Search results for "Morphogen"

showing 10 items of 258 documents

Regulation of Rooting Ability of Solanum tuberosum L. Explants by Gaseous Environment, In Vitro

1997

It has been reported by many investigators that morphogenesis of expiant tissue can be regulated by the composition of the nutrient medium as well as by the gaseous environment (Buddendorf-Joosten and Woltering, 1994). The aim of the present study was to investigate different effects on rooting ability of potato expiants in vitro, caused by limited gas exchange and IBA and BAP treatment.

HorticultureNutrientfungiBotanyMorphogenesisfood and beveragesComposition (visual arts)BiologySolanum tuberosumcomplex mixturesIn vitroExplant culture
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Different effectors of dimorphism in Yarrowia lipolytica

2002

Yarrowia lipolytica is an ascomycete with biotechnological potential. In common media, the fungus grows as a mixture of yeast-like and short mycelial cells. The environmental factors that affect dimorphism in the wild-type strain, W29, and its auxotrophic derivative, PO1a, were analyzed. In both strains, pH was the most important factor regulating the dimorphic transition. Mycelium formation was maximal at pH near neutrality and decreased as pH was lowered to become almost null at pH 3. Carbon and nitrogen sources, namely glucose and ammonium, were also important for mycelium formation; and their effect was antagonized by some alternative carbon and nitrogen sources. Citrate was an importan…

Hot TemperatureNitrogenAuxotrophyYarrowiaFungusBiochemistryMicrobiologyCitric Acidchemistry.chemical_compoundBotanyCyclic AMPMorphogenesisGeneticsAmmoniumMolecular BiologyMyceliumSex CharacteristicsbiologyEffectorfungiYarrowiaGeneral MedicineHydrogen-Ion Concentrationbiology.organism_classificationCarbonYeastCulture MediaBiochemistrychemistryStarvationDimorphic fungusArchives of Microbiology
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Proteomic Analyses of Human Cytomegalovirus Strain AD169 Derivatives Reveal Highly Conserved Patterns of Viral and Cellular Proteins in Infected Fibr…

2014

Human cytomegalovirus (HCMV) particle morphogenesis in infected cells is an orchestrated process that eventually results in the release of enveloped virions. Proteomic analysis has been employed to reveal the complexity in the protein composition of these extracellular particles. Only limited information is however available regarding the proteome of infected cells preceding the release of HCMV virions. We used quantitative mass spectrometry to address the pattern of viral and cellular proteins in cells, infected with derivatives of the AD169 laboratory strain. Our analyses revealed a remarkable conservation in the patterns of viral and of abundant cellular proteins in cells, infected for 2…

Human cytomegalovirusTime FactorsProteomeviruseslcsh:QR1-502MorphogenesisCytomegalovirusBiologyVirus ReplicationProteomicslcsh:MicrobiologyMass SpectrometryArticleCell LineproteomicsVirologyExtracellularmedicineHumanshuman cytomegalovirus; proteomics; mass spectrometry; virions; expression patternProteinsViral tegumentFibroblastsmedicine.diseaseVirologyCell biologyInfectious DiseasesViral replicationhuman cytomegalovirusCell cultureexpression patternHost-Pathogen InteractionsProteomevirionsViruses
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Perlecan Maintains microvessel integrity in vivo and modulates their formation in vitro

2012

Perlecan is a heparan sulfate proteoglycan assembled into the vascular basement membranes (BMs) during vasculogenesis. In the present study we have investigated vessel formation in mice, teratomas and embryoid bodies (EBs) in the absence of perlecan. We found that perlecan was dispensable for blood vessel formation and maturation until embryonic day (E) 12.5. At later stages of development 40% of mutant embryos showed dilated microvessels in brain and skin, which ruptured and led to severe bleedings. Surprisingly, teratomas derived from perlecan-null ES cells showed efficient contribution of perlecan-deficient endothelial cells to an apparently normal tumor vasculature. However, in perlecan…

