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DESCRIPTION (provided by applicant): Voltage-gated calcium (Ca2+) channels play a central role in neuronal function and are essential for converting electrical activity into biochemical events. The main goal of this proposal is to identify the molecular mechanisms by which voltage-gated calcium channels activate signaling cascades that mediate gene expression and promote neuronal survival. Neurons and muscle cells express at least ten different kinds of voltage-gated calcium channels that vary in their subcellular localization and biophysical properties. L-type channels (LTCs) are particularly effective at activating transcriptional pathways and at promoting neuronal survival. The transcription factors CREB and MEF-2 are two important targets of LTC signaling that regulate differentiation and plasticity in the nervous system. The biophysical and biochemical features that allow LTCs to activate gene expression and suppress apoptosis are not well understood. To address the question of how LTCs are linked to signaling pathways the following specific aims are proposed: 1) To determine the structural and biophysical features that allow L-type calcium channels to activate transcription. 2) To determine whether specific L-type channel interacting proteins link the channel to signaling pathways that lead to the activation of transcription. 3) To determine what features of L-type calcium channels allow them to inhibit neuronal apoptosis and promote survival. Biochemical, cell biological and electrophysiological techniques will be used to develop these specific aims. We have recently developed a method of using dihydropyridine insensitive LTCs to investigate LTC signaling in primary neurons and we plan to use this approach for these studies. We have also identified several LTC-interacting proteins that may be important for channel regulation and signaling and we plan to investigate their importance for signaling to the nucleus. The results of these experiments will provide critical insights into how voltage-gated channels activate the signaling pathways that regulate the structure and function of the nervous system.
期刊论文(8)
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会议论文
DOI: 10.1371/journal.pone.0060526
发表时间: 2013
期刊: PloS one
影响因子: 3.7
作者: [Gomez-Ospina N, Panagiotakos G, Portmann T, Pasca SP, Rabah D, Budzillo A, Kinet JP, Dolmetsch RE]
通讯作者: Dolmetsch RE
PIKfyve regulates CaV1.2 degradation and prevents excitotoxic cell death.
PIKfyve 调节 CaV1.2 降解并防止兴奋毒性细胞死亡。
DOI: 10.1083/jcb.200903028
发表时间: 2009-10-19
期刊: The Journal of cell biology
影响因子: --
作者: [Tsuruta F, Green EM, Rousset M, Dolmetsch RE]
通讯作者: Dolmetsch RE
DOI: 10.1371/journal.pone.0000802
发表时间: 2007-08-29
期刊: PloS one
影响因子: 3.7
作者: [Brenner JS, Dolmetsch RE]
通讯作者: Dolmetsch RE
PIKfyve mediates the motility of late endosomes and lysosomes in neuronal dendrites.
PIKfyve 介导神经元树突中晚期内体和溶酶体的运动。
DOI: 10.1016/j.neulet.2015.07.021
发表时间: 2015
期刊: Neuroscience letters
影响因子: 2.5
作者: [Tsuruta,Fuminori, Dolmetsch,RicardoE]
通讯作者: Dolmetsch,RicardoE
Exploring the Neuronal Phenotype of Autism Spectrum Disorders Using Induced Pluri
  • 批准号:
    8609683
  • 项目类别:
  • 资助金额:
    $18.04万
  • 财政年份:
    2009
  • 负责人:
    Ricardo E. Dolmetsch
  • 依托单位:
Exploring the Neuronal Phenotype of Autism Spectrum Disorders Using Induced Pluri
  • 批准号:
    8321078
  • 项目类别:
  • 资助金额:
    $36.65万
  • 财政年份:
    2009
  • 负责人:
    Ricardo E. Dolmetsch
  • 依托单位:
Exploring the Neuronal Phenotype of Autism Spectrum Disorders Using Induced Pluri
  • 批准号:
    8206064
  • 项目类别:
  • 资助金额:
    $36.85万
  • 财政年份:
    2009
  • 负责人:
    Ricardo E. Dolmetsch
  • 依托单位:
Exploring the Neuronal Phenotype of Autism Spectrum Disorders Using Induced Pluri
  • 批准号:
    7939753
  • 项目类别:
  • 资助金额:
    $24.15万
  • 财政年份:
    2009
  • 负责人:
    Ricardo E. Dolmetsch
  • 依托单位:
国内基金
海外基金
Epac1/2通过蛋白酶体调控中性粒细胞NETosis和Apoptosis在急性肺损伤中的作用研究
  • 批准号:
    LBY21H010001
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2020
  • 负责人:
    郑绪阳
  • 依托单位:
基于Apoptosis/Ferroptosis双重激活效应的天然产物AlbiziabiosideA的抗肿瘤作用机制研究及其结构改造
  • 批准号:
    81703335
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    20.0万元
  • 批准年份:
    2017
  • 负责人:
    卫高菲
  • 依托单位:
双肝移植后Apoptosis和pyroptosis在移植物萎缩差异中的作用和供受者免疫微环境变化研究
  • 批准号:
    81670594
  • 项目类别:
    面上项目
  • 资助金额:
    58.0万元
  • 批准年份:
    2016
  • 负责人:
    陈昊
  • 依托单位:
Serp-2 调控apoptosis和pyroptosis 对肝脏缺血再灌注损伤的保护作用研究
  • 批准号:
    81470791
  • 项目类别:
    面上项目
  • 资助金额:
    73.0万元
  • 批准年份:
    2014
  • 负责人:
    董家鸿
  • 依托单位: