Search results for "Reticulum"

showing 10 items of 336 documents

Is Autophagy Altered in the Leukocytes of Type 2 Diabetic Patients?

2015

It is unknown whether autophagy is altered in the leukocytes of type 2 diabetes (T2D) patients and whether oxidative and endoplasmic reticulum (ER) stresses regulate this mechanism. We studied anthropometric and metabolic parameters and evaluated oxidative stress, chromatin condensation, ER stress, and autophagy parameters in leukocytes of 103 T2D patients versus 109 sex- and age-matched controls. Patients showed increases in glucose, insulin, homeostasis model assessment of insulin resistance, and glycated hemoglobin (HbA1c) compared with controls (p < 0.001). Leukocytes displayed enhanced total and mitochondrial reactive oxygen species (ROS), reduced mitochondrial mass, and increased chro…

Malemedicine.medical_specialtyCell Nucleus ShapePhysiologymedicine.medical_treatmentClinical BiochemistryBiologymedicine.disease_causeBiochemistryInsulin resistanceInternal medicinemedicineAutophagyLeukocytesHumansMolecular BiologyEndoplasmic Reticulum Chaperone BiPGeneral Environmental ScienceAgedchemistry.chemical_classificationReactive oxygen speciesATF6Endoplasmic reticulumInsulinAutophagyCell BiologyMiddle Agedmedicine.diseaseEndoplasmic Reticulum StressOxidative StressEndocrinologychemistryDiabetes Mellitus Type 2Case-Control StudiesUnfolded protein responseGeneral Earth and Planetary SciencesFemaleReactive Oxygen SpeciesOxidation-ReductionOxidative stressSignal TransductionAntioxidantsredox signaling
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Structure and function of prothoracic glands and oenocytes in embryos and last larval instars of Oncopeltus fasciatus Dallas (Insecta, Heteroptera).

1976

1. Active prothoracic glands and oenocytes of last larval stage are both characteristized by well-developed smooth and rough endoplasmic reticulum (ER). Prothoracic glands also show plasma membrane infoldings, but not oenocytes which contain a large number of pleomorphic vesicles. 2. The fine structure of embryonic oenocytes corresponds after blastokinesis with that of active larval and adult cells. Thus, an activity in the late embryo can be assumed. Embryonic prothoracic glands reveal no signs of activity: smooth and rough ER are absent. The subcellular structure resembles that of organ anlagen, i.e. not yet fully differentiated tissue. Hormone synthesis is not likely. 3. Ecdysone titer w…

Malemedicine.medical_specialtyEcdysoneHistologyInsectaEndoplasmic reticulumEmbryogenesisEmbryoCell BiologyBiologyProthoracic glandPathology and Forensic MedicineCell biologychemistry.chemical_compoundEndocrinologychemistryInternal medicineEcdysisUltrastructuremedicineEndocrine systemAnimalsFemaleEcdysoneCell and tissue research
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Studies on vinblastine-induced autophagocytosis in mouse liver. III. A quantitative study.

1982

The microtubule inhibitor vinblastine (25 mg/kg, i.p.) induces autophagocytosis in mouse hepatocytes. The formation of autophagic vacuoles, their contents, and other cellular changes after vinblastine injection in hepatocytes, were studied by light and electron microscopic morphometric analysis. The volume density of autophagic vacuoles increased significantly during the experimental period (24 h). This increase was due to the significant increase in their number, which was approximately 5-fold 4 h, 12 h and 24 h after vinblastine injection. The mean volume of the autophagic vacuoles increased significantly 1 h after vinblastine injection, at which time the formation of new autophagic vacuo…

Malemedicine.medical_specialtyTime FactorsLiver cytologymedicine.medical_treatmentIntraperitoneal injectionVacuoleBiologyVinblastinesymbols.namesakeMicePhagocytosisInternal medicinemedicineAutophagyAnimalsLobules of liverEndoplasmic reticulumAcid phosphataseGolgi apparatusVinblastineEndocrinologyBiochemistryLiverbiology.proteinsymbolsmedicine.drugVirchows Archiv. B, Cell pathology including molecular pathology
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Controlled Release of Metformin Hydrochloride from Core-Shell Nanofibers with Fish Sarcoplasmic Protein

