Follistatin-like protein 1 promotes arthritis by up-regulating IFN-gamma

J Immunol. 2009 Jan 1;182(1):234-9. doi: 10.4049/jimmunol.182.1.234.

Abstract

Follistatin-like protein-1 (FSTL-1) is a poorly characterized protein that is up-regulated in the early stage of collagen-induced arthritis and that exacerbates arthritis when delivered by gene transfer. The current study was designed to determine the mechanism by which FSTL-1 promotes arthritis. FSTL-1 was injected into mouse paws, resulting in severe paw swelling associated with up-regulation of IFN-gamma transcript and the IFN-gamma-induced chemokine, CXCL10. Mice depleted of T cells were protected. A central role for IFN-gamma was confirmed by the finding that mice deficient in IFN-gamma failed to exhibit paw swelling in response to injection of FSTL-1. Furthermore, IFN-gamma secretion from mouse spleen cells exposed to a weak TCR signal was increased 5-fold in the presence of FSTL-1. FSTL-1 could be induced by innate immune signals, including TLR4 agonists and the arthritogenic cytokine, IL-1beta, via an NFkappaB pathway. Finally, FSTL-1 was found to be overexpressed in human arthritis and its neutralization inhibited murine collagen-induced arthritis and suppressed IFN-gamma and CXCL10 production in arthritic joints. These findings demonstrate that FSTL-1 plays a critical role in arthritis by enhancing IFN-gamma signaling pathways and suggest a mechanism by which FSTL-1 bridges innate and adaptive immune responses.

Publication types

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

MeSH terms

  • Animals
  • Arthritis, Experimental / immunology*
  • Arthritis, Experimental / metabolism*
  • Arthritis, Rheumatoid / immunology
  • Arthritis, Rheumatoid / metabolism
  • Arthritis, Rheumatoid / surgery
  • Cell Line
  • Follistatin-Related Proteins / biosynthesis
  • Follistatin-Related Proteins / genetics
  • Follistatin-Related Proteins / physiology*
  • Humans
  • Inflammation Mediators / metabolism
  • Inflammation Mediators / physiology*
  • Interferon-gamma / biosynthesis*
  • Interferon-gamma / deficiency
  • Interferon-gamma / genetics
  • Interferon-gamma / metabolism
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred DBA
  • Mice, Knockout
  • Mice, Transgenic
  • RNA, Messenger / biosynthesis
  • Signal Transduction / genetics
  • Signal Transduction / immunology*
  • Up-Regulation / genetics
  • Up-Regulation / immunology*

Substances

  • Follistatin-Related Proteins
  • Fstl1 protein, mouse
  • Inflammation Mediators
  • RNA, Messenger
  • Interferon-gamma