Cell Molecular and Developmental Biology Program, University of California, Riverside, Riverside, CA, USA.
Photochem Photobiol. 2011 Mar-Apr;87(2):408-17. doi: 10.1111/j.1751-1097.2010.00873.x. Epub 2011 Jan 25.
We studied the three-dimensional (3D) distribution of actin filaments and mitochondria in relation to ACBT glioblastoma cells migration. We embedded the cells in the spheroid form within collagen hydrogels and imaged them by in situ multiphoton microscopy (MPM). The static 3D overlay of the distribution of actin filaments and mitochondria provided a greater understanding of cell-to-cell and cell-to-substrate interactions and morphology. While imaging mitochondria to obtain ratiometric redox index based on cellular fluorescence from reduced nicotinamide adenine dinucleotide and oxidized flavin adenine dinucleotide we observed differential sensitivity of the migrating ACBT glioblastoma cells to femtosecond laser irradiation employed in MPM. We imaged actin-green fluorescent protein fluorescence in live ACBT glioma cells and for the first time observed dynamic modulation of the pools of actin during migration in 3D. The MPM imaging, which probes cells directly within the 3D cancer models, could potentially aid in working out a link between the functional performance of mitochondria, actin distribution and cancer invasiveness.
我们研究了肌动蛋白丝和线粒体在与 ACBT 胶质母细胞瘤细胞迁移相关的三维(3D)分布。我们将细胞嵌入胶原水凝胶中形成球体,并通过原位多光子显微镜(MPM)对其进行成像。肌动蛋白丝和线粒体分布的静态 3D 叠加提供了对细胞间和细胞与基底相互作用和形态的更深入了解。在对线粒体进行成像以获得基于还原型烟酰胺腺嘌呤二核苷酸和氧化黄素腺嘌呤二核苷酸的细胞荧光的比率还原氧化指数时,我们观察到迁移的 ACBT 胶质母细胞瘤细胞对用于 MPM 的飞秒激光照射的敏感性不同。我们对活的 ACBT 神经胶质瘤细胞中的肌动蛋白-绿色荧光蛋白荧光进行成像,并首次观察到在 3D 中迁移过程中肌动蛋白池的动态调制。MPM 成像直接探测 3D 癌症模型中的细胞,可能有助于阐明线粒体、肌动蛋白分布和癌症侵袭性之间的功能关系。