Kneussel Matthias, Hausrat Torben Johann
Department of Molecular Neurogenetics, Center for Molecular Neurobiology, ZMNH, University Medical Center Hamburg-Eppendorf, Falkenried 94, 20251 Hamburg, Germany.
Department of Molecular Neurogenetics, Center for Molecular Neurobiology, ZMNH, University Medical Center Hamburg-Eppendorf, Falkenried 94, 20251 Hamburg, Germany.
Trends Neurosci. 2016 Mar;39(3):170-182. doi: 10.1016/j.tins.2016.01.002. Epub 2016 Jan 30.
At excitatory and inhibitory synapses, an immediate transfer of additional neurotransmitter receptors from non-synaptic positions to the synapse mediates synaptic long-term potentiation (LTP). Different types of non-synaptic reserve pools permit the rapid supply of transmembrane neurotransmitter receptors. Recycling endosomes (REs) serve as an intracellular reservoir of receptors that is delivered to the plasma membrane on LTP induction. Furthermore, AMPA receptors at the non-synaptic plasma membrane provide an extrasynaptic reserve pool that is also important to potentiate synapse function. Finally, bidirectional synaptic versus extrasynaptic trapping of freely diffusing plasma membrane GABAA receptors (GABAARs) by scaffolding proteins modulates synaptic transmission. Here we discuss novel findings regarding neurotransmitter receptor reservoirs and potential reserve pool mechanisms for synaptic potentiation.
在兴奋性和抑制性突触处,额外的神经递质受体从非突触位置立即转移至突触介导突触长期增强(LTP)。不同类型的非突触储备池可实现跨膜神经递质受体的快速供应。回收型内体(REs)作为受体的细胞内储存库,在LTP诱导时被转运至质膜。此外,非突触质膜上的AMPA受体提供了一个突触外储备池,这对增强突触功能也很重要。最后,支架蛋白对自由扩散的质膜GABAA受体(GABAARs)进行双向的突触与突触外捕获,从而调节突触传递。在此,我们讨论有关神经递质受体储存库的新发现以及突触增强的潜在储备池机制。