Dong Yan, Heien Michael L, Maxson Marc M, Ewing Andrew G
Department of Chemistry, The Pennsylvania State University, University Park, PA, USA.
J Neurochem. 2008 Dec;107(6):1589-95. doi: 10.1111/j.1471-4159.2008.05721.x.
MN9D cells have been used as a successful model to investigate dopamine pharmacology and to test the specific effects of drugs for the treatment of Parkinson's disease. However, quantitative measurements of quantal release from these cells have not been carried out. In this work, we used amperometry to investigate catecholamine release from MN9D cells. Amperometric events were observed in both undifferentiated and differentiated (butyric acid-treated) cells. An increase in quantal size and half-width was observed for differentiated cells versus undifferentiated cells; however, the number of events per cell and the amplitude remained constant. In transmission electron microscopy images, no obvious cluster of small synaptic vesicles was observed, and large dense-core vesicles were present in the cell body of undifferentiated cells; however, after differentiation, vesicles were concentrated in the cell processes. In differentiated cells, l-DOPA caused an increase in quantal size and half-width, which could be blocked by the vesicular monoamine transporter inhibitor, reserpine.
MN9D细胞已被用作研究多巴胺药理学和测试治疗帕金森病药物特定效果的成功模型。然而,尚未对这些细胞的量子释放进行定量测量。在这项工作中,我们使用安培法研究MN9D细胞中儿茶酚胺的释放。在未分化和分化(丁酸处理)的细胞中均观察到安培事件。与未分化细胞相比,分化细胞的量子大小和半高宽增加;然而,每个细胞的事件数量和幅度保持不变。在透射电子显微镜图像中,未观察到明显的小突触小泡簇,未分化细胞的细胞体中存在大的致密核心小泡;然而,分化后,小泡集中在细胞突起中。在分化细胞中,左旋多巴导致量子大小和半高宽增加,这可被囊泡单胺转运体抑制剂利血平阻断。