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微小RNA在肥厚性心脏中表达异常:它们在心肌肥厚中起作用吗?

MicroRNAs are aberrantly expressed in hypertrophic heart: do they play a role in cardiac hypertrophy?

作者信息

Cheng Yunhui, Ji Ruirui, Yue Junming, Yang Jian, Liu Xiaojun, Chen He, Dean David B, Zhang Chunxiang

机构信息

Cardiovascular Research Laboratory, Vascular Biology Center and Department of Surgery, University of Tennessee Health Science Center, 956 Court Avenue, Memphis, TN 38163, USA.

出版信息

Am J Pathol. 2007 Jun;170(6):1831-40. doi: 10.2353/ajpath.2007.061170.

Abstract

MicroRNAs (miRNAs) are a recently discovered class of endogenous, small, noncoding RNAs that regulate gene expression. Although miRNAs are highly expressed in the heart, their roles in heart diseases are currently unclear. Using microarray analysis designed to detect the majority of mammalian miRNAs identified thus far, we demonstrated that miRNAs are aberrantly expressed in hypertrophic mouse hearts. The time course of the aberrant miRNA expression was further identified in mouse hearts at 7, 14, and 21 days after aortic banding. Nineteen of the most significantly dysregulated miRNAs were further confirmed by Northern blot and/or real-time polymerase chain reaction, in which miR-21 was striking because of its more than fourfold increase when compared with the sham surgical group. Similar aberrant expression of the most up-regulated miRNA, miR-21, was also found in cultured neonatal hypertrophic cardiomyocytes stimulated by angiotensin II or phenylephrine. Modulating miR-21 expression via antisense-mediated depletion (knockdown) had a significant negative effect on cardiomyocyte hypertrophy. The results suggest that miRNAs are involved in cardiac hypertrophy formation. miRNAs might be a new therapeutic target for cardiovascular diseases involving cardiac hypertrophy such as hypertension, ischemic heart disease, valvular diseases, and endocrine disorders.

摘要

微小RNA(miRNA)是最近发现的一类内源性、小分子、非编码RNA,可调节基因表达。尽管miRNA在心脏中高度表达,但其在心脏病中的作用目前尚不清楚。通过旨在检测迄今为止已鉴定出的大多数哺乳动物miRNA的微阵列分析,我们证明了miRNA在肥厚型小鼠心脏中异常表达。在主动脉缩窄术后7天、14天和21天的小鼠心脏中进一步确定了异常miRNA表达的时间进程。通过Northern印迹和/或实时聚合酶链反应进一步证实了19种失调最明显的miRNA,其中miR-21尤为显著,因为与假手术组相比其增加了四倍多。在由血管紧张素II或去氧肾上腺素刺激的培养新生肥厚型心肌细胞中也发现了上调最明显的miRNA即miR-21的类似异常表达。通过反义介导的耗竭(敲低)来调节miR-21的表达对心肌细胞肥大有显著的负面影响。结果表明,miRNA参与了心肌肥大的形成。miRNA可能是涉及心肌肥大的心血管疾病(如高血压、缺血性心脏病、瓣膜疾病和内分泌紊乱)的新治疗靶点。

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