4.5 Article

The DEK nuclear autoantigen is a secreted chemotactic factor

Journal

MOLECULAR AND CELLULAR BIOLOGY
Volume 26, Issue 24, Pages 9484-9496

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/MCB.01030-06

Keywords

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Funding

  1. NCI NIH HHS [T32CA88784-03, T32 CA088784] Funding Source: Medline
  2. NCRR NIH HHS [M01-RR00042, M01 RR000042] Funding Source: Medline
  3. NHLBI NIH HHS [HL58694] Funding Source: Medline
  4. NIAID NIH HHS [AI40987, R01 AI040987] Funding Source: Medline
  5. NIAMS NIH HHS [AR48267, AR49907, R01 AR048267, P30 AR048310, R03 AR049907, 5 P30 AR48310-02] Funding Source: Medline
  6. NIGMS NIH HHS [T32 GM07863, T32 GM007863] Funding Source: Medline

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The nuclear DNA-binding protein DEK is an autoantigen that has been implicated in the regulation of transcription, chromatin architecture, and mRNA processing. We demonstrate here that DEK is actively secreted by macrophages and is also found in synovial fluid samples from patients with juvenile arthritis. Secretion of DEK is modulated by casein kinase 2, stimulated by interieukin-8, and inhibited by dexamethasone and cyclosporine A, consistent with a role as a proinflammatory molecule. DEK is secreted in both a free form and in exosomes, vesicular structures in which transcription-modulating factors such as DEK have not previously been found. Furthermore, DEK functions as a chemotactic factor, attracting neutrophils, CD8(+) T lymphocytes, and natural killer cells. Therefore, the DEK autoantigen, previously described as a strictly nuclear protein, is secreted and can act as an extracellular chemoattractant, suggesting a direct role for DEK in inflammation.

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