Neuregulins in Adult Neurogenesis and Migration
Neuregulins in Adult Neurogenesis and Migration
批准号:
6885238
负责人:
Hooman Troy Ghashghaei
金额:
$4.73万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-09-22 至 2006-09-21
关键词:
biological signal transductionbrain imaging /visualization /scanningcell differentiationcell growth regulationcell migrationcell proliferationcell typecerebral ventriclesgrowth factor receptorshistologylaboratory mousenerve stem cellneuregulinsneurogenesispostdoctoral investigatorprotein isoformsprotein structure functionprotein tyrosine kinasereceptor expression
中文摘要
描述(申请人提供):在这个项目中,我们建议研究受体酪氨酸激酶的一个亚型ErbB4及其配体神经调节蛋白(NRGs)在成人神经发生和形成嘴迁移流(RMS)的细胞迁移中的作用。在成年小鼠中,出生在侧脑室前区(SVZ)的神经前体细胞以RMS中的神经元链的形式迁移到嗅球,在那里它们分化为中间神经元。ErbB4受体主要在RMS中表达,而NRGs的所有异构体都在RMS周围的嗅觉和皮质结构中表达。在体外,NRG-1似乎阻止了迁移神经元链的形成,并分散了已经形成的链。另一方面,NRG-2在体外和体内诱导神经发生,表明它招募了增殖机制。在这里,我们建议通过将重组NRG注入成年小鼠的前脑室来阐明ErbB4受体在SVZ和RMS细胞的神经发生和迁移中的作用。然后,我们建议表征ErbB4激活对成年小鼠SVZ和RMS中的细胞类型的影响。最后,我们建议使用实时成像和固定的组织分析来确定RMS中迁移的神经母细胞的速率、组织和方向的潜在变化,以响应ErbB4的激活和失活。通过这些努力,我们希望对成人脑内神经前体细胞增殖、迁移和分化的分子机制有更好的了解。
英文摘要
DESCRIPTION (provided by applicant): In this project, we propose to study the role of one isoform of the receptor tyrosine kinases, ErbB4, and its ligands, the neuregulins (NRGs), in adult neurogenesis and migration of cells that form the rostral migratory stream (RMS). In adult mice, neural progenitor cells born in the anterior region of the lateral ventricle (SVZ) migrate as chains of neurons in the RMS to the olfactory bulb where they differentiate into interneurons. The ErbB4 receptor is prominently expressed in the RMS while all isoforms of NRGs are expressed in olfactory and cortical structures in the immediate surroundings of the RMS. In vitro, NRG-1 appears to block the formation of chains of migrating neurons and disperses chains that have already formed. NRG-2, on the other hand, induces neurogenesis in vitro and in vivo, suggesting that it recruits proliferative mechanisms. Here we propose to elucidate the role of the ErbB4 receptor in neurogenesis and migration of cells in the SVZ and RMS by infusing recombanant NRG's in the anterior ventricles of adult mice. We then propose to characterize the cell types affected by ErbB4 activation in the SVZ and RMS of adult mice. Finally, we propose to identify potential changes in rate, organization, and orientation of migrating neuroblasts in the RMS in response to ErbB4 activation and inactivation using real-time imaging as well as fixed tissue analyses. Through these efforts, we hope to gain an improved understanding of molecular mechanisms that regulate neural progenitor cell proliferation, migration and differentiation in the adult brain
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