Yang Boyi, Dormann Christof, Vogt Miriam A, Sprengel Rolf, Gass Peter, Inta Dragos
Department of Molecular Neurobiology, Max Planck Institute for Medical Research, Jahnstrasse 29, 69120, Heidelberg, Germany.
RG Animal Models in Psychiatry, Department of Psychiatry and Psychotherapy, Central Institute of Mental Health Medical Faculty Mannheim, Heidelberg University, J 5, 68159, Mannheim, Germany.
Cell Mol Neurobiol. 2016 Oct;36(7):1215-8. doi: 10.1007/s10571-015-0307-2. Epub 2015 Dec 8.
The recently identified Cystine-knot containing AMPAR-associated protein (Ckamp44) represents a novel AMPAR-related protein that critically controls AMPAR-mediated currents and short-term plasticity. However, the effects of the lack of this protein at network level are not entirely understood. Here we used c-Fos brain mapping to analyse whether the excitatory/inhibitory balance is altered in the absence of the Ckamp44. We found that Ckamp44(-/-) mice treated with an NMDAR antagonist exhibited a very robust c-Fos expression pattern, similar with that seen in mice lacking the GluN2A subunit of NMDAR treated with the same compound. This finding is unexpected, in particular, since Ckamp44 expression is strongest in dentate gyrus granule cells and less abundant in the rest of the brain.
最近发现的含有胱氨酸结的AMPA受体相关蛋白(Ckamp44)是一种新型的AMPA受体相关蛋白,它对AMPA受体介导的电流和短期可塑性起着关键的调控作用。然而,在网络水平上缺乏这种蛋白所产生的影响尚未完全明确。在此,我们利用c-Fos脑图谱分析在缺乏Ckamp44的情况下兴奋性/抑制性平衡是否发生改变。我们发现,用NMDAR拮抗剂处理的Ckamp44基因敲除小鼠表现出非常强烈的c-Fos表达模式,这与用相同化合物处理的缺乏NMDAR的GluN2A亚基的小鼠所观察到的模式相似。这一发现出乎意料,特别是因为Ckamp44在齿状回颗粒细胞中表达最强,而在大脑其他部位表达较少。