Detection of cell-type-enriched long noncoding RNAs in atherosclerosis using single-cell techniques: A brief review

生物 电池类型 计算生物学 细胞 免疫系统 破译 长非编码RNA 核糖核酸 细胞生物学 生物信息学 遗传学 基因
作者
Zhiyuan Wu,Yin HongZhuan,Guo Yongsheng,Hongchao Yin,Yongjun Li
出处
期刊:Life Sciences [Elsevier]
卷期号:333: 122138-122138 被引量:3
标识
DOI:10.1016/j.lfs.2023.122138
摘要

Cardiovascular diseases are the leading causes of mortality and morbidity worldwide. Atherosclerotic plaque underlies the predominant factors and is composed of various cell types, including structure cells, such as endothelial and smooth muscle cells, and immune cells, such as macrophages and T cells. Single-cell RNA sequencing (scRNA-seq) has been extensively applied to decipher these cellular heterogeneities to expand our understanding on the mechanisms of atherosclerosis (AS) and to facilitate identifying cell-type-specific long noncoding RNAs (LncRNAs). LncRNAs have been demonstrated to deeply regulate biological activities at the transcriptional and post-transcriptional levels. A group of well-documented functional lncRNAs in AS have been studied. In our review, we selectively described several lncRNAs involved in the critical process of AS. We highlighted four novel lncRNAs (lncRNA CARMN, LINC00607, PCAT19, LINC01235) detected in scRNA-seq datasets and their functions in AS. We also reviewed open web source and bioinformatic tools, as well as the latest methods to perform an in-depth study of lncRNAs. It is fundamental to annotate functional lncRNAs in the various biological activities of AS, as lncRNAs may represent promising targets in the future for treatment and diagnosis in clinical practice.
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