Department of Biochemistry I, Ruhr University Bochum, Universitätsstr. 150, 44780 Bochum, Germany.
Membranes (Basel). 2014 Aug 20;4(3):565-95. doi: 10.3390/membranes4030565.
Ionotropic glutamate receptors (iGluRs) mediate the vast majority of excitatory neurotransmission in the central nervous system of vertebrates. In the protein family of iGluRs, kainate receptors (KARs) comprise the probably least well understood receptor class. Although KARs act as key players in the regulation of synaptic network activity, many properties and functions of these proteins remain elusive until now. Especially the precise pre-, extra-, and postsynaptic localization of KARs plays a critical role for neuronal function, as an unbalanced localization of KARs would ultimately lead to dysregulated neuronal excitability. Recently, important advances in the understanding of the regulation of surface expression, function, and agonist-dependent endocytosis of KARs have been achieved. Post-translational modifications like PKC-mediated phosphorylation and SUMOylation have been reported to critically influence surface expression and endocytosis, while newly discovered auxiliary proteins were shown to shape the functional properties of KARs.
离子型谷氨酸受体(iGluRs)在脊椎动物中枢神经系统中介导绝大多数兴奋性神经递质传递。在 iGluR 蛋白家族中,红藻氨酸受体(KARs)是可能了解最少的受体类别。尽管 KARs 作为调节突触网络活动的关键参与者,但这些蛋白质的许多特性和功能至今仍不明确。特别是 KARs 的精确前、外和后突触定位对于神经元功能至关重要,因为 KARs 的不平衡定位最终会导致神经元兴奋性失调。最近,在理解 KAR 的表面表达、功能和激动剂依赖性内吞作用的调控方面取得了重要进展。已报道翻译后修饰,如 PKC 介导的磷酸化和 SUMO 化,对表面表达和内吞作用有重要影响,而新发现的辅助蛋白被证明可以塑造 KAR 的功能特性。