Search results for "CELLULAR"

showing 10 items of 6449 documents

A factor derived from chick embryo retina which inhibits DNA synthesis of retina itself.

1992

Chick embryo retinas contain a peptide factor that inhibits DNA synthesis in explants of chick embryo retina. The inhibitory factor, obtained by acid/ethanol extraction from 15-day-old chick embryo retinas, was partially purified by affinity chromatography on heparin-sepharose CL-6B and gel filtration on Sephadex G-100. The inhibitor reduced DNA synthesis with maximal effects observed in retinal explants from 7 to 8-day-old chick embryos. The inhibitory effect became apparent after 10 h of incubation and reached the maximum levels after 16 h. DNA-inhibiting activity was heat and acid-stable and was destroyed by trypsin and alkaline treatments. The inhibitory effect was observed in retinal e…

animal structuresChick EmbryoBiologyBiochemistryChromatography AffinityRetinaCellular and Molecular Neurosciencechemistry.chemical_compoundBiological Factorsinhibits DNA synthesisAffinity chromatographyCulture TechniquesmedicineAnimalsRetinaDNA synthesisTissue ExtractsEmbryogenesisEmbryoGeneral MedicineDNATrypsinMolecular biologymedicine.anatomical_structureBiochemistrychemistrySephadexembryonic structuresChromatography GelThymidineCell Divisionmedicine.drugThymidineNeurochemical research
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Clustering transmembrane-agrin induces filopodia-like processes on axons and dendrites

2005

The transmembrane form of agrin (TM-agrin) is primarily expressed in the CNS, particularly on neurites. To analyze its function, we clustered TM-agrin on neurons using anti-agrin antibodies. On axons from the chick CNS and PNS as well as on axons and dendrites from mouse hippocampal neurons anti-agrin antibodies induced the dose- and time-dependent formation of numerous filopodia-like processes. The processes appeared within minutes after antibody addition and contained a complex cytoskeleton. Formation of processes required calcium, could be inhibited by cytochalasine D, but was not influenced by staurosporine, heparin or pervanadate. Time-lapse video microscopy revealed that the processes…

animal structuresDendritic spineTime FactorsNeuriteCytochalasin BGrowth ConesVideo microscopyChick EmbryoBiologyNervous SystemAntibodiesCellular and Molecular NeuroscienceMicemedicineNeuritesAnimalsAgrinPseudopodiaGrowth coneCytoskeletonMolecular BiologyCells CulturedCytoskeletonAgrinMicroscopy VideoDose-Response Relationship DrugCell MembraneCell DifferentiationCell BiologyDendritesCell biologymedicine.anatomical_structurenervous systemAnimals NewbornNeuronFilopodia
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Procollagen C-proteinase Enhancer Stimulates Procollagen Processing by Binding to the C-propeptide Region Only*

2011

Background: Procollagen C-proteinase enhancer-1 (PCPE-1) is an extracellular glycoprotein that increases activity of certain zinc metalloproteinases involved in tissue development and repair. Results: PCPE-1 binds uniquely to the C-propeptide region of the procollagen molecule. Conclusion: PCPE-1 enhances proteolysis by binding solely to the procollagen C-propeptides. Significance: These data may lead to future applications in the development of antifibrotic therapies.

animal structuresGlycosylationBiologyBiochemistryBone morphogenetic protein 1Protein Structure SecondaryBone Morphogenetic Protein 103 medical and health scienceschemistry.chemical_compoundMetalloprotease0302 clinical medicineHumansBinding siteEnhancerMolecular Biology030304 developmental biologyCell Line TransformedGlycoproteinschemistry.chemical_classification0303 health sciencesMetalloproteinaseExtracellular Matrix ProteinsBinding Sitesintegumentary systemCell BiologyEnzymatic ProcessingFibrosisExtracellular MatrixProcollagen peptidaseCollagen Type IIIchemistryBiochemistry030220 oncology & carcinogenesisembryonic structuresEnzymologyCollagenGlycoproteinProtein Processing Post-TranslationalTriple helixThe Journal of Biological Chemistry
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Electron microscopy of a double helical tubular filament in keyhole limpet (Megathura crenulata) hemolymph.

