Nikodijevic B, Creveling C R, Koizumi S, Guroff G
Section on Growth Factors, National Institute of Child Health and Human Development, Bethesda, Maryland 20892.
J Neurosci Res. 1990 Jul;26(3):288-95. doi: 10.1002/jnr.490260304.
PC12 cells are a nerve growth factor-responsive clone derived from a rat pheochromocytoma. The cells contain catecholamines and secrete them in response to depolarizing stimuli and cholinergic agonists. Treatment of the cells with nerve growth factor produces a number of very rapid changes, including the structural rearrangement of the cell membrane, the generation of a number of different second messengers, and the phosphorylation of several proteins. The present studies show that nerve growth factor treatment increases the release of dopamine and norepinephrine from the cells within a few minutes and does so independently of its effect on their metabolism. The experiments indicate that this effect on nerve growth factor is dependent on the presence of extracellular calcium and can be blocked by calcium channel antagonists. K-252a, an alkaloid-like material, usually found to inhibit the actions of nerve growth factor on PC12 cells, also increases the release of catecholamines under these conditions.
PC12细胞是源自大鼠嗜铬细胞瘤的神经生长因子反应性克隆。这些细胞含有儿茶酚胺,并在受到去极化刺激和胆碱能激动剂作用时分泌它们。用神经生长因子处理这些细胞会产生许多非常迅速的变化,包括细胞膜的结构重排、多种不同第二信使的产生以及几种蛋白质的磷酸化。目前的研究表明,神经生长因子处理在几分钟内就能增加细胞中多巴胺和去甲肾上腺素的释放,且这种作用与其对细胞代谢的影响无关。实验表明,这种对神经生长因子的作用依赖于细胞外钙的存在,并且可被钙通道拮抗剂阻断。K-252a是一种类似生物碱的物质,通常被发现能抑制神经生长因子对PC12细胞的作用,但在这些条件下也会增加儿茶酚胺的释放。