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长非编码 RNA NR_045363 控制心肌细胞增殖和心脏修复。

A long noncoding RNA NR_045363 controls cardiomyocyte proliferation and cardiac repair.

机构信息

Department of Cardiac Surgery, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.

Children's Heart Center, The Second Affiliated Hospital and Yuying Children's Hospital, Institute of Cardiovascular Development and Translational Medicine, Wenzhou Medical University, Wenzhou, Zhejiang, China; State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Disease, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, China.

出版信息

J Mol Cell Cardiol. 2019 Feb;127:105-114. doi: 10.1016/j.yjmcc.2018.12.005. Epub 2018 Dec 13.

Abstract

Long noncoding RNAs (lncRNAs) play important roles in the regulation of genes involved in cell proliferation. We have previously sought to more globally understand the differences of lncRNA expression between human fetal heart and adult heart to identify some functional lncRNAs which involve in the process of heart repair. We found that a highly conserved long noncoding RNA NR_045363 was mainly expressed in cardiomyocytes and rarely in non-cardiomyocytes. NR_045363 overexpression in 7-day-old mice heart could improve cardiac function and stimulate cardiomyocyte proliferation after myocardial infarction. Furthermore, NR_045363 knockdown inhibited proliferation of primary embryonic cardiomyocytes, while NR_045363 overexpression enhanced DNA synthesis and cytokinesis in neonatal cardiomyocytes in vitro. Mechanistic analysis revealed that NR_045363 promoted cardiomyocyte proliferation through interaction with miR-216a, which regulated the JAK2-STAT3 pathway. Our results showed that NR_045363 is a potent lncRNA modulator essential for cardiomyocyte proliferation.

摘要

长链非编码 RNA(lncRNA)在调节细胞增殖相关基因方面发挥着重要作用。我们之前试图更全面地了解人胎儿心脏和成人心脏之间 lncRNA 表达的差异,以鉴定一些涉及心脏修复过程的功能性 lncRNA。我们发现一个高度保守的长链非编码 RNA NR_045363 主要在心肌细胞中表达,而在非心肌细胞中很少表达。在 7 天大的小鼠心脏中过表达 NR_045363 可以改善心脏功能,并在心肌梗死后刺激心肌细胞增殖。此外,NR_045363 敲低抑制原代胚胎心肌细胞的增殖,而 NR_045363 过表达在体外增强新生心肌细胞的 DNA 合成和胞质分裂。机制分析表明,NR_045363 通过与 miR-216a 相互作用促进心肌细胞增殖,后者调节 JAK2-STAT3 通路。我们的结果表明,NR_045363 是一种重要的 lncRNA 调节剂,对心肌细胞增殖至关重要。

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