Search results for "Helium"

showing 10 items of 1689 documents

Expression of the endothelial markers PECAM-1, vWf, and CD34 in vivo and in vitro.

2002

EC culture models are essential to study pathological alterations of endothelial cells (ECs) in pulmonary vascular diseases under standardized conditions. Nevertheless, little is known about the spectrum of alterations of vessel-specific endothelial phenotypes in monolayer cultures. For the comparative study of endothelial markers in vivo and in vitro we investigated immunohistochemically the expression of PECAM-1, vWf, and CD34 by pulmonary ECs in vivo and in stimulated/unstimulated human umbilical vein endothelial cells (HU-VEC) and human pulmonary microvascular endothelial cells (HPMEC). In vivo, vessel type-specific expression patterns were found for vWf and CD34, while PECAM-1 was homo…

Pathologymedicine.medical_specialtyEndotheliumClinical BiochemistryCD34Antigens CD34BiologyIn Vitro TechniquesUmbilical veinPathology and Forensic MedicineIn vivovon Willebrand FactormedicineHumansMolecular BiologyLungCells CulturedMicrocirculationImmunohistochemistryIn vitroCell biologyEndothelial stem cellPlatelet Endothelial Cell Adhesion Molecule-1medicine.anatomical_structurePhenotypeCell culturecardiovascular systemEndothelium VascularBiomarkersBlood vesselExperimental and molecular pathology
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Comparative Study of Adhesion Molecule Expression in Cultured Human Macro- and Microvascular Endothelial Cells

2002

Culture systems as models for disease are only valid as long as they are comparable to in vivo conditions. The phenotype of cultured endothelial cells (ECs) has only been sporadically compared to the corresponding phenotype in vivo. Thus, we compared by immunolocalization the endothelial expression of ICAM-1, VCAM, and E-selectin in vivo in stimulated/unstimulated human umbilical vein endothelial cells (HUVEC) as a model for macrovascular ECs and stimulated/unstimulated HPMEC (human pulmonary microvessel endothelial cells) as a model for pulmonary microvascular ECs with that in human lungs in vivo (normal and ARDS). Proinflammatory stimuli in vitro were used to stimulate conditions relevant…

Pathologymedicine.medical_specialtyEndotheliumClinical BiochemistryVascular Cell Adhesion Molecule-1Umbilical veinPathology and Forensic MedicineIn vivoE-selectinCell AdhesionmedicineHumansMolecular BiologyMicrovesselCells CulturedRespiratory Distress SyndromebiologyCell adhesion moleculeIntercellular Adhesion Molecule-1ImmunohistochemistryMolecular biologyEndothelial stem cellPhenotypemedicine.anatomical_structureCell culturecardiovascular systembiology.proteinEndothelium VascularE-SelectinExperimental and Molecular Pathology
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CD15 – A new marker of pathological villous immaturity of the term placenta

2014

Abstract Introduction Idiopathic immaturity is one of the main reasons for latent placental insufficiency and antenatal hypoxia. Postnatal identification of the immature placental phenotype may help early stratification of a heterogeneous population of newborns and individually identify risk of disease in the immediate postnatal life. The aim of the study was to determine the relevant diagnostic markers associated with pathological placental immaturity. Methods 111 tissue samples from normal and pathological term placentas with persisting villous immaturity comprised the comparative immunohistochemical study (CD15, CD34). Positive immunohistochemical reactions were quantitatively assessed i…

Pathologymedicine.medical_specialtyEndotheliumLewis X AntigenAntigens CD34Placental insufficiencyBiologyPregnancyChronic VillitisFetal macrosomiamedicineHumansPathologicalPlacental villous immaturityAsphyxiaObstetrics and GynecologyHypoxia (medical)FucosyltransferasesPlacental Insufficiencymedicine.diseasemedicine.anatomical_structureReproductive MedicineCase-Control Studiesembryonic structuresImmunologyFemalemedicine.symptomBiomarkersDevelopmental BiologyPlacenta
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Lung epithelial cell lines in coculture with human pulmonary microvascular endothelial cells: development of an alveolo-capillary barrier in vitro.

