Npgrj_ni_1457 487..496

نویسندگان

  • Jane Tian
  • Ana Maria Avalos
  • Su-Yau Mao
  • Bo Chen
  • Kannaki Senthil
  • Herren Wu
  • Peggy Parroche
  • Stacey Drabic
  • Douglas Golenbock
  • Cherilyn Sirois
  • Jing Hua
  • Ling Ling An
  • Laurent Audoly
  • Greg La Rosa
  • Angelika Bierhaus
  • Peter Naworth
  • Ann Marshak-Rothstein
  • Mary K Crow
  • Katherine A Fitzgerald
  • Eicke Latz
  • Peter A Kiener
  • Anthony J Coyle
چکیده

Increased concentrations of DNA-containing immune complexes in the serum are associated with systemic autoimmune diseases such as lupus. Stimulation of Toll-like receptor 9 (TLR9) by DNA is important in the activation of plasmacytoid dendritic cells and B cells. Here we show that HMGB1, a nuclear DNA-binding protein released from necrotic cells, was an essential component of DNA-containing immune complexes that stimulated cytokine production through a TLR9–MyD88 pathway involving the multivalent receptor RAGE. Moreover, binding of HMGB1 to class A CpG oligodeoxynucleotides considerably augmented cytokine production by means of TLR9 and RAGE. Our data demonstrate a mechanism by which HMGB1 and RAGE activate plasmacytoid dendritic cells and B cells in response to DNA and contribute to autoimmune pathogenesis.

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تاریخ انتشار 2007