Voltage-gated ion channels and synaptic integration by cerebellar Purkinje cells
小脑浦肯野细胞的电压门控离子通道和突触整合
基本信息
- 批准号:7993041
- 负责人:
- 金额:$ 4.18万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2009
- 资助国家:美国
- 起止时间:2009-01-13 至 2012-01-12
- 项目状态:已结题
- 来源:
- 关键词:AtaxiaCalcium SpikesCellsCerebellar cortex structureCerebellumDendritesDiseaseElectrophysiology (science)EquilibriumExhibitsGated Ion ChannelGlutamatesGoalsHereditary DiseaseIndividualInvestigationMembrane ProteinsMonitorMotorMovementNatureNeuronsOutputPharmacologyPhysiologicalPosturePreparationProcessPropertyPurkinje CellsRattusResearchRoleShapesSliceStimulusSymptomsSynapsesSynaptic PotentialsTestingToxinType 2 Spinocerebellar AtaxiaWorkdefined contributionextracellulargranule cellinterestneuroregulationpatch clamppresynapticresearch studyresponsevoltagevoltage gated channel
项目摘要
DESCRIPTION (provided by applicant): The role of voltage-gated channels in shaping synaptic integration in cerebellar Purkinje cells is little understood. Examination of their functional properties and interactions is of critical interest since many debilitating hereditary diseases presenting cerebellar symptoms, including episodic ataxia types 1 (EA1) and 2 (EA2), and spinocerebellar ataxia type 6 (SCA6), are disorders of these membrane proteins. The overall goal of this research plan is to define the contributions of select voltage-gated conductances to the integration of excitatory synaptic inputs by Purkinje cells. Purkinje cells integrate a massive convergence of excitatory and inhibitory inputs and are the sole output of the cerebellar cortex. They are thus the main computational units of the cerebellum, ultimately enabling proper motor coordination, posture, and balance. Prior work in the lab established that Purkinje cells linearly encode the strength of their presynaptic glutamatergic granule cell inputs in their maximum post-stimulus firing rate. This was surprising considering that Purkinje cells exhibit active dendritic calcium spikes brought about by various dendritic voltage-gated conductances, which are inherently nonlinear. How is the activity of voltage-gated channels in Purkinje cells choreographed to allow for the linear summation of their granule cell inputs? We propose two aims to begin answering this question: 1) To noninvasively assess the contribution of select voltage-gated ion channels to the granule cell input-Purkinje cell output function; and 2) To test the hypothesis that active dendritic conductances are balanced to achieve the linear granule cell input-Purkinje cell output relationship. We will accomplish this through experiments combining extracellular and whole-cell patch clamp electrophysiology, glutamate uncaging, and pharmacology applied to a rat cerebellar slice preparation. These investigations are not only crucial to understanding neural control of movement and the mechanisms underlying ataxia, but also will help elucidate neuronal computational processes in general.
描述(由申请人提供):电压门控通道在小脑浦肯野细胞中形成突触整合的作用尚不清楚。检查其功能特性和相互作用是至关重要的,因为许多衰弱的遗传性疾病,小脑症状,包括发作性共济失调1型(EA 1)和2型(EA 2),脊髓小脑共济失调6型(SCA 6),这些膜蛋白的疾病。本研究计划的总体目标是确定选择电压门控电导的贡献,兴奋性突触输入浦肯野细胞的整合。浦肯野细胞整合了大量的兴奋性和抑制性输入,是小脑皮质的唯一输出。因此,它们是小脑的主要计算单位,最终使适当的运动协调,姿势和平衡。实验室先前的工作确定,浦肯野细胞在其最大刺激后放电率中线性编码其突触前神经元能颗粒细胞输入的强度。考虑到浦肯野细胞表现出由各种树突电压门控电导引起的活性树突钙尖峰,这是令人惊讶的,所述树突电压门控电导本质上是非线性的。浦肯野细胞中电压门控通道的活动是如何被编排以允许其颗粒细胞输入的线性总和的?我们提出了两个目标开始回答这个问题:1)非侵入性评估选择电压门控离子通道的颗粒细胞输入-浦肯野细胞输出功能的贡献;和2)测试的假设,活性树突状细胞电导平衡,以实现线性颗粒细胞输入-浦肯野细胞输出关系。我们将通过结合细胞外和全细胞膜片钳电生理学、谷氨酸释放和应用于大鼠小脑切片制备的药理学的实验来实现这一点。这些研究不仅对于理解运动的神经控制和共济失调的潜在机制至关重要,而且还将有助于阐明一般的神经元计算过程。
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)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Maria-Johanna Dizon其他文献
Maria-Johanna Dizon的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Maria-Johanna Dizon', 18)}}的其他基金
Voltage-gated ion channels and synaptic integration by cerebellar Purkinje cells
小脑浦肯野细胞的电压门控离子通道和突触整合
- 批准号:
7616380 - 财政年份:2009
- 资助金额:
$ 4.18万 - 项目类别:
Voltage-gated ion channels and synaptic integration by cerebellar Purkinje cells
小脑浦肯野细胞的电压门控离子通道和突触整合
- 批准号:
7795864 - 财政年份:2009
- 资助金额:
$ 4.18万 - 项目类别:
相似海外基金
Intracellular calcium spikes trigger cytoskeletal reorganization, adhesion and migration
细胞内钙峰值触发细胞骨架重组、粘附和迁移
- 批准号:
RGPIN-2014-05064 - 财政年份:2018
- 资助金额:
$ 4.18万 - 项目类别:
Discovery Grants Program - Individual
Intracellular calcium spikes trigger cytoskeletal reorganization, adhesion and migration
细胞内钙峰值触发细胞骨架重组、粘附和迁移
- 批准号:
RGPIN-2014-05064 - 财政年份:2017
- 资助金额:
$ 4.18万 - 项目类别:
Discovery Grants Program - Individual
Intracellular calcium spikes trigger cytoskeletal reorganization, adhesion and migration
细胞内钙峰值触发细胞骨架重组、粘附和迁移
- 批准号:
RGPIN-2014-05064 - 财政年份:2016
- 资助金额:
$ 4.18万 - 项目类别:
Discovery Grants Program - Individual
Intracellular calcium spikes trigger cytoskeletal reorganization, adhesion and migration
细胞内钙峰值触发细胞骨架重组、粘附和迁移
- 批准号:
RGPIN-2014-05064 - 财政年份:2015
- 资助金额:
$ 4.18万 - 项目类别:
Discovery Grants Program - Individual
Intracellular calcium spikes trigger cytoskeletal reorganization, adhesion and migration
细胞内钙峰值触发细胞骨架重组、粘附和迁移
- 批准号:
RGPIN-2014-05064 - 财政年份:2014
- 资助金额:
$ 4.18万 - 项目类别:
Discovery Grants Program - Individual