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Human skeletal muscle fiber heterogeneity beyond myosin heavy chains

Author

Listed:
  • Roger Moreno-Justicia

    (University of Copenhagen)

  • Thibaux Van der Stede

    (Ghent University
    University of Copenhagen)

  • Ben Stocks

    (University of Copenhagen
    Karolinska Institutet)

  • Jenni Laitila

    (University of Copenhagen)

  • Robert A. Seaborne

    (University of Copenhagen
    King’s College London)

  • Alexia Van de Loock

    (Ghent University)

  • Eline Lievens

    (Ghent University)

  • Diana Samodova

    (University of Copenhagen)

  • Leyre Marín-Arraiza

    (University of Copenhagen)

  • Oksana Dmytriyeva

    (University of Copenhagen)

  • Robin Browaeys

    (VIB Center for Inflammation Research
    Ghent University)

  • Kim Van Vossel

    (Ghent University)

  • Lukas Moesgaard

    (University of Copenhagen)

  • Nurten Yigit

    (Ghent University)

  • Jasper Anckaert

    (Ghent University)

  • Anneleen Weyns

    (Ghent University)

  • Ruud Van Thienen

    (Ghent University)

  • Ronni E. Sahl

    (University of Copenhagen)

  • Edmar Zanoteli

    (Universidade de São Paulo)

  • Michael W. Lawlor

    (Medical College of Wisconsin
    Diverge Translational Science Laboratory)

  • Michael Wierer

    (University of Copenhagen)

  • Pieter Mestdagh

    (Ghent University)

  • Jo Vandesompele

    (Ghent University)

  • Julien Ochala

    (University of Copenhagen)

  • Morten Hostrup

    (University of Copenhagen)

  • Wim Derave

    (Ghent University)

  • Atul S. Deshmukh

    (University of Copenhagen)

Abstract

Skeletal muscle is a heterogenous tissue comprised primarily of myofibers, commonly classified into three fiber types in humans: one “slow” (type 1) and two “fast” (type 2A and type 2X). However, heterogeneity between and within traditional fiber types remains underexplored. We applied transcriptomic and proteomic workflows to 1050 and 1038 single myofibers from human vastus lateralis, respectively. Proteomics was conducted in males, while transcriptomics included ten males and two females. We identify metabolic, ribosomal, and cell junction proteins, in addition to myosin heavy chain isoforms, as sources of multi-dimensional variation between myofibers. Furthermore, whilst slow and fast fiber clusters are identified, our data suggests that type 2X fibers are not phenotypically distinct to other fast fibers. Moreover, myosin heavy chain-based classifications do not adequately describe the phenotype of myofibers in nemaline myopathy. Overall, our data indicates that myofiber heterogeneity is multi-dimensional with sources of variation beyond myosin heavy chain isoforms.

Suggested Citation

  • Roger Moreno-Justicia & Thibaux Van der Stede & Ben Stocks & Jenni Laitila & Robert A. Seaborne & Alexia Van de Loock & Eline Lievens & Diana Samodova & Leyre Marín-Arraiza & Oksana Dmytriyeva & Robin, 2025. "Human skeletal muscle fiber heterogeneity beyond myosin heavy chains," Nature Communications, Nature, vol. 16(1), pages 1-18, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-56896-6
    DOI: 10.1038/s41467-025-56896-6
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