Search results for "Extracellular"

showing 10 items of 1220 documents

Evaluation of a novel biomarker of type XXVIII collagen formation, PRO-C28, in samples from cancer and heart failure with preserved ejection fraction…

2020

Increased turnover of extracellular matrix proteins is seen in many different diseases and is an underlying and driving feature of pathogenesis. An increased ratio of formation over degradation of extracellular matrix proteins, such as collagens, leads to accumulation of proteins in the tissues, ultimately impairing organ function. Understanding how this balance is regulated is key to providing deeper insight into high extracellular matrix turnover diseases. Type XXVIII collagen is a novel collagen with limited information available in relation to expression, tissue prevalence and clinical implication. We generated a novel, technically robust ELISA to measure a C-terminal fragment of type X…

Heart Failuremedicine.medical_specialtyChemistryClinical BiochemistryPharmaceutical ScienceCancerStroke Volumemedicine.diseasePeptide FragmentsAnalytical ChemistryPathogenesisExtracellular matrixCollagen formationEndocrinologyInternal medicineNeoplasmsDrug DiscoverymedicineBiomarker (medicine)HumansIn patientLung cancerHeart failure with preserved ejection fractionSpectroscopyBiomarkersJournal of pharmaceutical and biomedical analysis
researchProduct

Heat inactivation of fetal bovine serum increases protein contamination of extracellular vesicles

2022

Introduction: Extracellular vesicles (EVs) released in cell cultures are influenced by the cell culture conditions, such as the use of fetal bovine serum (FBS). FBS contains EVs and it is usually depleted of EVs by ultracentrifugation (UC) and/or heat inactivated (HI). Several studies have evaluated the effect of different UC protocols for FBS by evaluating both cells and EVs. However, less is known about the effect of HI on the cells and the released EVs. The aim of this study was therefore to evaluate the effect of HI on EV purity. Methods: To determine the effect of heat inactivation, three different protocols were applied based on different combinations of: 1) UC at 118,000 × g for 18h …

Heat inactivationFetal bovine serumExtracellular vesicles
researchProduct

Exosomal Hsp60 in human colon cancer

2014

Heat shock proteincolon cancerExtracellular vescicle
researchProduct

EGF and HGF levels are increased during active HBV infection and enhance survival signaling through extracellular matrix interactions in primary huma…

2008

The hepatitis B virus (HBV) is a major causative agent of chronic liver disease and subsequent liver cirrhosis worldwide. The reduced sensitivity of virus-infected liver cells to apoptosis may play a role in the failure to remove virus-infected cells and eventually promote viral chronicity. The purpose of our study was to investigate whether survival factors induced during compensatory liver regeneration may protect hepatocytes against apoptosis. We evaluated the serum levels of hepatocyte growth factor (HGF) and epidermal growth factor (EGF) in HBV-infected patients and found significant increases in HGF and EGF in patients with active virus infection. In primary human hepatocytes we show …

Hepatitis B virusCancer ResearchProgrammed cell deathApoptosisBiologyMembrane PotentialsFocal adhesionWortmanninchemistry.chemical_compoundEpidermal growth factorCell AdhesionmedicineHumansfas ReceptorCells CulturedEpidermal Growth FactorHepatocyte Growth FactorHepatitis BLiver regenerationExtracellular Matrixmedicine.anatomical_structureOncologychemistryImmune SystemHepatocyteImmunologyHepatocytesCancer researchHepatocyte growth factorSignal transductionSignal TransductionT-Lymphocytes Cytotoxicmedicine.drugInternational Journal of Cancer
researchProduct

The new murine hepatic 3A cell line responds to stress stimuli by activating an efficient Unfolded Protein Response (UPR)

2012

In the present study we have investigated the properties of a novel cell line (3A cells) obtained from the liver of 14.5. days post coitum (dpc) wild-type mouse embryo. 3A cells morphology was characterized by fluorescent localization of F-actin and β-catenin. The expression of specific genes and proteins essential to liver function in these cells was comparable or even more efficient then in the differentiated hepatocytic cell line MMH-D6. 3A cells also showed the capability to excrete molecules in extracellular spaces resembling functional bile canaliculi, glycogen storage activity and the ability to control retinol-binding protein 4 secretion in response to retinol deprivation. Their re…

Hepatocytes; ER stress; RBP4BiologyToxicologyCellular modelCell LineMicechemistry.chemical_compoundStress PhysiologicalExtracellularAnimalsHepatocyteSecretionActinbeta CateninAnimalReverse Transcriptase Polymerase Chain ReactionRBP4Gene Expression ProfilingTunicamycinDays post coitumCellular model; ER stress; Hepatocytes; RBP4; Actins; Animals; Cell Line; Fluorescein; Gene Expression Profiling; Glycogen; Liver; Retinol-Binding Proteins Plasma; Reverse Transcriptase Polymerase Chain Reaction; Stress Physiological; Tunicamycin; Unfolded Protein Response; beta Catenin; Mice; ToxicologyGeneral MedicineTunicamycinMolecular biologyActinsLiverchemistryCell cultureUnfolded Protein ResponseUnfolded protein responseER streFluoresceinLiver functionCellular modelRetinol-Binding Proteins PlasmaGlycogenToxicology in Vitro
researchProduct

Macrophage MerTK promotes profibrogenic cross-talk with hepatic stellate cells via soluble mediators

