The Physiology of Extra Synaptic NMDA Receptors

突触外 NMDA 受体的生理学

基本信息

项目摘要

DESCRIPTION (provided by applicant): N-methyl-D-aspartate receptor (NMDAR) activation can result in both long and short-term plasticity, promote cell survival, initiate cell death, and is also critical for normal synaptogenesis during development. A number of studies suggest that the consequences of NMDAR activation can vary widely depending on receptor localization, temporal characteristics, and size of the signal (Bito et al., 1996; Fields et al., 1997; Hardingham et al., 1999; Chawla and Bading, 2001; Hardingham et al., 2001a, b). The focus of this study is the physiological role of extrasynaptic vs. synaptic NMDARs. Cultured neuron studies have suggested that NMDARs can exist as synaptic NR1/NR2A heteromers and extrasynaptic NR1/NR2B heteromers. These two receptor types may be coupled to very different cellular processes, with calcium entry through extrasynaptic NMDARs activating cell death mechanisms and LTD rather than LTP (Lu et al., 2001; Hardingham et al., 2002). Although these experiments have provided valuable clues about possible spatial and functional segregation of extrasynaptic NMDARs in neurons, the existence and physiological relevance of these receptors in intact tissue remains unclear. Our preliminary results, which are significantly different from culture measurements, suggest that approximately 40% of the NMDAR population is extrasynaptic in acute hippocampal slice dendrites. This indicates that there is a large pool of extrasynaptic receptors available for activation during periods of high presynaptic activity. Our underlying hypothesis is that extrasynaptic NMDARs participate in neuronal interactions under pathological and physiologically relevant conditions. This hypothesis will be tested by determining the size of the extrasynaptic NMDAR pool, subunit composition, and developmental expression in acute hippocampal brain slices. We will determine the conditions under which extrasynaptic receptors can participate in transmission and their role in the expression of long-term potentiation or depression.
描述(由申请人提供):n -甲基- d -天冬氨酸受体(NMDAR)激活可导致长期和短期可塑性,促进细胞存活,启动细胞死亡,对发育过程中正常的突触发生也至关重要。许多研究表明,NMDAR激活的后果可能因受体定位、时间特征和信号大小而有很大差异(Bito等人,1996;Fields等人,1997;Hardingham等人,1999;Chawla和Bading, 2001; Hardingham等人,2001a, b)。本研究的重点是突触外与突触内NMDARs的生理作用。培养神经元研究表明,NMDARs可以作为突触内NR1/NR2A异构体和突触外NR1/NR2B异构体存在。这两种受体可能与非常不同的细胞过程耦合,钙通过突触外NMDARs进入激活细胞死亡机制和LTD而不是LTP (Lu et al., 2001; Hardingham et al., 2002)。尽管这些实验为神经元中突触外NMDARs可能的空间和功能分离提供了有价值的线索,但这些受体在完整组织中的存在及其生理相关性仍不清楚。我们的初步结果与培养测量结果有很大不同,表明大约40%的NMDAR在急性海马切片树突中是突触外的。这表明在高突触前活动期间,有大量的突触外受体可被激活。我们的基本假设是突触外NMDARs在病理和生理相关条件下参与神经元相互作用。这一假设将通过确定急性海马脑切片中突触外NMDAR库的大小、亚基组成和发育表达来验证。我们将确定突触外受体参与传递的条件及其在长时程增强或抑制表达中的作用。

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 }}

DIANA Leslie PETTIT其他文献

DIANA Leslie PETTIT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('DIANA Leslie PETTIT', 18)}}的其他基金

