Gokhin David S, Fowler Velia M
Department of Cell and Molecular Biology, The Scripps Research Institute, La Jolla, California, U.S.A.
J Microsc. 2017 Jan;265(1):11-20. doi: 10.1111/jmi.12456. Epub 2016 Sep 19.
The periodically arranged thin filaments within the striated myofibrils of skeletal and cardiac muscle have precisely regulated lengths, which can change in response to developmental adaptations, pathophysiological states, and genetic perturbations. We have developed a user-friendly, open-source ImageJ plugin that provides a graphical user interface (GUI) for super-resolution measurement of thin filament lengths by applying Distributed Deconvolution (DDecon) analysis to periodic line scans collected from fluorescence images. In the workflow presented here, we demonstrate thin filament length measurement using a phalloidin-stained cryosection of mouse skeletal muscle. The DDecon plugin is also capable of measuring distances of any periodically localized fluorescent signal from the Z- or M-line, as well as distances between successive Z- or M-lines, providing a broadly applicable tool for quantitative analysis of muscle cytoarchitecture. These functionalities can also be used to analyse periodic fluorescence signals in nonmuscle cells.
在骨骼肌和心肌的横纹肌原纤维中,周期性排列的细肌丝具有精确调控的长度,其长度可因发育适应、病理生理状态和基因扰动而发生变化。我们开发了一个用户友好的开源ImageJ插件,该插件通过对从荧光图像收集的周期性线扫描应用分布式反卷积(DDecon)分析,为细肌丝长度的超分辨率测量提供图形用户界面(GUI)。在此处展示的工作流程中,我们使用鬼笔环肽染色的小鼠骨骼肌冷冻切片演示了细肌丝长度测量。DDecon插件还能够测量任何周期性定位的荧光信号与Z线或M线之间的距离,以及连续Z线或M线之间的距离,为肌肉细胞结构的定量分析提供了一个广泛适用的工具。这些功能也可用于分析非肌肉细胞中的周期性荧光信号。