open access publication

Article, 2023

Distinct myofibre domains of the human myotendinous junction revealed by single nucleus RNA-seq

Journal of Cell Science, ISSN 1477-9137, 0021-9533, Volume 136, 8, 10.1242/jcs.260913

Contributors

Karlsen, Anders Peder Højer 0000-0002-0338-3751 [1] [2] Yeung, Ching-Yan Chloé 0000-0002-7076-8109 [1] [2] Schjerling, Peter 0000-0001-7138-3211 [1] [2] Denz, Linda [2] Hoegsbjerg, Christian 0000-0003-3212-5388 [2] Jakobsen, Jens Rithamer [3] Krogsgaard, Michael Rindom [3] Koch, Manuel 0000-0002-2962-7814 [4] Schiaffino, Stefano 0000-0002-5607-6421 [5] Kjaer, Michaela 0000-0002-9195-7339 [1] [2] Mackey, Abigail Louise 0000-0002-2017-4580 [1] [2]

Affiliations

  1. [1] University of Copenhagen
  2. [NORA names: KU University of Copenhagen; University; Denmark; Europe, EU; Nordic; OECD];
  3. [2] Bispebjerg Hospital
  4. [NORA names: Capital Region of Denmark; Hospital; Denmark; Europe, EU; Nordic; OECD];
  5. [3] Copenhagen University Hospital
  6. [NORA names: Capital Region of Denmark; Hospital; Denmark; Europe, EU; Nordic; OECD];
  7. [4] University of Cologne
  8. [NORA names: Germany; Europe, EU; OECD];
  9. [5] Venetian Institute of Molecular Medicine
  10. [NORA names: Italy; Europe, EU; OECD]

Abstract

The myotendinous junction (MTJ) is a specialized domain of the multinucleated myofibre that is faced with the challenge of maintaining robust cell-matrix contact with the tendon under high mechanical stress and strain. Here, we profiled 24,124 nuclei in semitendinosus muscle-tendon samples from three healthy males by using single-nucleus RNA sequencing (snRNA-seq), alongside spatial transcriptomics, to gain insight into the genes characterizing this specialization in humans. We identified a cluster of MTJ myonuclei represented by 47 enriched transcripts, of which the presence of ABI3BP, ABLIM1, ADAMTSL1, BICD1, CPM, FHOD3, FRAS1 and FREM2 was confirmed at the MTJ at the protein level in immunofluorescence assays. Four distinct subclusters of MTJ myonuclei were apparent, comprising two COL22A1-expressing subclusters and two subclusters lacking COL22A1 expression but with differing fibre type profiles characterized by expression of either MYH7 or MYH1 and/or MYH2. Our findings reveal distinct myonuclei profiles of the human MTJ, which represents a weak link in the musculoskeletal system that is selectively affected in pathological conditions ranging from muscle strains to muscular dystrophies.

Keywords

ABI3BP, ABLIM1, ADAMTSL1, BICD1, COL22A1, CPM, FHOD3, FRAS1, FREM2, MYH1, MYH2, MYH7, RNA sequencing, RNA-seq, assay, cell-matrix contacts, clusters, conditions, contact, domain, dystrophy, expression, fibre type profile, fibres, findings, genes, healthy males, high mechanical stress, human MTJ, humans, immunofluorescence, immunofluorescence assay, junction, levels, links, male, mechanical stress, multinucleated myofibres, muscle, muscular dystrophy, musculoskeletal system, myofibres, myonuclei, myotendinous junction, nucleus, nucleus RNA-seq, pathological conditions, presence, profile, protein, protein levels, samples, semitendinosus, sequence, single-nucleus RNA sequencing, snRNA-seq, spatial transcriptomics, specialization, strain, stress, subclusters, system, tendon, transcription, transcriptome, type profile, weak links

Funders

  • Deutsche Forschungsgemeinschaft
  • Lundbeck Foundation
  • Nordea-fonden
  • Novo Nordisk Foundation

Data Provider: Digital Science