Emerging role of damage-associated molecular patterns derived from mitochondria in inflammation

被引:547
|
作者
Krysko, Dmitri V. [1 ,2 ]
Agostinis, Patrizia [3 ]
Krysko, Olga [4 ]
Garg, Abhishek D. [3 ]
Bachert, Claus [4 ]
Lambrecht, Bart N. [5 ]
Vandenabeele, Peter [1 ,2 ]
机构
[1] VIB, Mol Signaling & Cell Death Unit, Dept Mol Biomed Res, Ghent, Belgium
[2] Univ Ghent, Dept Biomed Mol Biol, Ghent, Belgium
[3] Catholic Univ Louvain, Dept Mol Cell Biol, B-3000 Louvain, Belgium
[4] UZ Gent, State Univ Ghent Hosp, Upper Airway Res Lab, Dept Otorhinolaryngol,MRB, Ghent, Belgium
[5] Ghent Univ Hosp, Dept Resp Dis, Lab Immunoregulat & Mucosal Immun, B-9000 Ghent, Belgium
关键词
FORMYL PEPTIDE RECEPTORS; PROTEIN-COUPLED RECEPTORS; INNATE IMMUNE-RESPONSES; NECROTIC CELL-DEATH; FIND-ME SIGNAL; CYTOCHROME-C; IN-VIVO; EXTRACELLULAR ATP; OXIDATIVE STRESS; APOPTOSIS;
D O I
10.1016/j.it.2011.01.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cell death and injury often lead to release or exposure of intracellular molecules called damage-associated molecular patterns (DAMPs) or cell death-associated molecules. These molecules are recognized by the innate immune system by pattern recognition receptors the same receptors that detect pathogen-associated molecular patterns, thus revealing similarities between pathogen-induced and non-infectious inflammatory responses. Many DAMPs are derived from the plasma membrane, nucleus, endoplasmic reticulum and cytosol. Recently, mitochondria have emerged as other organelles that function as a source of DAMPs. Here, we highlight the significance of mitochondria! DAMPs and discuss their contribution to inflammation and development of human pathologies.
引用
收藏
页码:157 / 164
页数:8
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