Bergersen Linda Hildegard, Magistretti Pierre J, Pellerin Luc
Anatomical Institute, Centre for Molecular Biology and Neuroscience, University of Oslo, Blindern, Oslo, Norway.
Cereb Cortex. 2005 Apr;15(4):361-70. doi: 10.1093/cercor/bhh138.
MCT2 is the main neuronal monocarboxylate transporter needed by neurons if they are to use lactate as an additional energy substrate. Previous evidence suggested that some MCT2 could be located in postsynaptic elements of glutamatergic synapses. Using post-embedding electron microscopic immunocytochemistry, it is demonstrated that MCT2 is present at postsynaptic density of asymmetric synapses, in the stratum radiatum of both rat hippocampal CA1 and CA3 regions, as well as at parallel fibre-Purkinje cell synapses in mouse cerebellum. MCT2 levels were significantly lower at mossy fibre synapses on CA3 neurons, and MCT2 was almost absent from symmetric synapses on CA1 pyramidal cells. It could also be demonstrated using quantitative double-labeling immunogold cytochemistry that MCT2 and AMPA receptor GluR2/3 subunits have a similar postsynaptic distribution at asymmetric synapses with high levels expressed within the postsynaptic density. In addition, as for AMPA receptors, a significant proportion of MCT2 is located on vesicular membranes within the postsynaptic spine, forming an intracellular pool available for a putative postsynaptic endo/exocytotic trafficking at these excitatory synapses. Altogether, the data presented provide evidence for MCT2 expression in the postsynaptic density area at specific subsets of glutamatergic synapses, and also suggest that MCT2, like AMPA receptors, could undergo membrane trafficking.
MCT2是神经元若要将乳酸用作额外能量底物时所需的主要神经元单羧酸转运体。先前的证据表明,一些MCT2可能位于谷氨酸能突触的突触后元件中。通过包埋后电子显微镜免疫细胞化学方法,证实MCT2存在于大鼠海马CA1和CA3区辐射层不对称突触的突触后致密部,以及小鼠小脑的平行纤维-浦肯野细胞突触中。在CA3神经元的苔藓纤维突触处,MCT2水平显著较低,而在CA1锥体细胞的对称突触中几乎不存在MCT2。使用定量双标记免疫金细胞化学方法还可证明,在不对称突触中,MCT2和AMPA受体GluR2/3亚基在突触后致密部高水平表达的情况下具有相似的突触后分布。此外,与AMPA受体一样,相当一部分MCT2位于突触后棘内的囊泡膜上,形成一个细胞内池,可用于这些兴奋性突触处假定的突触后内吞/外排运输。总之,所呈现的数据为MCT2在特定谷氨酸能突触亚群的突触后致密部区域表达提供了证据,并且还表明MCT2与AMPA受体一样,可能经历膜运输。