Environmental biosensor of transgenic zebrafish
Environmental biosensor of transgenic zebrafish
批准号:
6647551
负责人:
Shuo Lin
金额:
$15.04万
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:
2003-07-01 至 2006-03-31
关键词:
biosensor device biotechnology cell cycle proteins chemokine cytokine developmental genetics endocrine disorder environmental contamination environmental stressor estrogen analog estrogens flow cytometry gene environment interaction gene expression genetically modified animals green fluorescent proteins hormone regulation /control mechanism microarray technology second messengers serial analysis of gene expression technology /technique development toxicant screening vertebrate embryology zebrafish
中文摘要
描述(由申请人提供):内分泌干扰化学物质(EDCs)是可以模仿或改变体内激素功能的物质。以前的研究大多使用细胞培养来检测EDCs对特定激素反应的影响。我们建议使用转基因斑马鱼,可以直接检查活体动物内分泌器官和激素反应的细微变化,以分析暴露于EDCs后发生的细胞行为和基因表达变化。这些转基因斑马鱼的绿色荧光蛋白(GFP)报告基因分别在胰岛素启动子引导的胰腺、POMC启动子引导的垂体以及卵黄原蛋白B1启动子引导的所有对雌激素有反应的细胞中表达。通过微阵列和microSAGE进行的流式细胞术和基因表达分析将用于在细胞水平上提供EDCs激活的基因概况。在分离的表达gfp的细胞中,重点研究细胞因子、趋化因子、信号转导信使、蛋白酶、癌基因或细胞周期相关产物,并比较天然雌激素暴露组和异种雌激素暴露组之间的差异。为了提供更多的工具来研究内分泌器官发育和EDC诱导的反应,我们还将使用来自每个系的转基因胚胎进行大规模的化合物筛选。在内分泌细胞系发育或雌激素反应中具有特异性作用的小分子将被选择用于未来的研究。由于本提案中研究的生物过程高度保守,我们相信斑马鱼的研究结果将最终帮助我们了解环境压力如何对人类内分泌细胞的发育和反应产生影响。
英文摘要
DESCRIPTION (provided by applicant): Endocrine disrupting chemicals (EDCs) are substances that can mimic or alter the function of hormones in the body. Previous studies have mostly used cell culture to examine EDCs effects on specific hormone responses. We propose to use transgenic zebrafish allowing direct examination of subtle alterations in endocrine organs and hormone responses in living animals to analyze the cellular behavior and gene expression changes that occur following exposure to EDCs. These transgenic zebrafish have the green fluorescent protein (GFP) reporter gene expressed, respectively, in pancreas directed by the insulin promoter, in pituitary by the POMC promoter, and all cells that respond to estrogens by the vitellogenin B1 promoter. Flow cytometry and gene expression analysis by microarrays and microSAGE will be used to provide a profile of the genes activated by EDCs at the cellular level. Cytokines, chemokines, signal transduction messengers, proteases, oncogenes or cell cycle-related products will be the focus studied in the separated GFP-expressing cells and compared between the natural estrogen exposure and xenoestrogen exposure groups. To generate more tools to study endocrine organ development and EDC induced responses, we will also perform a large-scale chemical compound screen using the transgenic embryos from each line. Small molecules that have specific effect in either endocrine cell lineage development or estrogen responses will be selected for future studies. Due to the high conservation of the biological processes to be studied in this proposal, we believe that findings from zebrafish should ultimately help us understand how environmental stresses exert their impact on the human endocrine cell development and responses.
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