Search results for "Ultrastructure"

showing 10 items of 224 documents

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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Neuronal markers in the rodent pineal gland ? an immunohistochemical investigation

1990

Although some embryological and morphological features speak in favour of a neuronal character of rodent pinealocytes, histochemistry and ultrastructure let this issue appear controversial. Using antibodies to different neurofilaments, the neural adhesion molecule L1, synaptophysin and tubulin as neuronal markers, the pineal glands of rat and guinea-pig were studied by means of immunofluorescence. Neurofilament-immunoreactivity was present in some rat pineal nerve fibers and in the majority of guinea-pig pinealocytes, L1 decorated rat intrapineal nerve fibers, synaptophysin was almost ubiquitously distributed in the pineal of both species, while tubulin-immunofluorescence was seen in nerve …

Malemedicine.medical_specialtyHistologyNeurofilamentL1Cell Adhesion Molecules NeuronalGuinea PigsIntermediate FilamentsSynaptophysinNerve Tissue ProteinsPineal GlandPinealocyteGuinea pigPineal glandTubulinInternal medicinemedicineAnimalsMolecular BiologyCytoskeletonbiologyMembrane ProteinsRats Inbred StrainsCell BiologyGeneral MedicineImmunohistochemistryRatsCell biologyMedical Laboratory TechnologyEndocrinologymedicine.anatomical_structurenervous systemSynaptophysinbiology.proteinUltrastructureImmunohistochemistryAnatomyGeneral Agricultural and Biological SciencesBiomarkersHistochemistry
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Evidence for the presence of two 24-h rhythms 180 degrees out of phase in the pineal gland of male Pirbright-White guinea pigs as monitored by counti…

1987

Previous studies have shown that the "synaptic" bodies of mammalian pinealocytes are a heterogeneous group of organelles. Whereas "synaptic" ribbons (SR) exhibit a day/night rhythm with small numbers during daytime and high numbers at night, the so-called "synaptic" spherules (SS) show species-specific differences in their rhythmicity. In the present study the numbers of SR and SS were monitored in male guinea pigs over a full 24-h period at 4-hourly intervals (LD 12:12, lights on at 7:00). The results obtained show that the rhythms of SR numbers and SS numbers are out of phase by 180 degrees. SR numbers are small during daytime and high at night, whereas SS numbers are high during daytime …

Malemedicine.medical_specialtyPeriod (gene)Guinea PigsPineal GlandPinealocyteMelatoninGuinea pigDiencephalonPineal glandInternal medicinemedicineAnimalsCircadian rhythmMelatoninMonitoring PhysiologicChemistryGeneral NeuroscienceCircadian RhythmOrganoidsMicroscopy ElectronEndocrinologymedicine.anatomical_structureSynapsesUltrastructuremedicine.drugExperimental brain research
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Ultrastructure of embryonic envelopes and integument ofOncopeltus fasciatus dallas (Insecta, Heteroptera)

1978

The embryo ofOncopeltus fasciatus forms a typical secondary dorsal organ (SDO). It develops after katatrepsis from the contracting serosa, the cells of which decrease in diameter but increase considerably in height. After 66 h, the SDO represents a protrusion of the serosal epithelium above the head and is then reduced to a disc-shaped formation, which sinks into the yolk, where it disintegrates after 80 h. During its typical expression, between 66 and 78 h, the SDO shows a zonal arrangement of its cell organelles. The nucleus, which is located in the basal cell region, has a very irregular outline and includes several nucleoli and globular inclusion bodies. Rough and smooth ER are well dev…

Malpighian tubule systemfood.ingredientAnatomyApical cellBiologyCell biologyfoodCytoplasmExcretory systemYolkOrganelleUltrastructureAnimal Science and ZoologyIntegumentAnatomyDevelopmental BiologyZoomorphologie
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Chemical characterization and ultrastructure study of pulp fibers

2020

Abstract Understanding the ultrastructure and chemical characterization of pulp fibers is highly important in utilizing wood as a raw material in a wide scope of applications, such as forest biomass-based biorefineries and low-cost renewable materials. The observation of the ultrastructure is not possible without advanced microscopy and spectroscopy techniques. Therefore, this study focuses on exploring the ultrastructure of pulp fibers with helium ion microscopy (HIM) and scanning electron microscopy (SEM). For the analysis of chemical characterization in the pulp fibers, Raman spectroscopy, Fourier transform infrared spectroscopy (FT-IR), and X-ray photoelectron spectroscopy (XPS) were pe…

Materials sciencePolymers and PlasticsScanning electron microscope02 engineering and technologyengineering.material010402 general chemistry01 natural sciencesCatalysisBiomaterialschemistry.chemical_compoundColloid and Surface Chemistrystomatognathic systemMicroscopyMaterials ChemistryLigninCelluloseFourier transform infrared spectroscopyPulp (paper)021001 nanoscience & nanotechnology0104 chemical sciencesElectronic Optical and Magnetic Materialsstomatognathic diseaseschemistryKraft processChemical engineeringengineeringUltrastructure0210 nano-technologyMaterials Today Chemistry
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Incremental lines in root cementum of human teeth: an approach to their ultrastructural nature by microscopy.

