Katoh K, Hammar K, Smith P J, Oldenbourg R
Marine Biological Laboratory, Woods Hole, Massachusetts 02543-1015, USA.
Mol Biol Cell. 1999 Jan;10(1):197-210. doi: 10.1091/mbc.10.1.197.
We have investigated the dynamic behavior of cytoskeletal fine structure in the lamellipodium of nerve growth cones using a new type of polarized light microscope (the Pol-Scope). Pol-Scope images display with exquisite resolution and definition birefringent fine structures, such as filaments and membranes, without having to treat the cell with exogenous dyes or fluorescent labels. Furthermore, the measured birefringence of protein fibers in the thin lamellipodial region can be interpreted in terms of the number of filaments in the bundles. We confirmed that birefringent fibers are actin-based using conventional fluorescence-labeling methods. By recording movies of time-lapsed Pol-Scope images, we analyzed the creation and dynamic composition of radial fibers, filopodia, and intrapodia in advancing growth cones. The strictly quantitative information available in time-lapsed Pol-Scope images confirms previously deduced behavior and provides new insight into the architectural dynamics of filamentous actin.
我们使用一种新型偏光显微镜(Pol-Scope)研究了神经生长锥板状伪足中细胞骨架精细结构的动态行为。Pol-Scope图像能以极高的分辨率和清晰度显示双折射精细结构,如细丝和膜,而无需用外源染料或荧光标记处理细胞。此外,在薄的板状伪足区域测量的蛋白质纤维双折射可以根据束中细丝的数量来解释。我们使用传统荧光标记方法证实双折射纤维是以肌动蛋白为基础的。通过记录Pol-Scope图像的延时电影,我们分析了前进生长锥中径向纤维、丝状伪足和伪足内的形成及动态组成。延时Pol-Scope图像中可获得的严格定量信息证实了先前推断的行为,并为丝状肌动蛋白的结构动力学提供了新的见解。