Rastedt Danielle E, Vaughan Roxanne A, Foster James D
Department of Biomedical Sciences, University of North Dakota, School of Medicine and Health Sciences, Grand Forks, ND 58202, United States.
Department of Biomedical Sciences, University of North Dakota, School of Medicine and Health Sciences, Grand Forks, ND 58202, United States.
J Chem Neuroanat. 2017 Oct;83-84:3-9. doi: 10.1016/j.jchemneu.2017.01.002. Epub 2017 Jan 20.
The neurotransmitter dopamine (DA) plays a key role in several biological processes including reward, mood, motor activity and attention. Synaptic DA homeostasis is controlled by the dopamine transporter (DAT) which transports extracellular DA into the presynaptic neuron after release and regulates its availability to receptors. Many neurological disorders such as schizophrenia, bipolar disorder, Parkinson disease and attention-deficit hyperactivity disorder are associated with imbalances in DA homeostasis that may be related to DAT dysfunction. DAT is also a target of psychostimulant and therapeutic drugs that inhibit DA reuptake and lead to elevated dopaminergic neurotransmission. We have recently demonstrated the acute and chronic modulation of DA reuptake activity and DAT stability through S-palmitoylation, the linkage of a 16-carbon palmitate group to cysteine via a thioester bond. This review summarizes the properties and regulation of DAT palmitoylation and describes how it serves to affect various transporter functions. Better understanding of the role of palmitoylation in regulation of DAT function may lead to identification of therapeutic targets for modulation of DA homeostasis in the treatment of dopaminergic disorders.
神经递质多巴胺(DA)在包括奖赏、情绪、运动活动和注意力在内的多种生物学过程中起关键作用。突触多巴胺稳态由多巴胺转运体(DAT)控制,DAT在多巴胺释放后将细胞外多巴胺转运到突触前神经元中,并调节其对受体的可利用性。许多神经疾病,如精神分裂症、双相情感障碍、帕金森病和注意力缺陷多动障碍,都与多巴胺稳态失衡有关,这可能与DAT功能障碍有关。DAT也是抑制多巴胺再摄取并导致多巴胺能神经传递增强的精神兴奋剂和治疗药物的靶点。我们最近通过S-棕榈酰化证明了多巴胺再摄取活性和DAT稳定性的急性和慢性调节,即通过硫酯键将一个16碳的棕榈酸酯基团连接到半胱氨酸上。本综述总结了DAT棕榈酰化的特性和调节,并描述了它如何影响各种转运体功能。更好地理解棕榈酰化在调节DAT功能中的作用,可能有助于确定在治疗多巴胺能疾病中调节多巴胺稳态的治疗靶点。