0000000000286315

AUTHOR

Eeva-liisa Punnonen

showing 7 related works from this author

Isoproterenol inhibits fluid-phase endocytosis from early to late endosomes

1999

We have shown recently that isoproterenol affects both the cellular location and the morphology of late endosomes in a pH-dependent manner [Marjomäki et al., Eur. J. Cell Biol. 65, 1-13 (1994)]. In this study, using fluorescence and quantitative electron microscopy, we wanted to examine further what is the fate of internalized markers during their translocation from early to late endosomes under isoproterenol treatment. Fluorescein dextran internalized for 30 min (10-min pulse followed by a 20-min chase) showed accumulation in the cellular periphery during isoproterenol treatment in contrast to the control cells, which accumulated dextran in the perinuclear region. Quantitative electron mic…

HistologyEndosomeCell CountEndosomesBiologyEndocytosisPathology and Forensic Medicinechemistry.chemical_compoundCyclic AMPAnimalsFragmentation (cell biology)Cells CulturedVesicleIsoproterenolCell BiologyGeneral MedicineHydrogen-Ion ConcentrationMembrane transportEndocytosisIn vitroRatsCell biologyDextranchemistryBiochemistryCalciumRabbitsPercollBiomarkers
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Filipin labelling and intramembrane particles on the membranes of early and later autophagic vacuoles in Ehrlich ascites cells

1987

Cholesterol and intramembrane particle distribution on autophagic vacuole membranes was studied in Ehrlich ascites cells using filipin labelling and freeze-fracture electron microscopy. Unsaturated fatty acids were stained using imidazole-buffered osmium tetroxide. Autophagocytosis was induced with vinblastine, and early autophagic vacuoles were accumulated by lowering the ATP level in the cells with iodoacetate. Filipin labelling was observed in the limiting membranes of later, apparently hydrolase-containing autophagic vacuoles, whereas the most newly-formed, doublemembrane limited vacuoles were not labelled. The limiting membranes of late, residual body-type vacuoles either showed patchy…

Osmium TetroxideIodoacetatesPolyenesVacuoleBiologyVinblastineFilipinlaw.inventionMembrane LipidsMice03 medical and health scienceschemistry.chemical_compoundPhagocytosislawAutophagyAnimalsFreeze FracturingFilipinCarcinoma Ehrlich Tumor030304 developmental biology0303 health sciencesStaining and LabelingCholesterolEndoplasmic reticulum030302 biochemistry & molecular biologyAutophagyImidazolesMembrane ProteinsIntracellular MembranesCell biologyOrganoidsMicroscopy ElectronCholesterolMembranechemistryOsmium tetroxideVacuolesElectron microscopeVirchows Archiv B Cell Pathology Including Molecular Pathology
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Autophagy, cathepsin L transport, and acidification in cultured rat fibroblasts.

1992

The mechanisms of enzyme delivery to and acidification of early autophagic vacuoles in cultured fibroblasts were elucidated by cryoimmunoelectron microscopic methods. The cation-independent mannose-6-phosphate receptor (MPR) was used as a marker of the pre-lysosomal compartment, and cathepsin L and an acidotropic amine (3-(2,4-dinitroanilino)-3'-amino-N-methyl-dipropylamine (DAMP), a cytochemical probe for low-pH organelles) as markers of both pre-lysosomal and lysosomal compartments. In addition, cationized ferritin was used as an endocytic marker. In ultrastructural double labeling experiments, the bulk of all the antigens was found in vesicles containing tightly packed membrane material…

HistologyCathepsin LEndocytic cycleFluorescent Antibody TechniqueReceptors Cell SurfaceVacuoleReceptor IGF Type 2Cathepsin LEndopeptidasesOrganelleAutophagyAnimalsMicroscopy ImmunoelectronCells CulturedCathepsinMannosephosphatesbiologyVesicleBiological TransportFibroblastsHydrogen-Ion ConcentrationCathepsinsRatsCell biologyFerritinCysteine EndopeptidasesDinitrobenzenesBiochemistryCytoplasmbiology.proteinAnatomyJournal of Histochemistry & Cytochemistry
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Intramembrane particles and filipin labelling on the membranes of autophagic vacuoles and lysosomes in mouse liver

1989

Morphologically detectable protein (intramembrane particles) and cholesterol (filipin labelling) in the membranes of autophagic vacuoles and lysosomes were studied in mouse hepatocytes using thin-section and freeze-fracture electron microscopy. Both isolated autophagic vacuoles and lysosomes, and intact tissue blocks were used due to the facts (i) that lysosomes are difficult to recognize in freeze-fracture replicas of intact hepatocytes, and (i) that filipin penetration into the tissue blocks is unsatisfactory. Intramembrane particle density was low in the membranes of early autophagic vacuoles (defined as round-shaped vacuoles in which an inner membrane parallel with the outer limiting me…

