Effects of Lead on Calcium-Binding Proteins in Rats
Effects of Lead on Calcium-Binding Proteins in Rats
批准号:
7216675
负责人:
JONATHAN PEVSNER
金额:
$25.38万
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-05-02 至 2009-03-31
关键词:
AffectAnnexin A1AnnexinsAstrocytesBiochemical ProcessBiochemistryBiologicalBrainC2 DomainCalciumCalcium BindingCalcium-Binding ProteinsCell LineCellsChildClassComplementConditionDNADataData AnalysesDatabasesDepositionDivalent CationsEnvironmental HealthFamilyFibroblastsGene ExpressionGene Expression ProfilingGene ProteinsGenesGoalsHeterogeneityHippocampus (Brain)In Situ HybridizationIn VitroKidneyLeadLead PoisoningLiverMeasurementMeasuresMolecularNorthern BlottingPC12 CellsPatternPhospholipase A2PhospholipidsPolymerase Chain ReactionPrincipal Component AnalysisProtein BindingProtein FamilyProtein Kinase CProteinsRat Cell LineRattusRegulationResearchSamplingSecond Messenger SystemsSpecificityTechniquesTestingTimeTissuesToxic effectUnited Statesannexin A5basecalreticulincell typecellular targetingfrontal lobein vivoin vivo Modelkidney celllead exposurememberneurotoxicityneurotransmitter releasepuprepositoryresponsesecond messengersensorstatisticssynaptotagmin
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The major long-term objectives of the proposed research are [1] to test the hypothesis that lead interacts with calcium binding proteins of the C2 and annexin families, and [2] to identify genes and proteins of these calcium-binding families that are regulated following lead exposure of rats. Lead poisoning remains a pervasive problem in the United States, affecting at least 5% of all children. The proposed research is intended to elucidate molecular mechanisms underlying lead toxicity. Previous studies have demonstrated potent interactions between lead and proteins of the C2 domain family (e.g. protein kinase C and synaptotagmin) and annexins. Furthermore, lead exposure of cells has been shown to regulate the expression of genes encoding calcium-binding annexins. The four specific aims of this proposal are [1] to measure the interactions of lead with proteins of the C2 domain and annexin families, in order to determine the possible targets of lead. [2] To measure gene expression in the brain, kidney and liver of lead-exposed rats. This in vivo model may reveal whether lead exposure differentially regulates the expression of genes encoding calcium-binding proteins. [3] To extend gene expression studies to well characterized cell lines (astrocytes, PC12 cells, fibroblasts and normal rat kidney cells). These studies will complement gene expression measurements from the in vivo model. [4] To deposit gene expression data into a publicly accessible database. Together these studies may reveal which calcium binding proteins interact with lead, and which genes encoding calcium-binding proteins are regulated by lead exposure.
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