Human keratinocytes produce the complement inhibitor factor H: synthesis is regulated by interferon-gamma

Mol Immunol. 2006 Feb;43(4):317-25. doi: 10.1016/j.molimm.2005.02.009. Epub 2005 Mar 16.

Abstract

Locally synthesized complement is believed to play an important role in host defense and inflammation at organ level. In the epidermis, keratinocytes have so far been shown to synthesize two complement components, C3 and factor B. Here, we studied the synthesis of factor H by human keratinocytes. We also studied the regulation of factor H synthesis in keratinocytes by several cytokines, namely IL-1alpha, IL-2, IL-6, TGF-beta1, TNF-alpha and IFN-gamma. Human keratinocytes expressed factor H mRNA and constitutively released small amounts of factor H protein into the culture medium. This release was strongly upregulated by IFN-gamma but not by other cytokines tested. Western blot analysis revealed that IFN-gamma augments the synthesis of both molecular species, factor H (FH; 155kDa) and factor H-like protein-1 (FHL-1; 45kDa), of factor H. Factor H released in response to IFN-gamma was functionally active. In conclusion, we demonstrate that keratinocytes are capable of synthesizing factor H and that this synthesis is regulated by IFN-gamma.

MeSH terms

  • Blotting, Western
  • Carcinoma, Squamous Cell / pathology
  • Cell Line, Tumor / drug effects
  • Cell Line, Tumor / metabolism
  • Cells, Cultured / drug effects
  • Cells, Cultured / metabolism
  • Complement C3b / metabolism
  • Complement C3b Inactivator Proteins
  • Complement Factor H / biosynthesis
  • Complement Factor H / genetics
  • Complement Factor H / metabolism
  • Complement Factor I / metabolism
  • Cytokines / pharmacology*
  • Humans
  • Interferon-gamma / pharmacology*
  • Interferon-gamma / physiology*
  • Interleukin-1 / pharmacology
  • Interleukin-2 / pharmacology
  • Interleukin-6 / pharmacology
  • Keratinocytes / drug effects
  • Keratinocytes / metabolism*
  • RNA, Messenger / biosynthesis
  • Recombinant Proteins
  • Skin Neoplasms / pathology
  • Transforming Growth Factor beta / pharmacology
  • Transforming Growth Factor beta1
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • CFH protein, human
  • CFHR1 protein, human
  • Complement C3b Inactivator Proteins
  • Cytokines
  • Interleukin-1
  • Interleukin-2
  • Interleukin-6
  • RNA, Messenger
  • Recombinant Proteins
  • TGFB1 protein, human
  • Transforming Growth Factor beta
  • Transforming Growth Factor beta1
  • Tumor Necrosis Factor-alpha
  • Complement C3b
  • Complement Factor H
  • Interferon-gamma
  • Complement Factor I