Kruse Maria Sol, Prémont Joël, Krebs Marie-Odile, Jay Thérèse M
INSERM, U894, Physiopathologie des Maladies Psychiatriques, Centre de psychiatrie et Neurosciences, Paris, France.
Eur Neuropsychopharmacol. 2009 Apr;19(4):296-304. doi: 10.1016/j.euroneuro.2008.12.006. Epub 2009 Jan 31.
Despite the tremendous importance of D1 and NMDA receptors to cognition (working memory, executive functions) and synaptic plasticity in the prefrontal cortex (PFC), little is known about the molecular mechanisms underlying D1-NMDA receptors interactions in this brain area. Here, we show that D1 receptors and the NMDA receptor co-localize in single pyramidal neurons and interneurons in adult rat PFC. NR1 and NR2A expression are found in different neuronal types. Conversely, D1 receptors are predominantly localized in pyramidal-like cells and parvalbumin positive cells. NR1 co-immunoprecipitates with D1 receptor in adult medial PFC. In prefrontal primary cultures, NMDA does not affect the D1 receptor dependent-cAMP production. In contrast, activation of D1 receptor potentiates the NMDA mediated increase in cytosolic Ca2+, an effect that was blocked by a PKA inhibitor. We conclude that D1 receptor potentiates the NMDA-Ca2+ signal by a PKA-dependent mechanism.
尽管D1受体和N-甲基-D-天冬氨酸(NMDA)受体对前额叶皮质(PFC)的认知(工作记忆、执行功能)和突触可塑性极为重要,但对于该脑区中D1-NMDA受体相互作用的分子机制却知之甚少。在此,我们表明,D1受体和NMDA受体在成年大鼠PFC的单个锥体神经元和中间神经元中共定位。在不同的神经元类型中发现了NR1和NR2A的表达。相反,D1受体主要定位于锥体样细胞和小白蛋白阳性细胞中。在成年内侧PFC中,NR1与D1受体进行共免疫沉淀。在额叶前皮质原代培养物中,NMDA不影响D1受体依赖性环磷酸腺苷(cAMP)的产生。相反,D1受体的激活增强了NMDA介导的胞质Ca2+增加,这一效应被蛋白激酶A(PKA)抑制剂所阻断。我们得出结论,D1受体通过PKA依赖性机制增强NMDA-Ca2+信号。