Inhibitory Microcircuits in the Piriform Cortex
梨状皮层的抑制微电路
  • 批准号:
    8112514
  • 财政年份:
    2010
  • 资助金额:
    $ 18.67万
  • 项目类别:
Inhibitory Microcircuits in the Piriform Cortex
梨状皮层的抑制微电路
  • 批准号:
    7991093
  • 财政年份:
    2010
  • 资助金额:
    $ 18.67万
  • 项目类别:
The Physiology of Extra Synaptic NMDA Receptors
突触外 NMDA 受体的生理学
  • 批准号:
    7244067
  • 财政年份:
    2006
  • 资助金额:
    $ 18.67万
  • 项目类别:
Kainate Receptors in Synaptic Transmission
突触传递中的红藻氨酸受体
  • 批准号:
    6925015
  • 财政年份:
    2005
  • 资助金额:
    $ 18.67万
  • 项目类别:
Kainate Receptors in Synaptic Transmission
突触传递中的红藻氨酸受体
  • 批准号:
    7406671
  • 财政年份:
    2005
  • 资助金额:
    $ 18.67万
  • 项目类别:
Kainate Receptors in Synaptic Transmission
突触传递中的红藻氨酸受体
  • 批准号:
    7017687
  • 财政年份:
    2005
  • 资助金额:
    $ 18.67万
  • 项目类别:
Kainate Receptors in Synaptic Transmission
突触传递中的红藻氨酸受体
  • 批准号:
    7217913
  • 财政年份:
    2005
  • 资助金额:
    $ 18.67万
  • 项目类别:
MICROMAPPING OF LEAD INDUCED CHANGES TO NMDA RECEPTORS
铅引起的 NMDA 受体变化的微图谱
  • 批准号:
    6658035
  • 财政年份:
    2001
  • 资助金额:
    $ 18.67万
  • 项目类别:
MICROMAPPING OF LEAD INDUCED CHANGES TO NMDA RECEPTORS
铅引起的 NMDA 受体变化的微图谱
  • 批准号:
    6132592
  • 财政年份:
    2001
  • 资助金额:
    $ 18.67万
  • 项目类别:
MICROMAPPING OF LEAD INDUCED CHANGES TO NMDA RECEPTORS
铅引起的 NMDA 受体变化的微图谱
  • 批准号:
    6524699
  • 财政年份:
    2001
  • 资助金额:
    $ 18.67万
  • 项目类别:

相似海外基金

Molecular Physiology of NMDA Receptors
NMDA 受体的分子生理学
  • 批准号:
    10665371
  • 财政年份:
    2023
  • 资助金额:
    $ 18.67万
  • 项目类别:
Physiology and pharmacology of GluN3-containing NMDA receptors
含 GluN3 的 NMDA 受体的生理学和药理学
  • 批准号:
    10531915
  • 财政年份:
    2021
  • 资助金额:
    $ 18.67万
  • 项目类别:
Physiology and pharmacology of GluN3-containing NMDA receptors
含 GluN3 的 NMDA 受体的生理学和药理学
  • 批准号:
    10360476
  • 财政年份:
    2021
  • 资助金额:
    $ 18.67万
  • 项目类别:
Ca2+-Dependent Block by Mematine and Selective Inhibition of Overactive NMDA Receptors
Mematine 的 Ca2 依赖性阻断和过度活跃的 NMDA 受体的选择性抑制
  • 批准号:
    10622606
  • 财政年份:
    2020
  • 资助金额:
    $ 18.67万
  • 项目类别:
Ca2+-Dependent Block by Mematine and Selective Inhibition of Overactive NMDA Receptors
Mematine 的 Ca2 依赖性阻断和过度活跃的 NMDA 受体的选择性抑制
  • 批准号:
    10835208
  • 财政年份:
    2020
  • 资助金额:
    $ 18.67万
  • 项目类别:
Ca2+-Dependent Block by Mematine and Selective Inhibition of Overactive NMDA Receptors
Mematine 的 Ca2 依赖性阻断和过度活跃的 NMDA 受体的选择性抑制
  • 批准号:
    10260592
  • 财政年份:
    2020
  • 资助金额:
    $ 18.67万
  • 项目类别:
Ca2+-Dependent Block by Mematine and Selective Inhibition of Overactive NMDA Receptors
Mematine 的 Ca2 依赖性阻断和过度活跃的 NMDA 受体的选择性抑制
  • 批准号:
    10410546
  • 财政年份:
    2020
  • 资助金额:
    $ 18.67万
  • 项目类别:
Molecular and functional diversity of NMDA receptors in the thalamus
丘脑 NMDA 受体的分子和功能多样性
  • 批准号:
    9903474
  • 财政年份:
    2019
  • 资助金额:
    $ 18.67万
  • 项目类别:
Molecular and functional diversity of NMDA receptors in the thalamus
丘脑 NMDA 受体的分子和功能多样性
  • 批准号:
    10593091
  • 财政年份:
    2019
  • 资助金额:
    $ 18.67万
  • 项目类别:
Molecular and functional diversity of NMDA receptors in the thalamus
丘脑 NMDA 受体的分子和功能多样性
  • 批准号:
    10373037
  • 财政年份:
    2019
  • 资助金额:
    $ 18.67万
  • 项目类别:
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了