SPINE AND SYNAPTIC PLASTICITY IN MATURE HIPPOCAMPUS
成熟海马的脊柱和突触可塑性
基本信息
- 批准号:6539615
- 负责人:
- 金额:$ 3.51万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1984
- 资助国家:美国
- 起止时间:1984-07-01 至 2002-08-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
DESCRIPTION (Verbatim from the Applicant's Abstract): Dendritic spines are tiny
protrusions that stud the surface of principal neurons throughout the brain.
They are the primary sites of excitatory synapses, the sites of communication
between neurons. The goal of the proposed work is to ascertain the role of
synaptic activity in the formation and structure of dendritic spines and their
synapses. It had been thought that spines are generated when synaptic activity
is enhanced. Our findings show however that spines and synapses are stable
during long term enhancement of synaptic activity. Instead we have discovered
that dendrites of mature neurons become more spiny within hours after synapses
are inactivated. The specific aims of this project are: 1) Establish how soon
after inactivation dendrites of mature hippocampal neurons become more spiny.
2) Assess whether dendrites become less spiny after reinstatement of activity.
3) Determine how inactivation and reactivation affect the structure of spines,
synapses, and their associated astroglial processes. 4) Determine whether the
additional spine synapses are functional. In Aims 1, 2, and 4 quantitative
confocal microscopy will be used with field and whole-cell recordings in
hippocampal slices from adult rats. In Aim 3 quantitative serial electron
microscopy will be used to answer a series of related questions including: i)
Do all of the spiny protusions that are detected with confocal microscopy have
synapses? ii) Do the additional synapses occur on pre-existing axonal boutons?
iii) Is synaptic structure modified during inactivation or reactivation? iv)
Are the calcium-regulating organelles in dendritic spines modified by activity?
v) Does activity modify the degree of astroglial ensheathment of spine
synapses? The reported progress and proposed research present an important new
way of thinking about spines and synapses in the mature brain. They suggest
that mature neurons maintain an optimal level of activation by regulating spine
and synapse number. They could explain why spines are lost after excessive
activity, for example, during epileptic seizures. They are also relevant to
understanding how spines and synapses might be generated in the mature brain at
times when overall brain activity is low.
This outstanding renewal application formulates a new and novel view of
dendritic spine plasticity that runs counter to established dogma but is
consistent with recent findings of other innovative workers in the field, and
extends work carried out during the prior application period into significant
new areas. Light microscopic and ultrastructural findings as well as
neurophysiological data strongly suggest that spine density exhibits multiple
states, with certain levels of neuronal activity stabilizing both spine and
synaptic number, while increased activity down-regulates both and decreased
activity actually up-regulates both, as if neurons strive to maintain stable
"activation," irregardless of variations in input activity.
描述(来自申请人摘要的逐字描述):树突棘很小
遍布大脑的主要神经元表面的突起。
它们是兴奋性突触的主要部位,也就是通讯的部位
神经元之间。拟议工作的目标是确定
树突棘的形成和结构中的突触活动及其
突触人们一直认为,当突触活动
增强了。然而我们的发现表明棘和突触是稳定的
突触活动的长期增强。相反,我们发现
成熟神经元的树突在突触形成后几小时内变得更加多刺,
都被灭活了该项目的具体目标是:1)确定
失活后,成熟海马神经元的树突变得更加多刺。
2)评估恢复活动后树突是否变得不那么多刺。
3)确定失活和再活化如何影响棘的结构,
突触和与之相关的星形胶质细胞过程。4)确定是否
另外的棘突触是功能性的。在目标1、2和4中,定量
共聚焦显微镜将用于现场和全细胞记录,
成年大鼠海马切片。In Aim 3定量系列电子
显微镜将用于回答一系列相关问题,包括:i)
是否所有用共聚焦显微镜检测到的棘状突起
突触ii)额外的突触是否发生在预先存在的轴突终扣上?
iii)突触结构在失活或再激活过程中是否发生改变?iv)
树突棘中的钙调节细胞器是否被活性修饰?
v)活动是否改变脊柱星形胶质细胞鞘化的程度
突触报告的进展和拟议的研究提出了一个重要的新的
来思考成熟大脑中的棘和突触。他们建议
成熟的神经元通过调节脊髓
和突触数。它们可以解释为什么在过度的
活动,例如,在癫痫发作期间。它们也与
了解脊椎和突触是如何在成熟的大脑中产生的,
这是大脑整体活动较低的时候。
这一突出的续期申请制定了一个新的和新颖的观点,
树突棘的可塑性与既定的教条背道而驰,
与该领域其他创新工作者的最新发现一致,
将上一个申请期内开展的工作扩展到
新领域。光镜和超微结构检查结果以及
神经生理学数据强烈地表明,脊柱密度表现出多种
状态,具有一定水平的神经元活动稳定脊柱和
突触数量,而增加的活动下调两者,
活动实际上上调了两者,就好像神经元努力保持稳定,
“激活”,而不管输入活动的变化。
项目成果
期刊论文数量(0)
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会议论文数量(0)
专利数量(0)
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KRISTEN M HARRIS其他文献
KRISTEN M HARRIS的其他文献
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{{ truncateString('KRISTEN M HARRIS', 18)}}的其他基金
Synapse growth and elimination in mature CNS
成熟中枢神经系统中突触的生长和消除
- 批准号:
9306182 - 财政年份:2014
- 资助金额:
$ 3.51万 - 项目类别:
Synapse growth and elimination in mature CNS
成熟中枢神经系统中突触的生长和消除
- 批准号:
8855853 - 财政年份:2014
- 资助金额:
$ 3.51万 - 项目类别:
Synapse growth and elimination in mature CNS
成熟中枢神经系统中突触的生长和消除
- 批准号:
8935920 - 财政年份:2014
- 资助金额:
$ 3.51万 - 项目类别:
DEVELOPMENTAL CONTROL OF SYNAPSE STRUCTURE WITH LTP
利用 LTP 控制突触结构的发育
- 批准号:
8508316 - 财政年份:2012
- 资助金额:
$ 3.51万 - 项目类别:
DEVELOPMENTAL CONTROL OF SYNAPSE STRUCTURE WITH LTP
利用 LTP 控制突触结构的发育
- 批准号:
8373632 - 财政年份:2012
- 资助金额:
$ 3.51万 - 项目类别:
DEVELOPMENTAL CONTROL OF SYNAPSE STRUCTURE WITH LTP
利用 LTP 控制突触结构的发育
- 批准号:
9085412 - 财政年份:2012
- 资助金额:
$ 3.51万 - 项目类别:
Pre-Doctoral Training in Interdisciplinary Neuroscience
跨学科神经科学博士前培训
- 批准号:
8288915 - 财政年份:2004
- 资助金额:
$ 3.51万 - 项目类别:
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