Search results for " pigment epithelium"

showing 10 items of 65 documents

Role of retinal pigment epithelium-derived exosomes and autophagy in new blood vessel formation

2018

Autophagy and exosome secretion play important roles in a variety of physiological and disease states, including the development of age‐related macular degeneration. Previous studies have demonstrated that these cellular mechanisms share common pathways of activation. Low oxidative damage in ARPE‐19 cells, alters both autophagy and exosome biogenesis. Moreover, oxidative stress modifies the protein and genetic cargo of exosomes, possibly affecting the fate of surrounding cells. In order to understand the connection between these two mechanisms and their impact on angiogenesis, stressed ARPE‐19 cells were treated with a siRNA‐targeting Atg7, a key protein for the formation of autophagosomes.…

0301 basic medicineautophagyretinaAngiogenesisretinal pigment epitheliumNeovascularization PhysiologicexosomesExosomeMacular Degeneration03 medical and health sciencesangiogenesismedicineHumansGene silencingoxidative stressSecretionCells CulturedTube formationRetinal pigment epitheliumBiología molecularChemistryAutophagyAutophagosomesOriginal ArticlesCell BiologyVascular Endothelial Growth Factor Receptor-2MicrovesiclesCell biologyOxidative Stress030104 developmental biologymedicine.anatomical_structureVEGFR2siRNAMolecular MedicineOriginal Article
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Ocular autofluorescence in diabetes mellitus. A review

2016

Diabetes mellitus is a metabolic disease with a considerable impact on healthcare owing to its increased prevalence and high mortality rate. Structural, morphological, and physiological changes in each of the ocular components have been described in detail. Autofluorescence has been described as a good indicator of metabolic activity. The aim of the present review is to provide an overview of ocular endogenous fluorophores in the cornea, the crystalline lens, and the retinal pigment epithelium, the effects of diabetes mellitus and therefore the potential of autofluorescence assessment for screening and monitoring changes in diabetic patients.

0301 basic medicinemedicine.medical_specialtyRetinal pigment epitheliumbusiness.industryEndocrinology Diabetes and Metabolismmedicine.diseaseeye diseases03 medical and health sciencesAutofluorescence030104 developmental biology0302 clinical medicinemedicine.anatomical_structureOphthalmologyDiabetes mellitusCornea030221 ophthalmology & optometryMedicinesense organsMetabolic diseasebusinessMetabolic activityJournal of Diabetes
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Confocal scanning laser ophthalmoscopy versus modified conventional fundus camera for fundus autofluorescence.

2016

Fundus autofluorescence (FAF) is a noninvasive imaging method to detect fundus endogenous fluorophores, mainly lipofuscin located in the retinal pigment epithelium (RPE). The FAF provides information about lipofuscin distribution and RPE health, and consequently an increased accumulation of lipofuscin has been correlated with ageing and development of certain retinal conditions. Areas covered: An exhaustive literature search in MEDLINE (via OVID) and PUBMED for articles related to ocular FAF in retinal diseases and different devices used for acquiring FAF imaging was conducted. Expert commentary: This review aims to show an overview about autofluorescence in the RPE and the main devices use…

0301 basic medicinemedicine.medical_specialtygenetic structuresFundus OculiBiomedical EngineeringFundus (eye)Fundus cameraFluorescenceLipofuscin03 medical and health scienceschemistry.chemical_compound0302 clinical medicineOpticsOphthalmologymedicinePhotographyHumansFluorescent DyesRetinal pigment epitheliumbusiness.industryLasersRetinalGeneral Medicineeye diseasesFundus autofluorescenceConfocal scanning laser ophthalmoscopyOphthalmoscopyAutofluorescence030104 developmental biologymedicine.anatomical_structurechemistry030221 ophthalmology & optometrySurgerysense organsbusinessExpert review of medical devices
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Clinical patterns and electrophysiological findings in retinal pigment epithelium diseases. Does a correlation exist?

