Increased expression of the novel proinflammatory cytokine high mobility group box chromosomal protein 1 in skin lesions of patients with lupus erythematosus

Arthritis Rheum. 2005 Nov;52(11):3639-45. doi: 10.1002/art.21398.

Abstract

Objective: To investigate the role of the novel cytokine high mobility group box chromosomal protein 1 (HMGB-1) in the pathogenesis of cutaneous lupus erythematosus (CLE).

Methods: Punch biopsy specimens of lesional and unaffected skin from 10 patients with CLE and 3 healthy control subjects were investigated. Immunohistochemical staining for HMGB-1, tumor necrosis factor alpha (TNFalpha), and interleukin-1beta (IL-1beta) was performed on consecutive sections. Analysis of single-nucleotide polymorphisms of -308 TNF was performed on DNA extracted from peripheral blood mononuclear cells.

Results: An altered expression of HMGB-1 was observed both in the epidermis and in the dermal infiltrates of lesional skin. Expression of HMGB-1 in the epidermis and dermis was increased (P < 0.01 and P < 0.001, respectively, versus unaffected skin), and translocation to the cytoplasm as well as the extracellular presence of secreted HMGB-1 were found. Increased levels of TNFalpha and IL-1beta were also observed in the dermal infiltrates of lesional skin (P < 0.01 and P < 0.05, respectively, versus unaffected skin). The carrier frequency of the -308A TNF polymorphism was 80% in patients with subacute CLE, but this was not related to higher expression of TNFalpha in biopsy specimens from the CLE group.

Conclusion: The high amount of extracellular HMGB-1 observed in skin lesions indicates that HMGB-1 is involved in the inflammatory process of CLE. TNFalpha and IL-1beta may form a proinflammatory loop with HMGB-1, since they can induce the release of each other. The extracellular HMGB-1 observed by immunostaining of the epidermis indicates that keratinocytes may be an as yet unrecognized source of secreted HMGB-1, underscoring the role of the target organ in the rheumatoid autoimmune inflammatory process.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • DNA / genetics
  • Female
  • HMGB1 Protein / genetics
  • HMGB1 Protein / metabolism*
  • Humans
  • Immunohistochemistry
  • Interleukin-1 / metabolism
  • Keratinocytes / metabolism
  • Keratinocytes / pathology
  • Leukocytes, Mononuclear / chemistry
  • Leukocytes, Mononuclear / pathology
  • Lupus Erythematosus, Cutaneous / genetics
  • Lupus Erythematosus, Cutaneous / metabolism*
  • Lupus Erythematosus, Cutaneous / pathology
  • Male
  • Middle Aged
  • Polymorphism, Single Nucleotide / genetics
  • Skin / metabolism*
  • Skin / pathology
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • HMGB1 Protein
  • Interleukin-1
  • Tumor Necrosis Factor-alpha
  • DNA