Effects of Lead on Calcium-Binding Proteins in Rats

铅对大鼠钙结合蛋白的影响

• 批准号: 7216675
• 负责人: JONATHAN PEVSNER
• 金额: $ 25.38万
• 依托单位: HUGO W. MOSER RES INST KENNEDY KRIEGER
• 依托单位国家: 美国
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-05-02 至 2009-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7216675
• 关键词: Affect; Annexin A1; Annexins; Astrocytes; Biochemical Process; Biochemistry; Biological; Brain; C2 Domain; Calcium; Calcium Binding; Calcium-Binding Proteins; Cell Line; Cells; Child; Class; Complement; Condition; DNA; Data; Data Analyses; Databases; Deposition; Divalent Cations; Environmental Health; Family; Fibroblasts; Gene Expression; Gene Expression Profiling; Gene Proteins; Genes; Goals; Heterogeneity; Hippocampus (Brain); In Situ Hybridization; In Vitro; Kidney; Lead; Lead Poisoning; Liver; Measurement; Measures; Molecular; Northern Blotting; PC12 Cells; Pattern; Phospholipase A2; Phospholipids; Polymerase Chain Reaction; Principal Component Analysis; Protein Binding; Protein Family; Protein Kinase C; Proteins; Rat Cell Line; Rattus; Regulation; Research; Sampling; Second Messenger Systems; Specificity; Techniques; Testing; Time; Tissues; Toxic effect; United States; annexin A5; base; calreticulin; cell type; cellular targeting; frontal lobe; in vivo; in vivo Model; kidney cell; lead exposure; member; neurotoxicity; neurotransmitter release; pup; repository; response; second messenger; sensor; statistics; synaptotagmin

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.

描述（由申请人提供）：拟议研究的主要长期目标是[1]检验铅与C2和膜联蛋白家族的钙结合蛋白相互作用的假设，[2]鉴定大鼠铅暴露后受调节的这些钙结合蛋白家族的基因和蛋白。铅中毒在美国仍然是一个普遍存在的问题，影响至少5%的儿童。这项拟议的研究旨在阐明铅毒性的分子机制。先前的研究已经证明了铅与C2结构域家族的蛋白质（例如蛋白激酶C和突触结合蛋白）和膜联蛋白之间的有效相互作用。此外，铅暴露的细胞已被证明可以调节基因编码的钙结合膜联蛋白的表达。该提案的四个具体目标是[1]测量铅与C2结构域和膜联蛋白家族蛋白质的相互作用，以确定铅的可能靶点。[2]检测铅暴露大鼠脑、肾和肝中基因表达。这种体内模型可能揭示铅暴露是否差异调节编码钙结合蛋白的基因的表达。[3]将基因表达研究扩展至充分表征的细胞系（星形胶质细胞、PC12细胞、成纤维细胞和正常大鼠肾细胞）。这些研究将补充体内模型的基因表达测量。[4]将基因表达数据存款公共数据库。这些研究可能揭示哪些钙结合蛋白与铅相互作用，以及哪些编码钙结合蛋白的基因受到铅暴露的调控。