Search results for "Golgi apparatus"

showing 10 items of 87 documents

Organelle pH studies using targeted avidin and fluorescein–biotin

2000

Abstract Background: Mammalian organelles of the secretory pathway are of differing pH. The pH values form a decreasing gradient: the endoplasmic reticulum (ER) is nearly neutral, the Golgi is mildly acidic and the secretory granules are more acidic still (∼pH 5). The mechanisms that regulate pH in these organelles are still unknown. Results: Using a novel method, we tested whether differences in H + ‘leak' and/or counterion conductances contributed to the pH difference between two secretory pathway organelles. A pH-sensitive, membrane-permeable fluorescein–biotin was targeted to endoplasmic-reticulum- and Golgi-localized avidin-chimera proteins in HeLa cells. In live, intact cells, ER pH (…

Clinical BiochemistryBiotinGolgi ApparatusEndoplasmic ReticulumBiochemistrysymbols.namesakechemistry.chemical_compoundChloridesBiotinOrganelleDrug DiscoveryHumansMicroscopy ImmunoelectronMolecular BiologySecretory pathwayFluorescent DyesOrganellesPharmacologyIon TransportFlubi-2ChemistryEndoplasmic reticulumBafilomycinIntracellular MembranesGeneral MedicineHydrogen-Ion ConcentrationProton PumpsGolgi apparatusAvidinCytosolTargeted fluorescenceMembraneBiochemistryH+ pumpPotassiumsymbolsMolecular MedicineFluoresceinHeLa CellsH+ leakChemistry & Biology
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A closer look at the cholesterol sensor

2002

Abstract Transport of the sterol regulatory element-binding protein (SREBP) cleavage-activating protein (SCAP)–SREBP complex from the endoplasmic reticulum (ER) to the Golgi is the central event mediating the cholesterol-feedback process in mammalian cells. A conformational change in SCAP is a crucial step; when cholesterol levels are high, the conformation of SCAP enables the SCAP–SREBP complex to associate with an insulin-induced gene (INSIG) retention protein in the ER. By contrast, when cholesterol levels are low, SCAP switches to a conformation that enables the dissociation of the retention protein and the association of SCAP–SREBP with COP II vesicles.

Conformational changeCholesterolEndoplasmic reticulumVesicleBiologyGolgi apparatusBiochemistrySterolSterol regulatory element-binding proteinCell biologysymbols.namesakechemistry.chemical_compoundBiochemistryStructural biologychemistrypolycyclic compoundssymbolslipids (amino acids peptides and proteins)Molecular BiologyTrends in Biochemical Sciences
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Polyphosphoinositide Metabolism and Golgi Complex Morphology in Hippocampal Neurons in Primary Culture is Altered by Chronic Ethanol Exposure

2012

Aims : Ethanol affects not only the cytoskeletal organization and activity, but also intracellular trafficking in neurons in the primary culture. Polyphosphoinositide (PPIn) are essential regulators of many important cell functions, including those mentioned, cytoskeleton integrity and intracellular vesicle trafficking. Since information about the effect of chronic ethanol exposure on PPIn metabolism in neurons is scarce, this study analysed the effect of this treatment on three of these phospholipids. Methods : Phosphatidylinositol (PtdIns) levels as well as the activity and/or levels of enzymes involved in their metabolism were analysed in neurons chronically exposed to ethanol. The level…

Cytoskeleton organizationGolgi ApparatusBiologyHippocampuschemistry.chemical_compoundsymbols.namesakePhosphatidylinositol PhosphatesAnimalsPhosphatidylinositolCytoskeletonCells CulturedNeuronsEthanolKinaseIntracellular vesicleGeneral MedicineGolgi apparatusRatsCell biologychemistryBiochemistrysymbolsFemalePhosphatidylethanolIntracellularSignal TransductionAlcohol and Alcoholism
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ER-to-Golgi Transport: The COPII-Pathway