2019

Ficai, Anton/0000-0002-1777-0525; Karademir, Betul/0000-0003-1762-0284 WOS:000503463400074 PubMed ID: 31658758 Background and Objectives: A coaxial electrospinning technique was used to produce core/shell nanofibers of a polylactic acid (PLA) as a shell and a polyvinyl alcohol (PVA) containing metformin hydrochloride (MH) as a core. Materials and Methods: Fish sarcoplasmic protein (FSP) was extracted from fresh bonito and incorporated into nanofiber at various concentrations to investigate the influence on properties of the coaxial nanofibers. The morphology, chemical structure and thermal properties of the nanofibers were studied. Results: The results show that uniform and bead-free struct…

Medicine (General)POLYMERIC NANOFIBERSChemical structurewound healingIn Vitro Techniquescoaxial electrospinningPolyvinyl alcoholArticleDELIVERYCrystallinitychemistry.chemical_compoundcoaxial electrospinning; fish sarcoplasmic protein; nanofibers; wound healingR5-920Differential scanning calorimetryPolylactic acidnanofibersSpectroscopy Fourier Transform InfraredMedicineAnimalsbusiness.industryTunaGeneral MedicineControlled releaseMetforminfish sarcoplasmic proteinDrug LiberationSarcoplasmic ReticulumchemistryChemical engineeringNanofiberDelayed-Action PreparationsPolyvinyl AlcoholELECTROSPUN NANOFIBERSCoaxialbusinessFIBERSMATRICES
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Regulation of Calcium Channel Activity by Lipid Domain Formation in Planar Lipid Bilayers

2003

The sarcoplasmic reticulum channel (ryanodine receptor) from cardiac myocytes was reconstituted into planar lipid bilayers consisting of 1-palmitoyl-2-oleoyl-phosphatidylethanolamine (POPE) and 1-palmitoyl-2-oleoyl-phosphatidylcholine (POPC) in varying ratios. The channel activity parameters, i.e., open probability and average open time and its resolved short and long components, were determined as a function of POPE mole fraction (X(PE)) at 22.4 degrees C. Interestingly, all of these parameters exhibited a narrow and pronounced peak at X(PE) approximately 0.80. Differential scanning calorimetric measurements on POPE/POPC liposomes with increasing X(PE) indicated that the lipid bilayer ente…

Membrane FluidityProtein ConformationLipid BilayersBiophysicsAnalytical chemistryMolecular Conformation010402 general chemistryElectric Capacitance01 natural sciencesMembrane Potentials03 medical and health scienceschemistry.chemical_compoundStructure-Activity RelationshipProtein structureMembrane MicrodomainsChannels Receptors and TransportersMembrane fluidityLipid bilayer phase behaviorLipid bilayerPOPC030304 developmental biologyMembrane potential0303 health sciencesLiposomeEndoplasmic reticulumPhosphatidylethanolaminesMembranes ArtificialRyanodine Receptor Calcium Release Channel0104 chemical scienceschemistry13. Climate actionBiophysicsPhosphatidylcholineslipids (amino acids peptides and proteins)Calcium ChannelsIon Channel Gating
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Ultrastructure of differentiating hemocytes in the embryo of Oncopeltus fasciatus dallas (insecta, heteroptera).

1978

The hemocytes of Oncopeltus differentiate rather early during embryogenesis. They are segregated by the mesoderm soon after its formation (about 50h after egg deposition). Newly segregated hemocytes show the “typical” features of “embryonic” cells: many free ribosomes, a few strands of rough ER, the cisternae of which are considerably distended, electron lucent vacuoles around the periphery, and glycogen deposits. A few hours thereafter the hemocytes undergo striking subcellular changes. First, glycogen, electron lucent vacuoles and rough ER disappear and phagocytotic activity can be observed. Golgi complexes become well expressed and give rise to electron dense vesicles which fuse to large…

MesodermHistologyHemocytesInsectaGolgi ApparatusVacuoleBiologyEndoplasmic ReticulumPathology and Forensic Medicinesymbols.namesakePhagocytosismedicineAnimalsInclusion BodiesBlood CellsEndoplasmic reticulumVesicleEmbryogenesisCell DifferentiationCell BiologyAnatomyGolgi apparatusCell biologymedicine.anatomical_structureCytoplasmLarvaVacuolessymbolsUltrastructureRibosomesGlycogenCell and tissue research
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Establishment and characterization of a nontumorigenic cell line derived from a human hepatocellular adenoma expressing hepatocyte-specific markers.

