Caudal Dorian, Rame Marion, Jay Thérèse M, Godsil Bill P
Physiopathologie des Maladies Psychiatriques, UMR_S 894 Inserm, Centre de Psychiatrie et Neurosciences, 2ter rue d'Alesia, 75014, Paris, France.
Université Paris Descartes, Sorbonne Paris Cité, Paris, France.
Cell Mol Neurobiol. 2016 Nov;36(8):1331-1342. doi: 10.1007/s10571-016-0332-9. Epub 2016 Jan 27.
The tuning of glutamatergic transmission is an essential mechanism for neuronal communication. α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPARs) are ionotropic glutamate receptors that mediate fast synaptic transmission. The phosphorylation states of specific serine residues on the GluA1 and GluA2 AMPAR subunits are considered critical post-translational modifications that regulate AMPAR activity and subcellular trafficking. While behavioral stress, via stress hormones, exerts specific alterations on such glutamatergic processes, there have been conflicting data concerning the influence of stress on AMPAR phosphorylation in different brain regions, and the post-stress signaling mechanisms mediating these processes are not well delineated. Here, we examined the dynamics of phosphorylation at three AMPAR serine residues (ser831-GluA1, ser845-GluA1, and ser880-GluA2) in four brain regions [amygdala, medial prefrontal cortex (mPFC), dorsal hippocampus, and ventral hippocampus] of the rat during the hour following behavioral stress. We also tested the impact of post-stress corticosteroid receptor blockade on AMPAR phosphorylation. Both GluA1 subunit residues exhibited elevated phosphorylation after stress, yet post-stress administration of corticosteroid receptor antagonists curtailed these effects only at ser831-GluA1. In contrast, ser880-GluA2 displayed a time-dependent tendency for early decreased phosphorylation (that was selectively augmented by mifepristone treatment in the amygdala and mPFC of stressed animals) followed by increased phosphorylation later on. These findings show that the in vivo regulation of AMPAR phosphorylation after stress is a dynamic and subunit-specific process, and they provide support for the hypothesis that corticosteroid receptors have an ongoing role in the regulation of ser831-GluA1 phosphorylation during the post-stress interval.
谷氨酸能传递的调节是神经元通讯的重要机制。α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体(AMPARs)是介导快速突触传递的离子型谷氨酸受体。GluA1和GluA2 AMPAR亚基上特定丝氨酸残基的磷酸化状态被认为是调节AMPAR活性和亚细胞转运的关键翻译后修饰。虽然行为应激通过应激激素对这种谷氨酸能过程产生特定改变,但关于应激对不同脑区AMPAR磷酸化的影响存在相互矛盾的数据,且介导这些过程的应激后信号传导机制尚未明确。在此,我们研究了行为应激后一小时内大鼠四个脑区[杏仁核、内侧前额叶皮质(mPFC)、背侧海马体和腹侧海马体]中三个AMPAR丝氨酸残基(ser831-GluA1、ser845-GluA1和ser880-GluA2)的磷酸化动态变化。我们还测试了应激后皮质类固醇受体阻断对AMPAR磷酸化的影响。应激后GluA1亚基的两个残基磷酸化均升高,但应激后给予皮质类固醇受体拮抗剂仅在ser831-GluA1处减弱了这些作用。相比之下,ser880-GluA2显示出早期磷酸化降低的时间依赖性趋势(在应激动物的杏仁核和mPFC中米非司酮处理选择性增强了这种趋势),随后磷酸化增加。这些发现表明,应激后AMPAR磷酸化的体内调节是一个动态且亚基特异性的过程,它们为皮质类固醇受体在应激后间隔期间对ser831-GluA1磷酸化调节中持续发挥作用的假说提供了支持。