Search results for "Lysosome"

showing 10 items of 125 documents

Occurrence of Retinal Ganglion Cell Loss via Autophagy and Apoptotic Pathways in an Autoimmune Glaucoma Model

2020

In glaucoma, an apoptotic death of retinal ganglion cells (RGCs) has been shown. However, little is known about other cell death mechanisms, like autophagy or necrosis. Therefore, we investigated these mechanisms in addition to antibody deposits in an experimental autoimmune glaucoma model.Rats were immunized with a retinal ganglion cell-layer homogenate (RGA), while controls received sodium chloride. Untreated rats served as natїve group. After seven weeks, retinal cross-sections were stained with antibodies against RGCs (Brn-3a), apoptosis (cleaved caspase 2, cleaved caspase 3 as well as caspase 3, 8, and 9), autophagy (LC3BII and LAMP1), and necrosis (RIPK3) followed by cell counts. Auto…

MaleRetinal Ganglion CellsProgrammed cell deathNecrosisgenetic structuresGlaucomaApoptosisAutoantigensRetinal ganglionAutoimmune Diseases03 medical and health sciencesCellular and Molecular Neuroscience0302 clinical medicineMicroscopy Electron TransmissionAutophagymedicineAnimalsAutoantibodiesCaspase 8biologyCaspase 3business.industryAutophagyLysosome-Associated Membrane GlycoproteinsGlaucomamedicine.diseaseCaspase 9eye diseasesSensory SystemsRatsDisease Models AnimalOphthalmologymedicine.anatomical_structureMicroscopy FluorescenceRetinal ganglion cellRats Inbred LewApoptosisImmunoglobulin G030221 ophthalmology & optometryCancer researchbiology.proteinsense organsAntibodymedicine.symptombusinessMicrotubule-Associated Proteins030217 neurology & neurosurgeryCurrent Eye Research
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Incidence of Abcd1 level on the induction of cell death and organelle dysfunctions triggered by very long chain fatty acids and TNF-alpha on oligoden…

2012

X-linked adrenoleukodystrophy (X-ALD) is characterized by ABCD1 deficiency. This disease is associated with elevated concentrations of very long chain fatty acids (C24:0 and C26:0) in the plasma and tissues of patients. Under its severe form, brain demyelination and inflammation are observed. Therefore, we determined the effects of C24:0 and C26:0 on glial cells:oligodendrocytes, which synthesize myelin, and astrocytes, which participate in immune response. So, 158N murine oligodendrocytes, rat C6 glioma cells, rat primary cultures of neuronal-glial cells, and of oligodendrocytes were treated for various periods of time in the absence or presence of C24:0 and C26:0 used at plasmatic concent…

MaleTime FactorsVacuoleMitochondrionToxicologyATP Binding Cassette Transporter Subfamily D Member 1chemistry.chemical_compoundMice0302 clinical medicineRNA Small InterferingAdrenoleukodystrophyCells CulturedComputingMilieux_MISCELLANEOUSMembrane Potential MitochondrialNeurons0303 health sciencesGeneral NeuroscienceFatty AcidsBrainPeroxisomeCatalaseFlow Cytometry3. Good healthCell biologyMitochondriaOligodendrogliamedicine.anatomical_structureFemaleProgrammed cell deathChromatography GasBiologyGas Chromatography-Mass SpectrometryStatistics Nonparametric03 medical and health sciencesMicroscopy Electron TransmissionLysosomeOrganellemedicineAnimalsHumansPropidium iodideRNA MessengerRats Wistar030304 developmental biologyCell SizeChemokine CCL22OrganellesDose-Response Relationship DrugCell growthTumor Necrosis Factor-alphaRatschemistryAnimals NewbornAstrocytesATP-Binding Cassette Transporters[SDV.AEN]Life Sciences [q-bio]/Food and Nutrition030217 neurology & neurosurgery
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Lysosomal Signaling Licenses Embryonic Stem Cell Differentiation via Inactivation of Tfe3

2019

International audience; Self-renewal and differentiation of pluripotent murine embryonic stem cells (ESCs) is regulated by extrinsic signaling pathways. It is less clear whether cellular metabolism instructs developmental progression. In an unbiased genome-wide CRISPR/Cas9 screen, we identified components of a conserved amino-acid-sensing pathway as critical drivers of ESC differentiation. Functional analysis revealed that lysosome activity, the Ragulator protein complex, and the tumor-suppressor protein Folliculin enable the Rag GTPases C and D to bind and seclude the bHLH transcription factor Tfe3 in the cytoplasm. In contrast, ectopic nuclear Tfe3 represses specific developmental and met…