Antifungal AgentsHistologyVacuoleBiologyFilipinPathology and Forensic MedicineMice03 medical and health scienceschemistry.chemical_compoundPhagocytosisLysosomeOrganelleAutophagymedicineAnimalsFreeze FracturingFilipin030304 developmental biologyPhagosome0303 health sciencesVesicle030302 biochemistry & molecular biologyBiological membraneCell BiologyCell biologymedicine.anatomical_structureMembraneLiverchemistryVacuolesLysosomesCell and Tissue Research
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Selective targeting of avidin/mannose 6-phosphate receptor chimeras to early or late endosomes

2000

Summary In this study we have used the Semliki forest virus expression system to transiently express chimeric proteins that contain transmembrane and cytoplasmic domains of the cation-independent mannose 6-phosphate receptor (CI-MPR) fused to chicken avidin. Immunofluorescence and electron microscopy studies showed that the chimeric protein with the entire cytoplasmic domain of CI-MPR was transported to late endosomes, where it accumulated. We made use of the biotin-binding capacity of lumenal avidin, and found that, in agreement with this distribution, the chimeric protein could be labelled with biotinylated HRP endocytosed for a long, but not a brief, period of time. However, truncation o…

CytoplasmTime FactorsHistologyEndosomeRecombinant Fusion ProteinsAmino Acid MotifsGreen Fluorescent ProteinsEndosomesEndocytosisReceptor IGF Type 2Pathology and Forensic Medicine03 medical and health sciencesCationsCricetinaeAnimalsBiotinylation030304 developmental biologyProtein Synthesis Inhibitors0303 health sciencesBrefeldin AMannose 6-phosphate receptorbiologyCell Membrane030302 biochemistry & molecular biologyPovidoneBiological TransportCell BiologyGeneral MedicineAvidinSilicon DioxideSemliki forest virusFusion proteinMolecular biologyEndocytosisTransmembrane proteinProtein Structure TertiaryLuminescent ProteinsMicroscopy ElectronTransmembrane domainCross-Linking ReagentsMicroscopy FluorescenceBiotinylationbiology.proteinCattleChickensDimerizationAvidinEuropean Journal of Cell Biology
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Effects of vinblastine, leucine, and histidine, and 3-methyladenine on autophagy in Ehrlich ascites cells.

1990

The microtubule inhibitor vinblastine causes accumulation of autophagic vacuoles in many cell types. In hepatocytes, many of the accumulated vacuoles are nascent, which has been interpreted to suggest that vinblastine acts by inhibiting the fusion of hydrolase-containing lysosomes with early autophagic vacuoles. However, our previous results suggested that, in Ehrlich ascites cells, vinblastine causes accumulation mainly of older autophagic vacuoles (AVs). This study was undertaken to further characterize the mode of action of vinblastine in these cells. The vinblastine-accumulated AVs were quantified by electron-microscopic morphometry. In addition, the effects of inhibitors of autophagic …

Cell SurvivalPhagocytosisClinical BiochemistryVacuoleProtein degradationBiologyVinblastinePathology and Forensic MedicinePhagocytosisMicrotubuleLeucineLysosomemedicineAutophagyTumor Cells CulturedAnimalsHumansHistidineCarcinoma Ehrlich TumorChildMolecular BiologyAdenineAutophagyVinblastineCell biologyMicroscopy Electronmedicine.anatomical_structureBiochemistryLeucinemedicine.drugExperimental and molecular pathology
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At reduced temperature, endocytic membrane traffic is blocked in multivesicular carrier endosomes in rat cardiac myocytes.

1998

Temperatures around 20 degrees C are known to block degradation of endocytosed material by preventing its transport to lysosomes, accordingly reduced temperature has been widely used to define endosomes. Newer studies have revealed that the low temperature block is proximal to perinuclear late endosomes, but it is not clear whether the block is already in early endosomes, or whether the traffic proceeds to multivesicular carrier endosomes which mediate transport from early to late compartments. We have now focused on this problem using rat cardiac myocytes. First, cell fractionation on Percoll gradients showed that at reduced temperatures (22 degrees C and 26 degrees C), with prolonged chas…

HistologyEndosomeEndocytic cycleEndosomesBiologyEndocytosisPathology and Forensic MedicineAnimalsCells Culturedchemistry.chemical_classificationVesicleMyocardiumTemperatureCell BiologyGeneral MedicineIntracellular MembranesMembrane transportEmbryo MammalianEndocytosisRatsCold TemperaturechemistryBiochemistryMicroscopy FluorescenceTransferrinBiophysicsCell fractionationCarrier ProteinsPercollEuropean journal of cell biology
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