Reichenbach Nicole, Herrmann Ulrike, Kähne Thilo, Schicknick Horst, Pielot Rainer, Naumann Michael, Dieterich Daniela C, Gundelfinger Eckart D, Smalla Karl-Heinz, Tischmeyer Wolfgang
Special Lab Molecular Biological Techniques, Leibniz Institute for Neurobiology, Magdeburg, 39118 Germany ; Present address: Research Group Neurovascular Diseases, German Center for Neurodegenerative Diseases (DZNE), Ludwig-Erhard-Allee 2, Bonn, 53175 Germany.
Special Lab Molecular Biological Techniques, Leibniz Institute for Neurobiology, Magdeburg, 39118 Germany ; Present address: Division of Cellular Neurobiology, Zoological Institute, TU Braunschweig, Braunschweig, 38106 Germany.
Proteome Sci. 2015 Mar 18;13:13. doi: 10.1186/s12953-015-0069-2. eCollection 2015.
Using auditory discrimination learning in gerbils, we have previously shown that activation of auditory-cortical D1/D5 dopamine receptors facilitates mTOR-mediated, protein synthesis-dependent mechanisms of memory consolidation and anterograde memory formation. To understand molecular mechanisms of this facilitatory effect, we tested the impact of local pharmacological activation of different D1/D5 dopamine receptor signalling modes in the auditory cortex. To this end, protein patterns in soluble and synaptic protein-enriched fractions from cortical, hippocampal and striatal brain regions of ligand- and vehicle-treated gerbils were analysed by 2D gel electrophoresis and mass spectrometry 24 h after intervention.
After auditory-cortical injection of SKF38393 - a D1/D5 dopamine receptor-selective agonist reported to activate the downstream effectors adenylyl cyclase and phospholipase C - prominent proteomic alterations compared to vehicle-treated controls appeared in the auditory cortex, striatum, and hippocampus, whereas only minor changes were detectable in the frontal cortex. In contrast, auditory-cortical injection of SKF83959 - a D1/D5 agonist reported to preferentially stimulate phospholipase C - induced pronounced changes in the frontal cortex. At the molecular level, we detected altered regulation of cytoskeletal and scaffolding proteins, changes in proteins with functions in energy metabolism, local protein synthesis, and synaptic signalling. Interestingly, abundance and/or subcellular localisation of the predominantly presynaptic protein α-synuclein displayed dopaminergic regulation. To assess the role of α-synuclein for dopaminergic mechanisms of memory modulation, we tested the impact of post-conditioning systemic pharmacological activation of different D1/D5 dopamine receptor signalling modes on auditory discrimination learning in α-synuclein-mutant mice. In C57BL/6JOlaHsd mice, bearing a spontaneous deletion of the α-synuclein-encoding gene, but not in the related substrains C57BL/6JCrl and C57BL/6JRccHsd, adenylyl cyclase-mediated signalling affected acquisition rates over future learning episodes, whereas phospholipase C-mediated signalling affected final memory performance.
Dopamine signalling modes via D1/D5 receptors in the auditory cortex differentially impact protein profiles related to rearrangement of cytomatrices, energy metabolism, and synaptic neurotransmission in cortical, hippocampal, and basal brain structures. Altered dopamine neurotransmission in α-synuclein-deficient mice revealed that distinct D1/D5 receptor signalling modes may control different aspects of memory consolidation.
我们之前利用沙鼠的听觉辨别学习实验表明,听觉皮层中D1/D5多巴胺受体的激活促进了mTOR介导的、依赖蛋白质合成的记忆巩固机制和顺行性记忆形成。为了了解这种促进作用的分子机制,我们测试了听觉皮层中不同D1/D5多巴胺受体信号传导模式的局部药理学激活的影响。为此,在干预24小时后,通过二维凝胶电泳和质谱分析了配体处理和载体处理的沙鼠的皮质、海马和纹状体脑区的可溶性和突触蛋白富集组分中的蛋白质模式。
在听觉皮层注射SKF38393(一种据报道可激活下游效应器腺苷酸环化酶和磷脂酶C的D1/D5多巴胺受体选择性激动剂)后,与载体处理的对照组相比,听觉皮层、纹状体和海马中出现了显著的蛋白质组学改变,而在额叶皮层中仅检测到微小变化。相比之下,在听觉皮层注射SKF83959(一种据报道优先刺激磷脂酶C的D1/D5激动剂)后,额叶皮层出现了明显变化。在分子水平上,我们检测到细胞骨架和支架蛋白的调节改变,以及在能量代谢、局部蛋白质合成和突触信号传导中起作用的蛋白质的变化。有趣的是,主要位于突触前的蛋白质α-突触核蛋白的丰度和/或亚细胞定位显示出多巴胺能调节。为了评估α-突触核蛋白在多巴胺能记忆调节机制中的作用,我们测试了不同D1/D5多巴胺受体信号传导模式的条件后全身药理学激活对α-突触核蛋白突变小鼠听觉辨别学习的影响。在自发缺失α-突触核蛋白编码基因的C57BL/6JOlaHsd小鼠中,而不是在相关亚系C57BL/6JCrl和C57BL/6JRccHsd中,腺苷酸环化酶介导的信号传导影响了未来学习阶段的习得率,而磷脂酶C介导的信号传导影响了最终记忆表现。
听觉皮层中通过D1/D5受体的多巴胺信号传导模式对与细胞基质重排、能量代谢和皮质、海马及基底脑结构中的突触电传递相关的蛋白质谱有不同影响。α-突触核蛋白缺陷小鼠中多巴胺神经传递的改变表明,不同的D1/D5受体信号传导模式可能控制记忆巩固的不同方面。