1986

At present it is difficult to distinguish those human chorioretinal diseases in which the retinal pigment epithelium (RPE) is the primary site of dysfunction. This difficulty is caused by several factors such as scarcity of biochemical and histological information and a lack of correlation of basic science information available with the clinical body of knowledge. In the present study we examined 134 eyes at early or late stages of hereditary diseases involving the RPE. We tried to distinguish primary RPE involvement by using standard ERG (a- and b-wave) and EOG testing. We conclude that in general primary RPE damage can be better assessed by current electrophysiology in those diseases whic…

AdultMalePathologymedicine.medical_specialtyAdolescentBasic scienceEye diseasemacromolecular substancesBiologyCorrelationRetinal DiseasesPhysiology (medical)medicineElectroretinographyHumansChildPigment Epithelium of EyeAgedRetinaRetinal pigment epitheliummedicine.diagnostic_testMiddle Agedmedicine.diseaseSensory SystemsOphthalmologyElectrophysiologyElectrooculographymedicine.anatomical_structureFemalesense organsElectroretinographyRetinopathyDocumenta ophthalmologica. Advances in ophthalmology
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Bilateral maculopathy after exposure to a laser pointer: Optical coherence tomography angiography findings.

2018

Abstract Case report A 36-year-old man went to the emergency department the day after exposure to a laser pointer. Funduscopy revealed dispersed macular pigment alterations, and optical coherence tomography showed a disruption of the retinal layers. The visual acuity was counting fingers in both eyes. Nine months later, optical coherence tomography angiography showed a rarefaction in the choriocapillaris vascular flow in the area of the laser injuries. Discussion The retinal layer mainly damaged by the laser injury was the retinal pigment epithelium. However, it is suggested that the laser injury could involve tissues beyond the retinal pigment epithelium, since a rarefaction of the chorioc…

AdultMalemedicine.medical_specialtyVisual acuitygenetic structuresRetinal Pigment Epitheliumlaw.invention03 medical and health scienceschemistry.chemical_compound0302 clinical medicineEye InjuriesOptical coherence tomographylawOphthalmologymedicineHumansMacula LuteaFluorescein AngiographyRetinal pigment epitheliummedicine.diagnostic_testbusiness.industryChoroidCystsLasersRetinalGeneral MedicineOptical coherence tomography angiographymedicine.diseaseLasereye diseasesmedicine.anatomical_structurechemistry030221 ophthalmology & optometryLaser pointerMaculopathysense organsmedicine.symptomEmergenciesbusiness030217 neurology & neurosurgeryTomography Optical Coherence
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Optical coherence tomography of chorioretinal and choroidal folds

2007

. Purpose:  To report the optical coherence tomography (OCT) findings in cases of chorioretinal and choroidal folds. Methods:  Eight subjects with folds of the fundus of the eye were examined with fundus photography, fluorescein angiography, B-scan ultrasonography and Stratus OCT. Results:  Two types patterns were found on OCT. Five cases showed undulating retinal as well as retinal pigment epithelial lines of normal thickness; these were defined as chorioretinal folds. The posterior vitreous surface often adhered to the crests of the folds only. Three cases exhibited a wavy appearance of the retinal pigment epithelium and a flat retinal surface; these were classified as choroidal folds. Co…

AdultMalevisual acuitygenetic structuresFundus OculiDiagnosis Differentialchemistry.chemical_compoundRetinal DiseasesOptical coherence tomographyPhotographymedicineHumansFluorescein AngiographyPigment Epithelium of EyeAgedChoroidal foldsRetinal pigment epitheliummedicine.diagnostic_testSettore MED/30 - Malattie Apparato Visivobusiness.industryFundus photographyRetinalChoroid DiseasesAnatomyMiddle AgedFluorescein angiographyeye diseasesOphthalmologymedicine.anatomical_structureOCTchemistryFemalesense organsUltrasonographybusinessNormal thicknessTomography Optical CoherenceActa Ophthalmologica Scandinavica
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Congenital hypertrophy of the retinal pigment epithelium and familial polyposis of the colon.

1987

Inquiries to Manuel Diaz Llopis, M.D., Cl Cirilo Amoros No. 1 PTA 2, Valencia 46004, Spain. Familial polyposis of the colon is a dominant autosomal disorder that is characterized by hundreds and sometimes thousands of adenomatous polyps throughout the entire colon, which begin in adolescence. Virtually all pa­ tients with familial polyposis develop carcino­ ma of the colon by age 50 years. A total colectomy should be carried out early in adult life in affected persons. Because of the autosomal dominant inheritance pattern, an intensive sur­ vey of family members must be conducted. There is no phenotype biochemical abnormality or serologic marker that indicates whether a familial member will…

AdultPathologymedicine.medical_specialtyMicrocephalyRetinal pigment epitheliumEpidermal Cystbusiness.industryDiseaseHypertrophymedicine.diseaseMuscle hypertrophySerologyOphthalmologyCongenital hypertrophymedicine.anatomical_structureAdenomatous Polyposis ColiRetinal DiseasesmedicineHumansAbnormalityFluorescein AngiographybusinessPigment Epithelium of EyeAmerican journal of ophthalmology
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Binding of 11-cis retinaldehyde to the partially purified cellular retinaldehyde binding protein from bovine retinal pigment epithelium.

