Eulenburg Volker, Armsen Wencke, Betz Heinrich, Gomeza Jesús
Department of Neurochemistry, Max-Planck-Institute for Brain Research, Deutschordenstrasse 46, 60528 Frankfurt, Germany.
Trends Biochem Sci. 2005 Jun;30(6):325-33. doi: 10.1016/j.tibs.2005.04.004.
Glycine has important neurotransmitter functions at inhibitory and excitatory synapses in the vertebrate central nervous system. The effective synaptic concentrations of glycine are regulated by glycine transporters (GlyTs), which mediate its reuptake into nerve terminals and adjacent glial cells. GlyTs are members of the Na(+)/Cl(-)-dependent transporter family, whose activities and subcellular distributions are regulated by phosphorylation and interactions with other proteins. The analysis of GlyT knockout mice has revealed distinct functions of individual GlyT subtypes in synaptic transmission and provided animal models for two hereditary human diseases, glycine encephalopathy and hyperekplexia. Selective GlyT inhibitors could be of therapeutic value in cognitive disorders, schizophrenia and pain.
甘氨酸在脊椎动物中枢神经系统的抑制性和兴奋性突触中具有重要的神经递质功能。甘氨酸的有效突触浓度由甘氨酸转运体(GlyTs)调节,GlyTs介导其重新摄取到神经末梢和相邻的神经胶质细胞中。GlyTs是Na(+)/Cl(-)依赖性转运体家族的成员,其活性和亚细胞分布受磷酸化以及与其他蛋白质相互作用的调节。对GlyT基因敲除小鼠的分析揭示了各个GlyT亚型在突触传递中的不同功能,并为两种人类遗传性疾病——甘氨酸脑病和惊跳症提供了动物模型。选择性GlyT抑制剂在认知障碍、精神分裂症和疼痛方面可能具有治疗价值。