The Inflammasome in Myocardial Injury and Cardiac Remodeling

被引:133
|
作者
Toldo, Stefano [1 ,2 ]
Mezzaroma, Eleonora [2 ,3 ]
Mauro, Adolfo Gabriele [1 ,2 ]
Salloum, Fadi [1 ]
Van Tassell, Benjamin Wallace [2 ,3 ]
Abbate, Antonio [1 ,2 ]
机构
[1] Virginia Commonwealth Univ, VCU Pauley Heart Ctr, Richmond, VA 23298 USA
[2] Virginia Commonwealth Univ, Dept Internal Med, Victoria Johnson Res Labs, Richmond, VA 23298 USA
[3] Virginia Commonwealth Univ, Sch Pharm, Pharmacotherapy & Outcome Sci, Richmond, VA 23298 USA
关键词
INTERLEUKIN-1 RECEPTOR ANTAGONIST; ISCHEMIA-REPERFUSION INJURY; MOBILITY GROUP BOX-1; CORONARY-HEART-DISEASE; PUBLIC-HEALTH PRACTICE; TUMOR-NECROSIS-FACTOR; C-REACTIVE PROTEIN; NLRP3; INFLAMMASOME; CARDIOVASCULAR-DISEASE; MITOCHONDRIAL-DNA;
D O I
10.1089/ars.2014.5989
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Significance: An inflammatory response follows an injury of any nature, and while such a response is an attempt to promote healing, it may, itself, result in further injury. Recent Advances: The inflammasome is a macromolecular structure recently recognized as a central mediator in the acute inflammatory response. The inflammasome senses the injury and it amplifies the response by leading to the release of powerful pro-inflammatory cytokines, interleukin-1 beta (IL-1 beta) and IL-18. Critical Issues: The activation of the inflammasome in the heart during ischemic and nonischemic injury represents an exaggerated response to sterile injury and promotes adverse cardiac remodeling and failure. Future Directions: Pilot clinical trials have explored blockade of the inflammasome-derived IL-1 beta and have shown beneficial effects on cardiac function. Additional clinical studies testing this approach are warranted. Moreover, specific inflammasome inhibitors that are ready for clinical use are currently lacking. Antioxid. Redox Signal. 22, 1146-1161.
引用
收藏
页码:1146 / 1161
页数:16
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