Quantitative changes in focal adhesion kinase and its inhibitor, FRNK, drive load-dependent expression of costamere components

Am J Physiol Regul Integr Comp Physiol. 2013 Sep 15;305(6):R647-57. doi: 10.1152/ajpregu.00007.2013. Epub 2013 Jul 31.

Abstract

Costameres are mechanosensory sites of focal adhesion in the sarcolemma that reinforce the muscle-fiber composite and provide an anchor for myofibrillogenesis. We hypothesized that elevated content of the integrin-associated regulator of costamere turnover in culture, focal adhesion kinase (FAK), drives changes in costamere component content in antigravity muscle in a load-dependent way in correspondence with altered muscle weight. The content of FAK in soleus muscle being phosphorylated at autoregulatory tyrosine 397 (FAK-pY397) was increased after 20 s of stretch. FAK-pY397 content remained elevated after 24 h of stretch-overload due to upregulated FAK content. Overexpression of FAK in soleus muscle fibers by means of gene electrotransfer increased the β1-integrin (+56%) and meta-vinculin (+88%) content. α7-Integrin (P = 0.46) and γ-vinculin (P = 0.18) content was not altered after FAK overexpression. Co-overexpression of the FAK inhibitor FAK-related nonkinase (FRNK) reduced FAK-pY397 content by 33% and increased the percentage of fast-type fibers that arose in connection with hybrid fibers with gene transfer. Transplantation experiments confirmed the association of FRNK expression with slow-to-fast fiber transformation. Seven days of unloading blunted the elevation of FAK-pY397, β1-integrin, and meta-vinculin content with FAK overexpression, and this was reversed by 1 day of reloading. The results highlight that the expression of components for costameric attachment sites of myofibrils is under load- and fiber type-related control via FAK and its inhibitor FRNK.

Keywords: atrophy; focal adhesion; focal adhesion kinase; focal adhesion kinase-related nonkinase; hypertrophy; muscle; vinculin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Physiological / physiology
  • Animals
  • Cell Differentiation
  • Costameres
  • Female
  • Focal Adhesion Protein-Tyrosine Kinases / antagonists & inhibitors
  • Focal Adhesion Protein-Tyrosine Kinases / metabolism*
  • Gene Expression Regulation / physiology
  • Mechanotransduction, Cellular / physiology*
  • Muscle Fibers, Fast-Twitch / cytology*
  • Muscle Fibers, Fast-Twitch / metabolism*
  • Muscle Fibers, Slow-Twitch / cytology*
  • Muscle Fibers, Slow-Twitch / metabolism*
  • Protein-Tyrosine Kinases / metabolism*
  • Rats
  • Rats, Wistar

Substances

  • FAK-related nonkinase
  • Protein-Tyrosine Kinases
  • Focal Adhesion Protein-Tyrosine Kinases