IL-6 signaling blockade increases inflammation but does not affect muscle function in the mdx mouse

BMC Musculoskelet Disord. 2012 Jun 20;13:106. doi: 10.1186/1471-2474-13-106.

Abstract

Background: IL-6 is a pleiotropic cytokine that modulates inflammatory responses and plays critical roles in muscle maintenance and remodeling. In the mouse model (mdx) of Duchenne Muscular Dystrophy, IL-6 and muscle inflammation are elevated, which is believed to contribute to the chronic inflammation and failure of muscle regeneration in DMD. The purpose of the current study was to examine the effect of blocking IL-6 signaling on the muscle phenotype including muscle weakness and pathology in the mdx mouse.

Methods: A monoclonal antibody against the IL-6 receptor (IL-6r mAb) that blocks local and systemic IL-6 signaling was administered to mdx and BL-10 mice for 5 weeks and muscle function, histology, and inflammation were examined.

Results: IL-6r mAb treatment increased mdx muscle inflammation including total inflammation score and ICAM-1 positive lumens in muscles. There was no significant improvement in muscle strength nor muscle pathology due to IL-6r mAb treatment in mdx mice.

Conclusions: These results showed that instead of reducing inflammation, IL-6 signaling blockade for 5 weeks caused an increase in muscle inflammation, with no significant change in indices related to muscle regeneration and muscle function. The results suggest a potential anti-inflammatory instead of the original hypothesized pro-inflammatory role of IL-6 signaling in the mdx mice.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Antibodies, Monoclonal / toxicity
  • Inflammation / chemically induced
  • Inflammation / pathology
  • Inflammation Mediators / antagonists & inhibitors*
  • Inflammation Mediators / physiology*
  • Interleukin-6 / antagonists & inhibitors*
  • Interleukin-6 / metabolism
  • Interleukin-6 / physiology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred mdx
  • Muscle Strength / drug effects
  • Muscle Strength / physiology
  • Muscle, Skeletal / physiology*
  • Muscular Dystrophy, Duchenne / chemically induced
  • Muscular Dystrophy, Duchenne / drug therapy
  • Muscular Dystrophy, Duchenne / pathology*
  • Random Allocation
  • Receptors, Interleukin-6 / immunology
  • Signal Transduction / physiology*

Substances

  • Antibodies, Monoclonal
  • Inflammation Mediators
  • Interleukin-6
  • Receptors, Interleukin-6
  • interleukin-6, mouse