MaleTranscription GeneticGTPaseGTP PhosphohydrolasesPATHWAYMice0302 clinical medicineNeural Stem CellsCRISPRTUMOR-SUPPRESSORCell Self RenewalPhosphorylationSPECIFICATIONdevelopmental disorder0303 health sciencesGenomeBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsCell DifferentiationMouse Embryonic Stem CellsFlcndifferentiationCell biologymedicine.anatomical_structuremTORMolecular MedicineFemaleSignal transductionProtein BindingSignal TransductionRECRUITMENTBiology03 medical and health sciencesRag GTPasesLysosomeGeneticsmedicineAnimalsHumansPoint MutationNAIVE PLURIPOTENCYAMINO-ACID LEVELSTranscription factorAllelesPI3K/AKT/mTOR pathway030304 developmental biologyCOMPLEXFOLLICULINRagulatorCell Biologypluripotencyembryonic stem cellEmbryonic stem cellTfe3[SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human geneticsCytoplasmLysosomes030217 neurology & neurosurgeryCell Stem Cell
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Electron microscopic study on the larval and adult corpus allatum of Oncopeltus fasciatus dallas (insecta, heteroptera)

1973

1. The ultrastructure of the corpora allata of last larval instars and adults of Oncopeltus was studied. The unpaired gland undergoes submicroscopic alterations and shows signs of degradation in old animals. The organ is partly covered and penetrated by corpus cardiacum tissue. Axons with different types of neurosecretory granules form synaptoid contacts with the corpus allatum cells.

Maleendocrine systemInsectaHistologyGolgi ApparatusBiologyEndoplasmic ReticulumPathology and Forensic MedicineSex FactorsAnimalsElectron microscopicCell NucleusLarvaHeteropteraCell BiologyAnatomybiology.organism_classificationNeurosecretory SystemsCorpus CardiacumAxonsJuvenile HormonesMicroscopy ElectronUltrastructureInstarFemaleCorpus allatumLysosomesRibosomesCell NucleolusNeurosecretory granulesZeitschrift f�r Zellforschung und Mikroskopische Anatomie
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Lysosomal changes related to ageing and physical exercise in mouse cardiac and skeletal muscles.

1982

Physical exercise increased the activities of arylsulphatase, cathepsin D and β-glucuronidase in mouse skeletal muscle but not in cardiac muscle. Exercise-induced lysosomal response was more prominent in young adult than in senescent mice. The lipofuscin content of cardiac and skeletal muscles increased markedly during ageing and was also found to increase slightly after exertion in young mice, but not in senescent ones.

Malemedicine.medical_specialtyAgingPhysical ExertionCathepsin DPhysical exerciseCathepsin DLipofuscinLipofuscinCellular and Molecular NeuroscienceMiceInternal medicinemedicineAnimalsExertionYoung adultMolecular BiologyArylsulfatasesGlucuronidasePharmacologybusiness.industryMusclesMyocardiumCardiac muscleSkeletal muscleCell BiologyAnatomyCathepsinsmedicine.anatomical_structureEndocrinologyAgeingMolecular MedicinebusinessLysosomesExperientia
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Mucolipidosis I — A sialidosis

1977

Mucolipidosis I is characterized by Hurler-like features and skeletal dysplasia with a cherry-red macular spot and signs of neurodegeneration involving neuronal cells and myelin. Excessive amounts of sialic acid-containing compounds were found in cultured fibroblasts, leukocytes, and urine of a patient with a clinical phenotype of mucolipidosis I. In cultured fibroblasts, profoundly diminished activity of an alpha-N-acetylneuraminidase (sialidase) was found. Mucolipidosis I thus appears to be a distinct disorder of complex carbohydrate catabolism caused by the genetic deficiency of a neuraminidase.

Malemedicine.medical_specialtyHydrolasesNeuraminidaseSialidaseMyelinMucolipidosesInternal medicinemedicineHumansSialidosisChildCells CulturedGenetics (clinical)SkinbiologyMucolipidosisCatabolismNeurodegenerationmedicine.diseasePhenotypeEndocrinologymedicine.anatomical_structureDysplasiaChild PreschoolImmunologySialic Acidsbiology.proteinLysosomesNeuraminidaseFollow-Up StudiesAmerican Journal of Medical Genetics
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N-Acetylneuraminic acid storage disease

1985

Increased amounts of free sialic acid were found in body fluids, leukocytes, cultured fibroblasts, and liver tissue of a four-year-old boy with mental retardation, ataxia, and clinical and radiologic findings of a mild mucopolysaccharidosis. A diagnosis of Salla disease was made though in contrast to earlier reports, recurrent upper respiratory infections and hepatosplenomegaly were present already in infancy, and skeletal abnormalities of dysostosis multiplex were found in early childhood. Free sialic acid in the urine was identified as N-acetylneuraminic acid by 1H-NMR spectroscopy. Sialidase activities were normal. Increased amounts of bound sialic acid were found in liver and cultured f…

