NMDA receptor-mediated excitation and inhibition balance is required for somatosensory development and maturation
NMDA receptor-mediated excitation and inhibition balance is required for somatosensory development and maturation
批准号:
24790187
负责人:
YAMASAKI Miwako
金额:
$2.91万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Young Scientists (B)
财政年份:
2012
资助国家:
日本
项目状态:
已结题
起止时间:
2012-04-01 至 2014-03-31
中文摘要
在本研究中,我们比较了GluN 2B和GluN 2D在桶发育中的功能作用。与对照组相比,GluN 2B +/-小鼠体感皮层中胡须相关图案的出现和关键期可塑性(CPP)的终止均延迟了近一天,但GluN 2D-/-小鼠提前了近一天。在两种小鼠的三叉神经通路的皮层下中继站也发现了类似的时间转移。相比之下,两种小鼠的桶皮质中的CPP的幅度是正常的。因此,GluN 2B和GluN 2D在桶的时间发育和成熟中起反作用,而不影响CPP的大小。在各中继站,谷氨酸能神经元突触中GluN 2B占优势,而GABA能神经元突触中GluN 2D则有选择性。总之,这些结果表明,谷氨酸能神经元中表达的GluN 2B促进体感发育,而GABA能神经元中表达的GluN 2D延迟体感发育。
英文摘要
In the present study, we compared functional roles of GluN2B and GluN2D in barrel development. Compared to control littermates, both the appearance of whisker-related patterning and the termination of critical period plasticity (CPP) were delayed by nearly a day in the somatosensory cortex of GluN2B+/- mice, but advanced by nearly a day in GluN2D-/- mice. Similar temporal shifts were also found at subcortical relay stations of the trigeminal pathway in both mice. By contrast, the magnitude of CPP in the barrel cortex was normal in both mice. Thus, GluN2B and GluN2D play counteractive roles in temporal development and maturation of barrels without affecting the magnitude of CPP. At each relay station, GluN2B was predominant at synapses of glutamatergic neurons while GluN2D was selective in GABAergic neurons. Taken together, these results indicate that GluN2B expressed in glutamatergic neurons facilitates somatosensory development, whereas GluN2D expressed in GABAergic neurons delays it.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
登录
查看更多内容
DOI:
10.1016/j.neuron.2013.02.031
发表时间:
2013-05-22
期刊:
Neuron
影响因子:
16.2
作者:
[Yan D, Yamasaki M, Straub C, Watanabe M, Tomita S]
通讯作者:
Tomita S
海馬CA1におけるAMPA受容体配分格差の分子機構Molecular determinants underlying heterogeneity in AMPAR content across CA1 Schaffer collateral synapses
CA1 Schaffer 侧支突触 AMPAR 含量异质性的分子决定因素
DOI:
--
发表时间:
2012
期刊:
影响因子:
--
作者:
[山崎美和子, 深谷昌弘, 山崎真弥, 阿部学, 畦地裕統, 崎村建司, 渡辺雅彦]
通讯作者:
渡辺雅彦
DOI:
10.1016/j.neuron.2013.03.031
发表时间:
2013-06-05
期刊:
NEURON
影响因子:
16.2
作者:
[Hoshina, Naosuke, Tanimura, Asami, Yamamoto, Tadashi]
通讯作者:
Yamamoto, Tadashi
海馬CA1領域におけるAMPA型グルタミン酸受容体の分配格差とその分子機構
海马CA1区AMPA型谷氨酸受体的差异分布及其分子机制
DOI:
--
发表时间:
2014
期刊:
影响因子:
--
作者:
[山崎美和子]
通讯作者:
山崎美和子
Molecular determinants underlying heterogeneity in AMPAR content across CA1 Schaffer collateral synapses
CA1 Schaffer 侧支突触 AMPAR 含量异质性的分子决定因素
DOI:
--
发表时间:
2015
期刊:
影响因子:
--
作者:
[Yamasaki M, Fukaya M, Yamazaki M, Azechi H, Natsume R, Abe M, Sakimura K, Watanabe M]
通讯作者:
Watanabe M
共 9 条
Surplus CF synapse elimination requires mGluR1-dependent CF synapse strengthening
-
批准号:19700285
-
项目类别:Grant-in-Aid for Young Scientists (B)
-
资助金额:$2.36万
-
财政年份:2007
-
负责人:YAMASAKI Miwako
-
依托单位:
海外基金