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骨骼肌中原纤维的自动和无偏分割与定量。

Automatic and unbiased segmentation and quantification of myofibers in skeletal muscle.

机构信息

CONICET - Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia (FLENI), Laboratorio de Investigación Aplicada a Neurociencias (LIAN), Buenos Aires, Argentina.

Department of Pharmacology and Therapeutics, University of Florida College of Medicine, Gainesville, 32610, FL, USA.

出版信息

Sci Rep. 2021 Jun 3;11(1):11793. doi: 10.1038/s41598-021-91191-6.

Abstract

Skeletal muscle has the remarkable ability to regenerate. However, with age and disease muscle strength and function decline. Myofiber size, which is affected by injury and disease, is a critical measurement to assess muscle health. Here, we test and apply Cellpose, a recently developed deep learning algorithm, to automatically segment myofibers within murine skeletal muscle. We first show that tissue fixation is necessary to preserve cellular structures such as primary cilia, small cellular antennae, and adipocyte lipid droplets. However, fixation generates heterogeneous myofiber labeling, which impedes intensity-based segmentation. We demonstrate that Cellpose efficiently delineates thousands of individual myofibers outlined by a variety of markers, even within fixed tissue with highly uneven myofiber staining. We created a novel ImageJ plugin (LabelsToRois) that allows processing of multiple Cellpose segmentation images in batch. The plugin also contains a semi-automatic erosion function to correct for the area bias introduced by the different stainings, thereby identifying myofibers as accurately as human experts. We successfully applied our segmentation pipeline to uncover myofiber regeneration differences between two different muscle injury models, cardiotoxin and glycerol. Thus, Cellpose combined with LabelsToRois allows for fast, unbiased, and reproducible myofiber quantification for a variety of staining and fixation conditions.

摘要

骨骼肌具有很强的再生能力。然而,随着年龄的增长和疾病的发生,肌肉力量和功能会下降。肌纤维大小受损伤和疾病的影响,是评估肌肉健康的一个重要指标。在这里,我们测试并应用了最近开发的深度学习算法 Cellpose,以自动分割鼠类骨骼肌中的肌纤维。我们首先表明,组织固定对于保存初级纤毛、小细胞天线和脂肪细胞脂质滴等细胞结构是必要的。然而,固定会导致肌纤维标记不均匀,这会阻碍基于强度的分割。我们证明了 Cellpose 可以有效地对几千个肌纤维进行分割,即使在固定组织中存在高度不均匀的肌纤维染色,它也能很好地工作。我们创建了一个新的 ImageJ 插件(LabelsToRois),可以批量处理多个 Cellpose 分割图像。该插件还包含半自动侵蚀功能,可以纠正不同染色引起的面积偏差,从而像人类专家一样准确地识别肌纤维。我们成功地将我们的分割管道应用于两种不同的肌肉损伤模型(心脏毒素和甘油),以揭示肌纤维再生的差异。因此,Cellpose 结合 LabelsToRois 可以快速、无偏和可重复地对各种染色和固定条件下的肌纤维进行定量分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f35/8175575/8ee1b7b4b45b/41598_2021_91191_Fig1_HTML.jpg

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