A glitch in the matrix: the pivotal role for extracellular matrix remodeling during muscle hypertrophy

Camille R. Brightwell, Christine M. Latham, Nicholas T. Thomas, Alexander R. Keeble, Kevin A. Murach, Christopher S. Fry

Research output: Contribution to journalReview articlepeer-review

25 Scopus citations

Abstract

Multinuclear muscle fibers are the most voluminous cells in skeletal muscle and the primary drivers of growth in response to loading. Outside the muscle fiber, however, is a diversity of mononuclear cell types that reside in the extracellular matrix (ECM). These muscle-resident cells are exercise-responsive and produce the scaffolding for successful myofibrillar growth. Without proper remodeling and maintenance of this ECM scaffolding, the ability to mount an appropriate response to resistance training in adult muscles is severely hindered. Complex cellular choreography takes place in muscles following a loading stimulus. These interactions have been recently revealed by single-cell explorations into muscle adaptation with loading. The intricate ballet of ECM remodeling involves collagen production from fibrogenic cells and ECM modifying signals initiated by satellite cells, immune cells, and the muscle fibers themselves. The acellular collagen-rich ECM is also a mechanical signal-transducer and rich repository of growth factors that may directly influence muscle fiber hypertrophy once liberated. Collectively, high levels of collagen expression, deposition, and turnover characterize a well-trained muscle phenotype. The purpose of this review is to highlight the most recent evidence for how the ECM and its cellular components affect loading-induced muscle hypertrophy. We also address how the muscle fiber may directly take part in ECM remodeling, and whether ECM dynamics are rate limiting for muscle fiber growth.

Original languageEnglish
Pages (from-to)C763-C771
JournalAmerican Journal of Physiology - Cell Physiology
Volume323
Issue number3
DOIs
StatePublished - Sep 1 2022

Keywords

  • collagen
  • fibro/adipogenic progenitors
  • mechanical overload
  • satellite cells
  • skeletal muscle

ASJC Scopus subject areas

  • Physiology
  • Cell Biology

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