Lu Wei, Bromley-Coolidge Samantha, Li Jun
Synapse and Neural Circuit Research Unit, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.
Synapse and Neural Circuit Research Unit, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.
Brain Res Bull. 2017 Mar;129:30-42. doi: 10.1016/j.brainresbull.2016.07.004. Epub 2016 Jul 21.
In the adult mammalian brain, GABAergic neurotransmission provides the majority of synaptic inhibition that balances glutamatergic excitatory drive and thereby controls neuronal output. It is generally accepted that synaptogenesis is initiated through highly specific protein-protein interactions mediated by membrane proteins expressed in developing presynaptic terminals and postsynaptic membranes. Accumulating studies have uncovered a number of membrane proteins that regulate different aspects of GABAergic synapse development. In this review, we summarize recent advances in understanding of GABAergic synapse development with a focus on postsynaptic membrane molecules, including receptors, synaptogenic cell adhesion molecules and immunoglobulin superfamily proteins.
在成年哺乳动物大脑中,γ-氨基丁酸(GABA)能神经传递提供了大部分的突触抑制,这种抑制平衡了谷氨酸能兴奋性驱动,从而控制神经元输出。人们普遍认为,突触发生是通过发育中的突触前终末和突触后膜中表达的膜蛋白介导的高度特异性蛋白质-蛋白质相互作用而启动的。越来越多的研究发现了许多调节GABA能突触发育不同方面的膜蛋白。在本综述中,我们总结了对GABA能突触发育理解的最新进展,重点关注突触后膜分子,包括受体、促突触形成的细胞粘附分子和免疫球蛋白超家族蛋白。