Zerby S E, Ewing A G
Department of Chemistry, Pennsylvania State University, University Park 16802, USA.
Brain Res. 1996 Mar 11;712(1):1-10. doi: 10.1016/0006-8993(95)01383-0.
Rat pheochromocytoma (PC12) cells have been used as a model of developing neurons to study exocytosis during differentiation. Upon treatment with nerve growth factor, PC12 cells become more neuronal-like. Using amperometric detection at carbon fiber microelectrodes, time-resolved exocytosis of electroactive catecholamines can be observed. The site of exocytosis has been compared for differentiated and undifferentiated cells. Upon differentiation, cells release catecholamines primarily from varicosities along their neurites with no release from the cell body. In addition, the mean vesicular content is not significantly altered upon differentiation although it appears that the distribution of vesicle content becomes more narrow. The number of release events observed also decreases as the cells become more neuronal in character. It is possible that the smaller range of vesicle dopamine content and the decreased number of release events observed after differentiation are a result of the relocation of the site of exocytosis.
大鼠嗜铬细胞瘤(PC12)细胞已被用作发育中神经元的模型,以研究分化过程中的胞吐作用。用神经生长因子处理后,PC12细胞变得更像神经元。使用碳纤维微电极进行安培检测,可以观察到电活性儿茶酚胺的时间分辨胞吐作用。已比较了分化细胞和未分化细胞的胞吐位点。分化后,细胞主要从神经突上的膨体释放儿茶酚胺,而细胞体不释放。此外,尽管囊泡内容物的分布似乎变得更窄,但分化后平均囊泡内容物没有显著改变。随着细胞在性质上变得更具神经元特征,观察到的释放事件数量也会减少。分化后观察到的囊泡多巴胺含量范围较小以及释放事件数量减少,可能是胞吐位点重新定位的结果。