Malemedicine.medical_specialtyMagnetic Resonance SpectroscopyMucopolysaccharidosisHepatosplenomegalyNeuraminidaseBiologySialidaseDiagnosis Differentialchemistry.chemical_compoundInternal medicineNeuraminic acidGeneticsmedicineHumansCells CulturedGenetics (clinical)Respiratory infectionmedicine.diseaseSialic acidRadiographySalla diseaseEndocrinologyLiverchemistryBiochemistryChild PreschoolSialic Acidsbiology.proteinChromatography Thin Layermedicine.symptomLysosomesNeuraminidaseMetabolism Inborn ErrorsHuman Genetics
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Nephrosis in two siblings with infantile sialic acid storage disease

1990

The diagnosis of infantile sialic acid storage disease (ISSD) was established in two siblings on the basis of typical clinical signs and the biochemical findings of hyperexcretion and intracellular storage of free sialic acid. A severe, steroid resistant nephrosis occurred in both siblings. The activities of lysosomal enzymes, including sialidase, were normal. A combined detection method for sialic acids with Limax flavus agglutinin labelling and phosphotungstic acid staining showed severely alterated sialic acid components in epithelial kidney cells and indicate a causal relationship between the nephrosis and the underlying biochemical defect. Further observations of ISSD patients with ren…

Malemedicine.medical_specialtyNephrosisKidney GlomerulusBiologyCarbohydrate metabolismSialidasechemistry.chemical_compoundInternal medicinemedicineHumansFamilychemistry.chemical_classificationKidneyInfant Newbornmedicine.diseasePhenotypeStainingSialic acidcarbohydrates (lipids)Microscopy Electronmedicine.anatomical_structureEnzymeEndocrinologychemistryBiochemistryPediatrics Perinatology and Child HealthSialic AcidsNephrosisFemaleLysosomesCarbohydrate Metabolism Inborn ErrorsEuropean Journal of Pediatrics
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Oxidative and lysosomal capacity in skeletal muscle of mice after endurance training of different intensities

1978

The activity of certain enzymes of energy metabolism (cytochrome c oxidase, citrate synthase, malate dehydrogenase, and lactate dehydrogenase) and of lysosomes (beta-glucuronidase, beta-N-acetylglucosamindase, arylsuphatase, ribonuclease, deoxyribonuclease, acid phosphatase, and cathepsin D) was assayed from m. rectus femoris of mice trained 5 days per week, 1 hr per day for 4 weeks according to 4 different programmes: I. running speed 20 m/min, horizontal track, II. 25 m/min, horizontal track, III. 20 m/min 8 degrees uphill inclination, and IV. 25 m/min 8 degrees uphill inclination. Oxidative capacity increased and anaerobic capacity decreased without distinction between the different tran…

Malemedicine.medical_specialtyPhysiologyAcid PhosphataseCathepsin DCitrate (si)-SynthaseMalate dehydrogenaseElectron Transport Complex IVMicechemistry.chemical_compoundRibonucleasesMalate DehydrogenaseEndurance trainingLactate dehydrogenaseInternal medicineAcetylglucosaminidasemedicineAnimalsCitrate synthaseCytochrome c oxidaseArylsulfatasesGlucuronidaseDeoxyribonucleasesPhysical Education and TrainingL-Lactate DehydrogenasebiologyHistocytochemistryMusclesAcid phosphataseSkeletal muscleCathepsinsEndocrinologymedicine.anatomical_structurechemistryBiochemistrybiology.proteinEnergy MetabolismLysosomesActa Physiologica Scandinavica
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Acid hydrolase activities in mouse cardiac and skeletal muscle following exhaustive exercise

1981

Acid hydrolase activities in skeletal and cardiac muscle were studied 5, 10 and 20 days after exhaustive intermittent running by untrained and endurance-trained mice. Exhaustion increased the activities of cathepsin D, beta-glucuronidase and ribonuclease, but not that of p-nitrophenylphosphatase in skeletal muscle of untrained mice. Activities were highest on the fifth day after exhaustion and decreased during the following two weeks. More intensive loading produced no changes in acid hydrolytic capacity in skeletal muscle of endurance-trained mice. Acid hydrolase activities in cardiac muscle of both untrained and trained mice were unaffected by exhaustive running. It is suggested that exha…

Malemedicine.medical_specialtyTime FactorsHydrolasesPhysiologyPhysical ExertionCathepsin DMicePhysiology (medical)Internal medicinemedicineAnimalsOrthopedics and Sports MedicineExertionGlucuronidasebiologyMusclesMyocardiumFiber necrosisPublic Health Environmental and Occupational HealthCardiac muscleSkeletal muscleGeneral MedicineHuman physiologyCathepsinsEndocrinologymedicine.anatomical_structureBiochemistrybiology.proteinLysosomesAcid hydrolaseEuropean Journal of Applied Physiology and Occupational Physiology
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