Mechanosensors control skeletal muscle mass, molecular clocks, and metabolism

Cell Mol Life Sci. 2022 May 27;79(6):321. doi: 10.1007/s00018-022-04346-7.

Abstract

Background: Skeletal muscles (SkM) are mechanosensitive, with mechanical unloading resulting in muscle-devastating conditions and altered metabolic properties. However, it remains unexplored whether these atrophic conditions affect SkM mechanosensors and molecular clocks, both crucial for their homeostasis and consequent physiological metabolism.

Methods: We induced SkM atrophy through 14 days of hindlimb suspension (HS) in 10 male C57BL/6J mice and 10 controls (CTR). SkM histology, gene expressions and protein levels of mechanosensors, molecular clocks and metabolism-related players were examined in the m. Gastrocnemius and m. Soleus. Furthermore, we genetically reduced the expression of mechanosensors integrin-linked kinase (Ilk1) and kindlin-2 (Fermt2) in myogenic C2C12 cells and analyzed the gene expression of mechanosensors, clock components and metabolism-controlling genes.

Results: Upon hindlimb suspension, gene expression levels of both core molecular clocks and mechanosensors were moderately upregulated in m. Gastrocnemius but strongly downregulated in m. Soleus. Upon unloading, metabolism- and protein biosynthesis-related genes were moderately upregulated in m. Gastrocnemius but downregulated in m. Soleus. Furthermore, we identified very strong correlations between mechanosensors, metabolism- and circadian clock-regulating genes. Finally, genetically induced downregulations of mechanosensors Ilk1 and Fermt2 caused a downregulated mechanosensor, molecular clock and metabolism-related gene expression in the C2C12 model.

Conclusions: Collectively, these data shed new lights on mechanisms that control muscle loss. Mechanosensors are identified to crucially control these processes, specifically through commanding molecular clock components and metabolism.

Keywords: Atrophy; Hindlimb suspension; Mechanosensing; Molecular clock; Skeletal muscle metabolism.

MeSH terms

  • Animals
  • Biological Clocks* / genetics
  • Biological Clocks* / physiology
  • Cytoskeletal Proteins / genetics
  • Cytoskeletal Proteins / metabolism
  • Gene Expression
  • Hindlimb Suspension
  • Male
  • Mechanoreceptors* / metabolism
  • Mechanotransduction, Cellular / genetics
  • Mechanotransduction, Cellular / physiology
  • Mice
  • Mice, Inbred C57BL
  • Models, Animal
  • Muscle Proteins / genetics
  • Muscle Proteins / metabolism
  • Muscle, Skeletal* / metabolism
  • Muscular Atrophy* / genetics
  • Muscular Atrophy* / metabolism
  • Muscular Diseases / genetics
  • Muscular Diseases / metabolism
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism

Substances

  • Cytoskeletal Proteins
  • Muscle Proteins
  • kindlin-2 protein, mouse
  • integrin-linked kinase
  • Protein Serine-Threonine Kinases