2006

The endoplasmic reticulum (ER) is the starting site of the journey of newly synthesized proteinsto the apoplast, plasma membrane and to the vacuolar compartments. Transport between these membranecompartments of the secretory pathway in eukaryotic cells is mediated by vesicles, which are producedby a budding mechanism involving coat proteins that capture specific cargo molecules and helppackage them into coated vesicles. These vesicles are known as COPII-coated vesicles, and are usuallyisolated after their induction in vitro using microsomal membranes, cytosol and a non-hydrolyzableGTP-analogue. COPII-coated vesicles are formed at specific sites in the ER known as ER-exit sites(ERES). ERES a…

Cytosolsymbols.namesakeChemistryEndoplasmic reticulumVesicleMicrosomesymbolsCoated vesicleGolgi apparatusCOPIISecretory pathwayCell biology
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Dynamic changes in the subcellular distribution of the tobacco ROS-producing enzyme RBOHD in response to the oomycete elicitor cryptogein.

2014

Highlight text The oomycete elicitor cryptogein triggers the relocation of RBOHD from intracellular compartments to the plasma membrane in tobacco cells. This suggests that intracellular trafficking is a potential determinant of RBOHD activity.

DETERGENT-RESISTANT MEMBRANESPhysiologyNicotiana tabacum[SDV]Life Sciences [q-bio]BY-2 cellsPlant SciencecryptogeinCell membranechemistry.chemical_compoundAPOPLASTIC OXIDATIVE BURSTCELL-SURFACEDISEASE RESISTANCE[MATH]Mathematics [math]Plant Proteinsreactive oxygen speciesFungal proteinNADPH oxidaseMicroscopy Confocalbiologyfood and beveragesElicitorCell biologymedicine.anatomical_structureBiochemistryprotein trafficking.[SDE]Environmental SciencessymbolsNADPH OXIDASE RBOHDprotein traffickingResearch PaperPhytophthoraCycloheximiderespiratory burst oxidase homolog D (RBOHD)Real-Time Polymerase Chain ReactionFungal Proteinssymbols.namesakeNICOTIANA-BENTHAMIANAMicroscopy Electron TransmissionTobaccomedicine[SDV.BV]Life Sciences [q-bio]/Vegetal Biology[INFO]Computer Science [cs]NITRIC-OXIDENicotiana tabacumCell MembraneNADPH OxidasesGolgi apparatusbiology.organism_classificationSubcellular localizationLIPID RAFTSchemistryPLASMA-MEMBRANEbiology.proteinPLANT DEFENSE
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Ultrastructural changes of the oenocytes of Gryllus bimaculatus DEG (Saltatoria, Insecta) during the moulting cycle

1974

1. The oenocytes of Gryllus bimaculatus are characterized by an abundant smooth-surfaced ER (ATER). In spite of the great cell size the plasma membrane never shows extensive infoldings during the moulting cycle. In addition to mitochondria there are very large numbers of microbodies containing peroxidase but apparently not uricase. Within the second part of the instar the microbodies lie along the clefts which run through the whole cell. 2. The following changes are observed in the course of a moulting cycle: Immediately after hatching the ATER is scarcely developed, some liposomes are located within areas of ATER disappearing some hours later. 20 hours after emergence glycogen deposits app…

EcdysoneInsectaTime FactorsHistologyGolgi ApparatusMicrobodiesPathology and Forensic Medicinechemistry.chemical_compoundAnimalsMicrobodyOvumCell NucleusStaining and LabelingGlycogenbiologyHistocytochemistryHatchingGryllus bimaculatusCell MembraneMetamorphosis BiologicalCell BiologyAnatomybiology.organism_classificationMitochondriaCell biologyMicroscopy ElectronchemistryLarvaUltrastructureInstarFemaleLysosomesMoultingReticulumGlycogenCell and Tissue Research
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Microbial strategies to exploit host cells

2005

The European Research Conference (EURESCO) on Spatial and Temporal Dynamics of the Endomembrane System was held in sunny San Feliu de Guixols, Spain, between 16 and 21 October 2004. The conference was organized by D. Holden and H. Stenmark ![][1] By bringing together scientists from the fields of microbiology and cell biology, the European Research Conference (EURESCO) on ‘Spatial and Temporal Dynamics of the Endomembrane System’ combined the best of both worlds at the intersection where intracellular pathogens and host cells meet. The mixture of studies, which focused on the molecular mechanisms behind endocytic and secretory transport, and the pathogenic microbes that exploit these pathwa…

