Pathophysiology of interieukin-1 receptor-associated kinase-M:: implications in refractory state

被引:22
作者
Lopez-Collazo, Eduardo [1 ]
Fuentes-Prior, Pablo
Arnalich, Francisco
del Fresno, Carlos
机构
[1] La Paz Hosp, Res Unit, Madrid 28046, Spain
[2] CSIC, ICCC, Cardiovasc Res Ctr, Barcelona, Spain
关键词
cancer tolerance; endotoxin tolerance; human monocytes; inflammation; interlukin-1 receptor-associated kinase-M; toll-like receptor;
D O I
10.1097/01.qco.0000224817.35105.7d
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Purpose of review The pseudo-kinase interleukin-1 receptor-associated kinase-M has emerged as a critical molecule in the down-regulation of inflammatory responses. Dysregulation of the toll-like receptor-interleukin-1 receptor-associated kinase-M up-regulation, are associated with a number of pathologies. This review highlights recent findings on interleukin-1 receptor-associated kinease-M reported in biomedical literature. Recent findings Interleukin-1 receptor-associated kinease-M plays a critical role in generating refractory state of the immune system following monocytes/macrophages encounter with bacteria or tumor cells. This state has been demonstrated so far in patients who suffer from sepsis,leukemia, and acute coronary syndrome, and seems to be associated with interleukin-1 receptor-associated kinase-M overexpression in their circulating monocytes. In addition, the pseudo-kinase represents a central regulator of osteoclast differentiation and activation, and might thus be related to the onset of osteoporosis. Summary Interleukin-1 receptor-associated kinase-M is involved in the control of endotoxin tolerance in monocytes, in osteoporsis, as well as in the deactivation of tumor-infiltrating macrophages. Additionally, patients who suffer from several pathologies related to inflammatory responses express high levels of this molecule in their circulating monocytes. Human monocytes treated with a nitric oxide donor also express large amounts of interleukin-1 receptor-associated kinase-M, apparently under the control of tumor necrosis factor-alpha. This mechanism could explain the induction of interleukin-1 receptor-associated kinase-M in monocytes from patients who suffer from an inflammatory pathology.
引用
收藏
页码:237 / 244
页数:8
相关论文
共 67 条
[1]   IL-4 abrogates osteoclastogenesis through STAT6-dependent inhibition of NF-κB [J].
Abu-Amer, Y .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (11) :1375-1385
[2]   Toll-like receptor signalling [J].
Akira, S ;
Takeda, K .
NATURE REVIEWS IMMUNOLOGY, 2004, 4 (07) :499-511
[3]   A low molecular weight mimic of the Toll/IL-1 receptor/resistance domain inhibits IL-1 receptor-mediated responses [J].
Bartfai, T ;
Behrens, MM ;
Gaidarova, S ;
Pemberton, J ;
Shivanyuk, A ;
Rebek, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (13) :7971-7976
[4]   Innate immune sensing and its roots: the story of endotoxin [J].
Beutler, B ;
Rietschel, ET .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (02) :169-176
[5]   Inhibition of interleukin 1 receptor/toll-like receptor signaling through the alternatively spliced, short form of MyD88 is due to its failure to recruit IRAK-4 [J].
Burns, K ;
Janssens, S ;
Brissoni, B ;
Olivos, N ;
Beyaert, R ;
Tschopp, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (02) :263-268
[6]  
Calvano SE, 2005, NATURE, V438, P696, DOI 10.1038/nature04362
[7]   IRAK: A kinase associated with the interleukin-1 receptor [J].
Cao, ZD ;
Henzel, WJ ;
Gao, XO .
SCIENCE, 1996, 271 (5252) :1128-1131
[8]   Achieving stability of lipopolysaccharide-induced NF-κB activation [J].
Covert, MW ;
Leung, TH ;
Gaston, JE ;
Baltimore, D .
SCIENCE, 2005, 309 (5742) :1854-1857
[9]   Tumor cells deactivate human monocytes by up-regulating IL-1 receptor associated kinase-M expression via CD44 and TLR4 [J].
del Fresno, C ;
Otero, K ;
Gómez-García, L ;
González-León, MC ;
Soler-Ranger, L ;
Fuentes-Prior, P ;
Escoll, P ;
Baos, R ;
Caveda, L ;
García, F ;
Arnalich, F ;
López-Collazo, E .
JOURNAL OF IMMUNOLOGY, 2005, 174 (05) :3032-3040
[10]   Nitric oxide activates the expression of IRAK-M via the release of TNF-α in human monocytes [J].
del Fresno, C ;
Gömez-García, L ;
Caveda, L ;
Escoll, P ;
Arnalich, F ;
Zamora, R ;
López-Collazo, E .
NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2004, 10 (04) :213-220