Burke N V, Han W, Li D, Takimoto K, Watkins S C, Levitan E S
Department of Pharmacology, University of Pittsburgh, Pennsylvania 15261, USA.
Neuron. 1997 Nov;19(5):1095-102. doi: 10.1016/s0896-6273(00)80400-6.
Neuropeptides are slowly released from a limited pool of secretory granules. To visualize this process, GFP-tagged preproatrial natriuretic factor (ANF) was expressed in nerve growth factor-treated PC12 cells. Biochemical and microfluorimetric experiments demonstrate that proANF-EGFP is packaged in granules that accumulate at neurite endings and is released in a Ca2+-dependent manner by secretagogs. Confocal microscopy shows that secretion is associated with depletion of granules distributed throughout the terminal. Fluorescence recovery after photobleaching and time-lapse particle tracking reveal that only a subpopulation of cytoplasmic secretory granules, similar in size to the releasable pool, can move quickly enough (D = 6 x 10(-11) cm2/s) to support release. Therefore, sustained secretory responses are limited by the number of mobile granules and their slow rate of diffusion.
神经肽从有限的分泌颗粒池中缓慢释放。为了观察这一过程,在经神经生长因子处理的PC12细胞中表达了绿色荧光蛋白标记的前心钠素原(ANF)。生化和显微荧光实验表明,前心钠素原-增强绿色荧光蛋白(proANF-EGFP)被包装在聚集于神经突末端的颗粒中,并通过促分泌剂以钙离子依赖的方式释放。共聚焦显微镜显示,分泌与分布在整个末端的颗粒耗尽有关。光漂白后的荧光恢复和延时粒子追踪表明,只有一部分细胞质分泌颗粒能够快速移动(扩散系数D = 6×10⁻¹¹ cm²/s)以支持释放,这些颗粒的大小与可释放池相似。因此,持续的分泌反应受到可移动颗粒数量及其缓慢扩散速率的限制。