Search results for "Outer plexiform layer"

showing 10 items of 12 documents

Strain differences in the ratio of synaptic body types in photoreceptors of the rat retina.

1993

In the retinal outer plexiform layer of seven different rat strains, synaptic bodies (SB) were counted and, according to their morphology, characterized as synaptic ribbons (SR), synaptic spheres (SS) or intermediate structures. It was found that absolute SB numbers showed relatively small variations while SR/SS ratios differed considerably between the strains investigated. These results are discussed with respect to retinal pigmentation and to formation and degradation, respectively, of synaptic ribbons.

MaleMorphology (linguistics)Outer plexiform layerlaw.inventionSynapsechemistry.chemical_compoundSpecies SpecificitylawmedicineAnimalsPhotoreceptor CellsSynaptic ribbonRetinaStrain (chemistry)PigmentationRetinalRats Inbred StrainsSensory SystemsRatsOphthalmologyMicroscopy Electronmedicine.anatomical_structurechemistryBiophysicsFemalesense organsSynaptic VesiclesElectron microscopeNeuroscienceVision research
researchProduct

Deletion of myosin VI causes slow retinal optic neuropathy and age-related macular degeneration (AMD)-relevant retinal phenotype

2015

The unconventional myosin VI, a member of the actin-based motor protein family of myosins, is expressed in the retina. Its deletion was previously shown to reduce amplitudes of the a- and b-waves of the electroretinogram. Analyzing wild-type and myosin VI-deficient Snell’s Waltzer mice in more detail, the expression pattern of myosin VI in retinal pigment epithelium, outer limiting membrane, and outer plexiform layer could be linked with differential progressing ocular deficits. These encompassed reduced a-waves and b-waves and disturbed oscillatory potentials in the electroretinogram, photoreceptor cell death, retinal microglia infiltration, and formation of basal laminar deposits. A pheno…

Genotypegenetic structuresOuter retinaTranslocator protein TSPOOuter plexiform layermacromolecular substancesBiologyRetinaPhotoreceptor cellMouse modelStereociliaMacular DegenerationMiceCellular and Molecular Neurosciencechemistry.chemical_compoundOptic Nerve DiseasesMyosinmedicineAnimalsBipolar cellMolecular BiologyPharmacologyRetinaRetinal pigment epitheliumMyosin Heavy ChainsNeurodegenerationInner retinaChoriocapillarisRetinalCell BiologyAnatomyMacular degenerationmedicine.diseaseSynapseeye diseasesCell biologyMice Inbred C57BLmedicine.anatomical_structurechemistryMolecular MedicineMicrogliasense organsGene DeletionResearch ArticlePhotoreceptor Cells VertebrateCellular and Molecular Life Sciences
researchProduct

Identification of a β-Dystroglycan Immunoreactive Subcompartment in Photoreceptor Terminals

2005

PURPOSE Mutations in the dystrophin-associated glycoprotein complex (DGC) cause various forms of muscular dystrophy. These diseases are characterized by progressive loss of skeletal muscle tissue and by dysfunctions in the central nervous system (CNS). The CNS deficits include an altered electroretinogram, caused by an impaired synaptic transmission between photoreceptors and their postsynaptic target cells in the outer plexiform layer (OPL). The DGC is concentrated in the OPL but its exact distribution is controversial. Therefore, the precise distribution of beta-dystroglycan, the central component of the DGC, within the OPL of the mature chick retina, was determined. METHODS Double immuno…

Retinal Bipolar Cellsgenetic structuresPresynaptic TerminalsOuter plexiform layerNerve Tissue ProteinsRetinal Horizontal CellsNeurotransmissionRibbon synapseImaging Three-DimensionalGlycoprotein complexImage Processing Computer-AssistedmedicineDystroglycanAnimalsActive zoneDystroglycansFluorescent Antibody Technique IndirectSynaptic ribbonRetinabiologyAnatomyCell CompartmentationCell biologyMicroscopy Electronmedicine.anatomical_structureMicroscopy Fluorescencebiology.proteinsense organsChickensPhotoreceptor Cells VertebrateInvestigative Opthalmology & Visual Science
researchProduct

AAV-Mediated Clarin-1 Expression in the Mouse Retina: Implications for USH3A Gene Therapy

