猫左心的MicroRNA谱识别健康和晚期肥厚性心肌病的腔特异性表达特征

Jessica Joshua , Jeff L. Caswell , Josep M. Monné Rodriguez , Anja Kipar , M. Lynne O'Sullivan , Geoffrey Wood , Sonja Fonfara
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引用次数: 0

摘要

肥厚性心肌病(HCM)是人类和猫常见的心脏病,然而,其发病机制仍知之甚少。怀疑microRNA参与疾病过程,但尚未确定猫心肌microRNA的表达模式。我们假设健康猫和患有HCM的猫的microRNA谱不同。对健康猫(8 LV, 8 LA)和HCM猫(7 LV, 5 LA)的左心室(LV)和左心房(LA)样本进行小RNA测序。我们鉴定了1039个差异表达的microrna(错误发现率<0.01,倍数变化>2)。发现HCM猫具有明显的microRNA表达谱,具有明显的区域异质性。比较HCM和对照心脏,我们检测到HCM左室有80个差异表达的microrna, LA有37个差异表达的microrna。其中包括LV和LA富集的miR-21、miR-146b和降低的miR-122-5p,这些最近被认为是HCM发病机制的关键microrna,以及可能具有治疗意义的miR-132。几种最富集的microrna: miR-3958, miR-382-5p, miR-487a-5p (HCM LV);miR-chrD4_30107-3p (HCM LA);miR-3548 (HCM LV和LA)在心脏中要么没有报道,要么知之甚少。我们发现了潜在的相关microrna,需要进一步研究它们的作用。与健康心脏相比,已知被差异表达的microrna靶向的基因与HCM左室和左室的炎症和生长途径、左室的心脏保护途径以及左室的纤维化和结构变化相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

MicroRNA profiling of the feline left heart identifies chamber-specific expression signatures in health and in advanced hypertrophic cardiomyopathy

MicroRNA profiling of the feline left heart identifies chamber-specific expression signatures in health and in advanced hypertrophic cardiomyopathy

Hypertrophic cardiomyopathy (HCM) is a common heart disease in humans and cats, nonetheless, the disease pathogenesis is still poorly understood. MicroRNAs are suspected to be involved in the disease process but the myocardial microRNA expression pattern in cats has not been identified. We hypothesized that microRNA profiles differ between healthy cats and cats with HCM. Small RNA sequencing on left ventricle (LV) and left atria (LA) samples from healthy cats (8 LV, 8 LA) and cats with HCM (7 LV, 5 LA) was performed. We identified 1039 differentially expressed microRNAs (False Discovery Rate <0.01, fold change >2). Cats with HCM were found to have a distinct microRNA expression profile with apparent regional heterogeneity. Comparing the HCM and control hearts, we detected 80 differentially expressed microRNAs for the HCM LV, and 37 for the LA. These included LV and LA enriched miR-21, miR-146b, and reduced miR-122-5p, which were recently suggested as key microRNAs for the HCM pathogenesis, and miR-132, which might be of therapeutic interest. Several top enriched microRNAs: miR-3958, miR-382-5p, miR-487a-5p (HCM LV); miR-chrD4_30107-3p (HCM LA); miR-3548 (HCM LV and LA) have either not been reported in the heart or only little is known. We identified potentially relevant microRNAs and further investigations into their role are required. Genes known to be targeted by the differentially expressed microRNAs were associated with inflammation and growth pathways in the HCM LV and LA, cardioprotective pathways in the LV, and fibrosis and structural changes in the LA when compared to healthy hearts.

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来源期刊
Journal of molecular and cellular cardiology plus
Journal of molecular and cellular cardiology plus Cardiology and Cardiovascular Medicine
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