Li Dongdong, Xiong Jun, Qu Anlian, Xu Tao
Institute of Biophysics and Biochemistry, School of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074, People's Republic of China.
Biophys J. 2004 Sep;87(3):1991-2001. doi: 10.1529/biophysj.104.043281.
Deconvolution wide-field fluorescence microscopy and single-particle tracking were used to study the three-dimensional mobility of single secretory granules in live PC12 cells. Acridine orange-labeled granules were found to travel primarily in random and caged diffusion, whereas only a small fraction of granules traveled in directed fashion. High K(+) stimulation increased significantly the percentage of granules traveling in directed fashion. By dividing granules into the near-membrane group (within 1 microm from the plasma membrane) and cytosolic group, we have revealed significant differences between these two groups of granules in their mobility. The mobility of these two groups of granules is also differentially affected by disruption of F-actin, suggesting different mechanisms are involved in the motion of the two groups of granules. Our results demonstrate that combined deconvolution and single-particle tracking may find its application in three-dimensional tracking of long-term motion of granules and elucidating the underlying mechanisms.
反卷积宽场荧光显微镜和单颗粒追踪技术被用于研究活PC12细胞中单个分泌颗粒的三维运动性。发现吖啶橙标记的颗粒主要以随机和受限扩散的方式移动,而只有一小部分颗粒以定向方式移动。高钾刺激显著增加了以定向方式移动的颗粒的百分比。通过将颗粒分为近膜组(距质膜1微米以内)和胞质组,我们揭示了这两组颗粒在运动性上的显著差异。这两组颗粒的运动性也受到F-肌动蛋白破坏的不同影响,表明两组颗粒的运动涉及不同机制。我们的结果表明,反卷积和单颗粒追踪相结合可能在颗粒长期运动的三维追踪以及阐明潜在机制方面找到应用。