Search results for "Fibronectins"

showing 10 items of 89 documents

Perlecan-Induced Suppression of Smooth Muscle Cell Proliferation Is Mediated Through Increased Activity of the Tumor Suppressor PTEN

2004

We were interested in the elucidation of the interaction between the heparan sulfate proteoglycan, perlecan, and PTEN in the regulation of vascular smooth muscle cell (SMC) growth. We verified serum-stimulated DNA synthesis, and Akt and FAK phosphorylation were significantly reduced in SMCs overexpressing wild-type PTEN. Our previous studies showed perlecan is a potent inhibitor of serum-stimulated SMC growth. We report in the present study, compared with SMCs plated on fibronectin, serum-stimulated SMCs plated on perlecan exhibited increased PTEN activity, decreased FAK and Akt activities, and high levels of p27, consistent with SMC growth arrest. Adenoviral-mediated overexpression of cons…

MaleVascular smooth musclePhysiology:CIENCIAS MÉDICAS ::Farmacodinámica [UNESCO]Aorta ThoracicBasement MembraneCulture Media Serum-FreeMuscle Smooth VascularRats Sprague-DawleyMicePhosphorylationCells CulturedGlycosaminoglycansbiologyProtein-Tyrosine KinasesCell cycle:CIENCIAS MÉDICAS [UNESCO]musculoskeletal systemUNESCO::CIENCIAS MÉDICAS ::FarmacodinámicaUNESCO::CIENCIAS MÉDICAScardiovascular systemPhosphorylationSmooth muscle cell proliferationCardiology and Cardiovascular MedicineCell DivisionDNA ReplicationBasement membraneRecombinant Fusion ProteinsPerlecanProtein Serine-Threonine KinasesVascular injurySmooth muscle cell proliferation ; Restenosis ; Vascular injury ; Vascular development ; Basement membraneCatheterizationProto-Oncogene ProteinsAnimalsPTENProtein kinase BRestenosisCell growthVascular developmentOligonucleotides AntisenseFibronectinsRatsFibronectinFocal Adhesion Kinase 1Focal Adhesion Protein-Tyrosine Kinasesbiology.proteinCancer researchHeparitin SulfateCarotid Artery InjuriesProtein Processing Post-TranslationalProto-Oncogene Proteins c-aktHeparan Sulfate ProteoglycansCirculation Research
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Coagulation factors and proteinase inhibitors in the plasma of children with acute lymphoblastic leukoses. Behaviour before and during treatment acco…

1984

The thrombocyte count, the factor XIII (F XIII) activity, the concentration of fibrinogen (F I), prothrombin (F II), fibronectin (CIG), albumin and the proteinase inhibitors antithrombin III (AT III), alpha 2-macroglobulin (A2M), alpha 1-antitrypsin (A1A) and Cl-esterase inactivator (Cl-INA) were determined in ten children with acute lymphoblastic leukaemia (ALL). Changes due to the disease and to therapy were observed. Before the start of treatment the patients had thrombocytopenia secondary to the disease, and the proteinase inhibitors--especially Cl-INA and A1A--were raised. During the induction phase the thrombocyte count rose but there was also a marked increase in the concentration of…

Malemedicine.medical_specialtyAdolescentAntithrombin IIIAlpha (ethology)Complement C1 Inactivator ProteinsFibrinogenMaintenance therapyInternal medicineDrug DiscoveryAntineoplastic Combined Chemotherapy ProtocolsmedicineHumansProtease Inhibitorsalpha-MacroglobulinsChildGenetics (clinical)Factor XIIIbusiness.industryAntithrombinAlbuminFibrinogenGeneral MedicineFactor XIIIMolecular medicineBlood Coagulation FactorsFibronectinsLeukemia LymphoidEndocrinologyCoagulationChild Preschoolalpha 1-AntitrypsinImmunologyMolecular MedicineFemaleProthrombinbusinessmedicine.drugKlinische Wochenschrift
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The disruption of myofibre structures in rat skeletal muscle after forced lengthening contractions.

1998

Specific antibodies against structural proteins (actin, desmin, dystrophin, fibronectin) of muscle fibres were used to study the effect of forced lengthening contractions on muscle microarchitecture. Tibialis anterior (TA) muscle of male Wistar rats were subjected to 240 forced lengthening contractions. At consecutive time points (0, and 6 h, 2, 4, and 7 days) after stimulation, the TA muscle was excised for biochemical and histological assays. Beta-Glucuronidase activity, a quantitative indicator of muscle damage, showed increased values 2-7 days after the lengthening, peaking on day 4 (11.7-fold increase). A typical course of histopathological changes (myofibre swelling, necrosis and rege…

Malemedicine.medical_specialtyNecrosisPhysiologyClinical BiochemistryDesminDystrophinMyofibrilsPhysiology (medical)Internal medicinemedicineMyocyteAnimalsRats WistarIntermediate filamentMuscle SkeletalActinGlucuronidasebiologyChemistrySkeletal muscleImmunohistochemistryActinsElectric StimulationFibronectinsRatsEnzyme ActivationEndocrinologymedicine.anatomical_structurebiology.proteinDesminStress Mechanicalmedicine.symptomMyofibrilDystrophinMuscle ContractionPflugers Archiv : European journal of physiology
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Fibronectin-mediated endothelialisation of chitosan porous matrices.