1992

A approximately 25 nm hollow double helical filament has been detected ultrastructurally in the cell-free supernatant from hemolymph of the keyhole limpet Megathura crenulata (Gastropoda: Prosobranchia: Fissurellidae). Subsequently, much higher concentrations of this material were found in the cell pellet from hemolymph. Both negative staining and thin sectioning have been performed in an attempt to obtain a preliminary structural characterization of this new filament. It is proposed that the filaments are released or secreted from blood hemocytes in response to bleeding, but it has not been possible to define absolutely an intracellular organelle containing this material. It is shown that …

animal structuresHistologymedicine.medical_treatmentchemical and pharmacologic phenomenamacromolecular substancesMegathura crenulataMicrotubulesPathology and Forensic MedicineProtein filamentIntracellular organelleHemolymphHemolymphmedicineAnimalsFissurellidaebiologyCell-Free SystemLimpetHemocyaninCell BiologyAnatomybiology.organism_classificationActin CytoskeletonMicroscopy ElectronMolluscaHemocyaninsbiology.proteinBiophysicsCollagenKeyhole limpet hemocyaninCell and tissue research
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Long-Term Potentiation in the Neonatal Rat Barrel Cortex In Vivo

2012

Long-term potentiation (LTP) is important for the activity-dependent formation of early cortical circuits. In the neonatal rodent barrel cortex, LTP has been studied only in vitro . We combined voltage-sensitive dye imaging with extracellular multielectrode recordings to study whisker stimulation-induced LTP in the whisker-to-barrel cortex pathway of the neonatal rat barrel cortex in vivo . Single whisker stimulation at 2 Hz for 10 min induced an age-dependent expression of LTP in postnatal day (P) 0 to P14 rats, with the strongest expression of LTP at P3–P5. The magnitude of LTP was largest in the activated barrel-related column, smaller in the surrounding septal region, and no LTP could b…

animal structuresPatch-Clamp TechniquesLong-Term PotentiationBiophysicsStimulationBiologyIn Vitro TechniquesStatistics NonparametricIn vivoCortex (anatomy)Evoked Potentials SomatosensoryExtracellularmedicineAnimalsNeuronsSerotonin Plasma Membrane Transport ProteinsCortical circuitsNeonatal ratAfferent PathwaysGeneral Neurosciencemusculoskeletal neural and ocular physiologyAge FactorsLong-term potentiationSomatosensory CortexBarrel cortexElectric StimulationVoltage-Sensitive Dye ImagingRatsmedicine.anatomical_structurenervous systemAnimals NewbornVibrissaeBiophysicsBrief CommunicationsNeuroscience
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Hyperplastic Conotruncal Endocardial Cushions and Transposition of Great Arteries in Perlecan-Null Mice

2002

Perlecan is a heparan-sulfate proteoglycan abundantly expressed in pericellular matrices and basement membranes during development. Inactivation of the perlecan gene in mice is lethal at two developmental stages: around E10 and around birth. We report a high incidence of malformations of the cardiac outflow tract in perlecan-deficient embryos. Complete transposition of great arteries was diagnosed in 11 out of 15 late embryos studied (73%). Three of these 11 embryos also showed malformations of semilunar valves. Mesenchymal cells in the outflow tract were abnormally abundant in mutant embryos by E9.5, when the endocardial-mesenchymal transformation starts in wild-type embryos. At E10.5, mut…

animal structuresPhysiologyTransposition of Great VesselsMesenchymeMorphogenesisPerlecanBiologyMesodermExtracellular matrixMiceCoronary CirculationmedicineAnimalsEndocardiumMice KnockoutHyperplasiaMyocardiumEmbryogenesisMesenchymal stem cellNeural crestHeartArteriesAnatomyEmbryo MammalianImmunohistochemistryCell biologyKineticsPhenotypemedicine.anatomical_structureembryonic structuresbiology.proteinCardiology and Cardiovascular MedicineHeparan Sulfate ProteoglycansEndocardial Cushion DefectsCirculation Research
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In vitro differentiation of E-N-CAM expressing rat neural precursor cells isolated by FACS during prenatal development

1994

Most fetal rat brain cells expressing the embryonal, highly sialylated form of the cell adhesion molecule N-CAM (E-N-CAM) are precursor cells, as judged from the absence of marker molecules specific for mature neural cell types. However, the detection of E-N-CAM+ cells in frozen sections does not provide information on the lineage-specific differentiation of these cells during development. To investigate their differentiation behaviour in vitro, E-N-CAM+ cells were isolated at different times of brain development by fluorescence-activated cell sorting (FACS), using a monoclonal antibody (Mab RB21-7) which specifically recognizes polysialic acid (PSA) residues on E-N-CAM. Double-immunofluore…

animal structuresPolysialic acidCell adhesion moleculeBiologyCell sortingCell biologyCellular and Molecular Neurosciencemedicine.anatomical_structureCell culturePrecursor cellImmunologymedicineProgenitor cellAstrocyteGliogenesisJournal of Neuroscience Research
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Sonic hedgehog promotes the migration and proliferation of optic nerve oligodendrocyte precursors.

