Damage-Associated Molecular Patterns in Inflammatory Diseases

被引:702
作者
Roh, Jong Seong [1 ]
Sohn, Dong Hyun [1 ]
机构
[1] Pusan Natl Univ, Sch Med, Dept Microbiol & Immunol, 49 Busandaehak Ro, Yangsan 50612, South Korea
关键词
Damage-associated molecular patterns; Inflammation; Pattern recognition receptors; Inflammatory diseases; TOLL-LIKE RECEPTOR; SMOOTH-MUSCLE-CELLS; RHEUMATOID-ARTHRITIS; IMMUNE-SYSTEM; HMGB1; EXPRESSION; LUPUS NEPHRITIS; SYNOVIAL-FLUID; SERUM-LEVELS; DANGER; ATHEROSCLEROSIS;
D O I
10.4110/in.2018.18.e27
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Damage-associated molecular patterns (DAMPs) are endogenous danger molecules that are released from damaged or dying cells and activate the innate immune system by interacting with pattern recognition receptors (PRRs). Although DAMPs contribute to the host's defense, they promote pathological inflammatory responses. Recent studies have suggested that various DAMPs, such as high-mobility group box 1 (HMGB1), S100 proteins, and heat shock proteins (HSPs), are increased and considered to have a pathogenic role in inflammatory diseases. Here, we review current research on the role of DAMPs in inflammatory diseases, including rheumatoid arthritis, systemic lupus erythematosus, osteoarthritis, atherosclerosis, Alzheimer's disease, Parkinson's disease, and cancer. We also discuss the possibility of DAMPs as biomarkers and therapeutic targets for these diseases.
引用
收藏
页数:14
相关论文
共 92 条
  • [41] Innate immune sensing of microbes by Nod proteins
    Kufer, Thomas A.
    Banks, Diana J.
    Philpott, Dana J.
    [J]. INFLAMMATORY BOWEL DISEASE: GENETICS, BARRIER FUNCTION, IMMUNOLOGIC MECHANISMS, AND MICROBIAL PATHWAYS, 2006, 1072 : 19 - 27
  • [42] Land Walter G, 2015, Sultan Qaboos Univ Med J, V15, pe157
  • [43] Lee MS, 2007, MOL CELLS, V23, P1
  • [44] Methotrexate affects HMGB1 expression in rheumatoid arthritis, and the downregulation of HMGB1 prevents rheumatoid arthritis progression
    Li, Yuan-bo
    Xu, Peng
    Xu, Ke
    Cai, Yong-Song
    Sun, Meng-yao
    Yang, Le
    Sun, Jian
    Lu, She-min
    [J]. MOLECULAR AND CELLULAR BIOCHEMISTRY, 2016, 420 (1-2) : 161 - 170
  • [45] EN-RAGE A Novel Inflammatory Marker for Incident Coronary Heart Disease
    Ligthart, Symen
    Sedaghat, Sanaz
    Ikram, M. Arfan
    Hofman, Albert
    Franco, Oscar H.
    Dehghan, Abbas
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2014, 34 (12) : 2695 - 2699
  • [46] Immune Signaling by RIG-I-like Receptors
    Loo, Yueh-Ming
    Gale, Michael, Jr.
    [J]. IMMUNITY, 2011, 34 (05) : 680 - 692
  • [47] Neutrophil extracellular traps enriched in oxidized mitochondrial DNA are interferogenic and contribute to lupus-like disease
    Lood, Christian
    Blanco, Luz P.
    Purmalek, Monica M.
    Carmona-Rivera, Carmelo
    De Ravin, Suk S.
    Smith, Carolyne K.
    Malech, Harry L.
    Ledbetter, Jeffrey A.
    Elkon, Keith B.
    Kaplan, Mariana J.
    [J]. NATURE MEDICINE, 2016, 22 (02) : 146 - 153
  • [48] Increased alpha-defensin expression is associated with risk of coronary heart disease: a feasible predictive inflammatory biomarker of coronary heart disease in hyperlipidemia patients
    Maneerat, Yaowapa
    Prasongsukarn, Kriengchai
    Benjathummarak, Surachet
    Dechkhajorn, Wilanee
    Chaisri, Urai
    [J]. LIPIDS IN HEALTH AND DISEASE, 2016, 15
  • [49] Systemic lupus erythematosus
    Manson, Jessica J.
    Rahman, Anisur
    [J]. ORPHANET JOURNAL OF RARE DISEASES, 2006, 1 (1)
  • [50] Mariathasan S, 2006, NATURE, V440, P228, DOI 10.1038/nature04515