The Wnt pathway: A macrophage effector molecule that triggers inflammation

被引:77
作者
Pereira, Claudia P. [1 ]
Bachli, Esther B. [1 ]
Schoedon, Gabriele [1 ]
机构
[1] Univ Zurich Hosp, Dept Med, CH-8091 Zurich, Switzerland
关键词
ACTIVATED PROTEIN-C; NF-KAPPA-B; SIGNALING PATHWAY; GENE-EXPRESSION; MONONUCLEAR-CELLS; TISSUE FACTOR; RECEPTOR; INHIBITION; WINGLESS; POLARITY;
D O I
10.1007/s11883-009-0036-4
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Wnt proteins are members of the highly conserved wingless family of proteins responsible for cell differentiation and development and for neoplastic and degenerative processes. Recently, Toll-like receptor-mediated Wnt signaling was found to be associated with innate immunity in Drosophila. Upregulation of Wnt5A in human macrophages upon microbial challenge indicated a similar mechanism. Toll-like receptor-mediated Wnt5A expression is a key process for sustained inflammatory macrophage activation through autocrine and paracrine signaling. Downregulation of Wnt5A expression and subsequent attenuation of inflammatory macrophage responses by activated protein C supports the link between inflammation and coagulation, another highly conserved biologic system. Direct evidence for the relevance of Wnt5A in severe systemic inflammation is provided by the finding of higher Wnt5A levels in patients with sepsis than in healthy individuals. The fact that Wnt5A signaling can be modulated by anti-inflammatory mediators makes this effector molecule an attractive target for therapeutic intervention in inflammatory diseases.
引用
收藏
页码:236 / 242
页数:7
相关论文
共 50 条
[1]   Epidemiology of severe sepsis in the United States: Analysis of incidence, outcome, and associated costs of care [J].
Angus, DC ;
Linde-Zwirble, WT ;
Lidicker, J ;
Clermont, G ;
Carcillo, J ;
Pinsky, MR .
CRITICAL CARE MEDICINE, 2001, 29 (07) :1303-1310
[2]   The profibrinolytic effect of activated protein C in clots formed from plasma is TAFI-dependent [J].
Bajzar, L ;
Nesheim, ME ;
Tracy, PB .
BLOOD, 1996, 88 (06) :2093-2100
[3]   Efficacy and safety of recombinant human activated protein C for severe sepsis. [J].
Bernard, GR ;
Vincent, JL ;
Laterre, P ;
LaRosa, SP ;
Dhainaut, JF ;
Lopez-Rodriguez, A ;
Steingrub, JS ;
Garber, GE ;
Helterbrand, JD ;
Ely, EW ;
Fisher, CJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (10) :699-709
[4]   The Wingless homolog, WNT5A and its receptor Frizzled-5 regulate inflammatory responses of human mononuclear cells induced by microbial stimulation [J].
Blumenthal, Antje ;
Ehlers, Stefan ;
Lauber, Jorg ;
Buer, Jan ;
Lange, Christoph ;
Goldmann, Torsten ;
Heine, Holger ;
Brandt, Ernst ;
Reiling, Norbert .
BLOOD, 2006, 108 (03) :965-973
[5]   BINDING OF HUMAN FACTOR-VII AND FACTOR-VIIA TO MONOCYTES [J].
BROZE, GJ .
JOURNAL OF CLINICAL INVESTIGATION, 1982, 70 (03) :526-535
[6]   Drotrecogin alfa (activated) inhibits NF-kappa B activation and MIP-1-alpha release from isolated mononuclear cells of patients with severe sepsis [J].
Brueckmann, M ;
Hoffmann, U ;
Dvortsak, E ;
Lang, S ;
Kaden, JJ ;
Borggrefe, M ;
Haase, KK .
INFLAMMATION RESEARCH, 2004, 53 (10) :528-533
[7]   Activated protein C inhibits the release of macrophage inflammatory protein-1-alpha from THP-1 cells and from human monocytes [J].
Brueckmann, M ;
Hoffmann, U ;
de Rossi, L ;
Weller, HM ;
Liebe, V ;
Lang, S ;
Kaden, JJ ;
Borggrefe, M ;
Haase, KK ;
Huhle, G .
CYTOKINE, 2004, 26 (03) :106-113
[8]   Monocytes/macrophages and sepsis [J].
Cavaillon, JM ;
Adib-Conquy, M .
CRITICAL CARE MEDICINE, 2005, 33 (12) :S506-S509
[9]   Unique gene expression profiles of human macrophages and dendritic cells to phylogenetically distinct parasites [J].
Chaussabel, D ;
Semnani, RT ;
McDowell, MA ;
Sacks, D ;
Sher, A ;
Nutman, TB .
BLOOD, 2003, 102 (02) :672-681
[10]   The immunopathogenesis of sepsis [J].
Cohen, J .
NATURE, 2002, 420 (6917) :885-891