Haglerød C, Kapic A, Boulland J-L, Hussain S, Holen T, Skare O, Laake P, Ottersen O P, Haug F-M S, Davanger S
Institute of Basic Medical Sciences, Department of Anatomy, and Centre for Molecular Biology and Neuroscience, University of Oslo, P.O. Box 1105 Blindern, 0317 Oslo, Norway.
Neuroscience. 2009 Jan 12;158(1):242-52. doi: 10.1016/j.neuroscience.2008.11.029. Epub 2008 Nov 27.
AMPA receptors have been identified in different populations of presynaptic terminals and found to be involved in the modulation of neurotransmitter release. The mechanisms that govern the expression of presynaptic AMPA receptors are not known. One possibility is that pre- and postsynaptic AMPA receptors are regulated according to the same principles. To address this hypothesis we investigated whether protein interacting with C kinase 1 (PICK1), known to interact with AMPA receptors postsynaptically, also is expressed presynaptically, together with AMPA receptors. Subfractionation and high-resolution immunogold analyses of the rat hippocampus revealed that GluR2 and PICK1 are enriched postsynaptically, but also in presynaptic membrane compartments, including the active zone and vesicular membranes. PICK1 and GluR2 are associated with the same vesicles, which are immunopositive also for synaptophysin and vesicle-associated membrane protein 2. Based on what is known about the function of PICK1 postsynaptically, the present data suggest that PICK1 is involved in the regulation of presynaptic AMPA receptor trafficking and in determining the size of the AMPA receptor pool that modulates presynaptic glutamate release.
α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体已在不同群体的突触前终末中被鉴定出来,并发现其参与神经递质释放的调节。目前尚不清楚调控突触前AMPA受体表达的机制。一种可能性是,突触前和突触后AMPA受体按照相同的原则进行调节。为了验证这一假设,我们研究了已知在突触后与AMPA受体相互作用的蛋白激酶C相互作用蛋白1(PICK1)是否也与AMPA受体一起在突触前表达。对大鼠海马体进行亚分级分离和高分辨率免疫金分析显示,谷氨酸受体2(GluR2)和PICK1在突触后富集,但在突触前膜区室中也有富集,包括活性区和囊泡膜。PICK1和GluR2与相同的囊泡相关,这些囊泡对突触素和囊泡相关膜蛋白2也呈免疫阳性。基于已知的PICK1在突触后的功能,目前的数据表明,PICK1参与突触前AMPA受体运输的调节,并决定调节突触前谷氨酸释放的AMPA受体池的大小。