2009

Chitosan (Ch) porous matrices were investigated regarding their ability to be colonized by human microvascular endothelial cells (HPMEC-ST1.6R cell line) and macrovascular endothelial cells namely HUVECs. Specifically we assessed if previous incubation of Ch in a fibronectin (FN) solution was effective in promoting endothelial cell (EC) adhesion to Ch matrices with different degrees of acetylation (DAs). Upon FN physiadsorption, marked differences were found between the two DAs investigated, namely DA 4% and 15%. While cell adhesion was impaired on Ch with DA 15%, ECs were able to not only adhere to Ch with DA 4%, but also to spread and colonize the scaffolds, with retention of the EC pheno…

Materials scienceAngiogenesisCell SurvivalBiophysicsNeovascularization PhysiologicBioengineeringBiocompatible MaterialsCell LineBiomaterialsMaterials TestingHumansCell adhesionCell ProliferationCell SizeChitosanbiologyCell growthEndothelial CellsAdhesionFibronectinsEndothelial stem cellFibronectinBiochemistryMechanics of MaterialsCell cultureCeramics and Compositesbiology.proteinBiophysicsPorosityProtein adsorptionBiomaterials
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The effect of extracellular matrix proteins on the cellular response of HUVECS and HOBS after covalent immobilization onto titanium

2014

Biomimetic surface modifications are regarded as promising approach to stimulate cellular behavior at the interface of implant materials. Aim of the study was an evaluation of the cellular response of human umbilical cord cells (HUVECS) and human osteoblasts (HOBS) on titanium covalently coated with the extracellular matrix (ECM) proteins fibrinogen, collagen, laminin, and osteopontin. For the surface modification, titanium discs were first amino-functionalized by plasma polymerization of allylamine. The ECM protein conjugation was performed using the linker molecule α, ω-bis-N-hydroxysuccinimide polyethylene glycol (Di-NHS linker). For surface characterization, infrared spectroscopy and fl…

Materials sciencePlasma GasesSpectrophotometry InfraredBiomedical EngineeringAllylaminePolymerizationAllylamineBiomaterialsExtracellular matrixchemistry.chemical_compoundLamininCell AdhesionHuman Umbilical Vein Endothelial CellsHumansSurface plasmon resonanceCell adhesionFluorescein isothiocyanateTitaniumExtracellular Matrix ProteinsOsteoblastsbiologyMetals and AlloysSurface Plasmon ResonanceFibronectinsFibronectinKineticsImmobilized ProteinschemistryBiochemistryCeramics and Compositesbiology.proteinBiophysicsSurface modificationOsteopontinCollagenLamininJournal of Biomedical Materials Research Part A
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Endothelialization of chitosan porous conduits via immobilization of a recombinant fibronectin fragment (rhFNIII7–10)

2013

Abstract The present study aimed to develop a pre-endothelialized chitosan (CH) porous hollowed scaffold for application in spinal cord regenerative therapies. CH conduits with different degrees of acetylation (DA; 4% and 15%) were prepared, characterized (microstructure, porosity and water uptake) and functionalized with a recombinant fragment of human fibronectin (rhFNIII 7–10 ). Immobilized rhFNIII 7–10 was characterized in terms of amount ( 125 I-radiolabelling), exposure of cell-binding domains (immunofluorescence) and ability to mediate endothelial cell (EC) adhesion and cytoskeletal rearrangement. Functionalized conduits revealed a linear increase in immobilized rhFNIII 7–10 with rhF…

Materials scienceProtein radiolabellingBiomedical EngineeringNeovascularization PhysiologicSpinal cord injuryBiochemistrylaw.inventionBiomaterialsChitosanchemistry.chemical_compoundTissue engineeringlawSpectroscopy Fourier Transform InfraredPolymer chemistryHumansSurface graftingCytoskeletonMolecular BiologyFluorescent DyesChitosanTissue ScaffoldsbiologyThree-dimensional scaffoldsEndothelial CellsDNAGeneral MedicineAdhesionGraftingRecombinant ProteinsFibronectinsProtein Structure TertiaryFibronectinEndothelial stem cellImmobilized ProteinschemistryProtein conformationMicroscopy Electron Scanningbiology.proteinRecombinant DNABiophysicsAdsorptionPorosityBiotechnology
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Localization and mRNA steady-state level of cellular fibronectin in rat liver undergoing a CCl4-induced acute damage or fibrosis.

