PICK1 interacts with α7 neuronal nicotinic acetylcholine receptors and controls their clustering

被引:29
|
作者
Baer, Kristin
Buerli, Thomas
Huh, Kyung-Hye
Wiesner, Andreas
Erb-Voegtli, Susanne
Goeckeritz-Dujmovic, Dubravka
Moransard, Martijn
Nishimune, Atsushi
Rees, Mark I.
Henley, Jeremy M.
Fritschy, Jean-Marc
Fuhrer, Christian
机构
[1] Univ Zurich, Dept Neurochem, Inst Brain Res, CH-8057 Zurich, Switzerland
[2] Univ Coll Swansea, Sch Med, Swansea SA2 8PP, W Glam, Wales
[3] Univ Zurich, Inst Pharmacol & Toxicol, CH-8057 Zurich, Switzerland
[4] Univ Bristol, Dept Anat, MRC, Ctr Synapt Plast, Bristol BS8 1TD, Avon, England
基金
英国医学研究理事会;
关键词
nicotinic receptor; alpha; 7; nAChR; PICK1; clustering; hippocampus; GABAergic interneuron;
D O I
10.1016/j.mcn.2007.03.009
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Central to synaptic function are protein scaffolds associated with neurotransmitter receptors. alpha 7 neuronal nicotinic acetylcholine receptors (nAChRs) modulate network activity, neuronal survival and cognitive processes in the CNS, but protein scaffolds that interact with these receptors are unknown. Here we show that the PDZ-domain containing protein PICK1 binds to alpha 7 nAChRs and plays a role in their clustering. PICK1 interacted with the alpha 7 cytoplasmic loop in yeast in a PDZ-dependent way, and the interaction was confirmed in recombinant pull-down experiments and by co-precipitation of native proteins. Some alpha 7 and PICK1 clusters were adjacent at the surface of SH-SY5Y cells and GABAergic interneurons in hippocampal cultures. Expression of PICK1 caused decreased alpha 7 clustering on the surface of the interneurons in a PDZ-dependent way. These data show that PICK1 negatively regulates surface clustering of alpha 7 nAChRs on hippocampal interneurons, which may be important in inhibitory functions of OL7 in the hippocampus. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:339 / 355
页数:17
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