Search results for "membrane permeability"

showing 10 items of 134 documents

Fetuin-B, a liver-derived plasma protein is essential for fertilization.

2013

SummaryThe zona pellucida (ZP) is a glycoprotein matrix surrounding mammalian oocytes. Upon fertilization, ZP hardening prevents sperm from binding to and penetrating the ZP. Here, we report that targeted gene deletion of the liver-derived plasma protein fetuin-B causes premature ZP hardening and, consequently, female infertility. Transplanting fetuin-B-deficient ovaries into wild-type recipients restores fertility, indicating that plasma fetuin-B is necessary and sufficient for fertilization. In vitro fertilization of oocytes from fetuin-B-deficient mice only worked after rendering the ZP penetrable by laser perforation. Mechanistically, fetuin-B sustains fertility by inhibiting ovastacin,…

Malemedicine.medical_specialtyCell Membrane Permeabilitymedicine.medical_treatmentmacromolecular substancesFertilization in VitroBiologyGeneral Biochemistry Genetics and Molecular BiologyMiceHuman fertilizationPregnancyInternal medicinemedicineAnimalsZona pellucidaMolecular BiologyZona Pellucidachemistry.chemical_classificationProteaseOvaryGene Expression Regulation DevelopmentalEmbryoCell BiologyEmbryo TransferEmbryo MammalianSpermFetuinSpermatozoaFetuin-BRecombinant ProteinsCell biologyEnzyme ActivationMice Inbred C57BLmedicine.anatomical_structureEndocrinologychemistryFertilizationMetalloproteasesOocytesGameteFemaleGlycoproteinInfertility FemaleDevelopmental BiologyDevelopmental cell
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Coagulation bath composition and desiccation environment as tuning parameters to prepare skinless membranes via diffusion induced phase separation

2015

Diffusion Induced Phase Separation (DIPS) is a currently used technique to produce porous membranes for a large variety of applications. A strong limitation is represented by the occurrence of a dense skin, which is formed during the process, highly reducing the membrane permeability. To overcome this issue, two modifications of the standard DIPS protocol were investigated: the use of coagulation baths composed by a solvent/nonsolvent mixture and the desiccation in a controlled environment, by modulating the partial pressure of nonsolvent vapor. An appropriate choice of coagulation bath composition, together with an appropriate desiccation protocol (i.e., the use of a nonsolvent vapor), wil…

Materials Chemistry2506 Metals and AlloyMaterials scienceChromatographyPolymers and PlasticPolymers and PlasticsMembrane permeabilityDiffusionChemistry (all)Surfaces Coatings and FilmGeneral ChemistryPartial pressureSurfaces Coatings and FilmsSolventMembraneChemical engineeringmorphologyMaterials Chemistryphase behaviorCoagulation (water treatment)porous materialPorous mediumDesiccationmembrane
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Bacterial Cytolysin Perturbs Round Window Membrane Permeability Barrier In Vivo: Possible Cause of Sensorineural Hearing Loss in Acute Otitis Media

1998

ABSTRACT The passage of radioiodinated streptolysin-O (SLO) and albumin through the round window membrane (RWM) was studied in vivo. When applied to the middle ear, SLO became quantitatively entrapped in this compartment and no passage to the cochlea occurred. However, flux of radioiodinated albumin through the toxin-damaged RWM was observed. We propose that the passage of noxious macromolecules, such as proteases, from a purulent middle-ear effusion may be facilitated by pore-forming toxins, resulting in cochlear damage and sensorineural hearing loss.

Membrane permeabilityHearing lossHearing Loss SensorineuralImmunologyGuinea PigsBiologyIn Vitro TechniquesMicrobiologyPermeabilityBacterial ProteinsIn vivoAlbuminsmedicineotorhinolaryngologic diseasesAnimalsCochleaRound windowMembranesOtitis Media with EffusionAnatomyBacterial Infectionsmedicine.diseaseCochleaInfectious Diseasesmedicine.anatomical_structureRound Window EarStreptolysinsBiophysicsMiddle earParasitologySensorineural hearing lossCytolysinsense organsmedicine.symptom
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Performance of industrial scale hollow-fibre membranes in a submerged anaerobic MBR (HF-SAnMBR) system at mesophilic and psychrophilic conditions

