Division of Biological Science, Graduate School of Science, Nagoya University, Nagoya, 464-8602, Japan.
Genes Cells. 2013 Mar;18(3):211-24. doi: 10.1111/gtc.12032. Epub 2013 Jan 25.
Synaptic transmission-dependent regulation of neurotransmitter receptor accumulation at postsynaptic sites underlies the formation, maintenance and maturation of synaptic function. Previous in vitro studies showed that glycine receptor (GlyR) clustering requires synaptic inputs. However, in vivo GlyR regulation by synaptic transmission is not fully understood. Here, we established a model system using developing zebrafish, in which GlyRs are expressed in Mauthner cells (M-cells), a pair of giant, reticulospinal, hindbrain neurons, thereby enabling analysis of GlyR clusters over time in identifiable cells. Bath application of a glycinergic blocker, strychnine, to developing zebrafish prevented postsynaptic GlyR cluster formation in the M-cells. After strychnine removal, the GlyR clusters appeared in the M-cells. At a later stage, glycinergic transmission blockade impaired maintenance of GlyR clusters. We also found that pharmacological blockade of either L-type Ca(2+) channels or calcium-/calmodulin-dependent protein kinase II (CaMKII) disturbed GlyR clustering. In addition, the M-cell-specific CaMKII inactivation using the Gal4-UAS system significantly impaired GlyR clustering in the M-cells. Thus, the formation and maintenance of GlyR clusters in the M-cells in the developing animals are regulated in a synaptic transmission-dependent manner, and CaMKII activation at the postsynapse is essential for GlyR clustering. This is the first demonstration of synaptic transmission-dependent modulation of synaptic GlyRs in vivo.
突触传递依赖性调节神经递质受体在突触后部位的聚集是突触功能形成、维持和成熟的基础。先前的体外研究表明甘氨酸受体 (GlyR) 的聚集需要突触输入。然而,体内突触传递对 GlyR 的调节还不完全清楚。在这里,我们使用发育中的斑马鱼建立了一个模型系统,其中 GlyRs 在 Mauthner 细胞 (M-cells) 中表达,M-cells 是一对巨大的、网状的、后脑神经元,从而能够在可识别的细胞中随时间分析 GlyR 簇。将甘氨酸能阻滞剂士的宁应用于发育中的斑马鱼可防止 M-cells 中的突触后 GlyR 簇形成。士的宁去除后,GlyR 簇出现在 M-cells 中。在稍后的阶段,甘氨酸能传递的阻断会损害 GlyR 簇的维持。我们还发现,L 型钙 (Ca 2+ ) 通道或钙/钙调蛋白依赖性蛋白激酶 II (CaMKII) 的药理学阻断会干扰 GlyR 聚集。此外,使用 Gal4-UAS 系统特异性地使 M 细胞中的 CaMKII 失活,会显著损害 M 细胞中的 GlyR 聚集。因此,发育中动物 M 细胞中的 GlyR 簇的形成和维持受突触传递依赖性调节,而突触后 CaMKII 的激活对于 GlyR 聚集是必需的。这是体内突触传递依赖性调节突触 GlyRs 的首次证明。