IntegrinsAnatomy and PhysiologyGlycobiologylcsh:MedicineCardiovascularurologic and male genital diseasesCardiovascular SystemBiochemistryBiotecnologiaBasement MembraneMicePregnancyMolecular Cell BiologyMorphogenesisHistochemistrylcsh:ScienceSkinMice KnockoutPeripheral Vascular DiseasesExtracellular Matrix ProteinsNeovascularization PathologicTeratomaProteïnes de membranaBrainCell DifferentiationExtracellular MatrixConnective TissueCytochemistryMedicineFemaleFibroblast Growth Factor 2ProteoglycansResearch Articleendocrine systemMice 129 StrainCèl·lulesNeovascularization PhysiologicCell MigrationGrowth FactorsCell AdhesionAnimalsBirth DefectsBiologyExtracellular Matrix AdhesionsEmbryoid BodiesEmbryonic Stem Cellslcsh:RfungiProteinsExtracellular Matrix CompositionMice Inbred C57BLcarbohydrates (lipids)Cancer and OncologyMicrovesselsCardiovascular Anatomylcsh:QHeparan Sulfate ProteoglycansDevelopmental Biology
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The Dorsocross T-box transcription factors promote tissue morphogenesis in the Drosophila wing imaginal disc.

2012

The Drosophila wing imaginal disc is subdivided into notum, hinge and blade territories during the third larval instar by formation of several deep apical folds. The molecular mechanisms of these subdivisions and the subsequent initiation of morphogenic processes during metamorphosis are poorly understood. Here, we demonstrate that the Dorsocross (Doc) T-box genes promote the progression of epithelial folds that not only separate the hinge and blade regions of the wing disc but also contribute to metamorphic development by changing cell shapes and bending the wing disc. We found that Doc expression was restricted by two inhibitors, Vestigial and Homothorax, leading to two narrow Doc stripes…

Integrinsanimal structuresTime FactorsMorphogenesisBiologyMicrotubulesExtracellular matrixMicrotubuleMorphogenesisAnimalsDrosophila ProteinsWings AnimalTransgenesMolecular BiologyAllelesWingAnatomyNotumCell biologyExtracellular MatrixImaginal discT-boxDrosophila melanogasterMutationMatrix Metalloproteinase 2RNA InterferenceDrosophila ProteinDevelopmental BiologyProtein BindingSignal TransductionTranscription FactorsDevelopment (Cambridge, England)
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Cultivation of primmorphs from the marine sponge Suberites domuncula: morphogenetic potential of silicon and iron.

2002

Abstract Marine demosponges (phylum Porifera) are rich sources for potent bioactive compounds. With the establishment of the primmorph system from sponges, especially from Suberites domuncula , the technology to cultivate sponge cells in vitro improved considerably. This progress was possible after the elucidation that sponges are provided with characteristic metazoan cell adhesion receptors and extracellular matrix molecules which allow their cells a positioning in a complex organization pattern. This review summarizes recent data on the cultivation of sponges in aquaria and—with main emphasis—of primmorphs in vitro. It is outlined that silicon and Fe(+++) contribute substantially to the f…

IronCell Culture TechniquesBioengineeringApplied Microbiology and BiotechnologyBioreactorsSpecies SpecificityFood supplyMorphogenesisAnimalsGrowth SubstancesEcosystemCell AggregationPhylum PoriferabiologyEcologySilicatesGeneral MedicineExtracellular matrix moleculesbiology.organism_classificationCanal systemCell biologyPoriferaSuberites domunculaSpongeGene Expression RegulationFerritinsCell DivisionBiotechnologySuberitesJournal of biotechnology
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α-parvin is required for epidermal morphogenesis, hair follicle development and basal keratinocyte polarity

2020

Epidermal morphogenesis and hair follicle (HF) development depend on the ability of keratinocytes to adhere to the basement membrane (BM) and migrate along the extracellular matrix. Integrins are cell-matrix receptors that control keratinocyte adhesion and migration, and are recognized as major regulators of epidermal homeostasis. How integrins regulate the behavior of keratinocytes during epidermal morphogenesis remains insufficiently understood. Here, we show that alpha-parvin (alpha-pv), a focal adhesion protein that couples integrins to actin cytoskeleton, is indispensable for epidermal morphogenesis and HF development. Inactivation of the murine alpha-pv gene in basal keratinocytes res…

