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谷氨酸转运体的阻断促进小脑突触长时程抑制。

Blockade of glutamate transporters facilitates cerebellar synaptic long-term depression.

作者信息

Su Li-Da, Shen Ying

机构信息

Department of Neurobiology/Institute of Neuroscience, Key Laboratory of Medical Neurobiology of Ministry of Health of China, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.

出版信息

Neuroreport. 2009 Mar 25;20(5):502-7. doi: 10.1097/WNR.0b013e328328f397.

Abstract

Excitatory amino acid transporters (EAATs) are believed to limit extracellular glutamate concentrations with specific roles poorly understood. At cerebellar climbing fiber-Purkinje cell synapse, EAAT4 and metabotropic glutamate receptor 1 (mGluR1) are closely expressed in surrounding postsynaptic locations, suggesting that EAAT4 may regulate mGluR1 activation. We examined the actions of EAAT4 on synaptic plasticity by applying blockers of glutamate transporters, DL-threo-beta-benzyloxyaspartic acid and D-aspartate. Inhibition of EAAT4 markedly prolonged AMPA receptor-mediated excitatory postsynaptic currents evoked by stimulating climbing fibers. Impairing glutamate uptake facilitated mGluR1-dependent climbing fiber-Purkinje cell synaptic long-term depression (LTD). Glutamate uptake blockers also sufficiently rescued climbing fiber-Purkinje cell synaptic LTD that failed to be induced by a weaker tetanus. Our results suggest that neuronal glutamate transporters strongly influence mGluR1-dependent cerebellar LTD.

摘要

兴奋性氨基酸转运体(EAATs)被认为可限制细胞外谷氨酸浓度,但其具体作用尚不清楚。在小脑攀缘纤维-浦肯野细胞突触处,EAAT4和代谢型谷氨酸受体1(mGluR1)在周围突触后位置紧密表达,这表明EAAT4可能调节mGluR1的激活。我们通过应用谷氨酸转运体阻滞剂DL-苏式-β-苄氧基天冬氨酸和D-天冬氨酸来研究EAAT4对突触可塑性的作用。抑制EAAT4可显著延长刺激攀缘纤维诱发的AMPA受体介导的兴奋性突触后电流。损害谷氨酸摄取促进了mGluR1依赖的攀缘纤维-浦肯野细胞突触长时程抑制(LTD)。谷氨酸摄取阻滞剂也充分挽救了由较弱强直刺激未能诱导出的攀缘纤维-浦肯野细胞突触LTD。我们的结果表明,神经元谷氨酸转运体强烈影响mGluR1依赖的小脑LTD。

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