2013

The aim of this work was to evaluate the effect of temperature on the performance of industrial hollow-fibre (HF) membranes treating urban wastewater in a submerged anaerobic MBR system (SAnMBR). To this end, a demonstration plant with two commercial HF ultrafiltration membrane modules (PURON®, Koch Membrane Systems, PUR-PSH31) was operated at 20, 25 and 33 °C. The mixed liquor total solid (MLTS) level was a key factor affecting membrane permeability (K). K was higher under psychrophilic than mesophilic conditions when operating at similar transmembrane fluxes and MLTS, because the biomass activity of the psychrophilic mixed liquor was lower than the mesophilic mixed liquor. Thus, lower ext…

Mesophilic and psychrophilic anaerobic conditionsSoluble microbial products (SMPs)INGENIERIA HIDRAULICAMembrane permeabilityFoulingChemistryEnvironmental engineeringUltrafiltrationFiltration and SeparationPulp and paper industryAnalytical ChemistryMembraneExtracellular polymeric substanceMembrane permeabilityWastewaterExtracellular polymeric substances (EPSs)PsychrophileIndustrial hollow-fibre membranesTECNOLOGIA DEL MEDIO AMBIENTEMesophile
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A guide to the use of pore-forming toxins for controlled permeabilization of cell membranes

1993

Depending on the size of the pores one wishes to produce in plasma membranes, the choice will probably fall on one of the three toxins discussed above. S. aureus alpha-toxin should be tried first when pores of 1-1.5 nm diameter are required. This is generally the case when Ca2+ and nucleotide dependence of a given process is being studied. If alpha-toxin does not work, this is probably due to the fact that the toxin either does not produce pores, or that the pores are too small. In this case, high concentrations of alpha-toxin should be tried. If this still does not work, we recommend the use of HlyA. When very large pores are to be created, e.g. for introduction of antibodies into the cell…

Microbiology (medical)TetanolysinPore-forming toxinCell Membrane PermeabilityEscherichia coli ProteinsEscherichia coli ProteinsBacterial ToxinsCell MembraneImmunologyGeneral MedicineMembrane transportBiologyHemolysin Proteinschemistry.chemical_compoundMembraneBacterial ProteinschemistryBiochemistryStreptolysinsBiophysicsImmunology and AllergyCell permeabilityMedical Microbiology and Immunology
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Active surfaces engineered by immobilizing protein-polymer nanoreactors for selectively detecting sugar alcohols.

2016

We introduce active surfaces generated by immobilizing protein-polymer nanoreactors on a solid support for sensitive sugar alcohols detection. First, such selective nanoreactors were engineered in solution by simultaneous encapsulation of specific enzymes in copolymer polymersomes, and insertion of membrane proteins for selective conduct of sugar alcohols. Despite the artificial surroundings, and the thickness of the copolymer membrane, functionality of reconstituted Escherichia coli glycerol facilitator (GlpF) was preserved, and allowed selective diffusion of sugar alcohols to the inner cavity of the polymersome, where encapsulated ribitol dehydrogenase (RDH) enzymes served as biosensing e…

Models MolecularMaterials scienceMembrane permeabilityPolymersSurface PropertiesBiophysicsBioengineering02 engineering and technologyNanoreactorBiosensing Techniques010402 general chemistryRibitolAquaporins01 natural sciencesPermeabilityBiomaterialschemistry.chemical_compoundSugar AlcoholsEscherichia coliOrganic chemistrySugar alcoholRibitolchemistry.chemical_classificationEscherichia coli Proteins021001 nanoscience & nanotechnology0104 chemical sciencesNanostructuresMembraneImmobilized ProteinschemistryMechanics of MaterialsPolymersomeCeramics and Composites0210 nano-technologyBiosensorSugar Alcohol DehydrogenasesSugar Alcohol DehydrogenasesBiomaterials
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Complement lysis: a hole is a hole.

1991

recent experimental advances 21, it is now possible to produce MACs with a precise molecular composition 7 for better designed experiments. In my judgement, however, it will always be problematic to propose a single unifying mechanism for MAC action simply because MAC effects are not uniform. The reason for attempting to classify MACs as leaky patch or channel formers is a desire to wield Occam's razor and carve out the simplest unifying theory. But this razor often cuts one's throat, especially when it comes to immunological processes. A system that degranulates platelets, 'kills' such widely diverse targets as artificial liposomes, 'dead' viruses and erythrocytes, metabolically active cel…

Molecular compositionCell Membrane PermeabilityComputer scienceNuclear EnvelopeCarve outImmunologyoccamComplement System ProteinsTopologyHemolysisModels BiologicalIon ChannelsComplement (complexity)Patch formationAction (philosophy)Channel (programming)Humanscomputercomputer.programming_languageSimple (philosophy)Immunology today
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Modulation of drug transport by selected flavonoids: Involvement of P-gp and OCT?