KeratinocytesIntegrinsEpitheliumBasement MembraneExtracellular matrixMiceAnimal CellsCell MovementMedicine and Health SciencesMorphogenesisCells CulturedSkinMultidisciplinarybiologyintegumentary systemChemistryQMicrofilament ProteinsMorfogènesiRCell DifferentiationDermisCell biologyExtracellular Matrixmedicine.anatomical_structureMedicineCellular TypesAnatomyCellular Structures and OrganellesIntegumentary SystemKeratinocyteHair FollicleResearch ArticleCèl·lulesCellsScienceIntegrinMorphogenesisMice TransgenicActin cytoskeleton organizationFocal adhesionHair FolliclesmedicineCell AdhesionAnimalsFocal AdhesionsBiology and Life SciencesEpithelial CellsCell BiologyActin cytoskeletonActinsBiological Tissuebiology.proteinEpidermisEpidermal thickeningDevelopmental BiologyHairPLoS ONE
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The Influence of Adalimumab and Cyclosporine A on the Expression Profile of the Genes Related to TGFβ Signaling Pathways in Keratinocyte Cells Treate…

2020

Background. In the treatment of moderate to severe psoriasis, cyclosporine A (CsA) conventional therapy is used and biological, anti-cytokine treatment using, for example, anti-TNF drug—adalimumab. Aim. This study aimed at investigating the effect of CsA and adalimumab on the profile of mRNAs and protein expression associated with transforming growth factor β (TGFβ) pathways in human keratinocyte (HaCaT) culture previously exposed to lipopolysaccharide (LPS). Materials and Methods. HaCaT culture was exposed to 1 ng/ml LPS for 8 hours+8 μg/ml adalimumab for 2, 8, and 24 hours or 1 ng/ml LPS for 8 hours+100 ng/ml CsA for 2, 8, and 24 hours and compared to the control culture. Sulphorodamine B…

KeratinocytesLipopolysaccharidesArticle SubjectLipopolysaccharideMicroarrayImmunologyPharmacologychemistry.chemical_compoundTransforming Growth Factor betaCell Line TumorCyclosporin aPathologymedicineRB1-214Humansskin and connective tissue diseasesCytotoxicityRhodaminesAdalimumabCell BiologyBone morphogenetic protein 6HaCaTmedicine.anatomical_structurechemistryCyclosporineKeratinocyteResearch ArticleSignal TransductionTransforming growth factorMediators of Inflammation
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Processing of procollagen III by meprins: new players in extracellular matrix assembly?

2010

Meprins α and β, a subgroup of zinc metalloproteinases belonging to the astacin family, are known to cleave components of the extracellular matrix, either during physiological remodeling or in pathological situations. In this study we present a new role for meprins in matrix assembly, namely the proteolytic processing of procollagens. Both meprins α and β release the N- and C-propeptides from procollagen III, with such processing events being critical steps in collagen fibril formation. In addition, both meprins cleave procollagen III at exactly the same site as the procollagen C-proteinases, including bone morphogenetic protein-1 (BMP-1) and other members of the tolloid proteinase family. …

Keratinocytesmacromolecular substancesDermatologyMatrix metalloproteinaseCleavage (embryo)BiochemistryBone Morphogenetic Protein 1Substrate SpecificityExtracellular matrix03 medical and health sciencesDermismedicineHumansEnhancerMolecular BiologyCells Cultured030304 developmental biology0303 health sciencesExtracellular Matrix Proteinsintegumentary systemChemistryExtracellular matrix assembly030302 biochemistry & molecular biologyMetalloendopeptidasesCell BiologyDermisFibroblastsFibrosisProcollagen peptidasemedicine.anatomical_structureCollagen Type IIIHEK293 CellsBiochemistryKeloidAstacinThe Journal of investigative dermatology
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MEK1 Required for Invasive Growth of mIMCD3 renal Cells in a 3D Collagen Matrix

2004

Branching morphogenesis is an essential process during kidney development: This process controls epithelialization of the metanephric mesenchyme during the induction of branching structures and in this way determines the number of nephrons. Various grow factors, such HGF, have been implicated in branching morphogenesis in renal cells, including mIMCD3 ( murine inner medullary collecting duct) and MDCK cells. Growth factors which induce branching morphogenesis in renal cells also activate the MEK1/ERK pathway. The authors analyzed the potential role that this pathway might play in branching morphogenesis. The authors show that PD98059, a specific inhibitor of MEK1,inhibits branching of mIMCD…

Kidney development branching morphogenesis in renal cells MEK1/ERK pathway
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