Mice deficient in plasminogen activator inhibitor-1 have improved skeletal muscle regeneration

Am J Physiol Cell Physiol. 2005 Jul;289(1):C217-23. doi: 10.1152/ajpcell.00555.2004. Epub 2005 Feb 16.

Abstract

Skeletal muscle possesses a remarkable capacity for regeneration. Although the regulation of this process at the molecular level remains largely undefined, the plasminogen system appears to play a critical role. Specifically, mice deficient in either urokinase-type plasminogen activator (uPA-/- mice) or plasminogen demonstrate markedly impaired muscle regeneration after injury. In the present study, we tested the hypothesis that loss of the primary inhibitor of uPA, plasminogen activator inhibitor-1 (PAI-1), would improve muscle regeneration. Repair of the extensor digitorum longus muscle was assessed after cardiotoxin injury in wild-type, uPA-/-, and PAI-1-deficient (PAI-1-/-) mice. As expected, there was no uPA activity in the injured muscles of uPA-/- mice, and muscles from these transgenic animals demonstrated impaired regeneration. On the other hand, uPA activity was increased in injured muscle from PAI-1-/- mice to a greater extent than in wild-type controls. Furthermore, PAI-1-/- mice demonstrated increased expression of MyoD and developmental myosin after injury as well as accelerated recovery of muscle morphology, protein levels, and muscle force compared with wild-type animals. The injured muscles of PAI-1-null mice also demonstrated increased macrophage accumulation, contrasting with impaired macrophage accumulation in uPA-deficient mice. The extent of macrophage accumulation correlated with both the clearance of protein after injury and the efficiency of regeneration. Taken together, these results indicate that PAI-1 deficiency promotes muscle regeneration, and this protease inhibitor represents a therapeutic target for enhancing muscle regeneration.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cobra Cardiotoxin Proteins / pharmacology
  • Hindlimb
  • Macrophages / pathology
  • Mice
  • Mice, Knockout
  • Muscle Proteins / metabolism
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / pathology
  • Muscle, Skeletal / physiopathology*
  • Neutrophils / pathology
  • Plasminogen Activator Inhibitor 1 / deficiency*
  • Plasminogen Activators / metabolism
  • Regeneration*
  • Toes
  • Urokinase-Type Plasminogen Activator / metabolism

Substances

  • Cobra Cardiotoxin Proteins
  • Muscle Proteins
  • Plasminogen Activator Inhibitor 1
  • Plasminogen Activators
  • Urokinase-Type Plasminogen Activator