Department of Surgery, Davis Heart and Lung Research Institute, Biomedical Sciences Graduate Program, Biophysics Graduate Program, The Ohio State University Wexner Medical Center, Columbus, OH, 43210, USA.
Skelet Muscle. 2018 Oct 18;8(1):32. doi: 10.1186/s13395-018-0178-6.
Histological assessment of skeletal muscle sections is important for the research of muscle physiology and diseases. Quantifiable measures of skeletal muscle often include mean fiber diameter, fiber size distribution, and centrally nucleated muscle fibers. These parameters offer insights into the dynamic adaptation of skeletal muscle cells during repeated cycles of degeneration and regeneration associated with many muscle diseases and injuries. Computational programs designed to obtain these parameters would greatly facilitate such efforts and offer significant advantage over manual image analysis, which is very labor-intensive and often subjective. Here, we describe a customized pipeline termed MuscleAnalyzer for muscle histology analysis based upon CellProfiler, a free, open-source software for measuring and analyzing cell images.
The MuscleAnalyzer pipeline consists of loading, adjusting, and running a series of image-processing modules provided by CellProfiler. This pipeline was evaluated using wild-type and mdx muscle sections co-stained with laminin (to demarcate the muscle fiber boundaries) and 4',6-diamidino-2-phenylindole (DAPI, to label the nuclei). The immunofluorescence images analyzed using the MuscleAnalyzer pipeline or manually yielded similar results in the number of muscle fibers per image (p = 0.42) and central nucleated fiber (CNF) percentage (p = 0.29) in mdx mice. However, for a total of 67 images, CellProfiler completed the analysis in ~ 10 min on a regular PC while it took an investigator ~ 3 h using the manual approach in order to quantify the number of muscle fibers and CNF. Moreover, the MuscleAnalyzer pipeline also provided the measurement of the cross-sectional area (CSA) and minimal Feret's diameter (MFD) of muscle fibers, and thus fiber size distribution can be plotted.
Our data indicate that the MuscleAnalyzer pipeline can efficiently and accurately analyze laminin and DAPI co-stained muscle images in a batch format and provide quantitative measurements for muscle histological properties such as muscle fiber diameters, fiber size distribution, and CNF percentage.
骨骼肌切片的组织学评估对于肌肉生理学和疾病的研究很重要。骨骼肌的可量化指标通常包括平均纤维直径、纤维大小分布和中央核肌纤维。这些参数可以深入了解骨骼肌细胞在与许多肌肉疾病和损伤相关的反复退化和再生循环中的动态适应。设计用于获取这些参数的计算程序将极大地促进这些努力,并提供比手动图像分析显著的优势,手动图像分析非常耗时且常常具有主观性。在这里,我们描述了一种基于 CellProfiler 的定制流水线,称为 MuscleAnalyzer,用于肌肉组织学分析,CellProfiler 是一种用于测量和分析细胞图像的免费、开源软件。
MuscleAnalyzer 流水线由加载、调整和运行一系列 CellProfiler 提供的图像处理模块组成。使用 laminin(用于划定肌肉纤维边界)和 4',6-二脒基-2-苯基吲哚(DAPI,用于标记核)双重免疫荧光染色的野生型和 mdx 肌肉切片评估了该流水线。使用 MuscleAnalyzer 流水线或手动分析的免疫荧光图像在每张图像中的肌纤维数量(p=0.42)和中央核肌纤维(CNF)百分比(p=0.29)方面产生了相似的结果。然而,对于总共 67 张图像,CellProfiler 在常规 PC 上完成分析大约需要 10 分钟,而使用手动方法则需要调查员大约 3 小时才能定量肌纤维和 CNF 的数量。此外,MuscleAnalyzer 流水线还提供了肌纤维横截面积(CSA)和最小 Feret 直径(MFD)的测量值,因此可以绘制纤维大小分布。
我们的数据表明,MuscleAnalyzer 流水线可以以批处理格式高效、准确地分析 laminin 和 DAPI 双重免疫荧光染色的肌肉图像,并提供肌肉组织学特性的定量测量值,例如纤维直径、纤维大小分布和 CNF 百分比。