Microparticles as a source of extracellular DNA

被引:68
作者
Pisetsky, David S. [1 ,2 ,3 ]
Gauley, Julie [1 ,2 ,3 ]
Ullal, Anirudh J. [1 ,2 ,3 ]
机构
[1] Durham VAMC, Med Res Serv, Durham, NC 27705 USA
[2] Duke Univ, Med Ctr, Div Rheumatol & Immunol, Durham, NC 27705 USA
[3] Duke Univ, Med Ctr, Dept Immunol, Durham, NC 27705 USA
关键词
Microparticles; DNA; Apoptosis; Systemic lupus erythematosus; Innate immunity; MURINE MACROPHAGES; PROTEIN HMGB1; CELLS; RELEASE; AUTOANTIGENS; COMPLEXES; JURKAT;
D O I
10.1007/s12026-010-8184-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Microparticles are small membrane-bound vesicles that display pro-inflammatory and pro-thrombotic activities important in the pathogenesis of a wide variety of diseases. These particles are released from activated and dying cells and incorporate nuclear and cytoplasmic molecules for extracellular export. Of these molecules, DNA is a central autoantigen in systemic lupus erythematosus (SLE). As studies in our laboratory show, DNA occurs prominently in microparticles, translocating into these structures during apoptotic cell death. This DNA is antigenically active and can bind to lupus anti-DNA autoantibodies. These findings suggest that microparticles are an important source of extracellular DNA to serve as an autoantigen and autoadjuvant in SLE.
引用
收藏
页码:227 / 234
页数:8
相关论文
共 25 条
[1]
The role of HMGB1 in the pathogenesis of rheumatic disease [J].
Andersson, Ulf ;
Harris, Helena Erlandsson .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS, 2010, 1799 (1-2) :141-148
[2]
The role of microparticles in the pathogenesis of rheumatic diseases [J].
Beyer, Christian ;
Pisetsky, David S. .
NATURE REVIEWS RHEUMATOLOGY, 2010, 6 (01) :21-29
[3]
Monocytic cells hyperacetylate chromatin protein HMGB1 to redirect it towards secretion [J].
Bonaldi, T ;
Talamo, F ;
Scaffidi, P ;
Ferrera, D ;
Porto, A ;
Bachi, A ;
Rubartelli, A ;
Agresti, A ;
Bianchi, ME .
EMBO JOURNAL, 2003, 22 (20) :5551-5560
[4]
AUTOANTIGENS TARGETED IN SYSTEMIC LUPUS-ERYTHEMATOSUS ARE CLUSTERED IN 2 POPULATIONS OF SURFACE-STRUCTURES ON APOPTOTIC KERATINOCYTES [J].
CASCIOLAROSEN, LA ;
ANHALT, G ;
ROSEN, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (04) :1317-1330
[5]
Shedding microvesicles: artefacts no more [J].
Cocucci, Emanuele ;
Racchetti, Gabriella ;
Meldolesi, Jacopo .
TRENDS IN CELL BIOLOGY, 2009, 19 (02) :43-51
[6]
The nuclear protein HMGB1 is secreted by monocytes via a non-classical, vesicle-mediated secretory pathway [J].
Gardella, S ;
Andrei, C ;
Ferrera, D ;
Lotti, LV ;
Torrisi, MR ;
Bianchi, ME ;
Rubartelli, A .
EMBO REPORTS, 2002, 3 (10) :995-1001
[7]
The release of microparticles by RAW 264.7 macrophage cells stimulated with TLR ligands [J].
Gauley, Julie ;
Pisetsky, David S. .
JOURNAL OF LEUKOCYTE BIOLOGY, 2010, 87 (06) :1115-1123
[8]
Antibodies to DNA [J].
Hahn, BH .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (19) :1359-1368
[9]
Alarmin(g) news about danger - Workshop on innate danger signals and HMGB1 [J].
Harris, Helena Erlandsson ;
Raucci, Angela .
EMBO REPORTS, 2006, 7 (08) :774-778
[10]
The relationship between apoptosis and high-mobility group protein 1 release from murine macrophages stimulated with lipopolysaccharide or polyinosinic-polycytidylic acid [J].
Jiang, Weiwen ;
Bell, Charles W. ;
Pisetsky, David S. .
JOURNAL OF IMMUNOLOGY, 2007, 178 (10) :6495-6503