1993

Abstract In an attempt to investigate cellular fibronectin synthesis and deposition during acute liver damage and fibrogenesis, we used the presence of the additional type III-related ED-A domain of cellular fibronectin as a characteristic for distinguishing it from the plasma form. Using site-specific antibodies, we localized cellular fibronectin deposition in the necrotic pericentral areas of acutely damaged liver tissue after a single CCl 4 -gavage, whereas in control liver only trace amounts of cellular fibronectin were detectable along the sinusoids. Upon several CCl 4 -administrations leading to liver fibrosis, cellular fibronectin deposits were accumulated in the fibrotic septa. Nort…

Messenger RNAbiologyMesenchymal stem cellIn situ hybridizationmedicine.diseaseLiver Cirrhosis ExperimentalMolecular biologyFibronectinsRatsFibronectinLiverFibrosisImmunologyGene expressionbiology.proteinmedicineMolecular MedicineImmunohistochemistryAnimalsFemaleNorthern blotRNA MessengerRats WistarMolecular BiologyCarbon TetrachlorideBiochimica et biophysica acta
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Expression of Staphylococcus saprophyticus surface properties is modulated by composition of the atmosphere.

1995

Expression of two major surface proteins of Staphylococcus saprophyticus, the haemagglutinin and the Staphylococcus saprophyticus surface-associated protein (Ssp), requires carefully defined culture conditions. The Ssp is produced when bacteria are grown on agar, whereas expression of the haemagglutinin requires growth in broth. We sought to identify the environmental signals that are responsible for this modulation. Varying the pH, the osmolarity of the growth medium or the temperature did not influence expression of the proteins. In contrast, growth in an anaerobic atmosphere increased haemagglutination titres and fibronectin binding (both mediated by the haemagglutinin) but suppressed pr…

Microbiology (medical)food.ingredientStaphylococcusImmunologyBiologyMicrobiologychemistry.chemical_compoundfoodBacterial ProteinsImmunology and AllergyAgarAdhesins Bacterialchemistry.chemical_classificationGrowth mediumStaphylococcus saprophyticusOsmotic concentrationGeneral MedicineHemagglutininbiology.organism_classificationFibronectinsMolecular WeightHemagglutininsFibronectin bindingchemistryBiochemistryGlycoproteinCarrier ProteinsBacteriaBacterial Outer Membrane ProteinsMedical microbiology and immunology
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Unexpected multivalent display of proteins by temperature triggered self-assembly of elastin-like polypeptide block copolymers

2012

We report herein the unexpected temperature triggered self-assembly of proteins fused to thermally responsive elastin-like polypeptides (ELPs) into spherical micelles. A set of six ELP block copolymers (ELP(BC)) differing in hydrophilic and hydrophobic block lengths were genetically fused to two single domain proteins, thioredoxin (Trx) and a fibronectin type III domain (Fn3) that binds the α(v)β(3) integrin. The self-assembly of these protein-ELP(BC) fusions as a function of temperature was investigated by UV spectroscopy, light scattering, and cryo-TEM. Self-assembly of the ELP(BC) was unexpectedly retained upon fusion to the two proteins, resulting in the formation of spherical micelles …

Models MolecularHydrodynamic radiusPolymers and PlasticsIntegrinBioengineeringFibronectin type III domainMicelleArticleBiomaterialsThioredoxinsMaterials ChemistryCopolymerTumor Cells CulturedHumansParticle SizeMicellesbiologyChemistryTemperatureFibronectinsElastinFibronectinsBiochemistryBiophysicsbiology.proteinSelf-assemblyThioredoxinK562 CellsPeptidesHydrophobic and Hydrophilic Interactions
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Receptor protein-tyrosine phosphatases: origin of domains (catalytic domain, Ig-related domain, fibronectin type III module) based on the sequence of…

2001

Abstract Reversible tyrosine phosphorylation of proteins is one of the major regulatory physiological events in response to cell-cell- and cell-matrix contact in Metazoa. Previously it was documented that the tyrosine phosphorylating enzymes, the tyrosine kinases (TKs), are autapomorphic characters of Metazoa, including sponges. In this paper the tyrosine dephosphorylating enzymes, the protein-tyrosine phosphatases (PTPs), are studied which can be grouped into two subfamilies, the soluble PTPs and the receptor PTPs (RPTPs). PTPs are characterized by one PTPase domain which interestingly comprises sequence similarity to yeast PTPs. In contrast to the PTPs, the RPTPs – which have been found o…

Molecular Sequence DataImmunoglobulinsBiologyPolymerase Chain ReactionEvolution Molecularchemistry.chemical_compoundCatalytic DomainGene duplicationGeneticsAnimalsAmino Acid SequenceTyrosineCloning MolecularPhylogenychemistry.chemical_classificationPhylogenetic treeSequence Homology Amino AcidTyrosine phosphorylationGeneral MedicineProtein-Tyrosine KinasesAmino acidFibronectinsPoriferaProtein Structure TertiaryOpen reading framechemistryBiochemistryPhosphorylationProtein Tyrosine PhosphatasesTyrosine kinaseSequence AnalysisGene
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