Search results for "Dispase"

showing 4 items of 4 documents

Influence of different types of pulp treatment during isolation in the obtention of human dental pulp stem cells

2016

Background: Different methods have been used in order to isolate dental pulp stem cells. The aim of this study was to study the effect of different types of pulp treatment during isolation, under 3% O 2 conditions, in the time needed and the efficacy for obtaining dental pulp stem cells. Material and Methods: One hundred and twenty dental pulps were used to isolate dental pulp stem cells treating the pulp tissue during isolation using 9 different methods, using digestive, disgregation, or mechanical agents, or combining them. The cells were positive for CD133, Oct4, Nestin, Stro-1, CD34 markers, and negative for the hematopoietic cell marker CD-45, thus confirming the presence of mesenchyma…

0301 basic medicineCD34DentistryOdontologíaAndrology03 medical and health sciences0302 clinical medicinestomatognathic systemDental pulp stem cellsDispasemedicineHumansGeneral DentistryCells CulturedDental PulpPulp treatmentbusiness.industryResearchMesenchymal stem cellEpithelial CellsMesenchymal Stem Cells030206 dentistryNestin:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludstomatognathic diseases030104 developmental biologyOtorhinolaryngologyUNESCO::CIENCIAS MÉDICASCollagenasePulp (tooth)SurgeryOral SurgerybusinessStem Cell Transplantationmedicine.drug
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Improved yield and functionality of parathyroid cells separated by using collagenase-digestion with cold pre-incubation.

2001

Preparation of cells from solid organs often induces a functional impairment due to the proteolytic cell damage by the applied digestive enzyme like collagenase, trypsin or dispase. To preserve the tissue and to enhance the yield of cells, Laue et al. reported an islet cell isolation with pre-incubation at 4 C permitting the enzyme to diffuse into the tissue and explicite activity equally throughout the whole particle. The aim of this study was to investigate whether this procedure can be applied to parathyroid glands. Therefore porcine parathyroid glands were dissected into 1 mm3 pieces. Subsequently one group of these pieces was incubated 22 h at 4 C in 2 mg/ml collagenase before activati…

Cell SurvivalSwineEndocrinology Diabetes and MetabolismParathyroid hormoneCell CountCell SeparationParathyroid GlandsEndocrinologyDispasemedicineAnimalsCollagenasesbiologyParathyroid chief cellTrypsinMolecular biologyCold TemperatureBiochemistryCell cultureParathyroid HormoneDigestive enzymebiology.proteinCollagenaseInterstitial collagenaseCalciummedicine.drugJournal of endocrinological investigation
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Hypoxia-induced reduction of sVEGFR-2 levels in human colonic microvascular endothelial cells in vitro: Comparative study with HUVEC.

2008

The functionality of large-vessel endothelial cells, such as human umbilical vein endothelial cells (HUVEC), may differ significantly from that in the microvasculature. We established a method for the isolation of human colonic microvascular endothelial cells (HCMEC). Since colonic diseases are often accompanied by hypoxia we examined its effects on HCMEC of five individuals in comparison with HUVEC, with respect to the secretion of the soluble form of the two important vascular endothelial growth factor (VEGF) receptors, VEGFR-1 and 2. After dissociation by dispase/collagenase of mucosal and submucosal tissue obtained from normal adult colon, HCMEC were isolated using CD31-coated magnetic …

ColonBiologyUmbilical veinAndrologychemistry.chemical_compoundDispaseGeneticsmedicineHumansReceptorCells CulturedVascular Endothelial Growth Factor Receptor-1Endothelial CellsKinase insert domain receptorGeneral MedicineHypoxia (medical)Vascular Endothelial Growth Factor Receptor-2In vitroCell HypoxiaCell biologyVascular endothelial growth factorchemistryGene Expression RegulationApoptosiscardiovascular systemmedicine.symptomInternational journal of molecular medicine
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Isolation and subsequent analysis of murine lamina propria mononuclear cells from colonic tissue

2007

Studies on colonic cells in the lamina propria (LP) of mice are important for understanding the cellular and immune responses in the gut, especially in inflammatory bowel diseases (such as morbus crohn and colitis ulcerosa). This protocol details a method to isolate LP cells and characterize freshly isolated cells by quality control experiments to obtain cells that can be used for further investigations. After different steps of digestion of the tissue using collagenase, DNase and dispase, the resulting cells are purified using Percoll gradient. The success of the isolation can be analyzed by cell viability test (Trypan Blue exclusion test) and by flow cytometric analysis to assess apoptosi…

Lamina propriabiologyColonCell Culture Techniquesfood and beveragesCell SeparationTransfectionGeneral Biochemistry Genetics and Molecular BiologyCell biologyTissue Culture TechniquesMicemedicine.anatomical_structureImmune systemCell cultureDispasemedicinebiology.proteinAnimalsLymphocytesViability assayIntestinal MucosaAntibodyPercollCryoultramicrotomyNature Protocols
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