2004

Flavonoids, as a common component of daily nutrition, are a possible source of interference with absorption processes, due to modulation of transporting proteins. In this study, the influence of selected flavonoids (quercetin, isoquercitrin, spiraeoside, rutin, kaempferol, naringenin, naringin, and kaempferol) on the transport of the P-gp substrate [3H]talinolol across Caco-2 cell monolayers was investigated. To elucidate the mechanism behind the interaction observed in this system the potency of the flavonoids to replace [3H]talinolol from its P-gp binding site as well as their activity to inhibit OCT2-mediated [14C]TEA uptake into LLC-PK(1) cells were measured, as P-gp and OCT have been s…

NaringeninCell Membrane PermeabilityOrganic Cation Transport ProteinsFlavonoidPharmaceutical ScienceBinding CompetitivePropanolaminesFood-Drug InteractionsRadioligand Assaychemistry.chemical_compoundRutinHumansheterocyclic compoundsATP Binding Cassette Transporter Subfamily B Member 1NaringinFlavonoidschemistry.chemical_classificationHesperetinfood and beveragesBiological TransportchemistryBiochemistryCaco-2 CellsKaempferolQuercetinTalinololEuropean Journal of Pharmaceutical Sciences
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Nature of sterols affects plasma membrane behavior and yeast survival during dehydration.

2011

International audience; The plasma membrane (PM) is a main site of injury during osmotic perturbation. Sterols, major lipids of the PM structure in eukaryotes, are thought to play a role in ensuring the stability of the lipid bilayer during physicochemical perturbations. Here, we investigated the relationship between the nature of PM sterols and resistance of the yeast Saccharomyces cerevisiae to hyperosmotic treatment. We compared the responses to osmotic dehydration (viability, sterol quantification, ultrastructure, cell volume, and membrane permeability) in the wild-type (WT) strain and the ergosterol mutant erg6Δ strain. Our main results suggest that the nature of membrane sterols gover…

Osmotic stressCell Membrane PermeabilityChromatography GasSaccharomyces cerevisiae ProteinsOsmotic shockMembrane permeabilitySaccharomyces cerevisiaeBiophysicsSterol evolutionSaccharomyces cerevisiaeBiologyBiochemistryCell survival03 medical and health scienceschemistry.chemical_compoundOsmotic Pressure[ SDV.MP ] Life Sciences [q-bio]/Microbiology and ParasitologyErgosterolpolycyclic compoundsLipid bilayer030304 developmental biology0303 health sciencesErgosterolOsmotic concentrationDehydration030306 microbiologyCell MembraneMethyltransferasesCell Biologybiology.organism_classificationSterolMicroscopy ElectronSterols[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyBiochemistrychemistryMutationlipids (amino acids peptides and proteins)Osmotic dehydrationPlasma membrane
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Infarct Size Measurement by Triphenyltetrazolium Chloride StainingVersus In VivoInjection of Propidium Iodide

1997

Infarct size delineation by triphenyltetrazolium chloride (TTC) staining is dependent on sufficient reperfusion. We therefore evaluated the possibility of using propidium iodide (PI), a reagent conventionally used in flow cytometry to fluorescently stain dead cells, for infarct size analysis after short periods of reperfusion. Forty-five rabbits were subjected to either 15 min, 2 h or 4.5 h of coronary artery occlusion without reperfusion, or to 15 min, 30 min and 2 h of coronary artery occlusion followed by 30 min, 1 h and 3 h of reperfusion. Fifteen min before terminating the experiment, PI was injected into the left atrium. Patent blue violet was used to delineate the area at risk. Follo…

Pathologymedicine.medical_specialtyCell Membrane PermeabilityMyocardial InfarctionTetrazolium SaltsMyocardial ReperfusionStainFlow cytometrychemistry.chemical_compoundIn vivoOcclusionmedicineAnimalscardiovascular diseasesPropidium iodideColoring AgentsMolecular BiologyStaining and Labelingmedicine.diagnostic_testChemistrybusiness.industryMyocardiumHistologymedicine.diseaseCoronary VesselsStainingInjections Intra-ArterialRabbitsCardiology and Cardiovascular MedicineNuclear medicinebusinessReperfusion injuryPropidiumJournal of Molecular and Cellular Cardiology
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