Search results for "live cell"

showing 9 items of 19 documents

Live imaging of stem cell and progeny behaviour in physiological hair-follicle regeneration

2012

Tissue development and regeneration depend on cell-cell interactions and signals that target stem cells and their immediate progeny. However, the cellular behaviours that lead to a properly regenerated tissue are not well understood. Using a new, non-invasive, intravital two-photon imaging approach we study physiological hair-follicle regeneration over time in live mice. By these means we have monitored the behaviour of epithelial stem cells and their progeny during physiological hair regeneration and addressed how the mesenchyme influences their behaviour. Consistent with earlier studies, stem cells are quiescent during the initial stages of hair regeneration, whereas the progeny are more …

MesodermCell divisionCell SurvivalMesenchymeMice TransgenicBiologyArticleMesodermMiceCell MovementStem CellLive cell imagingmedicineAnimalsRegenerationMultidisciplinaryintegumentary systemAnimalStem CellsMedicine (all)Regeneration (biology)DermisHair follicleCell biologyMicroscopy Fluorescence Multiphotonmedicine.anatomical_structureAnimals; Cell Division; Cell Movement; Cell Survival; Cell Tracking; Dermis; Hair Follicle; Laser Therapy; Mesoderm; Mice; Mice Transgenic; Microscopy Fluorescence Multiphoton; Regeneration; Stem Cells; Medicine (all); MultidisciplinaryCell TrackingDermiLaser TherapyStem cellHair FollicleDevelopmental biologyCell DivisionNature
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Site-specific incorporation of perylene into an N-terminally modified light-harvesting complex II.

2010

Employing the utility of the native chemical ligation, site-specific attachment of an ultrastable perylene dye to a derivative of the major light-harvesting complex (LHCII) was demonstrated. Biochemical analysis of the conjugate indicated that the structure and function of LHCII remain largely unaffected by the N-terminal modification.

Molecular Sequence DataLight-Harvesting Protein Complexes010402 general chemistryPhotochemistry01 natural sciencesBiochemistry03 medical and health scienceschemistry.chemical_compoundPhysical and Theoretical ChemistryFLUORESCENCEPROTEIN LIGATIONPerylene030304 developmental biologyFluorescent DyesPlant Proteins0303 health sciencesSTABILITYOrganic ChemistryMICROSCOPYPlantsNative chemical ligationFluorescenceLIVE CELLS0104 chemical sciencesStructure and functionchemistryBiophysicsSMALL-MOLECULE PROBESCYSTEINEPeryleneDerivative (chemistry)DYESCysteineConjugateLight harvesting complex IIOrganicbiomolecular chemistry
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Dye selection for live cell imaging of intact siRNA

2011

Abstract Investigations into the fate of small interfering RNA (siRNA) after transfection may unravel new ways to improve RNA interference (RNAi) efficiency. Because intracellular degradation of RNA may prevent reliable observation of fluorescence-labeled siRNA, new tools for fluorescence microscopy are warranted to cover the considerable duration of the RNAi effect. Here, the characterization and application of new fluorescence resonance energy transfer (FRET) dye pairs for sensing the integrity of duplex siRNA is reported, which allows an assessment of the degradation status of an siRNA cell population by live cell imaging. A panel of high-yield fluorescent dyes has been investigated for …

Small interfering RNACell SurvivalClinical BiochemistryPopulationBiologyBiochemistryLive cell imagingRNA interferenceFluorescence Resonance Energy TransferFluorescence microscopeAnimalsRNA Small InterferingeducationMolecular BiologyCells CulturedFluorescent Dyeseducation.field_of_studyMicroscopy ConfocalBrainEndothelial CellsRNATransfectionHydrogen-Ion ConcentrationMolecular biologyRatsFörster resonance energy transferBiophysicsBiological Chemistry
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Fluctuation Methods To Study Protein Aggregation in Live Cells: Concanavalin A Oligomers Formation

2011

Prefibrillar oligomers of proteins are suspected to be the primary pathogenic agents in several neurodegenerative diseases. A key approach for elucidating the pathogenic mechanisms is to probe the existence of oligomers directly in living cells. In this work, we were able to monitor the process of aggregation of Concanavalin A in live cells. We used number and brightness analysis, two-color cross number and brightness analysis, and Raster image correlation spectroscopy to obtain the number of molecules, aggregation state, and diffusion coefficient as a function of time and cell location. We observed that binding of Concanavalin A to the membrane and the formation of small aggregates paralle…

Time FactorsCell SurvivalCellSpectroscopy Imaging and Other TechniquesBiophysicsProtein aggregationCell morphologyCell membraneDiffusion03 medical and health scienceschemistry.chemical_compoundMice0302 clinical medicineProtein structure2-NaphthylaminemedicineConcanavalin AAnimalsconfocal microscopy super resolution protein aggregation kinetics in live cells amyloid related pathologiesAnnexin A5Protein Structure QuaternaryCell Shape030304 developmental biology0303 health sciencesbiologySpectrum AnalysisCell MembraneFibroblastsEmbryo MammalianCell biologyMembranemedicine.anatomical_structurechemistryConcanavalin Abiology.proteinLaurdan030217 neurology & neurosurgeryFluorescein-5-isothiocyanateLaurates
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Imaging of Keratin Dynamics during the Cell Cycle and in Response to Phosphatase Inhibition