EffectorEndocytic cycleCDC42Golgi apparatusBiologyEndocytosisBiochemistryCell biologysymbols.namesakeGeneticssymbolsEndomembrane systemSecretionMolecular BiologyPhagosomeEMBO reports
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The serosa of Manduca sexta (Insecta, Lepidoptera): ontogeny, secretory activity, structural changes, and functional considerations

2001

In Manduca sexta, the blastoderm forms successively and becomes immediately cellularized as the cleavage energids reach the surface of the oocyte. Presumptive serosal cells are large and contain 2 or 4 large polyploid nuclei; presumptive embryonic cells are small and mononuclear. All parts of the blastoderm participate in the uptake and digestion of yolk material. About 10 h post-oviposition, the blastoderm breaks at the amnioserosal fold and the extraembryonic part closes above the germ band and constitutes the serosa (12 h post-oviposition, i.e. 10% development completed). At once, the serosa starts to secrete a cuticle consisting of an epi- and a lamellated endocuticle. Detachment of the…

Embryo Nonmammalianfood.ingredientApolysisBiologysymbols.namesakefoodManducaYolkLipid dropletparasitic diseasesAnimalsYolk SacVesiclefungiEmbryogenesisCell BiologyGeneral MedicineAnatomyGolgi apparatusbiology.organism_classificationCell biologyMicroscopy ElectronManduca sextaOocytessymbolsInsect ProteinsBlastodermDevelopmental BiologyTissue and Cell
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Quantitative electron microscopic observations on Paneth cells of germfree and ex-germfree Wistar rats.

1986

Ultrastructural changes of Paneth cells of germfree (Gf) rats which had been inoculated with bacteria-containing feces from conventionally-reared (SPF) rats were quantitatively examined. 12 and 24 h after inoculation, the Paneth cells showed a striking decrease in the number of secretory granules and the occurrence of large vacuoles. Phagosomes containing bacteria were not seen. After 4 days, the secretory granules reaccumulated and smooth-surfaced apical vesicles increased in number. It is discussed that the large vacuoles may be related to membrane-retrieval events following the massive extrusion of secretory granules whereas the apical vesicles appear to serve this function when exocytos…

EmbryologyPathologymedicine.medical_specialtyTime FactorsGolgi ApparatusVacuoleBiologyCytoplasmic Granulesdigestive systemExocytosislaw.inventionlawIntestine SmallmedicineAnimalsGerm-Free LifeIntestinal MucosaCell NucleusGerm-free animalVesicleCell BiologyMolecular biologySmall intestineRatsMicroscopy Electronmedicine.anatomical_structurePaneth cellUltrastructureAnatomyElectron microscopeLysosomesDevelopmental BiologyAnatomy and embryology
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Effects of Ga3 and Ca2+ on barley aleurone protoplasts: a freeze-fracture study

1988

Freeze-fracture electron microscopy was used to study changes in the endomembrane system of barley (Hordeum vulgare L. cv. Himalaya) aleurone protoplasts. Protoplasts were used for this study because their response to calcium and the plant hormone gibberellic acid (Ga3) can be monitored prior to rapid freezing of cells for electron microscopy. Protoplasts incubated in Ga3 plus Ca2+ secrete elevated levels of a-amylase relative to cells incubated in Ga3 or Ca2+ alone. The endoplasmic reticulum (ER) and Golgi apparatus of protoplasts incubated in Ga3 plus Ca2+ undergo changes that are well correlated with the synthesis and secretion of a-amylase. The ER, which appears as short, single sheets …

Endoplasmic reticulumfungifood and beveragesCell BiologyPlant ScienceGeneral Medicinebiochemical phenomena metabolism and nutritionGolgi apparatusBiologyCell biologysymbols.namesakeBiochemistryAleuroneOrganelleGolgi cisternasymbolsSecretionEndomembrane systemHordeum vulgareProtoplasma
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