首页> 美国卫生研究院文献>PLoS Clinical Trials >Quantitative Organization of GABAergic Synapses in the Molecular Layer of the Mouse Cerebellar Cortex
【2h】

Quantitative Organization of GABAergic Synapses in the Molecular Layer of the Mouse Cerebellar Cortex

机译:小鼠小脑皮层分子层中GABA能突触的定量组织。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

In the cerebellar cortex, interneurons of the molecular layer (stellate and basket cells) provide GABAergic input to Purkinje cells, as well as to each other and possibly to other interneurons. GABAergic inhibition in the molecular layer has mainly been investigated at the interneuron to Purkinje cell synapse. In this study, we used complementary subtractive strategies to quantitatively assess the ratio of GABAergic synapses on Purkinje cell dendrites versus those on interneurons. We generated a mouse model in which the GABAA receptor α1 subunit (GABAARα1) was selectively removed from Purkinje cells using the Cre/loxP system. Deletion of the α1 subunit resulted in a complete loss of GABAAR aggregates from Purkinje cells, allowing us to determine the density of GABAAR clusters in interneurons. In a complementary approach, we determined the density of GABA synapses impinging on Purkinje cells using α-dystroglycan as a specific marker of inhibitory postsynaptic sites. Combining these inverse approaches, we found that synapses received by interneurons represent approximately 40% of all GABAergic synapses in the molecular layer. Notably, this proportion was stable during postnatal development, indicating synchronized synaptogenesis. Based on the pure quantity of GABAergic synapses onto interneurons, we propose that mutual inhibition must play an important, yet largely neglected, computational role in the cerebellar cortex.
机译:在小脑皮质中,分子层的中间神经元(星状和篮状细胞)为浦肯野细胞,彼此之间以及可能与其他中间神经元提供GABA能输入。主要在中间神经元对浦肯野细胞突触中研究了分子层中的GABA能抑制。在这项研究中,我们使用互补的消减策略来定量评估Purkinje细胞树突上的GABA能突触与中间神经元上的GABA能突触的比率。我们生成了一个小鼠模型,其中使用Cre / loxP系统从Purkinje细胞中选择性去除了GABAA受体α1亚基(GABAARα1)。 α1亚基的缺失导致浦肯野细胞的GABAAR聚集体完全丧失,这使我们能够确定中间神经元中GABAAR簇的密度。在一种补充方法中,我们使用α-dystroglycan作为抑制突触后位点的特定标记,确定了撞击Purkinje细胞的GABA突触的密度。结合这些逆方法,我们发现由中间神经元接收的突触约占分子层中所有GABA能突触的40%。值得注意的是,该比例在产后发育期间是稳定的,表明突触发生同步。基于纯净量的GABA能突触到神经元上,我们建议相互抑制必须在小脑皮质中发挥重要但很大程度上被忽略的计算作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号