DAMP-sensing receptors in sterile inflammation and inflammatory diseases

被引:1222
作者
Gong, Tao [1 ]
Liu, Lei [1 ]
Jiang, Wei [1 ]
Zhou, Rongbin [1 ,2 ]
机构
[1] Univ Sci & Technol China,, Hefei Natl Lab, CAS Key Lab Innate Immun & Chron Dis, Sch Basic,Div Life Sci & Med, Hefei, Peoples R China
[2] Univ Sci & Technol Chona, CAS Ctr Excellence Cell & Mol Biol, Hefei, Peoples R China
基金
中国国家自然科学基金;
关键词
CGAS/STING-DEPENDENT INNATE; GLYCATION END-PRODUCTS; FOAM CELL-FORMATION; TOLL-LIKE RECEPTORS; NLRP3; INFLAMMASOME; P2X7; RECEPTOR; AIM2; DENDRITIC CELLS; CUTTING EDGE; AMYLOID-BETA;
D O I
10.1038/s41577-019-0215-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The innate immune system has the capacity to detect 'non-self' molecules derived from pathogens, known as pathogen-associated molecular patterns, via pattern recognition receptors. In addition, an increasing number of endogenous host-derived molecules, termed damage-associated molecular patterns (DAMPs), have been found to be sensed by various innate immune receptors. The recognition of DAMPs, which are produced or released by damaged and dying cells, promotes sterile inflammation, which is important for tissue repair and regeneration, but can also lead to the development of numerous inflammatory diseases, such as metabolic disorders, neurodegenerative diseases, autoimmune diseases and cancer. Here we examine recent discoveries concerning the roles of DAMP-sensing receptors in sterile inflammation and in diseases resulting from dysregulated sterile inflammation, and then discuss insights into the cross-regulation of these receptors and their ligands. Host-derived molecules, the so-called damage-associated molecular patterns (DAMPs), can induce sterile inflammation. This Review provides an overview of DAMP-sensing receptors, discusses the crosstalk between these receptors and explores their role in disease.
引用
收藏
页码:95 / 112
页数:18
相关论文
共 214 条
[31]   Inhibiting DNA Methylation Causes an Interferon Response in Cancer via dsRNA Including Endogenous Retroviruses [J].
Chiappinelli, Katherine B. ;
Strissel, Pamela L. ;
Desrichard, Alexis ;
Li, Huili ;
Henke, Christine ;
Akman, Benjamin ;
Hein, Alexander ;
Rote, Neal S. ;
Cope, Leslie M. ;
Snyder, Alexandra ;
Makarov, Vladimir ;
Buhu, Sadna ;
Slamon, Dennis J. ;
Wolchok, Jedd D. ;
Pardoll, Drew M. ;
Beckmann, Matthias W. ;
Zahnow, Cynthia A. ;
Mergoub, Taha ;
Chan, Timothy A. ;
Baylin, Stephen B. ;
Strick, Reiner .
CELL, 2015, 162 (05) :974-986
[32]   Recognition of tumor cells by Dectin-1 orchestrates innate immune cells for anti-tumor responses [J].
Chiba, Shiho ;
Ikushima, Hiroaki ;
Ueki, Hiroshi ;
Yanai, Hideyuki ;
Kimura, Yoshitaka ;
Hangai, Sho ;
Nishio, Junko ;
Negishi, Hideo ;
Tamura, Tomohiko ;
Saijo, Shinobu ;
Iwakura, Yoichiro ;
Taniguchi, Tadatsugu .
ELIFE, 2014, 3 :1-20
[33]   Toll-like receptor 7 and TLR9 dictate autoantibody specificity and have opposing inflammatory and regulatory roles in a murine model of lupus [J].
Christensen, Sean R. ;
Shupe, Jonathan ;
Nickerson, Kevin ;
Kashgarian, Michael ;
Flavell, Richard A. ;
Shlomchik, Mark J. .
IMMUNITY, 2006, 25 (03) :417-428
[34]   Receptor for Advanced Glycation End Products and Its Involvement in Inflammatory Diseases [J].
