Kato-Negishi Midori, Muramoto Kazuyo, Kawahara Masahiro, Kuroda Yoichiro, Ichikawa Masumi
Laboratory of Anatomy and Cell Biology, Department of Basic Technique and Facilities, Tokyo Metropolitan Institute for Neuroscience, Tokyo Metropolitan Organization for Medical Research, 2-6 Musashi-dai, Fuchu, Tokyo 183-8526, Japan.
Brain Res Dev Brain Res. 2004 Sep 17;152(2):99-108. doi: 10.1016/j.devbrainres.2004.05.013.
The characteristics of functional changes of GABAergic synapses between cultured rat cortical neurons were observed by monitoring intracellular calcium level ([Ca2+]in) during development in vitro. After 5 days in vitro (DIV), cultured cortical neurons spontaneously exhibited synchronous oscillatory changes in [Ca2+]in, which were derived from synaptic activity. Exposure to bicuculline, antagonist of gamma-aminobutyric acid (GABA)(A) receptors, caused a marked decrease in the frequency of [Ca2+]in oscillations at 7-20 DIV. Although the frequency of spontaneous oscillations increased during this culture period, the ratio of the decrease in the frequency following bicuculline treatment did not significantly change. Thereafter, to investigate the detailed morphological changes of GABAergic synapses during development in vitro, the cultured neurons were immunostained with antibodies to glutamic acid decarboxylase (GAD), synaptophysin and GABA(A) receptor and were observed under a confocal laser microscope. Most of the GAD-positive puncta colocalized with synaptophysin-positive puncta and were opposed to GABA(A) receptor-positive structures. The images of GAD-positive puncta were reconstructed from the confocal three-dimensional data to analyze their number, volume, and surface area. The number of these puncta increased with culture time at 7-20 DIV. Although the volume of individual GAD-positive puncta did not significantly change, the surface area decreased in a time-dependent manner over the culture period. This system that we developed enabled us to investigate in detail the morphological and functional changes of GABAergic synapses during neuronal development.
通过监测体外培养大鼠皮质神经元发育过程中的细胞内钙水平([Ca2+]in),观察了γ-氨基丁酸(GABA)能突触功能变化的特征。体外培养5天(DIV)后,培养的皮质神经元自发地表现出[Ca2+]in的同步振荡变化,这些变化源于突触活动。暴露于γ-氨基丁酸(GABA)(A)受体拮抗剂荷包牡丹碱,导致7 - 20 DIV时[Ca2+]in振荡频率显著降低。尽管在此培养期间自发振荡频率增加,但荷包牡丹碱处理后频率降低的比例没有显著变化。此后,为了研究体外发育过程中GABA能突触的详细形态变化,用谷氨酸脱羧酶(GAD)、突触素和GABA(A)受体抗体对培养的神经元进行免疫染色,并在共聚焦激光显微镜下观察。大多数GAD阳性斑点与突触素阳性斑点共定位,并与GABA(A)受体阳性结构相对。从共聚焦三维数据重建GAD阳性斑点的图像,以分析其数量、体积和表面积。在7 - 20 DIV时,这些斑点的数量随培养时间增加。尽管单个GAD阳性斑点的体积没有显著变化,但在培养期间表面积以时间依赖的方式减小。我们开发的这个系统使我们能够详细研究神经元发育过程中GABA能突触的形态和功能变化。