Localization of organic cation transporter 2 (OCT2) in monoaminergic and cholinergic axon terminals of the mouse brain

• Published in: Neuroscience letters Vol. 633; pp. 118 - 124
• Main Authors: Matsui, Toshiyasu, Nakata, Takahiro, Kobayashi, Yasushi
• Format: Journal Article
• Language: English
• Published: Ireland Elsevier B.V 28.10.2016
• Subjects: Acetylcholine; Animals; Brain - metabolism; Cholinergic Neurons - metabolism; Dopaminergic Neurons - metabolism; Female; Locus Coeruleus - metabolism; Male; Mice, Inbred ICR; Monoamine; Neurotransmitter reuptake; Neurotransmitter transporter; Organic Cation Transport Proteins - metabolism; Organic cation transporter; Organic Cation Transporter 2; Presynaptic Terminals - metabolism; Prosencephalon - metabolism; Serotonergic Neurons - metabolism; Monoamine; Organic cation transporter; Acetylcholine; Neurotransmitter transporter; Neurotransmitter reuptake
• ISSN: 0304-3940; 1872-7972
• DOI: 10.1016/j.neulet.2016.09.025

•OCT2 is widely distributed throughout the mouse forebrain.•OCT2-positive cell bodies are located in cholinergic and monoaminergic nuclei.•OCT2 is localized in cholinergic, dopaminergic, and serotonergic synaptic terminals.•OCT2 is also localized in anterogradely labeled terminals from the locus coeruleus.•These data imply that presynaptic OCT2 might mediate choline and monoamine reuptake. Organic cation transporters (OCTs) are low-affinity, high-capacity carriers that mediate sodium-independent transport for biogenic cations, including catecholamine, serotonin, histamine, and choline/acetylcholine. Among them, OCT2 is expressed in neurons of the central nervous system. Although previous studies show OCT2 expression in several populations of cholinergic and monoaminergic neurons, the regional distribution of OCT2 in the brain remains largely unknown. Here we performed immunohistochemical analyses to reveal the distribution of OCT2 throughout the mouse forebrain. OCT2 immunoreactivity was widely distributed, with substantial regional specificity in cortical and subcortical structures including the hippocampus, striatum, and some subdivisions of the amygdala and extended amygdala. Interestingly, OCT2 appeared as punctate, bouton-like labeling in cholinergic, dopaminergic, and serotonergic axon terminals that were co-labeled with presynaptic neurochemical markers. We also co-labeled OCT2 and an anterograde tract-tracer injected into the locus coeruleus, demonstrating that OCT2 was localized to presumptive noradrenergic terminals in the forebrain. Together, our results demonstrated that the polyspecific cation transporter OCT2 is distributed in cholinergic and monoaminergic terminals in various forebrain regions, suggesting that OCT2 could play a role in regulating presynaptic reuptake and recycling of choline and monoamines.