Cardiovascular inflammation: RNA takes the lead

被引:21
作者
Martens, Colton R. [1 ]
Bansal, Shyam S. [1 ]
Accornero, Federica [1 ]
机构
[1] Ohio State Univ, Dept Physiol & Cell Biol, Dorothy M Davis Heart & Lung Res Inst, Columbus, OH 43210 USA
关键词
TUMOR-NECROSIS-FACTOR; TRISTETRAPROLIN-DEFICIENT MICE; AU-RICH ELEMENTS; MESSENGER-RNA; NONCODING RNA; TNF-ALPHA; CARDIAC INFLAMMATION; ATHEROSCLEROTIC LESIONS; MYOCARDIAL-INFARCTION; NLRP3; INFLAMMASOME;
D O I
10.1016/j.yjmcc.2019.03.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Inflammation has recently gained tremendous attention as a key contributor in several chronic diseases. While physiological inflammation is essential to counter a wide variety of damaging stimuli and to improve wound healing, dysregulated inflammation such as in the myocardium and vasculature can promote cardiovascular diseases. Given the high severity, prevalence, and economic burden of these diseases, understanding the factors involved in the regulation of physiological inflammation is essential. Like other complex biological phenomena, RNA-based processes are emerging as major regulators of inflammatory responses. Among such processes are cis-regulatory elements in the mRNA of inflammatory genes, noncoding RNAs directing the production or localization of inflammatory cytokines/chemokines, or pathogenic RNA driving inflammatory responses. In this review, we describe several specific RNA-based molecular mechanisms by which physiological inflammation pertaining to cardiovascular diseases is regulated. These include the role of AU-rich element-containing mRNAs, long non-coding RNAs, microRNAs, and viral RNAs.
引用
收藏
页码:247 / 256
页数:10
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