Electrophysiology Laboratory, Multidisciplinary Institute of Cell Biology, Universidad Nacional de La Plata, Consejo de Investigaciones Científicas y Técnicas, Comisión de Investigaciones de la Provincia de Buenos Aires, Buenos Aires, Argentina.
Instituto de Investigaciones Farmacológicas, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Buenos Aires, Argentina.
J Gen Physiol. 2020 May 4;152(5). doi: 10.1085/jgp.201912492.
Alterations in dopamine receptor type 1 (D1R) density are associated with cognitive deficits of aging and schizophrenia. In the prefrontal cortex (PFC), D1R plays a critical role in the regulation of working memory, which is impaired in these cognitive deficit states, but the cellular events triggered by changes in D1R expression remain unknown. A previous report demonstrated that interaction between voltage-gated calcium channel type 2.2 (CaV2.2) and D1R stimulates CaV2.2 postsynaptic surface location in medial PFC pyramidal neurons. Here, we show that in addition to the occurrence of the physical receptor-channel interaction, constitutive D1R activity mediates up-regulation of functional CaV2.2 surface density. We performed patch-clamp experiments on transfected HEK293T cells and wild-type C57BL/6 mouse brain slices, as well as imaging experiments and cAMP measurements. We found that D1R coexpression led to ∼60% increase in CaV2.2 currents in HEK293T cells. This effect was occluded by preincubation with a D1/D5R inverse agonist, chlorpromazine, and by replacing D1R with a D1R mutant lacking constitutive activity. Moreover, D1R-induced increase in CaV2.2 currents required basally active Gs protein, as well as D1R-CaV2.2 interaction. In mice, intraperitoneal administration of chlorpromazine reduced native CaV currents' sensitivity to ω-conotoxin-GVIA and their size by ∼49% in layer V/VI pyramidal neurons from medial PFC, indicating a selective effect on CaV2.2. Additionally, we found that reducing D1/D5R constitutive activity correlates with a decrease in the agonist-induced D1/D5R inhibitory effect on native CaV currents. Our results could be interpreted as a stimulatory effect of D1R constitutive activity on the number of CaV2.2 channels available for dopamine-mediated modulation. Our results contribute to the understanding of the physiological role of D1R constitutive activity and may explain the noncanonical postsynaptic distribution of functional CaV2.2 in PFC neurons.
多巴胺受体 1 型(D1R)密度的改变与衰老和精神分裂症的认知缺陷有关。在前额叶皮层(PFC)中,D1R 在调节工作记忆中起着关键作用,而在这些认知缺陷状态下,工作记忆受损,但D1R 表达变化引发的细胞事件仍不清楚。先前的一份报告表明,电压门控钙通道 2.2 型(CaV2.2)与 D1R 之间的相互作用刺激了内侧 PFC 锥体神经元中 CaV2.2 的突触后表面位置。在这里,我们表明,除了发生物理受体-通道相互作用之外,组成型 D1R 活性还介导功能性 CaV2.2 表面密度的上调。我们在转染的 HEK293T 细胞和野生型 C57BL/6 小鼠脑片中进行了膜片钳实验,以及成像实验和 cAMP 测量。我们发现,D1R 共表达导致 HEK293T 细胞中 CaV2.2 电流增加约 60%。这种效应被 D1/D5R 反向激动剂氯丙嗪预孵育所阻断,并且用缺乏组成型活性的 D1R 突变体替代 D1R 也会阻断。此外,D1R 诱导的 CaV2.2 电流增加需要基础活性 Gs 蛋白以及 D1R-CaV2.2 相互作用。在小鼠中,腹腔内给予氯丙嗪可使内侧 PFC 层 V/VI 锥体神经元中内源性 CaV 电流对 ω-芋螺毒素-GVIA 的敏感性降低约 49%,表明其对 CaV2.2 具有选择性作用。此外,我们发现降低 D1/D5R 的组成型活性与激动剂诱导的 D1/D5R 对内源性 CaV 电流的抑制作用降低相关。我们的结果可以解释为 D1R 组成型活性对可用于多巴胺介导调节的 CaV2.2 通道数量的刺激作用。我们的结果有助于理解 D1R 组成型活性的生理作用,并可能解释 PFC 神经元中功能性 CaV2.2 的非典型突触后分布。