Eriksen Jacob, Rasmussen Søren G F, Rasmussen Trine Nygaard, Vaegter Christian Bjerggaard, Cha Joo Hwan, Zou Mu-Fa, Newman Amy Hauck, Gether Ulrik
Molecular Neuropharmacology Group and Center for Pharmacogenomics, Department of Neuroscience and Pharmacology, The Panum Institute, University of Copenhagen, DK-2200 Copenhagen N, Denmark.
J Neurosci. 2009 May 27;29(21):6794-808. doi: 10.1523/JNEUROSCI.4177-08.2009.
The dopamine transporter (DAT) mediates reuptake of dopamine from the synaptic cleft and is a target for widely abused psychostimulants such as cocaine and amphetamine. Nonetheless, little is known about the cellular distribution and trafficking of natively expressed DAT. Here we use novel fluorescently tagged cocaine analogs to visualize DAT and DAT trafficking in cultured live midbrain dopaminergic neurons. The fluorescent tags were extended from the tropane N-position of 2beta-carbomethoxy-3beta-(3,4-dichlorophenyl)tropane using an ethylamino-linker. The rhodamine-, OR Green-, or Cy3-labeled ligands had high binding affinity for DAT and enabled specific labeling of DAT in live neurons and visualization by confocal imaging. In the dopaminergic neurons, DAT was uniformly distributed in the plasma membrane of the soma, the neuronal extensions, and varicosities along these extensions. FRAP (fluorescence recovery after photobleaching) experiments demonstrated bidirectional movement of DAT in the extensions and indicated that DAT is highly mobile both in the extensions and in the varicosities (immobile fraction less than approximately 30%). DAT was constitutively internalized into vesicular structures likely representing intracellular transporter pools. The internalization was blocked by lentiviral-mediated expression of dominant-negative dynamin and internalized DAT displayed partial colocalization with the early endosomal marker EGFP-Rab5 and with the transferrin receptor. DAT internalization and function was not affected by activation of protein kinase C (PKC) with phorbol-12-myristate-13-acetate (PMA) or by inhibition with staurosporine or GF109203X. These data are in contrast to findings for DAT in transfected heterologous cells and challenge the paradigm that trafficking and cellular distribution of endogenous DAT is subject to regulation by PKC.
多巴胺转运体(DAT)介导从突触间隙重新摄取多巴胺,并且是可卡因和苯丙胺等广泛滥用的精神兴奋剂的作用靶点。尽管如此,对于天然表达的DAT的细胞分布和转运情况却知之甚少。在此,我们使用新型荧光标记的可卡因类似物来观察培养的活中脑多巴胺能神经元中的DAT及其转运情况。荧光标签通过一个乙氨基连接子从2β-甲氧羰基-3β-(3,4-二氯苯基)托烷的托烷N位延伸而来。罗丹明、OR Green或Cy3标记的配体对DAT具有高结合亲和力,能够在活神经元中特异性标记DAT,并通过共聚焦成像进行观察。在多巴胺能神经元中,DAT均匀分布于胞体的质膜、神经元突起以及沿这些突起的膨体中。光漂白后荧光恢复(FRAP)实验表明DAT在突起中双向移动,并且表明DAT在突起和膨体中都具有高度的流动性(固定部分小于约30%)。DAT持续内化到可能代表细胞内转运体池的囊泡结构中。这种内化被慢病毒介导表达的显性负性发动蛋白所阻断,并且内化的DAT与早期内体标记物EGFP-Rab5以及转铁蛋白受体部分共定位。DAT的内化和功能不受佛波醇-12-肉豆蔻酸酯-13-乙酸酯(PMA)激活蛋白激酶C(PKC)或星形孢菌素或GF109203X抑制的影响。这些数据与转染异源细胞中DAT的研究结果相反,并对内源性DAT的转运和细胞分布受PKC调节的范式提出了挑战。