首页> 美国卫生研究院文献>The Journal of Neuroscience >Functional Coupling between mGluR1 and Cav3.1 T-Type Calcium Channels Contributes to Parallel Fiber-Induced Fast Calcium Signaling within Purkinje Cell Dendritic Spines
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Functional Coupling between mGluR1 and Cav3.1 T-Type Calcium Channels Contributes to Parallel Fiber-Induced Fast Calcium Signaling within Purkinje Cell Dendritic Spines

机译:mGluR1和Cav3.1 T型钙通道之间的功能性耦合有助于浦肯野细胞树突棘内的平行纤维诱导的快速钙信号传导。

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摘要

T-type voltage-gated calcium channels are expressed in the dendrites of many neurons, although their functional interactions with postsynaptic receptors and contributions to synaptic signaling are not well understood. We combine electrophysiological and ultrafast two-photon calcium imaging to demonstrate that mGluR1 activation potentiates cerebellar Purkinje cell Cav3.1 T-type currents via a G-protein- and tyrosine-phosphatase-dependent pathway. Immunohistochemical and electron microscopic investigations on wild-type and Cav3.1 gene knock-out animals show that Cav3.1 T-type channels are preferentially expressed in Purkinje cell dendritic spines and colocalize with mGluR1s. We further demonstrate that parallel fiber stimulation induces fast subthreshold calcium signaling in dendritic spines and that the synaptic Cav3.1-mediated calcium transients are potentiated by mGluR1 selectively during bursts of excitatory parallel fiber inputs. Our data identify a new fast calcium signaling pathway in Purkinje cell dendritic spines triggered by short burst of parallel fiber inputs and mediated by T-type calcium channels and mGluR1s.
机译:T型电压门控钙通道在许多神经元的树突中表达,尽管它们与突触后受体的功能相互作用以及对突触信号的贡献尚不十分清楚。我们结合电生理学和超快的两光子钙成像,以证明mGluR1激活通过G蛋白和酪氨酸磷酸酶依赖性途径增强小脑Purkinje细胞Cav3.1 T型电流。对野生型和Cav3.1基因敲除动物的免疫组织化学和电子显微镜研究表明,Cav3.1 T型通道在Purkinje细胞树突棘中优先表达,并与mGluR1s共定位。我们进一步证明,平行纤维刺激在树突棘中诱导快速的亚阈值钙信号传导,并且在兴奋性平行纤维输入的爆发期间,mGluR1选择性地增强了突触Cav3.1介导的钙瞬变。我们的数据在浦肯野细胞树突棘中发现了一条新的快速钙信号传导途径,该信号由平行纤维输入的短脉冲触发并由T型钙通道和mGluR1s介导。

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