ORGANIZATION OF ACTIVE ZONE WITHIN PRESYNAPTIC TERMINALS ON HIPPOCAMPAL NEURONS
海马神经元突触前末梢内活动区的组织
基本信息
- 批准号:6469034
- 负责人:
- 金额:$ 10.66万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2001
- 资助国家:美国
- 起止时间:2001-05-01 至 2002-04-30
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
During the development of the nervous system, a number of cellular
processes which include cell proliferation, cell differentiation, cell
adhesion, cell migration and cell death are required for the correct
formation of neural structures and to obtain functional and
reproducible connectivity between them. In the nervous system some of
these cellular processes have been shown to be mediated or modulated
by growth factors and their receptors. The receptors transduce
responses upon activation its ligand through their tyrosine kinase
domain the cytoplasmic tail. Examples of such growth factors/receptor
pairs are NGF/trk, BDNK/trkB, and NT3/trkC. A yet uncharacterized
receptor Tyro-3, belongs to this class and is the subject of our
study. The overall goal of this project is to understand some of the
functions, primarily in cell adhesion and to identify signal
transduction pathways affected by the tyrosine kinas Tyro-3. This
receptor has two immunoglobulin-like repeats and two fibronectin
type-III repeats in its extracellular portion and intracellularly a
functional tyrosine kinase domain, shown to be phosphorylated upon
binding of its known ligand gas-6. We will determine the
ultrastructural localization of Tyro-3 in the hoppocampus, in order to
establish a possible role of Tyro-3 in synaptogenesis and synaptic
plasticity. Preliminary data suggests that the Tyro-3 protein and
mRNA are preferentially localizd in the dendritic layer of CA1
neurons. This structure has been demonstrated to be crucial for the
establishment of short term memory and to be affected in Alzheimers
disease. We will also analyze the cell adhesive properties of Tyro-3
and the ability of this adhesion to affect its kinase activity. Cel l
adhesion plays a major role in neuronal patterning during development
and can affect remodeling of synaptic connections in the adult CNS.
We will study the observation that Tyro-3 is phosphorylated upon
addition of glutamate to hippocampal neurons in culture. Through
these efforts we hope to understand the role of Tyro-3, one of the few
nervous ysstem specific tyrosine kinases described so far, and gain
insight into the role played by tyrosine kinases in general in the
signal transduction events important for the development and
functioning of the nervous system.
在神经系统的发育过程中,有许多细胞
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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THOMAS SCHIKORSKI其他文献
THOMAS SCHIKORSKI的其他文献
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{{ truncateString('THOMAS SCHIKORSKI', 18)}}的其他基金
Synaptic Vesicle Dynamics at Hippocampal Synapses
海马突触的突触小泡动力学
- 批准号:
9170987 - 财政年份:2016
- 资助金额:
$ 10.66万 - 项目类别:
Synaptic Vesicle Dynamics at Excitatory Hippocampal Synapses
兴奋性海马突触的突触小泡动力学
- 批准号:
8079279 - 财政年份:2011
- 资助金额:
$ 10.66万 - 项目类别:
Synaptic Vesicle Dynamics at Excitatory Hippocampal Synapses
兴奋性海马突触的突触小泡动力学
- 批准号:
8469588 - 财政年份:2011
- 资助金额:
$ 10.66万 - 项目类别:
Synaptic Vesicle Dynamics at Excitatory Hippocampal Synapses
兴奋性海马突触的突触小泡动力学
- 批准号:
8320864 - 财政年份:2011
- 资助金额:
$ 10.66万 - 项目类别:
HRP cDNA expression: a label for modern electron microscopy on neuroscience
HRP cDNA 表达:现代电子显微镜神经科学的标签
- 批准号:
7845476 - 财政年份:2009
- 资助金额:
$ 10.66万 - 项目类别:
ORGANIZATION OF ACTIVE ZONE WITHIN PRESYNAPTIC TERMINALS ON HIPPOCAMPAL NEURONS
海马神经元突触前末梢内活动区的组织
- 批准号:
6354285 - 财政年份:2000
- 资助金额:
$ 10.66万 - 项目类别:
ORGANIZATION OF ACTIVE ZONE WITHIN PRESYNAPTIC TERMINALS ON HIPPOCAMPAL NEURONS
海马神经元突触前末梢内活动区的组织
- 批准号:
6220673 - 财政年份:1999
- 资助金额:
$ 10.66万 - 项目类别:
ORGANIZATION OF ACTIVE ZONE WITHIN PRESYNAPTIC TERMINALS ON HIPPOCAMPAL NEURONS
海马神经元突触前末梢内活动区的组织
- 批准号:
6121825 - 财政年份:1999
- 资助金额:
$ 10.66万 - 项目类别:
ORGANIZATION OF ACTIVE ZONE WITHIN PRESYNAPTIC TERMINALS ON HIPPOCAMPAL NEURONS
海马神经元突触前末梢内活动区的组织
- 批准号:
6282138 - 财政年份:1998
- 资助金额:
$ 10.66万 - 项目类别:
ORGANIZATION OF ACTIVE ZONE WITHIN PRESYNAPTIC TERMINALS ON HIPPOCAMPAL NEURONS
海马神经元突触前末梢内活动区的组织
- 批准号:
6252933 - 财政年份:1997
- 资助金额:
$ 10.66万 - 项目类别:
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