2022

Background & aims: Activation of Kupffer cells and recruitment of monocytes are key events in fibrogenesis. These cells release soluble mediators which induce the activation of hepatic stellate cells (HSCs), the main fibrogenic cell type within the liver. Mer tyrosine kinase (MerTK) signaling regulates multiple processes in macrophages and has been implicated in the pathogenesis of non-alcoholic steatohepatitis-related fibrosis. In this study, we explored if MerTK activation in macrophages influences the profibrogenic phenotype of HSCs. Methods: Macrophages were derived from THP-1 cells or differentiated from peripheral blood monocytes towards MerTK+/CD206+/CD163+/CD209- macrophages. Th…

HepatologyCM conditioned medium ECM extracellular matrix Gas-6 Gas-6 growth arrest-specific gene 6 HSC(s) hepatic stellate cells KC(s) Kupffer cell(s) M-CSF macrophage colony-stimulating factor M2c-like macrophages MerTK Myeloid-epithelial-reproductive tyrosine kinase NAFLD non-alcoholic fatty liver disease NASH NASH non-alcoholic steatohepatitis PMA phorbol 12-myristate 13-acetate TGFβ1 transforming growth factor-β1 THP-1 TIMP1 tissue inhibitor of metalloproteinase 1 VEGF-A vascular endothelial growth factor-A liver fibrosis siRNA small-interfering RNAGas-6; liver fibrosis; M2c-like macrophages; NASH; THP-1GastroenterologyInternal MedicineImmunology and AllergyJHEP Reports
researchProduct

Exploration of extracellular vesicles from Ascaris suum provides evidence of parasite–host cross talk

2019

The prevalent porcine helminth, Ascaris suum, compromises pig health and reduces farm productivity worldwide. The closely related human parasite, A. lumbricoides, infects more than 800 million people representing a disease burden of 1.31 million disability-adjusted life years. The infections are often chronic in nature, and the parasites have a profound ability to modulate their hosts' immune responses. This study provides the first in-depth characterisation of extracellular vesicles (EVs) from different developmental stages and body parts of A. suum and proposes the role of these vesicles in the host-parasite interplay. The release of EVs from the third- (L3) and fourth-stage (L4) larvae a…

Histology030231 tropical medicineascaris suumProteomicsMicrobiology03 medical and health sciences0302 clinical medicineImmune systemproteomicsAntigenImmunityhost–parasite interactionsParasite hostinglcsh:QH573-671Ascaris suumAscaris suum030304 developmental biologymiRNA0303 health sciencesbiologylcsh:CytologyCell Biologybiology.organism_classificationimmunityMicrovesicleshost-parasite interactionsHuman parasiteextracellular vesiclesmirna
researchProduct

Distribution patterns of neoglycoprotein-binding sites (endogenous lectins) and lectin-reactive glycoconjugates during cartilage and bone formation i…

1995

The distribution of endogenous lectins, visualized by labelled neoglycoproteins, and of defined oligosaccharide structures, reactive with plant lectins, during fetal development of the fingers was analyzed in sections of human 3- to 8-month-old fetal specimens. Chondrogenesis as well as ossification were correlated with characteristic modulations in the expression of both glycoligand-binding molecules and characteristic carbohydrate structures. Occurrence of xylose-specific receptors was judged to be an early sign of cartilage development. Similarly, α-mannosyl residues that had been attached to labelled carrier proteins were strongly bound by the extracellular matrix already during early s…

HistologyCartilage metabolismBone tissueFingersExtracellular matrixPregnancyLectinsmedicineHumansGlycoproteinsBinding SitesBone DevelopmentbiologyHistocytochemistryChemistryOssificationOsteoidCartilageLectinChondrogenesisCartilagemedicine.anatomical_structureBiochemistrybiology.proteinFemaleAnatomymedicine.symptomGlycoconjugates
researchProduct

Elektronenmikroskopische Studien �ber eine extrazellul�r auftretende Substanz in der Muskulatur des Insekts Oncopeltus fasciatus Dallas

1973

Im Stroma von Aorta und Retrocerebralkomplex sowie von verschiedenen Muskeln (Oberschenkel-, Mitteldarm-, Speicheldrusen-, Samenleiter- und Eileitermuskeln), jedoch nicht im Stroma der Flugmuskulatur und des Herzschlauches, kommt eine fibrillar strukturierte Substanz (X-Substanz) von auserordentlich hoher Elektronendichte vor.

HistologyChemistryExtracellularUltrastructureCell BiologyAnatomyElectron microscopicMolecular biologyPathology and Forensic MedicineZeitschrift f�r Zellforschung und Mikroskopische Anatomie
researchProduct

Localization of Ca(2+)-stores and tissue compartments with a Ca(2+)-binding capacity in the organ of Corti of the guinea-pig by electron energy-loss …

1992

SUMMARY The addition of 10 mM CaCl2 to glutaraldehyde fixative leads to the formation of small electron-dense deposits in the organ of Corti of the guinea-pig. These precipitates are mainly attached to cell membranes in contact with different extracellular lymphatic fluids. A higher number of precipitates is localized in the acellular parts of tectorial and basilar membrane. Electron energy-loss spectroscopy (EELS) was used to determine the elemental composition of the deposits formed. The spectra showed a prominent signal at the Ca2+ L2,3 ionization edge. Oxygen could also be detected in all the precipitates analysed. EELS analysis of mitochondria of the inner and outer hair cells after co…

HistologyGuinea PigsAnalytical chemistrychemistry.chemical_elementCalciumPathology and Forensic Medicinechemistry.chemical_compoundCalcium ChlorideHair Cells AuditorymedicineExtracellularAnimalsInner earOrgan of CortiFixativeOrganellesElectron energy loss spectroscopyMitochondriaOxygenMicroscopy ElectronMembranemedicine.anatomical_structurechemistryOrgan of CortiBiophysicsCalciumGlutaraldehydeElectron Probe MicroanalysisJournal of microscopy
researchProduct