2015

Usher syndrome type III (USH3A) is an autosomal recessive disorder caused by mutations in clarin-1 (CLRN1) gene, leading to progressive retinal degeneration and sensorineural deafness. Efforts to develop therapies for preventing photoreceptor cell loss are hampered by the lack of a retinal phenotype in the existing USH3 mouse models and by conflicting reports regarding the endogenous retinal localization of clarin-1, a transmembrane protein of unknown function. In this study, we used an AAV-based approach to express CLRN1 in the mouse retina in order to determine the pattern of its subcellular localization in different cell types. We found that all major classes of retinal cells express AAV…

Photoreceptors0301 basic medicineRetinal degenerationSensory ReceptorsPhysiologyUsher syndromeCell Membraneslcsh:MedicineSocial SciencesNervous SystemPhotoreceptor cellMicechemistry.chemical_compound0302 clinical medicineAnimal CellsMedicine and Health SciencesPsychologylcsh:ScienceNeuronsRegulation of gene expressionGeneticsMultidisciplinaryRetinal DegenerationAnimal ModelsDependovirusCell biologyElectrophysiologymedicine.anatomical_structureSensory PerceptionCellular TypesAnatomyCellular Structures and OrganellesUsher SyndromesResearch ArticleSignal TransductionCell typeImaging TechniquesOcular AnatomyNeurophysiologyOuter plexiform layerMouse ModelsBiologyResearch and Analysis MethodsRetina03 medical and health sciencesModel OrganismsOcular SystemFluorescence ImagingmedicineAnimalsHumansRetinalcsh:RMembrane ProteinsBiology and Life SciencesAfferent NeuronsRetinalGenetic TherapyCell Biologymedicine.diseaseDisease Models Animal030104 developmental biologyGene Expression RegulationchemistrySynapsesEyeslcsh:QHead030217 neurology & neurosurgeryNeurosciencePLOS ONE
researchProduct

Long-spined polymorphic neurons of the medial cortex of lizards: a Golgi, Timm, and electron-microscopic study.

1988

The morphology, ultrastructure, and principal synaptic input of longspined neurons located in the inner plexiform layer of the medial cortex in three related species of lizards is described. Golgi impregnations have been used to define the external morphology of these neurons and their axonal trajectories. Their most striking characteristic is the presence of very long spines or “microdendrites” especially abundant on the distal dendritic segments. Axons have ascendent trajectories, pass through the cell layer, and ramify in the outer plexiform layer. Combined Golgi-electron microscopy as well as standard electron microscopy permitted the definition of the ultrastructure of these neurons. T…

Cerebral CortexNeuronsDendritic spineMedial cortexHistocytochemistryGeneral NeuroscienceOuter plexiform layerDendriteLizardsAnatomyDendritesBiologyInner plexiform layerMicroscopy ElectronZincmedicine.anatomical_structurenervous systemCerebral cortexMetalsmedicineBiophysicsUltrastructureAnimalsFascia dentataThe Journal of comparative neurology
researchProduct

Tomographic reconstruction reveals the morphology of a unique cellular organelle, the aggregated macrotubules (Macrotubuli aggregati) of human retina…

2014

Abstract Horizontal cells of the human retina contain unique tubular organelles that have a diameter which is about 10 times larger than that of microtubules (∼230 nm). These macrotubuli in most cases form regular aggregates. Therefore we propose to introduce them as Macrotubuli aggregati in the Terminologia histologica. Tomographic investigation of the structures revealed that the walls of the tubules most probably consist of intermediate filaments running nearly parallel to each other and show somewhat regularly attached ribosomes on their inner and also outer surface. About 2% of the organelles exhibit double- to multiple layered walls and less than 1% resemble large scrolls. The tubules…

MaleCytoplasmMedizinOuter plexiform layerBiologyRetinal Horizontal CellsMicrotubulesRetinaMicrotubuleOrganellemedicineHumansIntermediate filamentAged 80 and overNeuronsOrganellesRetinaCell BiologyGeneral MedicineAnatomyMiddle Agedmedicine.anatomical_structureCytoplasmInner nuclear layerUltrastructureBiophysicsDevelopmental BiologyTissuecell
researchProduct

Retinal neurodegenerative changes in the adult insulin receptor substrate-2 deficient mouse.

