No retraction, correction or concern found when last checked on Oct 30, 2026.
Automatic and unbiased segmentation and quantification of myofibers in skeletal muscle
Ariel Waisman, Alessandra Marie Norris, Martín Elías Costa and 1 more
Scientific Reports · 2021 · CC BY
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.
References 69
- 1.
Lepper C, Partridge TA, Fan CM. An absolute requirement for pax7-positive satellite cells in acute injury-induced skeletal muscle regeneration. Development. 2011;138:3639-3646.
Not in our library10.1242/dev.067595
- 2.
Murphy MM, Lawson JA, Mathew SJ, Hutcheson DA, Kardon G. Satellite cells, connective tissue fibroblasts and their interactions are crucial for muscle regeneration. Development. 2011.
Not in our library10.1242/dev.064162
- 3.
Relaix F, Zammit PS. Satellite cells are essential for skeletal muscle regeneration: The cell on the edge returns centre stage. Development. 2012.
Not in our library10.1242/dev.069088
- 4.
Sambasivan R, et al. Pax7-expressing satellite cells are indispensable for adult skeletal muscle regeneration. Development. 2011;138:3647-3656.
Not in our library10.1242/dev.067587
- 5.
Joe AW, et al. Muscle injury activates resident fibro/adipogenic progenitors that facilitate myogenesis. Nat. Cell Biol. 2010;12:2015.
Not in our library10.1038/ncb2015
- 6.
Kopinke D, Roberson EC, Reiter JF. Ciliary hedgehog signaling restricts injury-induced adipogenesis. Cell. 2017;170:340-351.
Not in our library10.1016/j.cell.2017.06.035
- 7.
Lukjanenko L, et al. Aging disrupts muscle stem cell function by impairing matricellular WISP1 secretion from fibro-adipogenic progenitors. Cell Stem Cell. 2019;24:433-446.
Not in our library10.1016/j.stem.2018.12.014
- 8.
Murphy M, Kardon G. Origin of vertebrate limb muscle: The role of progenitor and myoblast populations. Curr. Top. Dev. Biol. 2011;96:1-32.
Not in our library10.1016/b978-0-12-385940-2.00001-2
- 9.
Santini MP, et al. Tissue-resident PDGFR\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\alpha$$\end{document}α+ progenitor cells contribute to fibrosis versus healing in a context- and spatiotemporally dependent manner. Cell Rep. 2020;30:555-570.
Not in our library10.1016/j.celrep.2019.12.045
- 10.
Uezumi A, Fukada SI, Yamamoto N, Takeda S, Tsuchida K. Mesenchymal progenitors distinct from satellite cells contribute to ectopic fat cell formation in skeletal muscle. Nat. Cell Biol. 2010;12:14.
Not in our library10.1038/ncb2014
- 11.
Uezumi A, et al. Fibrosis and adipogenesis originate from a common mesenchymal progenitor in skeletal muscle. J. Cell Sci. 2011;124:86629.
Not in our library10.1242/jcs.086629
- 12.
Wosczyna MN, et al. Mesenchymal stromal cells are required for regeneration and homeostatic maintenance of article mesenchymal stromal cells are required for regeneration and homeostatic maintenance of skeletal muscle. Cell Rep. 2019;27:2029-2035.
Not in our library10.1016/j.celrep.2019.04.074
- 13.
- 14.
Liu W, Liu Y, Lai X, Kuang S. Intramuscular adipose is derived from a non-Pax3 lineage and required for efficient regeneration of skeletal muscles. Dev. Biol. 2012.
Not in our library10.1016/j.ydbio.2011.10.011
- 15.
Scott RW, Arostegui M, Schweitzer R, Rossi FM, Underhill TM. Hic1 defines quiescent mesenchymal progenitor subpopulations with distinct functions and fates in skeletal muscle regeneration. Cell Stem Cell. 2019;25:797-813.
Not in our library10.1016/j.stem.2019.11.004
- 16.
Stumm J, et al. Odd skipped-related 1 (Osr1) identifies muscle-interstitial fibro-adipogenic progenitors (FAPs) activated by acute injury. Stem Cell Res. 2018;32:8-16.
Not in our library10.1016/j.scr.2018.08.010
- 17.
- 18.
Goodpaster BH, et al. Obesity, regional body fat distribution, and the metabolic syndrome in older men and women. Arch. Intern. Med. 2005;165:777-783.
Not in our library10.1001/archinte.165.7.777
- 19.
Goodpaster BH, et al. Tissue distribution and both type 2 diabetes and impaired glucose. Diabetes Care. 2003;26:372-379.
Not in our library10.2337/diacare.26.2.372
- 20.
