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climbing fiber 介导的向中间神经元的溢出传递受 EAAT4 调节。

Climbing Fiber-Mediated Spillover Transmission to Interneurons Is Regulated by EAAT4.

机构信息

Department of Neurobiology and McKnight Brain Institute, University of Alabama at Birmingham, Birmingham, Alabama 35294.

Department of Systems Neurophysiology, Tokyo Medical and Dental University Graduate School of Medical and Dental Sciences, Tokyo, 113-8519, Japan.

出版信息

J Neurosci. 2021 Sep 29;41(39):8126-8133. doi: 10.1523/JNEUROSCI.0616-21.2021. Epub 2021 Aug 16.

Abstract

Neurotransmitter spillover is a form of communication not readily predicted by anatomic structure. In the cerebellum, glutamate spillover from climbing fibers recruits molecular layer interneurons in the absence of conventional synaptic connections. Spillover-mediated signaling is typically limited by transporters that bind and reuptake glutamate. Here, we show that patterned expression of the excitatory amino acid transporter 4 (EAAT4) in Purkinje cells regulates glutamate spillover to molecular layer interneurons. Using male and female Aldolase C-Venus knock-in mice to visualize zebrin microzones, we find larger climbing fiber-evoked spillover EPSCs in regions with low levels of EAAT4 compared with regions with high EAAT4. This difference is not explained by presynaptic glutamate release properties or postsynaptic receptor density but rather by differences in the glutamate concentration reaching receptors on interneurons. Inhibiting glutamate transport normalizes the differences between microzones, suggesting that heterogeneity in EAAT4 expression is a primary determinant of differential spillover. These results show that neuronal glutamate transporters limit extrasynaptic transmission in a non-cell-autonomous manner and provide new insight into the functional specialization of cerebellar microzones. Excitatory amino acid transporters (EAATs) help maintain the fidelity and independence of point-to-point synaptic transmission. Whereas glial transporters are critical to maintain low ambient levels of extracellular glutamate to prevent excitotoxicity, neuronal transporters have more subtle roles in shaping excitatory synaptic transmission. Here we show that the patterned expression of neuronal EAAT4 in cerebellar microzones controls glutamate spillover from cerebellar climbing fibers to nearby interneurons. These results contribute to fundamental understanding of neuronal transporter functions and specialization of cerebellar microzones.

摘要

神经递质溢出是一种不易通过解剖结构预测的通讯形式。在小脑,来自 climbing fibers 的谷氨酸溢出会在没有传统突触连接的情况下招募分子层中间神经元。溢出介导的信号传递通常受到结合并重新摄取谷氨酸的转运体限制。在这里,我们表明,兴奋性氨基酸转运体 4 (EAAT4) 在浦肯野细胞中的模式表达调节谷氨酸对分子层中间神经元的溢出。使用雄性和雌性 Aldolase C-Venus 敲入小鼠来可视化 zebrin 微区,我们发现与 EAAT4 水平较高的区域相比,EAAT4 水平较低的区域中 climbing fiber 诱发的溢出 EPSC 较大。这种差异不能用突触前谷氨酸释放特性或突触后受体密度来解释,而是由到达中间神经元受体的谷氨酸浓度差异来解释。抑制谷氨酸转运使微区之间的差异正常化,这表明 EAAT4 表达的异质性是溢出差异的主要决定因素。这些结果表明神经元谷氨酸转运体以非细胞自主的方式限制了突触外传递,并为小脑微区的功能特化提供了新的见解。兴奋性氨基酸转运体 (EAATs) 有助于保持点对点突触传递的保真度和独立性。虽然胶质转运体对于维持低水平的细胞外谷氨酸以防止兴奋毒性至关重要,但神经元转运体在塑造兴奋性突触传递方面具有更微妙的作用。在这里,我们表明小脑微区中神经元 EAAT4 的模式表达控制来自小脑 climbing fibers 的谷氨酸溢出到附近的中间神经元。这些结果有助于理解神经元转运体的功能和小脑微区的特化。

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