2004

We have established a coculture system of human distal lung epithelial cells and human microvascular endothelial cells in order to study the cellular interactions of epithelium and endothelium at the alveolocapillary barrier in both pathogenesis and recovery from acute lung injury. The aim was to determine conditions for the development of functional cellular junctions and the formation of a tight epithelial barrier similar to that observed in vivo. The in vitro coculture system consisted of monolayers of human lung epithelial cell lines (A549 or NCI H441) and primary human pulmonary microvascular endothelial cells (HPMEC) on opposite sides of a permeable filter membrane. A549 failed to sho…

Pathologymedicine.medical_specialtyEndotheliummedicine.medical_treatmentBiologyLung injuryCell junctionDexamethasonePathology and Forensic MedicineCell LineTight JunctionsAdherens junctionmedicineElectric ImpedanceHumansMolecular BiologyLungLungBlood-Air BarrierTumor Necrosis Factor-alphaEpithelial CellsCell BiologyAdherens JunctionsEpitheliumCoculture TechniquesCell biologyEndothelial stem cellPulmonary AlveoliMicroscopy Electronmedicine.anatomical_structureCytokineEndothelium VascularInflammation MediatorsLaboratory investigation; a journal of technical methods and pathology
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Microvascular in vivo assessment of reperfusion injury: significance of prostaglandin E1 and I2 in postischemic “no-reflow” and “reflow-paradox”

2004

Microvascular ischemia-reperfusion (I/R) injury is characterized by failure of capillary perfusion ("no-reflow") and reoxygenation-associated phenomena ("reflow-paradox"), including activation of leukocyte-endothelium interaction with cytotoxic mediator-induced loss of endothelial integrity. The objectives of this study were to elucidate the impact of both prostaglandins E(1) (PGE(1)) and I(2) (PGI(2)) in microvascular reperfusion injury, with special focus on the distinct pathophysiology of no-reflow- and reflow-paradox phenomena.By use of the hamster dorsal skinfold preparation and in vivo fluorescence microscopy, the microcirculation of a striated skin muscle was assessed before 4 h of p…

Pathologymedicine.medical_specialtyEndotheliummedicine.medical_treatmentIschemiaPharmacologyMicrocirculationCapillary Permeabilitychemistry.chemical_compoundIn vivoCricetinaemedicineAnimalsVascular Diseasescardiovascular diseasesAlprostadilMuscle SkeletalProstaglandin E1SkinMicroscopyMesocricetusbusiness.industryMicrocirculationmedicine.diseaseEpoprostenolPathophysiologyCapillariesChemotaxis Leukocytemedicine.anatomical_structurechemistryReperfusion InjuryModels Animalcardiovascular systemSurgeryEndothelium VascularbusinessReperfusion injuryPlatelet Aggregation InhibitorsProstaglandin EJournal of Surgical Research
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Wharton's Jelly Stem Cells: A Novel Cell Source for Oral Mucosa and Skin Epithelia Regeneration

2013

Abstract Perinatal stem cells such as human umbilical cord Wharton's jelly stem cells (HWJSCs) are excellent candidates for tissue engineering because of their proliferation and differentiation capabilities. However, their differentiation potential into epithelial cells at in vitro and in vivo levels has not yet been reported. In this work we have studied the capability of HWJSCs to differentiate in vitro and in vivo to oral mucosa and skin epithelial cells using a bioactive three-dimensional model that mimics the native epithelial-mesenchymal interaction. To achieve this, primary cell cultures of HWJSCs, oral mucosa, and skin fibroblasts were obtained in order to generate a three-dimension…

Pathologymedicine.medical_specialtyFluorescent Antibody TechniqueMice NudeFilaggrin ProteinsBiologyModels BiologicalEpitheliumMiceIntermediate Filament ProteinsTissue engineeringTissue Engineering and Regenerative MedicineWharton's jellymedicineAnimalsHumansRegenerationWharton JellyProtein PrecursorsOral mucosaInvolucrinSkinRegeneration (biology)Mouth MucosaCell DifferentiationEpithelial CellsMesenchymal Stem CellsCell BiologyGeneral MedicineFlow CytometryCell biologymedicine.anatomical_structureCell cultureKeratinsLeukocyte Common AntigensThy-1 Antigensgamma CateninStem cellDevelopmental BiologyAdult stem cellStem Cells Translational Medicine
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Serum antibodies to thymus epithelial cells in non-A, non-B and cryptogenic chronic liver disease

