Karataeva Anna R, Klaassen Remco V, Ströder Jasper, Ruiperez-Alonso Marta, Hjorth Johannes J J, van Nierop Pim, Spijker Sabine, Mansvelder Huibert D, Smit August B
Department of Molecular and Cellular Neurobiology, Center for Neurogenomics and Cognitive Research, Neuroscience Campus Amsterdam, Vrije Universiteit University, Amsterdam, The Netherlands.
Department of Molecular and Cellular Neurobiology, Center for Neurogenomics and Cognitive Research, Neuroscience Campus Amsterdam, Vrije Universiteit University, Amsterdam, The Netherlands ; Department of Integrative Neurophysiology, Center for Neurogenomics and Cognitive Research, Neuroscience Campus Amsterdam, Vrije Universiteit University, Amsterdam, The Netherlands.
PLoS One. 2014 Feb 3;9(2):e87360. doi: 10.1371/journal.pone.0087360. eCollection 2014.
Shisa9 (initially named CKAMP44) has been identified as auxiliary subunit of the AMPA-type glutamate receptors and was shown to modulate its physiological properties. Shisa9 is a type-I transmembrane protein and contains a C-terminal PDZ domain that potentially interacts with cytosolic proteins. In this study, we performed a yeast two-hybrid screening that yielded eight PDZ domain-containing interactors of Shisa9, which were independently validated. The identified interactors are known scaffolding proteins residing in the neuronal postsynaptic density. To test whether C-terminal scaffolding interactions of Shisa9 affect synaptic AMPA receptor function in the hippocampus, we disrupted these interactions using a Shisa9 C-terminal mimetic peptide. In the absence of scaffolding interactions of Shisa9, glutamatergic AMPA receptor-mediated synaptic currents in the lateral perforant path of the mouse hippocampus had a faster decay time, and paired-pulse facilitation was reduced. Furthermore, disruption of the PDZ interactions between Shisa9 and its binding partners affected hippocampal network activity. Taken together, our data identifies novel interaction partners of Shisa9, and shows that the C-terminal interactions of Shisa9 through its PDZ domain interaction motif are important for AMPA receptor synaptic and network functions.
Shisa9(最初命名为CKAMP44)已被鉴定为AMPA型谷氨酸受体的辅助亚基,并被证明可调节其生理特性。Shisa9是一种I型跨膜蛋白,含有一个可能与胞质蛋白相互作用的C末端PDZ结构域。在本研究中,我们进行了酵母双杂交筛选,得到了八个与Shisa9相互作用的含PDZ结构域的蛋白,并对其进行了独立验证。所鉴定的相互作用蛋白是位于神经元突触后致密区的已知支架蛋白。为了测试Shisa9的C末端支架相互作用是否影响海马体中的突触AMPA受体功能,我们使用Shisa9 C末端模拟肽破坏了这些相互作用。在没有Shisa9支架相互作用的情况下,小鼠海马体外侧穿通路径中谷氨酸能AMPA受体介导的突触电流具有更快的衰减时间,并且双脉冲易化作用降低。此外,Shisa9与其结合伙伴之间的PDZ相互作用的破坏影响了海马体网络活动。综上所述,我们的数据鉴定了Shisa9的新相互作用伙伴,并表明Shisa9通过其PDZ结构域相互作用基序的C末端相互作用对AMPA受体突触和网络功能很重要。