The DEK Nuclear Autoantigen Is a Secreted Chemotactic Factor

Author:

Mor-Vaknin Nirit1,Punturieri Antonello234,Sitwala Kajal15,Faulkner Neil15,Legendre Maureen1,Khodadoust Michael S.13,Kappes Ferdinand1,Ruth Jeffrey H.6,Koch Alisa63,Glass David7,Petruzzelli Lilli83,Adams Barbara S.9,Markovitz David M.135

Affiliation:

1. Department of Internal Medicine, Division of Infectious Diseases

2. Department of Internal Medicine, Division of Pulmonary Medicine

3. Program in Immunology

4. Division of Lung Diseases, NHLBI, Bethesda, Maryland

5. Cellular and Molecular Biology Program, University of Michigan Medical Center, Ann Arbor, Michigan 48109

6. Department of Internal Medicine, Division of Rheumatology

7. Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio 45229

8. Department of Internal Medicine, Division of Hematology and Oncology

9. Department of Pediatrics, Division of Rheumatology

Abstract

ABSTRACT 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 interleukin-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.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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