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首页> 外文期刊>Neuroscience Research: The Official Journal of the Japan Neuroscience Society >Facilitated activation of metabotropic glutamate receptors in cerebellar Purkinje cells in glutamate transporter EAAT4-deficient mice.
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Facilitated activation of metabotropic glutamate receptors in cerebellar Purkinje cells in glutamate transporter EAAT4-deficient mice.

机译:促进谷氨酸转运蛋白EAAT4缺陷小鼠小脑浦肯野细胞中代谢型谷氨酸受体的激活。

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摘要

Around excitatory synapses in cerebellar Purkinje cells (PCs), GLAST and EAAT4 are expressed as predominant glial and neuronal glutamate transporters, respectively. EAAC1, another subtype of neuronal glutamate transporter, is also expressed in PCs. EAAT4 is co-localized with metabotropic glutamate receptors (mGluRs) at perisynaptic sites in excitatory synapses in PCs, and this neuronal transporter was reported to be involved in the regulation of mGluR activation induced by the stimulation of parallel fibers (PFs). However, it remains to be elucidated whether only EAAT4 is specifically involved in mGluR activation among the glutamate transporters expressed near excitatory synapses in PCs. Here we examined mGluR-mediated excitatory postsynaptic currents (mGluR-EPSCs) evoked by PF stimulation in cerebellar slices of mice deficient in EAAT4, EAAC1, or GLAST. PF-evoked mGluR-EPSCs showed larger amplitude and faster rising kinetics in EAAT4-deficient mice than in the wild-type mice. In contrast, there was nosignificant difference in either the amplitude or the rising kinetics of mGluR-EPSCs in GLAST- or EAAC1-deficient mice compared to wild-type mice. We conclude that EAAT4 is most closely involved in mGluR activation in PCs among the glutamate transporters.
机译:小脑浦肯野细胞(PCs)的兴奋性突触周围,GLAST和EAAT4分别表示为主要的神经胶质和谷氨酸转运蛋白。 EAAC1,神经元谷氨酸转运蛋白的另一种亚型,也在PC中表达。 EAAT4与代谢型谷氨酸受体(mGluRs)共同定位在PC兴奋性突触的突触周围位点上,据报道该神经元转运蛋白参与了对平行纤维(PFs)的刺激诱导的mGluR激活的调节。但是,尚需阐明在PCs兴奋性突触附近表达的谷氨酸转运蛋白中,是否只有EAAT4专门参与了mGluR激活。在这里,我们检查了在EAAT4,EAAC1或GLAST缺乏的小鼠小脑切片中PF刺激引起的mGluR介导的兴奋性突触后电流(mGluR-EPSCs)。与野生型小鼠相比,PF诱发的mGluR-EPSC在EAAT4缺陷型小鼠中显示出更大的振幅和更快的上升动力学。相反,与野生型小鼠相比,在GLAST或EAAC1缺陷型小鼠中,mGluR-EPSC的振幅或上升动力学没有显着差异。我们得出的结论是,EAAT4与谷氨酸转运蛋白中PC中的mGluR激活最密切相关。

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