Université Catholique de Louvain, Institute of Neuroscience, Cell Physiology, av. Mounier 53/B1.53.17, B-1200 Brussels, Belgium.
Université Catholique de Louvain, de Duve Institute, Transgenic Core Facility, av. Hippocrate 75/B1.75.09, B-1200 Brussels, Belgium.
Int J Mol Sci. 2020 Mar 3;21(5):1712. doi: 10.3390/ijms21051712.
Group I metabotropic glutamate receptors (mGluR) are involved in various forms of synaptic plasticity that are believed to underlie declarative memory. We previously showed that mGluR5 specifically activates channels containing TRPC1, an isoform of the canonical family of Transient Receptor Potential channels highly expressed in the CA1-3 regions of the hippocampus. Using a tamoxifen-inducible conditional knockout model, we show here that the acute deletion of the gene alters the extinction of spatial reference memory. mGluR-induced long-term depression, which is partially responsible for memory extinction, was impaired in these mice. Similar results were obtained in vitro and in vivo by inhibiting the channel by its most specific inhibitor, Pico145. Among the numerous known postsynaptic pathways activated by type I mGluR, we observed that the deletion of impaired the activation of ERK1/2 and the subsequent expression of Arc, an immediate early gene that plays a key role in AMPA receptors endocytosis and subsequent long-term depression.
I 型代谢型谷氨酸受体(mGluR)参与各种形式的突触可塑性,这些可塑性被认为是陈述性记忆的基础。我们之前的研究表明,mGluR5 特异性激活包含 TRPC1 的通道,TRPC1 是经典瞬时受体电位通道家族的一个同工型,在海马 CA1-3 区高度表达。使用他莫昔芬诱导的条件性基因敲除模型,我们在此表明,基因的急性缺失改变了空间参考记忆的消退。在这些小鼠中,mGluR 诱导的长时程抑制,这部分负责记忆消退,受损。通过其最特异性的抑制剂 Pico145 抑制通道,在体外和体内也得到了类似的结果。在 I 型 mGluR 激活的众多已知的突触后途径中,我们观察到,的缺失损害了 ERK1/2 的激活,以及随后的 Arc 的表达,Arc 是一种立即早期基因,在 AMPA 受体内吞作用和随后的长时程抑制中起关键作用。