Lee Frank J S, Pei Lin, Moszczynska Anna, Vukusic Brian, Fletcher Paul J, Liu Fang
Department of Neuroscience, Centre for Addiction and Mental Health, University of Toronto, Toronto, Ontario, Canada.
EMBO J. 2007 Apr 18;26(8):2127-36. doi: 10.1038/sj.emboj.7601656. Epub 2007 Mar 22.
Altered synaptic dopamine levels have been implicated in several neurological/neuropsychiatric disorders, including drug addiction and schizophrenia. However, it is unclear what precipitates these changes in synaptic dopamine levels. One of the key presynaptic components involved in regulating dopaminergic tone is the dopamine transporter (DAT). Here, we report that the DAT is also regulated by the dopamine D2 receptor through a direct protein-protein interaction involving the DAT amino-terminus and the third intracellular loop of the D2 receptor. This physical coupling facilitates the recruitment of intracellular DAT to the plasma membrane and leads to enhanced dopamine reuptake. Moreover, mice injected with peptides that disrupt D2-DAT interaction exhibit decreased synaptosomal dopamine uptake and significantly increased locomotor activity, reminiscent of DAT knockout mice. Our data highlight a novel mechanism through which neurotransmitter receptors can functionally modulate neurotransmitter transporters, an interaction that can affect the synaptic neurotransmitter levels in the brain.
突触多巴胺水平的改变与多种神经/神经精神疾病有关,包括药物成瘾和精神分裂症。然而,尚不清楚是什么导致了突触多巴胺水平的这些变化。调节多巴胺能张力的关键突触前成分之一是多巴胺转运体(DAT)。在此,我们报告DAT也受多巴胺D2受体调节,通过涉及DAT氨基末端和D2受体第三细胞内环的直接蛋白质-蛋白质相互作用。这种物理偶联促进细胞内DAT募集到质膜,并导致多巴胺再摄取增强。此外,注射破坏D2-DAT相互作用肽的小鼠表现出突触体多巴胺摄取减少和运动活性显著增加,这与DAT基因敲除小鼠相似。我们的数据突出了一种新机制,通过该机制神经递质受体可在功能上调节神经递质转运体,这种相互作用可影响大脑中的突触神经递质水平。