Inflammatory response in human skeletal muscle cells: CXCL10 as a potential therapeutic target

Eur J Cell Biol. 2012 Feb;91(2):139-49. doi: 10.1016/j.ejcb.2011.09.011. Epub 2011 Dec 15.

Abstract

Inflammatory myopathies (IMs) are systemic diseases characterized by a T helper (Th) 1 type inflammatory response and cell infiltrates within skeletal muscles. The mainstay of treatment is drugs aimed at suppressing the immune system - corticosteroids and immunosuppressants. About 25% of patients are non-responders. Skeletal muscle cells seem actively involved in the immune-inflammatory response and not only a target; understanding the molecular bases of IMs might help drug development strategies. Within muscles the interaction between the chemokine interferon (IFN)γ inducible 10 kDa protein, CXCL10 or IP-10, and its specific receptor CXCR3, present on Th1 type infiltrating cells, likely plays a pivotal role, potentially offering the opportunity for therapeutic intervention. We aimed to clarify the involvement of human skeletal muscle cells in inflammatory processes in terms of CXCL10 secretion, to elucidate the engaged molecular mechanism(s) and, finally, to evaluate muscular cell responses, if any, to some immunosuppressants routinely used in IM treatment, such as methylprednisolone, methotrexate, cyclosporin A and Infliximab. We first isolated and characterized human fetal skeletal muscle cells (Hfsmc), which expressed the specific lineage markers and showed the competence to react in the context of an in vitro alloresponse. CXCL10 protein secretion by Hfsmc was similarly induced by the inflammatory cytokines interferon (IFN)γ and tumor necrosis factor (TNF)α, above undetectable control levels, through the activation of Stat1 and NF-kB pathways, respectively; CXCL10 secretion was significantly magnified by cytokine combination, and this synergy was associated to a significant up-regulation of TNFαRII; cytokine-induced CXCL10 secretion was considerably affected only by Infliximab. Our data suggested that human skeletal muscle cells might actively self-promote muscular inflammation by eliciting CXCL10 secretion, which is known to amplify Th1 cell tissue infiltration in vivo. In conclusion, we sustain that pharmacological targeting of CXCL10 within muscular cells might contribute to keep in control pro-Th1 polarization of the immune/inflammatory response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal / pharmacology
  • Cells, Cultured
  • Chemokine CXCL10 / immunology
  • Chemokine CXCL10 / metabolism*
  • Cyclosporine / pharmacology
  • Fetus
  • Humans
  • Immunosuppressive Agents / pharmacology
  • Infliximab
  • Interferon-gamma / pharmacology
  • Lymphocyte Activation
  • Methylprednisolone / pharmacology
  • Muscle Cells / drug effects
  • Muscle Cells / immunology
  • Muscle Cells / metabolism*
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / immunology
  • Muscle, Skeletal / metabolism*
  • Myositis / immunology
  • Myositis / metabolism*
  • NF-kappa B / metabolism
  • Receptors, CXCR3 / immunology
  • Receptors, CXCR3 / metabolism*
  • STAT1 Transcription Factor / metabolism
  • Signal Transduction
  • Th1 Cells / immunology
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Antibodies, Monoclonal
  • CXCL10 protein, human
  • CXCR3 protein, human
  • Chemokine CXCL10
  • Immunosuppressive Agents
  • NF-kappa B
  • Receptors, CXCR3
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma
  • Cyclosporine
  • Infliximab
  • Methylprednisolone