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staphylococcus aureus biofilms mediate keratinocyte apoptosis

staphylococcus aureus biofilms mediate keratinocyte apoptosis
金黄色葡萄球菌生物膜介导角质形成细胞凋亡
批准号:
8702084
负责人:
KELLY R KIRKER
金额:
$7.06万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-07-01 至 2016-06-30
关键词:
ATM geneATM wt AlleleAbbreviationsAffectAlkanesulfonatesApoptosisApoptosis InhibitorApoptoticBiological AssayBiologyCaringCaspaseCell Culture TechniquesCell DeathCellsCharacteristicsChronicCoculture TechniquesConditioned Culture MediaCulture MediaDNA FragmentationDNA NucleotidylexotransferaseDataDevelopmentDiabetes MellitusDiagnosticFermentationFluoresceinFluorescein-5-isothiocyanateFutureGlyceraldehyde-3-Phosphate DehydrogenasesGoalsGrowthHealthHealth Care CostsHigh Pressure Liquid ChromatographyHumanIn Situ Nick-End LabelingIncidenceInduction of ApoptosisInfectionInvestigationIsothiocyanatesLabelLeadMammalian CellMass Spectrum AnalysisMediatingMetabolicMetabolismMethodsMicrobial BiofilmsMicroscopicMolecularMolecular AnalysisMolecular BiologyMontanaMorbidity - disease rateNOESYNecrosisNuclear Magnetic ResonanceObesityOutcomePathogenesisPathway interactionsPatientsPenicillinsPhosphate BufferPhosphatidylserinesPolymerase Chain ReactionPopulationPropidium DiiodideResearchResearch PersonnelResourcesReverse TranscriptionSalineSignal PathwaySkinSodiumSodium ChlorideSpectrum AnalysisStaining methodStainsStaphylococcus aureusStreptomycinTNF Receptor-Associated FactorsTNF geneTechniquesTestingTetrazoliumTherapeutic InterventionTimeTumor Necrosis Factor-alphaUnited StatesUniversitiesWorkWound Healingaging populationapoptosis inducing factoraspartyl-glutamyl-valyl-aspartyl-p-nitroanilideaspartylglutamatecareerexperiencegel electrophoresiskeratinocytekillingsliquid chromatography mass spectrometrymetabolomicsmultidisciplinarynuclear Overhauser enhancementpreventresponsesmall moleculesocialsoystemwound

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DESCRIPTION (provided by applicant): PROJECT SUMMARY/ABSTRACT Chronic wounds affect approximately 6.5 million patients in the United States and represent $25 billion in annual health care costs. This burden is rapidly increasing due to escalating health care costs, an aging population, and the rising incidence of diabetes and obesity. Studies demonstrate that biofilms contribute to wound chronicity, and that Staphylococcus aureus is a prevalent species found in chronic wound biofilms; however, how biofilms contribute to the delayed re-epithelialization remains unclear. It was recently demonstrated that planktonic S. aureus and S. aureus biofilms have differential lethal effects on keratinocytes (KC). Therefore, it is hypothesized that planktonic S. aureus produce soluble factors that induce KC necrosis; whereas S. aureus biofilms produce soluble factors that mediate specific apoptotic pathways in KC. This hypothesis will be tested by comprehensively investigating KC cultures exposed to either biofilm-conditioned medium or planktonic-conditioned medium for apoptotic characteristics, including phosphatidylserine translocation and DNA fragmentation. Next, KC cultures will also be analyzed for the induction of the intrinsic and/or extrinsic apoptotic pathways. More specific molecular analysis of KC apoptosis will be investigated using a large format quantitative polymerase chain reaction array. Finally, bacterial products produced by S. aureus biofilms will be identified using nuclear magnetic resonance and mass spectrometry analysis, and the identified products will be screened to determine if they are apoptosis-inducing factors. The goals of this investigation include identifying the molecular pathways mediated by S. aureus biofilms and the specific bacterial products that induce KC apoptosis. Indentifying clearly defined signaling pathways and apoptosis- inducing bacterial products may provide a molecular rational for future chronic wound therapies and diagnostics, which may have a significant impact on patient health.
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staphylococcus aureus biofilms mediate keratinocyte apoptosis
staphylococcus aureus biofilms mediate keratinocyte apoptosis