动脉粥样硬化中氧化-LDL诱导血管平滑肌细胞衍生泡沫细胞的最新进展。

IF 4.6 2区 生物学 Q2 CELL BIOLOGY
Frontiers in Cell and Developmental Biology Pub Date : 2024-10-25 eCollection Date: 2024-01-01 DOI:10.3389/fcell.2024.1481505
Jingjing Guo, Laijing Du
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引用次数: 0

摘要

过量胆固醇的积聚会诱发泡沫细胞的积聚,最终加速动脉粥样硬化的发展。从历史上看,巨噬细胞衍生泡沫细胞的机制因其在斑块形成中的核心作用而备受关注,而结合单细胞测序(sc-seq)进行的系谱追踪则对这一机制提出了挑战。大量研究揭示了血管平滑肌细胞(VSMC)是如何增殖和迁移到血管内膜并积聚,然后在过剩脂质的诱导下转化为泡沫细胞,最终占小鼠和人类斑块内泡沫细胞总数的 30% 至 70%。因此,VSMC 衍生泡沫细胞的机制越来越受到关注。本综述旨在总结动脉粥样硬化中氧化低密度脂蛋白(ox-LDL)诱导 VSMC 转化为泡沫细胞的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An update on ox-LDL-inducing vascular smooth muscle cell-derived foam cells in atherosclerosis.

Excess cholesterol accumulation induces the accumulation of foam cells, eventually accelerating atherosclerosis progress. Historically, the mechanisms of macrophage-derived foam cells have attracted attention because of their central role in plaque development, which was challenged by lineage tracing in union with single-cell sequencing (sc-seq). Accumulated studies have uncovered how vascular smooth muscle cells (VSMCs) proliferate and migrate to the vascular intima and accumulate, then transform into foam cells induced by surplus lipids, finally accounting for 30% to 70% of the total foam cells within the plaque of both mice and humans. Therefore, the mechanisms of VSMC-derived foam cells have received increasing attention. The review intends to summarize the transformation mechanism of VSMCs into foam cells induced by oxidized low-density lipoproteins (ox-LDL) in atherosclerosis.

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来源期刊
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
9.70
自引率
3.60%
发文量
2531
审稿时长
12 weeks
期刊介绍: Frontiers in Cell and Developmental Biology is a broad-scope, interdisciplinary open-access journal, focusing on the fundamental processes of life, led by Prof Amanda Fisher and supported by a geographically diverse, high-quality editorial board. The journal welcomes submissions on a wide spectrum of cell and developmental biology, covering intracellular and extracellular dynamics, with sections focusing on signaling, adhesion, migration, cell death and survival and membrane trafficking. Additionally, the journal offers sections dedicated to the cutting edge of fundamental and translational research in molecular medicine and stem cell biology. With a collaborative, rigorous and transparent peer-review, the journal produces the highest scientific quality in both fundamental and applied research, and advanced article level metrics measure the real-time impact and influence of each publication.
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