Chuah, Yaw Kuang ;
Basir, Rusliza ;
Talib, Herni ;
Tie, Tung Hing ;
Nordin, Norshariza .
INTERNATIONAL JOURNAL OF INFLAMMATION, 2013, 2013
[35]   MCC950 directly targets the NLRP3 ATP- hydrolysis motif for inflammasome inhibition [J].
Coll, Rebecca C. ;
Hill, James R. ;
Day, Christopher J. ;
Zamoshnikova, Alina ;
Boucher, Dave ;
Massey, Nicholas L. ;
Chitty, Jessica L. ;
Fraser, James A. ;
Jennings, Michael P. ;
Robertson, Avril A. B. ;
Schroder, Kate .
NATURE CHEMICAL BIOLOGY, 2019, 15 (06) :556-+
[36]   A small-molecule inhibitor of the NLRP3 inflammasome for the treatment of inflammatory diseases [J].
Coll, Rebecca C. ;
Robertson, Avril A. B. ;
Chae, Jae Jin ;
Higgins, Sarah C. ;
Munoz-Planillo, Raul ;
Inserra, Marco C. ;
Vetter, Irina ;
Dungan, Lara S. ;
Monks, Brian G. ;
Stutz, Andrea ;
Croker, Daniel E. ;
Butler, Mark S. ;
Haneklaus, Moritz ;
Sutton, Caroline E. ;
Nunez, Gabriel ;
Latz, Eicke ;
Kastner, Daniel L. ;
Mills, Kingston H. G. ;
Masters, Seth L. ;
Schroder, Kate ;
Cooper, Matthew A. ;
O'Neill, Luke A. J. .
NATURE MEDICINE, 2015, 21 (03) :248-+
[37]   LC3-Associated Phagocytosis in Myeloid Cells Promotes Tumor Immune Tolerance [J].
Cunha, Larissa D. ;
Yang, Mao ;
Carter, Robert ;
Guy, Clifford ;
Harris, Lacie ;
Crawford, Jeremy C. ;
Quarato, Giovanni ;
Boada-Romero, Emilio ;
Kalkavan, Halime ;
Johnson, Michael Dl ;
Natarajan, Sivaraman ;
Turnis, Meghan E. ;
Finkelstein, David ;
Opferman, Joseph T. ;
Gawad, Charles ;
Green, Douglas R. .
CELL, 2018, 175 (02) :429-+
[38]   RAGE mediates amyloid-β peptide transport across the blood-brain barrier and accumulation in brain [J].
Deane, R ;
Yan, SD ;
Submamaryan, RK ;
LaRue, B ;
Jovanovic, S ;
Hogg, E ;
Welch, D ;
Manness, L ;
Lin, C ;
Yu, J ;
Zhu, H ;
Ghiso, J ;
Frangione, B ;
Stern, A ;
Schmidt, AM ;
Armstrong, DL ;
Arnold, B ;
Liliensiek, B ;
Nawroth, P ;
Hofman, F ;
Kindy, M ;
Stern, D ;
Zlokovic, B .
NATURE MEDICINE, 2003, 9 (07) :907-913
[39]   DNGR-1 in dendritic cells limits tissue damage by dampening neutrophil recruitment [J].
del Fresno, Carlos ;
Saz-Leal, Paula ;
Enamorado, Michel ;
Wculek, Stefanie K. ;
Martinez-Cano, Sarai ;
Blanco-Menendez, Noelia ;
Schulz, Oliver ;
Gallizioli, Mattia ;
Miro-Mur, Francesc ;
Cano, Eva ;
Planas, Anna ;
Sancho, David .
SCIENCE, 2018, 362 (6412) :351-+
[40]   Structural basis for m7G recognition and 2′-O-methyl discrimination in capped RNAs by the innate immune receptor RIG-I [J].
Devarkar, Swapnil C. ;
Wang, Chen ;
Miller, Matthew T. ;
Ramanathan, Anand ;
Jiang, Fuguo ;
Khan, Abdul G. ;
Patel, Smita S. ;
Marcotrigiano, Joseph .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2016, 113 (03) :596-601