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miRNA 表达分析在人心:未分化祖细胞与活检组织——对增殖和衰老的影响。

miRNA expression analysis in the human heart: Undifferentiated progenitors vs. bioptic tissues-Implications for proliferation and ageing.

机构信息

Department of Research, Istituto Mediterraneo per i Trapianti e Terapie ad alta specializzazione (ISMETT-IRCCS), Palermo, Italy.

Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome, Italy.

出版信息

J Cell Mol Med. 2021 Sep;25(18):8687-8700. doi: 10.1111/jcmm.16824. Epub 2021 Aug 13.

Abstract

In developed countries, cardiovascular diseases are currently the first cause of death. Cardiospheres (CSs) and cardiosphere-derived cells (CDCs) have been found to have the ability to regenerate the myocardium after myocardial infarction (MI). In recent years, much effort has been made to gain insight into the human heart repair mechanisms, in which miRNAs have been shown to play an important role. In this regard, to elucidate the involvement of miRNAs, we evaluated the miRNA expression profile across human heart biopsy, CSs and CDCs using microarray and next-generation sequencing (NGS) technologies. We identified several miRNAs more represented in the progenitors, where some of them can be responsible for the proliferation or the maintenance of an undifferentiated state, while others have been found to be downregulated in the undifferentiated progenitors compared with the biopsies. Moreover, we also found a correlation between downregulated miRNAs in CSs/CDCs and patient age (eg miR-490) and an inverse correlation among miRNAs upregulated in CSs/CDCs (eg miR-31).

摘要

在发达国家,心血管疾病目前是首要死因。研究发现,心肌球体(CSs)和心肌球体衍生细胞(CDCs)具有在心肌梗死(MI)后再生心肌的能力。近年来,人们做出了很多努力来深入了解人类心脏修复机制,其中 miRNA 被证明发挥了重要作用。在这方面,为了阐明 miRNA 的参与,我们使用微阵列和下一代测序(NGS)技术评估了人类心脏活检、CSs 和 CDCs 中的 miRNA 表达谱。我们鉴定了在祖细胞中表达更为丰富的几种 miRNA,其中一些可能负责增殖或维持未分化状态,而另一些则在未分化祖细胞中发现与活检相比被下调。此外,我们还发现 CSs/CDCs 中下调的 miRNA 与患者年龄之间存在相关性(例如 miR-490),而 CSs/CDCs 中上调的 miRNA 之间存在负相关(例如 miR-31)。

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