NFAT-mediated gene expression and striatal plasticity

NFAT 介导的基因表达和纹状体可塑性

• 批准号: 7417575
• 负责人: Paul G Mermelstein
• 金额: $ 23.6万
• 依托单位: UNIVERSITY OF MINNESOTA
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-06-15 至 2009-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7417575
• 关键词: Acute; Behavior; Behavioral; Biological Assay; Blood Vessels; Brain; Calcineurin; Calcium; Cardiac; Cells; Chronic; Class; Cocaine; Corpus striatum structure; Dopamine; Dopamine Receptor; Dorsal; Drug Addiction; Exposure to; Functional disorder; Gene Expression; Genetic Transcription; Goals; Growth; Immune response; Immune system; Injection of therapeutic agent; L-Type Calcium Channels; Lead; Learning; Link; Mediating; Mediator of activation protein; Modification; Molecular; Monitor; Muscle; Muscle Development; NF-AT; Nervous system structure; Neuronal Plasticity; Neurons; Nucleus Accumbens; Parkinson Disease; Pattern; Pharmaceutical Preparations; Play; Process; Production; Protein Biosynthesis; Protein Isoforms; Proteins; Range; Receptor Signaling; Regulation; Reporter Genes; Research; Research Personnel; Reverse Transcriptase Polymerase Chain Reaction; Rodent; Role; Self Administration; Shapes; Signal Pathway; Signal Transduction; Stimulus; Sum; Techniques; Transgenic Animals; Virus Diseases; base; behavioral sensitization; design; experience; in vivo; insight; nervous system disorder; neurotrophic factor; nuclear factors of activated T-cells; programs; psychostimulant; research study; response; transcription factor

DESCRIPTION (provided by applicant): The striatum contributes to our ability to learn sensorimotor tasks. It is also heavily involved in the wanting, seeking and self-administration of addictive drugs. Additionally, striatal dysfunction has been linked to a variety of neurological disorders. A major component to all these long-term alterations in brain function is modifications in striatal gene expression and protein synthesis. The diversity of transcription factors that direct these changes in neuronal plasticity are just now being appreciated. Outside of the nervous system, NFATc transcription factors are critical mediators of immune responses, vascular and cardiac development, and muscle growth. Recently, these transcription factors were discovered within brain, and it is the central hypothesis of this proposal that NFAT-dependent transcription is a critical mediator of striatal plasticity. Specific Aim 1 will characterize the expression of the 4, calcium/calcineurin-sensitive NFATc isoforms within the different neuronal subpopulations of the striatum. Specific Aim 2 will elucidate the intracellular signaling pathways triggered by dopamine receptor stimulation (D1- and D2-class) that lead to alterations in NFAT-dependent transcription. Specific Aim 3 will determine whether acute and/or chronic cocaine exposure leads to heightened NFAT-dependent transcription, and also whether inhibition of NFAT results in a diminution of cocaine-induced behavioral sensitization. In sum, utilizing modern cellular and molecular techniques, this study will reveal which NFATc proteins are expressed in the striatum, the stimuli that activate of NFAT-dependent transcription, and whether heightened NFAT activity can be linked to neuronal changes observed following exposure to addictive drugs. Ultimately, this project will lead to a better understanding of the role NFAT-dependent transcription plays in shaping long-term changes in brain function.

描述（由申请人提供）：纹状体有助于我们学习感觉运动任务的能力。它还与上瘾药物的欲望、寻求和自我管理密切相关。此外，纹状体功能障碍与多种神经系统疾病有关。脑功能所有这些长期改变的一个主要组成部分是纹状体基因表达和蛋白质合成的改变。指导这些神经元可塑性变化的转录因子的多样性现在才得到重视。在神经系统之外，NFATc转录因子是免疫反应、血管和心脏发育以及肌肉生长的关键介质。最近，这些转录因子在大脑中被发现，这一提议的中心假设是nfat依赖的转录是纹状体可塑性的关键介质。特异性Aim 1将表征4，钙/钙调磷酸酶敏感的NFATc亚型在纹状体的不同神经元亚群中的表达。特异性Aim 2将阐明由多巴胺受体刺激（D1-和d2 -类）引发的细胞内信号通路，导致nfat依赖性转录的改变。