1998

In ground sections of human teeth, root cementum shows under the light microscope as alternating, almost concentric, dark and light rings. In paleontology and forensic medicine, the number of these incremental lines or annulations is used to derive the age-at-death of the individual. To find the ultrastructural features underlying these cemental annulations, we used bright-field light microscopy (LM), confocal laser scanning microscopy (CLSM), transmission electron microscopy (TEM), and electron-dispersive x-radiation (EDX) in a scanning electron microscope (SEM). Annulations visible in ground sections of about 100-μm thickness were no longer visible in semi-thin sections (thickness, 1-2 μ…

Materials scienceScanning electron microscopeAnalytical chemistrylaw.inventionOpticsOptical microscopelawMicroscopyMicrotomeHumansBicuspidTooth RootDental CementumMicroscopyMicroscopy Confocalbusiness.industryScanning confocal electron microscopyGeneral MedicineMicrotomyDark field microscopyMicroscopy ElectronTransmission electron microscopyEvaluation Studies as TopicUltrastructureAge Determination by TeethbusinessElectron Probe MicroanalysisAdvances in dental research
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Microscopic observations of superficial ultrastructure of unworn siloxane-hydrogel contact lenses by cryo-scanning electron microscopy

2006

The purpose of this study was to analyze three commercial siloxane-hydrogel contact lens materials, lotrafilcon A, balafilcon A, and galyfilcon A, by cryogenic scanning electron microscopy (cryoSEM). The fully hydrated lenses were frozen in slush liquid nitrogen and qualitatively observed in a cryogenic scanning electron microscope. The superficial ultrastructure of the siloxane-hydrogels was observed at the areas where the lens fractured during sample cryogenic preparation. There are qualitative differences among the three examined materials in the complex polymer network structure existing between the outer layer and the underlying polymer. CryoSEM, although destructive, is a useful tool …

Materials scienceSiloxanesScanning electron microscopeSurface PropertiesBiomedical Engineering02 engineering and technologyContact lens materialsHydrogel Polyethylene Glycol Dimethacrylatelaw.inventionBiomaterials03 medical and health sciences0302 clinical medicineOpticssilicone-hydrogellawMicroscopyMaterials TestingHumansCryo-scanning electron microscopyComposite materialchemistry.chemical_classificationScience & Technologybusiness.industryCryoelectron MicroscopyCryoSEM microscopyPolymerLiquid nitrogenpolymer surface021001 nanoscience & nanotechnologyContact Lenses HydrophilicSiloxane-hydrogel contact lensescryoSEMLens (optics)Contact lenschemistry030221 ophthalmology & optometryUltrastructuremicroscopysiloxane-hydrogels0210 nano-technologybusiness
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Ultrastructure of the Perineurium

2014

The perineurium is composed of multiple concentric single-cell layers enclosing individual nerve fascicles. Each layer has a thickness equivalent to the width of a perineurial cell. Groups of these cells join by means of tight junctions and desmosomes to form layers that function as a barrier against diffusion of particles across them. Perineurial internal layers have more of these specialized unions among perineurial cells, which are proximal to nerve fascicles.

Materials sciencemedicine.anatomical_structureTight junctionUltrastructuremedicineBiophysicsDiffusion (business)PerineuriumPerineurial Cell
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Ultrastructure of Spinal Dura Mater

2014

Pia mater is the innermost of the three meningeal membranes, closely surrounding the brain, the spinal cord, and the portion of spinal nerve roots extending towards their exit across the dura mater. A cellular layer and a subpial compartment shape the structure of the pia mater. The cellular layer is made up of flat, overlapping pial cells with amorphous, fundamental substance interposed among them. The surface of the cellular plane appears smooth and bright under scanning electron microscopy (SEM). Transmission electron microscopy shows that the cellular component is about three to five pial cells thick at the medullary level and two to three cells thick at the level of the nerve roots. Th…

MembraneMaterials sciencemedicine.anatomical_structurenervous systemNerve rootPia materTransmission electron microscopyCompartment (ship)Dura materUltrastructuremedicineAnatomySpinal cord
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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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