2014

Abstract Insulin receptor substrate-2 (Irs2) mediates peripheral insulin action and is essential for retinal health. Previous investigations have reported severe photoreceptor degeneration and abnormal visual function in Irs2-deficient mice. However, molecular changes in the Irs2 − / −  mouse retina have not been described. In this study, we examined retinal degenerative changes in neuronal and glial cells of adult (9- and 12-week old) Irs2 − / −  mice by immunohistochemistry. 9-week old Irs2 − / −  mice showed significant thinning of outer retinal layers, concomitant to Muller and microglial cell activation. Photoreceptor cells displayed different signs of degeneration, such as outer/inner…

Retinal degenerationRetinal Ganglion CellsRetinal Bipolar Cellsgenetic structuresOuter plexiform layerBiologyRetinal ganglionCellular and Molecular Neurosciencechemistry.chemical_compoundMicemedicineElectroretinographyAnimalsVision OcularRetinaMicroscopy Confocalmedicine.diagnostic_testRetinal DegenerationRetinalmedicine.diseaseInner plexiform layerImmunohistochemistrySensory SystemsCell biologyMice Inbred C57BLOphthalmologyMicroglial cell activationDisease Models Animalmedicine.anatomical_structurechemistryInsulin Receptor Substrate Proteinssense organsNeuroscienceElectroretinographyPhotoreceptor Cells VertebrateExperimental eye research
researchProduct

Neurons of the medial cortex outer plexiform layer of the lizard Podarcis hispanica: Golgi and immunocytochemical studies.

1994

The study of Golgi-impregnated lizard brains has revealed a scarce but heterogeneous neuronal population in the outer plexiform layer of the medial cortex. Some of the neuronal types detected here resemble the neurons of the dentate molecular layer of the mammalian hippocampus. According to their morphology, five intrinsic neuronal types have been clearly identified: short axon aspinous bipolar neuron (type 1, or sarmentous neuron), short axon aspinous juxtasomatic neuron (type 2, or coral neuron), short axon sparsely spinous multipolar neuron (type 3, or stellate neuron), short axon sparsely spinous juxtasomatic multipolar neuron (type 4, or deep stellate neuron, and sparsely spinous juxta…

Cerebral CortexMaleNeuronsMedial cortexGeneral NeuroscienceHippocampusOuter plexiform layerLizardsBiologyImmunohistochemistryAxonsMultipolar neuronmedicine.anatomical_structureParvalbuminsnervous systemBipolar neuronmedicineAnimalsFemaleNeuronAxonUnipolar neuronNeurosciencegamma-Aminobutyric AcidThe Journal of comparative neurology
researchProduct

Projections from the medial cortex in the brain of lizards: correlation of anterograde and retrograde transport of horseradish peroxidase with Timm s…

1988

Efferent projections of the medial cortex of the lizards Podarcis hispanica and Gallotia stehlinii were studied by examining the transport of horseradish peroxidase; results were correlated with those from Timm-stained sections. Two efferent systems were found. The first reaches the distal part of the outer plexiform layer in the medial, dorsomedial, and dorsal cortices, i.e., zones that are negative to Timm staining, and possibly originates from horizontal fusiform neurons. The second reaches the Timm-positive zones in the cortex and septum and is topographically arranged: the vertical portion of the intermediate and caudal medial cortex and the entire rostral medial cortex project to the …

genetic structuresMedial cortexEfferentHippocampusOuter plexiform layerPodarcis hispanicaCortex (anatomy)Neural PathwaysmedicineAnimalsHorseradish PeroxidaseCerebral CortexBrain MappingStaining and LabelingbiologyHistocytochemistryGeneral NeuroscienceLizardsAnatomybiology.organism_classificationInner plexiform layerZincmedicine.anatomical_structurenervous systemMetalsCerebral cortexsense organs
researchProduct

Synaptic ribbons, spheres and intermediate structures in the developing rat retina

1992

The present study was conducted to investigate the qualitative and quantitative development of synaptic bodies in retinae of Wistar rats during postnatal days 4-28. In addition, the effects of different light regimens and of eye pigmentation on SB numbers were studied. Synaptic bodies were counted and measured in the outer plexiform layer of retinal tissue fixed and processed by routine electron microscopical techniques. At postnatal days 4 and 5, retinae showed only few synaptic bodies. The main numerical development of synaptic bodies occurred between postnatal days 4 and 9, numbers remaining more or less constant thereafter. The intracellular location of synaptic ribbons changed from pre…

MaleAgingLightgenetic structuresOuter plexiform layerRat retinaBiologyRetinaDevelopmental NeurosciencemedicineAnimalsRats WistarphotoperiodismSynaptic ribbonRetinaAnatomyDarknessEye pigmentationRatsMicroscopy Electronmedicine.anatomical_structureAnimals NewbornSynapsesDarknessBiophysicsFemalesense organsIntracellularDevelopmental BiologyInternational Journal of Developmental Neuroscience
researchProduct