miR-29a attenuates cardiac hypertrophy through inhibition of PPARδ expression.
Si ZhangZhongnan YinFei-Fei DaiHao WangMeng-Jiao ZhouMing-Hui YangShu-Feng ZhangZhi-Feng FuYing-Wu MeiMing-Xi ZangLixiang XuePublished in: Journal of cellular physiology (2018)
Although cardiac hypertrophy is widely recognized as a risk factor that leads to cardiac dysfunction and, ultimately, heart failure, the complex mechanisms underlying cardiac hypertrophy remain incompletely characterized. The nuclear receptor peroxisome proliferator-activated receptor δ (PPARδ) is involved in the regulation of cardiac lipid metabolism. Here, we describe a novel PPARδ-dependent molecular cascade involving microRNA-29a (miR-29a) and atrial natriuretic factor (ANF), which is reactivated in cardiac hypertrophy. In addition, we identify a novel role of miR-29a, in which it has a cardioprotective function in isoproterenol hydrochloride-induced cardiac hypertrophy by targeting PPARδ and downregulating ANF. Finally, we provide evidence that miR-29a reduces the isoproterenol hydrochloride-induced cardiac hypertrophy response, thereby underlining the potential clinical relevance of miR-29a in which it may serve as a potent therapeutic target for heart hypertrophy treatment.
Keyphrases
- cell proliferation
- long non coding rna
- long noncoding rna
- heart failure
- poor prognosis
- insulin resistance
- atrial fibrillation
- left ventricular
- fatty acid
- diabetic rats
- high glucose
- oxidative stress
- type diabetes
- risk factors
- risk assessment
- climate change
- adipose tissue
- metabolic syndrome
- endothelial cells
- anti inflammatory
- cardiac resynchronization therapy
- stress induced
- replacement therapy