2007

Optic nerve (ON) oligodendrocyte precursors (OPCs) are generated under the influence of the Sonic hedgehog (Shh) in the preoptic area from where they migrate to colonise the entire nerve. The molecular events that control this migration are still poorly understood. Recent studies suggested that Shh is often used by the same cell population to control different processes, including cell proliferation and migration, raising the possibility that Shh could contribute to these aspects of OPC development. In support of this idea, we show here that Shh induces the proliferation of OPCs derived from embryonic mouse ON explants and acts as a chemoattractant for their migration. In ovo injections of …

animal structuresPopulationCellChick EmbryoAntibodiesCellular and Molecular NeuroscienceMyelinMiceCell MovementCell Line TumormedicineAnimalsHedgehog ProteinsSonic hedgehogeducationMolecular BiologyCells CulturedMyelin SheathCell Proliferationeducation.field_of_studybiologyCell growthChemotaxisStem CellsCell DifferentiationOptic NerveCell BiologyEmbryonic stem cellOligodendrocyteCell biologystomatognathic diseasesOligodendrogliamedicine.anatomical_structurenervous systemembryonic structuresOptic nervebiology.proteinNeuroscienceSignal TransductionMolecular and cellular neurosciences
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Plexin-B1 activates NF-κB and IL-8 to promote a pro-angiogenic response in endothelial cells.

2011

Background The semaphorins and their receptors, the plexins, are proteins related to c-Met and the scatter factors that have been implicated in an expanding signal transduction network involving co-receptors, RhoA and Ras activation and deactivation, and phosphorylation events. Our previous work has demonstrated that Semaphorin 4D (Sema4D) acts through its receptor, Plexin-B1, on endothelial cells to promote angiogenesis in a RhoA and Akt-dependent manner. Since NF-κB has been linked to promotion of angiogenesis and can be activated by Akt in some contexts, we wanted to examine NF-κB in Sema4D treated cells to determine if there was biological significance for the pro-angiogenic phenotype o…

animal structuresRHOAProto-Oncogene Proteins c-aktAngiogenesisSignaling in cellular processesG-protein signalingCancer TreatmentSEMA4Dlcsh:MedicineSignal transductionBiology03 medical and health sciencesMolecular cell biology0302 clinical medicineSemaphorinSettore BIO/10 - BiochimicaAkt Signaling CascadeMembrane Receptor SignalingInterleukin 8lcsh:ScienceBiologyProtein kinase BGTPase signalingRas signaling030304 developmental biology0303 health sciencesMultidisciplinaryMechanisms of Signal Transductionlcsh:RSignaling Cascades3. Good healthCell biologyPlexin B1RNA interferencepro-angiogenicendothelial cellsOncology030220 oncology & carcinogenesisembryonic structuresCancer researchbiology.proteinMedicinelcsh:QAntiangiogenesis TherapyAntiapoptotic signalingSignal transductionResearch ArticlePLoS ONE
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Stretch-induced Intussuceptive and Sprouting Angiogenesis in the Chick Chorioallantoic Membrane

2014

Vascular systems grow and remodel in response to not only metabolic needs, but also mechanical influences as well. Here, we investigated the influence of tissue-level mechanical forces on the patterning and structure of the chick chorioallantoic membrane (CAM) microcirculation. A dipole stretch field was applied to the CAM using custom computer-controlled servomotors. The topography of the stretch field was mapped using finite element models. After 3 days of stretch, Sholl analysis of the CAM demonstrated a 7-fold increase in conducting vessel intersections within the stretch field (p 0.05). In contrast, corrosion casting and SEM of the stretch field capillary meshwork demonstrated intense …

animal structuresTime FactorsCapillary actionFinite Element AnalysisNeovascularization PhysiologicChick EmbryoCorrosion CastingBiochemistryMechanotransduction CellularArticleChorioallantoic MembraneChick chorioallantoic membraneMicrocirculationSholl analysisFluorescence microscopeAnimalsIntussusceptive angiogenesisSprouting angiogenesisMicroscopy VideoChemistryMicrocirculationModels CardiovascularCell BiologyAnatomyCapillariesChorioallantoic membraneMicroscopy FluorescenceBiophysicsMicroscopy Electrochemical ScanningStress MechanicalCardiology and Cardiovascular Medicine
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