2004

Publisher Summary The characterization and development of autofluorescent proteins, most prominently of the green florescent protein, have provided tools to label cellular structures such that they can be examined in living cells. This chapter highlights the potential of live cell imaging in providing novel and unprecedented insights into the dynamic organization of the keratin cytoskeleton and outlines the important aspects of this method. The live cell imaging experiments suggest that the driving force behind the vectorial and dynamic keratin distribution patterns relies both on microtubules and microfilaments and their associated factors. The studies on the dynamics of the keratin cytosk…

chemistry.chemical_classificationMotor proteinchemistryLive cell imagingMicrotubuleKeratinFluorescence recovery after photobleachingmacromolecular substancesBiologyIntermediate filamentCytoskeletonMicrofilamentCell biology
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A new method to value efficiency of enzyme blends for pancreatic tissue digestion.

2010

Islet transplantation, since the 90’s, has been resulting to be one of the best successful example of human cell therapy. Nevertheless, islet isolation procedure is not completely standardized; in fact, more than fifty percent of islets procedures don’t arrive to their transplantation. This is due both to the variability of donor’s pancreas and to an unpredictable enzymatic blend efficiency. Enzymes used in pancreas digestion are extracted from Clostridium histolyticum bacteria and digest several substrates. In particular they have strong collagenolytic activity compared to vertebrate collagenases. However, several impediments persist in human islet isolation success probably due to the var…

endocrine systemmedicine.medical_specialtyProteasesIslets transplantationmedicine.medical_treatmentCollagenaseIslets of Langerhans TransplantationThermolysinCell SeparationCell LineIslets of LangerhansClostridium histolyticumSettore BIO/10 - BiochimicaInternal medicinemedicineHumansCollagenasesPancreasTransplantationIslet cell transplantationgeographyEvaluation alive cellgeography.geographical_feature_categorybiologyPancreatic isletsREcombinant proteinProteolytic enzymesEndothelial Cellsproteolytic enzymesbiology.organism_classificationIsletTransplantationmedicine.anatomical_structureEndocrinologyBiochemistryGelatinasesSurgeryCollagenPancreasGelsPeptide HydrolasesTransplantation proceedings
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2014

Morphogenesis in plants is usually reconstructed by scanning electron microscopy and histology of meristematic structures. These techniques are destructive and require many samples to obtain a consecutive series of states. Unfortunately, using this methodology the absolute timing of growth and complete relative initiation of organs remain obscure. To overcome this limitation, an in vivo observational method based on Epi-Illumination Light Microscopy (ELM) was developed and tested with a male inflorescence meristem (floral unit) of the handkerchief tree Davidia involucrata Baill. (Nyssaceae). We asked whether the most basal flowers of this floral unit arise in a basipetal sequence or, altern…

fungiMorphogenesisfood and beveragesContext (language use)Plant ScienceBiologyMeristembiology.organism_classificationDavidia involucrataInflorescenceLive cell imagingBotanyPrimordiumNyssaceaeFrontiers in Plant Science
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Differential detection and quantification of cyclic AMP and other adenosine phosphates in live cell

2017

A new naphthol-based rhodamine derivative (NpRD) has been developed for the selective and differential detection of adenosine 3′,5′-cyclic monophosphate (cAMP) and adenosine phosphates (APs) (ATP, ADP, and AMP) from other nucleotides. The simple detection and quantification of cAMP in human blood cells and in other samples based on the ‘turn on’ fluorescence properties of this chemosensor through colorimetry or fluorometry makes it unique for probable application in high throughput screening. peerReviewed

quantification of cyclic AMPadenosine phosphatesdifferential detectionlive cell
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Molecular Mechanisms of the Blockage of Glioblastoma Motility

2021

Glioblastoma (GBM) is the most common and lethal brain tumor. GBM has a remarkable degree of motility and is able to infiltrate the healthy brain. In order to perform a rationale-based drug-repositioning study, we have used known inhibitors of two small Rho GTPases, Rac1 and Cdc42, which are upregulated in GBM and are involved in the signaling processes underlying the orchestration of the cytoskeleton and cellular motility. The selected inhibitors (R-ketorolac and ML141 for Cdc42 and R-ketorolac and EHT 1864 for Rac1) have been successfully employed to reduce the infiltration propensity of GBM in live cell imaging studies. Complementarily, all-atom simulations have elucidated the molecular …

rac1 GTP-Binding Proteinrho GTP-Binding ProteinsGeneral Chemical EngineeringBrain tumorMotilityRAC1CDC42Library and Information SciencesBiologySettore BIO/09 - FisiologiaMicrotubules01 natural sciencesDownregulation and upregulationLive cell imaging0103 physical sciencesmedicineHumanscdc42 GTP-Binding Protein010304 chemical physicsDrug discoveryCancerGeneral Chemistrymedicine.disease0104 chemical sciencesComputer Science Applications010404 medicinal & biomolecular chemistrySettore CHIM/03 - Chimica Generale E InorganicaCancer researchGlioblastomaJournal of Chemical Information and Modeling
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