologiaChildDatabases ProteinFibroblastCytoskeletonCells CulturedActinbiologyperiodontal ligamentProteinsFibroblastsCell biologyCytoskeletal Proteinsmedicine.anatomical_structureSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationProteomebiology.proteinPeriodonticsFibroblastFemaleIsoelectric Focusing
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Dynamic changes of the microtubule system corresponding to the unequal and spiral cleavage modes in the embryo of the zebra mussel, Dreissena polymor…

1998

Unequal cleavage requires a highly organised cytoskeleton. We investigated the localisation of both tubulins and microtubular arrays in Dreissena eggs during and after fertilisation using confocal laser scanning microscopy. Freshly spawned eggs are arrested in metaphase I. A maternal pool of γ-tubulin is found mainly in the centre of the asters of the meiotic spindle. The paternal pool of γ-tubulin, present in the fertilising sperm, could not be traced within the egg, but a microtubule-organising centre forms near the male pronucleus at anaphase II. Male and female pronuclei grow as they migrate in the wake of their aster and rendezvous. First cleavage is unequal and starts without pronucle…

MaleZygoteSpindle ApparatusAster (cell biology)BiologyCleavage (embryo)MicrotubulesTubulinAnimalsCleavage furrowMetaphaseCytoskeletonAnaphaseCell NucleusPronuclear fusionMicroscopy ConfocalPronucleusCell BiologyAnatomyMale pronucleusImmunohistochemistrySpermatozoaCell biologyBivalviaFertilizationOocytesCell DivisionDevelopmental BiologyZygote (Cambridge, England)
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Ultrastructural changes of the intercellular relationship in impaired human spermatogenesis

1980

In seven hypo- or aspermic patients, electron microscopic investigations of the intercellular connections of the seminiferous tubule were performed. The analysis of cell junctions of Sertoli cells and germ cells revealed irregularities of the Sertoli-cell junctions, hypoplasias of occluding junctions, hypo- and hyperplasias of the Sertoli-spermatid cell junctions and abnormal formation of Sertoli cell junctions with early spermatids, spermatocytes, and spermatogonia. Gap junction-like cell membrane specializations were very rare. Intercellular cytoplasmic bridges of germ cells were always present together with these cells. One hypoplastic bridge connecting two spermatogonia was found. The r…

Maleendocrine systemBiologyCell junctionCell membraneGeneticsmedicineHumansSpermatogenesisCytoskeletonInfertility MaleGenetics (clinical)Blood–testis barrierSertoli CellsTight junctionurogenital systemDesmosomesSeminiferous TubulesSertoli cellSpermatidsSpermatozoaCell biologyMicroscopy ElectronIntercellular Junctionsmedicine.anatomical_structureSeminiferous tubuleSpermatogenesisGerm cellHuman Genetics
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Neuronal markers in the rodent pineal gland ? an immunohistochemical investigation

1990

Although some embryological and morphological features speak in favour of a neuronal character of rodent pinealocytes, histochemistry and ultrastructure let this issue appear controversial. Using antibodies to different neurofilaments, the neural adhesion molecule L1, synaptophysin and tubulin as neuronal markers, the pineal glands of rat and guinea-pig were studied by means of immunofluorescence. Neurofilament-immunoreactivity was present in some rat pineal nerve fibers and in the majority of guinea-pig pinealocytes, L1 decorated rat intrapineal nerve fibers, synaptophysin was almost ubiquitously distributed in the pineal of both species, while tubulin-immunofluorescence was seen in nerve …

Malemedicine.medical_specialtyHistologyNeurofilamentL1Cell Adhesion Molecules NeuronalGuinea PigsIntermediate FilamentsSynaptophysinNerve Tissue ProteinsPineal GlandPinealocyteGuinea pigPineal glandTubulinInternal medicinemedicineAnimalsMolecular BiologyCytoskeletonbiologyMembrane ProteinsRats Inbred StrainsCell BiologyGeneral MedicineImmunohistochemistryRatsCell biologyMedical Laboratory TechnologyEndocrinologymedicine.anatomical_structurenervous systemSynaptophysinbiology.proteinUltrastructureImmunohistochemistryAnatomyGeneral Agricultural and Biological SciencesBiomarkersHistochemistry
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The effect of surface charge on nonspecific uptake and cytotoxicity of CdSe/ZnS core/shell quantum dots

2015

In this work, cytotoxicity and cellular impedance response was compared for CdSe/ZnS core/shell quantum dots (QDs) with positively charged cysteamine–QDs, negatively charged dihydrolipoic acid–QDs and zwitterionic D-penicillamine–QDs exposed to canine kidney MDCKII cells. Pretreatment of cells with pharmacological inhibitors suggested that the uptake of nanoparticles was largely due to receptor-independent pathways or spontaneous entry for carboxylated and zwitterionic QDs, while for amine-functionalized particles involvement of cholesterol-enriched membrane domains is conceivable. Cysteamine–QDs were found to be the least cytotoxic, while D-penicillamine–QDs reduced the mitochondrial activ…

Materials scienceBiocompatibilityCellGeneral Physics and AstronomyNanoparticleNanotechnologyquantum dotslcsh:Chemical technologylcsh:TechnologyFull Research PaperbiocompatibilitymedicineNanotechnologyGeneral Materials Sciencelcsh:TP1-1185Surface chargeElectrical and Electronic EngineeringCytoskeletonCytotoxicitylcsh:ScienceECISlcsh:Ttechnology industry and agricultureequipment and supplieslcsh:QC1-999NanoscienceMembranemedicine.anatomical_structureQuantum dotBiophysicscytotoxicitysingle-particle trackinglcsh:QCdSe/ZnSlcsh:PhysicsBeilstein Journal of Nanotechnology
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Simultaneous imaging of the surface and the submembraneous cytoskeleton in living cells by tapping mode atomic force microscopy

