LncRNA SCARNA8通过抑制巨噬细胞efferocytosis促进动脉粥样硬化斑块不稳定。

IF 2.9 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Epigenetics Pub Date : 2025-12-01 Epub Date: 2025-05-13 DOI:10.1080/15592294.2025.2487317
Xiaoliang Yin, Xiaodong Chen, Tao Wang, Jianling Yang, Jiahui Yu, Jun Yang
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引用次数: 0

摘要

近年来研究发现,长链非编码rna (long noncoding RNAs, lncRNAs)与动脉粥样硬化(atherosclerosis, AS)的发生发展密切相关,但lncrna调控的细胞质埋藏是否参与AS的调控尚缺乏相关研究。在本研究中,我们研究了lncRNA SCARNA8通过影响巨噬细胞埋藏来调控AS的机制。lncRNA SCARNA8调控的胞质埋藏相关靶基因为PPARG。颈动脉不稳定斑块组LncRNA SCARNA8升高,而PPARG降低。Ox-LDL导致Raw264.7细胞中lncRNA SCARNA8表达上调和凋亡呈时间、浓度依赖性。lncRNA SCARNA8的下调上调了Raw264.7细胞的PPARG并减少了细胞凋亡。此外,lncRNA SCARNA8的敲低通过促进Raw264.7细胞的细胞埋藏,提高了动脉粥样硬化斑块的稳定性。LncRNA SCARNA8是斑块易损的关键调节因子,靶向LncRNA SCARNA8可能为预防和治疗AS提供新的手段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
LncRNA SCARNA8 promotes atherosclerotic plaque instability by inhibiting macrophage efferocytosis.

In recent years, findings suggest that long noncoding RNAs (lncRNAs) are closely related to the development of atherosclerosis (AS), but there is a lack of studies on the involvement of lncRNA-regulated cytosolic burial in the regulation of AS. In this study, we investigated the mechanism by which lncRNA SCARNA8 affects macrophage cell burial to regulate AS. The cytosolic burial-associated target gene regulated by lncRNA SCARNA8 was PPARG. LncRNA SCARNA8 was increased in the carotid unstable plaque group, whereas PPARG was decreased. Ox-LDL led to the up-regulation of lncRNA SCARNA8 expression and apoptosis in Raw264.7 cells in a time-, concentration-dependent manner. Knockdown of lncRNA SCARNA8 upregulated PPARG and reduced apoptosis in Raw264.7 cells. In addition, knockdown of lncRNA SCARNA8 improved the stability of atherosclerotic plaques by promoting cellular burial of Raw264.7 cells. LncRNA SCARNA8 is a key regulator of plaque vulnerability, and targeting lncRNA SCARNA8 May provide a novel means for the prevention and treatment of AS.

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来源期刊
Epigenetics
Epigenetics 生物-生化与分子生物学
CiteScore
6.80
自引率
2.70%
发文量
82
审稿时长
3-8 weeks
期刊介绍: Epigenetics publishes peer-reviewed original research and review articles that provide an unprecedented forum where epigenetic mechanisms and their role in diverse biological processes can be revealed, shared, and discussed. Epigenetics research studies heritable changes in gene expression caused by mechanisms others than the modification of the DNA sequence. Epigenetics therefore plays critical roles in a variety of biological systems, diseases, and disciplines. Topics of interest include (but are not limited to): DNA methylation Nucleosome positioning and modification Gene silencing Imprinting Nuclear reprogramming Chromatin remodeling Non-coding RNA Non-histone chromosomal elements Dosage compensation Nuclear organization Epigenetic therapy and diagnostics Nutrition and environmental epigenetics Cancer epigenetics Neuroepigenetics
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