1997

In the present study the establishment and characterization of a nontumorigenic liver epithelial cell line (HACL-1) derived from a human hepatocellular adenoma is described. The HACL-1 cells have a finite life span (i.e., they proliferate for a period of 2 months and then senesce), show cell-cell contact inhibition, do not grow in soft agar, are not tumorigenic when injected in nude mice, and possess a normal diploid karyotype. The cultured cells resemble hepatocytes, but exhibit some features of dedifferentiation. At the ultrastructural level the cells are endowed with round or oval nuclei, abundant cytoplasmic organelles, and varying amounts of glycogen. The rough endoplasmic reticulum is…

Mice NudeBiologymedicine.disease_causeAdenoma Liver CellCytokeratinMicemedicineBiomarkers TumorTumor Cells CulturedAnimalsHumansCellular SenescenceEndoplasmic reticulumLiver NeoplasmsContact inhibitionEpithelial CellsCell BiologySequence Analysis DNAHepatocellular adenomamedicine.diseaseGenes p53Cell biologymedicine.anatomical_structureCytoplasmCell cultureOrgan SpecificityHepatocyteKaryotypingCarcinogenesisExperimental cell research
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Lack of GDAP1 induces neuronal calcium and mitochondrial defects in a knockout mouse model of Charcot-Marie-tooth neuropathy

2015

27 páginas, 9 figuras.

Mitochondrial proteinCancer Researchlcsh:QH426-470Nerve Tissue ProteinsBiologyMitochondrionCharcot-Marie-Tooth diseaseGDAP1 geneMiceGeneticsAutophagyAnimalsCalcium SignalingMolecular BiologyGenetics (clinical)Ecology Evolution Behavior and SystematicsCytoskeletonCalcium signalingGeneticsVoltage-dependent calcium channelEndoplasmic reticulumAutophagyBiología y Biomedicina / BiologíaAxonsCell biologyMitochondriaMitochondrialMice Inbred C57BLAlpha tubulinlcsh:Geneticsmitochondrial fusionKnockout mouseMitochondrial fissionCalcium ChannelsAnimal cellGene DeletionResearch Article
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The Surfactant Peptide KL4 Sequence Is Inserted with a Transmembrane Orientation into the Endoplasmic Reticulum Membrane

2008

AbstractSurfactant protein B (SP-B) is an essential component of pulmonary surfactant. Synthetic surfactant peptide KL4, a peptide based on a C-terminal amphipathic helical region of human SP-B, efficiently mimics some functional properties of SP-B and is included in therapeutic surfactant preparations used in trials to treat respiratory distress syndrome. The membrane orientation of this peptide is controversial. We used an in vitro transcription-translation system to study the insertion of hydrophobic sequences into microsomal membranes, and showed that the KL4 sequence integrates efficiently with a transmembrane orientation despite the presence of intermittent lysines throughout the sequ…

Models MolecularBiophysical LettersProtein ConformationBiophysicsBiologyEndoplasmic ReticulumCell membraneProtein structurePulmonary surfactantMembranes (Biologia)medicineAnimalsHumansPulmonary surfactant-associated protein BAmino Acid SequencePeptide sequencePulmonary Surfactant-Associated Protein BEndoplasmic reticulumCell MembraneInfant NewbornTransmembrane proteinMembranemedicine.anatomical_structureBiochemistryBiophysicsPèptidsPeptidesHydrophobic and Hydrophilic InteractionsBiophysical Journal
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Distant downstream sequence determinants can control N-tail translocation during protein insertion into the endoplasmic reticulum membrane.

2000

We have studied the membrane insertion of ProW, an Escherichia coli inner membrane protein with seven transmembrane segments and a large periplasmic N-terminal tail, into endoplasmic reticulum (ER)-derived dog pancreas microsomes. Strikingly, significant levels of N-tail translocation is seen only when a minimum of four of the transmembrane segments are present; for constructs with fewer transmembrane segments, the N-tail remains mostly nontranslocated and the majority of the molecules adopt an 'inverted' topology where normally nontranslocated parts are translocated and vice versa. N-tail translocation can also be promoted by shortening of the N-tail and by the addition of positively charg…

Models MolecularBioquímicaGlycosylationChromosomal translocationBiologyEndoplasmic ReticulumBiochemistryBacterial ProteinsMembranes (Biologia)MicrosomesEscherichia coliAnimalsInner membranePancreasMolecular BiologyEscherichia coli ProteinsEndoplasmic reticulumMembrane ProteinsSTIM1Periplasmic spaceCell BiologyMolecular biologyTransmembrane proteinCell biologyMembrane proteinMutationCatsMicrosomeATP-Binding Cassette TransportersProteïnesJournal of Biological Chemistry
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