Program in Cellular Neuroscience, Neurodegeneration and Repair (CNNR), Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, CT 06510, USA.
J Physiol. 2012 May 15;590(10):2217-23. doi: 10.1113/jphysiol.2011.221101. Epub 2012 Mar 19.
Kainate receptors (KARs) are a subfamily of ionotropic glutamate receptors (iGluRs) that mediate excitatory synaptic transmission, regulate neurotransmitter release, and show a remarkably selective distribution in the brain. Compared to other iGluRs, the precise contribution of KARs to brain function is less understood. Unlike recombinant KARs, native KARs exhibit characteristically slow channel kinetics. The underlying explanation for this dissimilar kinetics has remained elusive until recently. New research has identified Neto1 and Neto2 as KAR auxiliary subunits that determine unique properties of synaptic KARs, including their slow kinetics and high affinity for agonist. Whether these auxiliary subunits regulate KAR trafficking and targeting at the synapse is less clear. By regulating channel gating, Neto1 and Neto2 can increase the diversity of KAR functional properties. These auxiliary subunits may represent a starting point for a better understanding of the role played by neuronal KARs under normal and pathological conditions, but also, they may provide an alternative target for the development of new drugs regulating KARs and brain function.
kainate 受体(KARs)是离子型谷氨酸受体(iGluRs)的一个亚家族,它们介导兴奋性突触传递、调节神经递质释放,并在大脑中表现出显著的选择性分布。与其他 iGluRs 相比,KARs 对大脑功能的确切贡献还不太清楚。与重组 KARs 不同,天然 KARs 表现出特征性的缓慢通道动力学。直到最近,这种不同动力学的根本解释仍然难以捉摸。新的研究已经确定了 Neto1 和 Neto2 是 KAR 辅助亚基,它们决定了突触 KARs 的独特特性,包括其缓慢的动力学和对激动剂的高亲和力。这些辅助亚基是否调节突触处的 KAR 运输和靶向尚不清楚。通过调节通道门控,Neto1 和 Neto2 可以增加 KAR 功能特性的多样性。这些辅助亚基可能代表了更好地理解正常和病理条件下神经元 KARs 所起作用的起点,但它们也可能为开发调节 KAR 和大脑功能的新药提供替代靶标。