1997

Contact and tapping mode atomic force microscopy have been used to visualize the surface of cultured CV-1 kidney cells in aqueous medium. The height images obtained from living cells were comparable when using contact and tapping modes. In contrast, the corresponding, and simultaneously acquired, deflection images differed markedly. Whereas, as expected, deflection images enhanced the surface features in the contact mode, they revealed the presence of a filamentous network when using the tapping mode. This network became disorganized upon addition of cytochalasin, which strongly suggests that it corresponded to the submembraneous cytoskeleton. Examination of fixed cells further supported th…

Materials scienceEcologyAqueous mediumAtomic force microscopyCell MembraneIn Vitro TechniquesKidneyMicroscopy Atomic ForceGeneral Biochemistry Genetics and Molecular BiologyCell membranechemistry.chemical_compoundMembranemedicine.anatomical_structurechemistryChlorocebus aethiopsBiophysicsContact modemedicineAnimalsTappingCytochalasinCytoskeletonCells CulturedCytoskeletonComptes Rendus de l'Académie des Sciences - Series III - Sciences de la Vie
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Endothelialization of chitosan porous conduits via immobilization of a recombinant fibronectin fragment (rhFNIII7–10)

2013

Abstract The present study aimed to develop a pre-endothelialized chitosan (CH) porous hollowed scaffold for application in spinal cord regenerative therapies. CH conduits with different degrees of acetylation (DA; 4% and 15%) were prepared, characterized (microstructure, porosity and water uptake) and functionalized with a recombinant fragment of human fibronectin (rhFNIII 7–10 ). Immobilized rhFNIII 7–10 was characterized in terms of amount ( 125 I-radiolabelling), exposure of cell-binding domains (immunofluorescence) and ability to mediate endothelial cell (EC) adhesion and cytoskeletal rearrangement. Functionalized conduits revealed a linear increase in immobilized rhFNIII 7–10 with rhF…

Materials scienceProtein radiolabellingBiomedical EngineeringNeovascularization PhysiologicSpinal cord injuryBiochemistrylaw.inventionBiomaterialsChitosanchemistry.chemical_compoundTissue engineeringlawSpectroscopy Fourier Transform InfraredPolymer chemistryHumansSurface graftingCytoskeletonMolecular BiologyFluorescent DyesChitosanTissue ScaffoldsbiologyThree-dimensional scaffoldsEndothelial CellsDNAGeneral MedicineAdhesionGraftingRecombinant ProteinsFibronectinsProtein Structure TertiaryFibronectinEndothelial stem cellImmobilized ProteinschemistryProtein conformationMicroscopy Electron Scanningbiology.proteinRecombinant DNABiophysicsAdsorptionPorosityBiotechnology
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Toxicity of gold-nanoparticles: Synergistic effects of shape and surface functionalization on micromotility of epithelial cells

2010

Nanoparticle exposure is monitored by a combination of two label-free and non-invasive biosensor devices which detect cellular shape and viscoelasticity (quartz crystal microbalance), cell motility and the dynamics of epithelial cell-cell contacts (electric cell-substrate impedance sensing). With these tools we have studied the impact of nanoparticle shape on cellular physiology. Gold (Au) nanoparticles coated with CTAB were synthesized and studied in two distinct shapes: Spheres with a diameter of (43 ± 4) nm and rods with a size of (38 ± 7) nm × (17 ± 3) nm. Dose-response experiments were accompanied by conventional cytotoxicity tests as well as fluorescence and dark-field microscopy to v…

Materials scienceSurface PropertiesBiomedical EngineeringAnalytical chemistryMetal NanoparticlesNanoparticle02 engineering and technology010402 general chemistryToxicology01 natural sciencesCell LineSurface-Active AgentsCell MovementMicroscopyAnimalsParticle SizeCytoskeletonDose-Response Relationship DrugCetrimoniumEpithelial CellsQuartz crystal microbalance021001 nanoscience & nanotechnology0104 chemical sciencesColloidal goldCetrimonium CompoundsBiophysicsParticleSurface modificationGoldParticle sizeReactive Oxygen Species0210 nano-technologyBiosensorNanotoxicology
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Interactions between cells and titanium surfaces.

2002

The interaction between cells and implant materials is determined by the surface structure and/or surface composition of the material. In the past years, titanium and titanium alloys have proved their superiority over other implant materials in many clinical applications. This predominant behaviour is caused by a dense passive oxide layer which forms within milliseconds in oxidizing media. Titanium dioxide layers of 100 nm thickness were produced on the surface of cp-titanium grade 2, and on an experimental alloy of high vanadium content (Ti1.5Al25V) as a harmful control. The layers were produced by thermal and anodic oxidation and by coating by means of the sol-gel process. The resulting o…

Materials scienceSurface PropertiesOxidechemistry.chemical_elementVanadiumBioengineeringSensitivity and SpecificityCell Linechemistry.chemical_compoundMiceCoated Materials BiocompatibleChlorocebus aethiopsMaterials TestingAlloysCell AdhesionAnimalsSurface layerMolecular BiologyVero CellsCytoskeletonTitaniumOsteoblastsMetallurgytechnology industry and agricultureTitanium alloyFibroblastsequipment and suppliesActinsTitanium oxidechemistryChemical engineeringTitanium dioxideLayer (electronics)Cell DivisionBiotechnologyTitaniumBiomolecular engineering
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