Goodpaster BH, Thaete FL, Kelley DE. Thigh adipose tissue distribution is associated with insulin resistance in obesity and in type 2 diabetes mellitus. Am. J. Clin. Nutr. 2000;71:885-892.
Not in our library10.1093/ajcn/71.4.885
- 21.
Goodpaster BH, et al. The loss of skeletal muscle strength, mass, and quality in older adults: The health, aging and body composition study. J. Gerontol. A. 2006;61:1059-1064.
Not in our library10.1093/gerona/61.10.1059
- 22.
Goodpaster BH, Theriault R, Watkins SC, Kelley DE. Intramuscular lipid content is increased in obesity and decreased by weight loss. Metab. Clin. Exp. 2000;49:467-472.
Not in our library10.1016/s0026-0495(00)80010-4
- 23.
- 24.
Murphy WA, Totty WG, Carroll JE. MRI of normal and pathologic skeletal muscle. Am. J. Roentgenol. 1986;146:565-574.
Not in our library10.2214/ajr.146.3.565
- 25.
Willcocks RJ, et al. Multicenter prospective longitudinal study of magnetic resonance biomarkers in a large Duchenne muscular dystrophy cohort. Ann. Neurol. 2016;79:535-547.
Not in our library10.1002/ana.24599
- 26.
Wokke BH, et al. Quantitative MRI and strength measurements in the assessment of muscle quality in Duchenne muscular dystrophy. Neuromuscular Disord. 2014;24:409-416.
Not in our library10.1016/j.nmd.2014.01.015
- 27.
- 28.
Mahdy MA, Lei HY, Wakamatsu JI, Hosaka YZ, Nishimura T. Comparative study of muscle regeneration following cardiotoxin and glycerol injury. Ann. Anat. 2015.
Not in our library10.1016/j.aanat.2015.07.002
- 29.
Miller MS, Bedrin NG, Ades PA, Palmer BM, Toth MJ. Molecular determinants of force production in human skeletal muscle fibers: Effects of myosin isoform expression and cross-sectional area. Am. J. Physiol. 2015;308:C473-C484.
Not in our library10.1152/ajpcell.00158.2014
- 30.
Virgilio KM, Martin KS, Peirce SM, Blemker SS. Agent-based model illustrates the role of the microenvironment in regeneration in healthy and mdx skeletal muscle. J. Appl. Physiol. 2018;125:1424-1439.
Not in our library10.1152/japplphysiol.00379.2018
- 31.
Briguet A, Courdier-Fruh I, Foster M, Meier T, Magyar JP. Histological parameters for the quantitative assessment of muscular dystrophy in the mdx-mouse. Neuromuscular Disord. 2004;14:675-682.
Not in our library10.1016/j.nmd.2004.06.008
- 32.
- 33.
Flück M. Functional, structural and molecular plasticity of mammalian skeletal muscle in response to exercise stimuli. J. Exp. Biol. 2006;209:2239-2248.
Not in our library10.1242/jeb.02149
- 34.
McDonald AA, Hebert SL, Kunz MD, Ralles SJ, McLoon LK. Disease course in mdx:Utrophin+/- mice: Comparison of three mouse models of duchenne muscular dystrophy. Physiol. Rep. 2015;3:1-22.
Not in our library10.14814/phy2.12391
- 35.
Encarnacion-Rivera L, Foltz S, Hartzell HC, Choo H. Myosoft: An automated muscle histology analysis tool using machine learning algorithm utilizing FIJI/ImageJ software. PLoS ONE. 2020;15:1-22.
Not in our library10.1371/journal.pone.0229041
- 36.
Kastenschmidt JM, et al. QuantiMus: A machine learning-based approach for high precision analysis of skeletal muscle morphology. Front. Physiol. 2019;10:1-10.
Not in our library10.3389/fphys.2019.01416
- 37.
- 38.
- 39.
Bergmeister KD, et al. A rapid automated protocol for muscle fiber population analysis in rat muscle cross sections using myosin heavy chain immunohistochemistry. J. Vis. Exp. 2017;2017:1-10.
Not in our library10.3791/55441
- 40.
Desgeorges T, et al. Open-CSAM, a new tool for semi-automated analysis of myofiber cross-sectional area in regenerating adult skeletal muscle. Skelet. Muscle. 2019;9:186.
Not in our library10.1186/s13395-018-0186-6
Cited by papers we hold 1
- Multimodal decoding of human liver regeneration · 2024No notice
Reads
Read by people on this page
None yet.
Checked or read by AI through naulon
None yet.
A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.
Are you an author?
Is this your paper?
Claim it to add your note and be paid when agents cite it. Free.