2008

Antibodies against thymus epithelial cells (anti-TEC) and the basal cell layer (BCLA) of squamous epithelia have been described in association with HDV-related chronic liver disease (CLD). Data are lacking on their presence during nAnB virus infection. Sera from 51 patients with nAnB post-transfusion hepatitis, including acute and chronic cases diagnosed during a prospective study on candidates for cardiac surgery, and 167 with various forms of CLD were tested for the presence of anti-TEC and BCLA using indirect immunofluorescence on human thymus and rat forestomach sections. Both antibodies mainly occurred in nAnB, HDV and cryptogenic CLD (anti-TEC: 51%, 47% and 42%; BCLA: 29%, 38% and 31%…

Pathologymedicine.medical_specialtyHepatitis Viral Humanmedicine.drug_classFluorescent Antibody TechniqueThymus GlandChronic liver diseaseMonoclonal antibodyEpitheliumSerologyPrimary biliary cirrhosisAntigenAntibody SpecificitymedicinePrevalenceHumansProspective StudiesChildAutoantibodiesHepatitis ChronicHepatitisHepatologybiologyLiver DiseasesAutoantibodyAntibodies MonoclonalTransfusion Reactionmedicine.diseaseHepatitis CImmunologyAcute Diseasebiology.proteinKeratinsAntibody
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Functional spectrum of sinusoidal endothelial liver cells

1992

Pathologymedicine.medical_specialtyHepatologyEndotheliumPhagocytosisInflammationBiologyEndocytosisCell biologylaw.inventionEndothelial stem cellmedicine.anatomical_structureCell–cell interactionlawmedicinemedicine.symptomIntracellularFiltrationJournal of Hepatology
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The distribution of blood group antigens in rodent epithelia

1984

The pattern of distribution of antigens cross-reacting with antibodies to human blood group antigens A and B and two precursor molecules was examined by immunofluorescence in the epidermis, oral mucosa and forestomach of rats and mice. Staining for blood group antigen A was negative. In all epithelia examined, blood group antigen B was present at the surface of basal and parabasal cells, and the H antigen at the surface of spinous cells. N-acetyllactosamine was present on the cell membranes in the upper spinous and granular cell layers of epidermis and forestomach epithelium and was not expressed in the oral epithelia except for a limited area in the dorsal tongue epithelium. Thus, the expr…

Pathologymedicine.medical_specialtyHistologyCellular differentiationBiologyH antigenImmunofluorescenceEpitheliumABO Blood-Group SystemPathology and Forensic MedicineEpitopesMiceAntigenABO blood group systemmedicineAnimalsTissue Distributionmedicine.diagnostic_testAntibodies MonoclonalCell DifferentiationCell BiologyMolecular biologyEpitheliumRatsmedicine.anatomical_structureCarbohydrate SequenceAntigens Surfacebiology.proteinEpidermisAntibodyCell and Tissue Research
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Patterns of cytokeratin and vimentin expression in the human eye

1988

We studied the expression of the various cytokeratin (CK) polypeptides and vimentin in tissues of the human eye by applying immunocytochemical procedures using a panel of monoclonal antibodies as well as by performing biochemical analyses of microdissected tissues. Adult corneal epithelium was found to contain significant amounts of the cornea-specific CKs nos. 3 and 12 as well as CK no. 5, and several additional minor CK components. Among these last CKs, no. 19 was found to exhibit an irregular mosaic-like staining pattern in the peripheral zone of the corneal epithelium, while having a predominantly basal distribution in the limbal epithelium. Both the fetal corneal epithelium and the con…

Pathologymedicine.medical_specialtyHistologyVimentinEyeCorneaCytokeratinFetusmedicineHumansVimentinPigment Epithelium of EyeMolecular BiologyCorneal epitheliumRetinal pigment epitheliumbiologyCiliary BodyCell BiologyGeneral MedicineImmunohistochemistryeye diseasesEpitheliumStainingMedical Laboratory Technologymedicine.anatomical_structurebiology.proteinKeratinsImmunohistochemistrysense organsAnatomyStem cellGeneral Agricultural and Biological SciencesConjunctivaHistochemistry
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