1987

11-cis retinaldehyde binding analysis was performed on a bovine retinal pigment epithelium preparation of cellular retinaldehyde binding protein (CRALBP), whose purity degree was estimated as 75%. Equilibrium binding studies were carried out measuring the replacement of tritium-labeled with unlabeled 11-cis retinaldehyde at 25 degrees C. Analysis of the experimental data both by a direct curve-fitting procedure utilizing a non linear least square regression analysis and by a conventional Scatchard plot revealed a single non-interacting binding site with an apparent equilibrium constant of 0.9 X 10(-7) M. A binding stoichiometry of approximately 1 mol of 11-cis retinaldehyde/mol of binding p…

Apparent Equilibrium ConstantBiologyBinding CompetitiveCellular and Molecular Neurosciencechemistry.chemical_compoundRetinoidsmedicineAnimalsBinding sitePigment Epithelium of EyeMolecular BiologyPharmacologyRetinaRetinal pigment epitheliumBinding proteinRetinalCell BiologyKineticsmedicine.anatomical_structureBiochemistrychemistryCELLULAR RETINALDEHYDE-BINDING PROTEINRetinaldehydeRetinaldehydeMolecular MedicineCattleCarrier ProteinsExperientia
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Retinyl ester hydrolases in retinal pigment epithelium.

1991

In bovine retinal pigment epithelium membranes we have found three hydrolases which were active against trans-retinyl palmitate. This was possible by assaying different subcellular fractions as a function of pH in the range 3-9. Detection of these activities has been favored by the use in the enzyme assay of Triton X-100, which has an activating effect up to a concentration of 0.03% at a detergent-protein ratio of about 1.5-3.0. Apparent kinetic parameters for the retinyl ester hydrolases have been determined after a study of the optimization of assay conditions. Vmax values for hydrolases acting at pH 4.5, 6.0, and 7.0 were, respectively, 156, 55, and 70 nmol/h/mg. To identify the subcellu…

BiophysicsBiochemistrysymbols.namesakechemistry.chemical_compoundCytosolHydrolasemedicineAnimalsPigment Epithelium of EyeMolecular Biologychemistry.chemical_classificationCell NucleusRetinal pigment epitheliumChromatographybiologyChemistryCell MembraneRetinolGolgi apparatusHydrogen-Ion ConcentrationEnzyme assayCytosolKineticsmedicine.anatomical_structureEnzymeBiochemistryMicrosomesymbolsbiology.proteinCattleCarboxylic Ester HydrolasesSubcellular FractionsArchives of biochemistry and biophysics
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A ciliopathy complex builds distal appendages to initiate ciliogenesis

2021

ABSTRACTCells inherit two centrioles, the older of which is uniquely capable of generating a cilium. Using proteomics and super-resolved imaging, we identified a module which we term DISCO (DIStal centriole COmplex). DISCO components CEP90, MNR and OFD1 underlie human ciliopathies. This complex localized to both distal centrioles and centriolar satellites, proteinaceous granules surrounding centrioles. Cells and mice lacking CEP90 or MNR did not generate cilia, failed to assemble distal appendages, and did not transduce Hedgehog signals. Disrupting the satellite pools did not affect distal appendage assembly, indicating that it is the centriolar populations of MNR and CEP90 that are critica…

BioquímicaCentrioleGreen Fluorescent ProteinsRetinal Pigment EpitheliumBiologyCiliopathiesCell LineMice03 medical and health sciences0302 clinical medicineBacterial ProteinsGenes ReporterCiliogenesismedicineAnimalsHumansbiochemistryCiliadevelopmentHedgehogCentrioles030304 developmental biologyMice KnockoutAppendage0303 health sciencesCiliumciliaProteinsEpithelial CellscytoskeletonCell BiologyEmbryo Mammalianmedicine.diseaseCiliopathiesCell biologyMice Inbred C57BLLuminescent ProteinsCiliopathyGene Expression RegulationMicrotubule-Associated Proteins030217 neurology & neurosurgerySignal TransductionJournal of Cell Biology
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