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本文引用的文献

1
Fate and State of Vascular Smooth Muscle Cells in Atherosclerosis.动脉粥样硬化中血管平滑肌细胞的命运和状态。
Circulation. 2021 May 25;143(21):2110-2116. doi: 10.1161/CIRCULATIONAHA.120.049922. Epub 2021 May 24.
2
Increased stem cell proliferation in atherosclerosis accelerates clonal hematopoiesis.动脉粥样硬化中干细胞增殖增加会加速克隆性造血。
Cell. 2021 Mar 4;184(5):1348-1361.e22. doi: 10.1016/j.cell.2021.01.049. Epub 2021 Feb 25.
3
Multiple cell types contribute to the atherosclerotic lesion fibrous cap by PDGFRβ and bioenergetic mechanisms.多种细胞类型通过 PDGFRβ 和生物能量机制促进动脉粥样硬化病变纤维帽的形成。
Nat Metab. 2021 Feb;3(2):166-181. doi: 10.1038/s42255-020-00338-8. Epub 2021 Feb 22.
4
Effect of CD47 Blockade on Vascular Inflammation.CD47阻断对血管炎症的影响。
N Engl J Med. 2021 Jan 28;384(4):382-383. doi: 10.1056/NEJMc2029834.
5
Inhibition of macrophage proliferation dominates plaque regression in response to cholesterol lowering.抑制巨噬细胞增殖在胆固醇降低引起的斑块消退中起主导作用。
Basic Res Cardiol. 2020 Dec 9;115(6):78. doi: 10.1007/s00395-020-00838-4.
6
Sca1 Cells Minimally Contribute to Smooth Muscle Cells in Atherosclerosis.Sca1细胞对动脉粥样硬化中平滑肌细胞的贡献极小。
Circ Res. 2021 Jan 8;128(1):133-135. doi: 10.1161/CIRCRESAHA.120.317972. Epub 2020 Nov 4.
7
Local M-CSF (Macrophage Colony-Stimulating Factor) Expression Regulates Macrophage Proliferation and Apoptosis in Atherosclerosis.局部 M-CSF(巨噬细胞集落刺激因子)表达调节动脉粥样硬化中的巨噬细胞增殖和凋亡。
Arterioscler Thromb Vasc Biol. 2021 Jan;41(1):220-233. doi: 10.1161/ATVBAHA.120.315255. Epub 2020 Oct 22.
8
Single-Cell Genomics Reveals a Novel Cell State During Smooth Muscle Cell Phenotypic Switching and Potential Therapeutic Targets for Atherosclerosis in Mouse and Human.单细胞基因组学揭示了平滑肌细胞表型转换过程中的一种新型细胞状态,以及在小鼠和人类动脉粥样硬化中的潜在治疗靶点。
Circulation. 2020 Nov 24;142(21):2060-2075. doi: 10.1161/CIRCULATIONAHA.120.048378. Epub 2020 Sep 23.
9
Limited proliferation capacity of aortic intima resident macrophages requires monocyte recruitment for atherosclerotic plaque progression.主动脉内膜驻留巨噬细胞的增殖能力有限,需要单核细胞募集来促进动脉粥样硬化斑块的进展。
Nat Immunol. 2020 Oct;21(10):1194-1204. doi: 10.1038/s41590-020-0768-4. Epub 2020 Sep 7.
10
A Notch3-Marked Subpopulation of Vascular Smooth Muscle Cells Is the Cell of Origin for Occlusive Pulmonary Vascular Lesions.Notch3 标记的血管平滑肌细胞亚群是闭塞性肺血管病变的起源细胞。
Circulation. 2020 Oct 20;142(16):1545-1561. doi: 10.1161/CIRCULATIONAHA.120.045750. Epub 2020 Aug 14.

动脉粥样硬化中血管细胞克隆扩增的新兴概念。

Emerging Concepts of Vascular Cell Clonal Expansion in Atherosclerosis.

机构信息

Heart Research Institute, Sydney, NSW, Australia (A.M., A.L., S.P.).

Faculty of Medicine and Health (A.M., R.R.), The University of Sydney, NSW, Australia.

出版信息

Arterioscler Thromb Vasc Biol. 2022 Mar;42(3):e74-e84. doi: 10.1161/ATVBAHA.121.316093. Epub 2022 Feb 3.

DOI:10.1161/ATVBAHA.121.316093
PMID:35109671
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8988894/
Abstract

Clonal expansion is a process that can drive pathogenesis in human diseases, with atherosclerosis being a prominent example. Despite advances in understanding the etiology of atherosclerosis, clonality studies of vascular cells remain in an early stage. Recently, several paradigm-shifting preclinical studies have identified clonal expansion of progenitor cells in the vasculature in response to atherosclerosis. This review provides an overview of cell clonality in atherosclerotic progression, focusing particularly on smooth muscle cells and macrophages. We discuss key findings from the latest research that give insight into the mechanisms by which clonal expansion of vascular cells contributes to disease pathology. The further probing of these mechanisms will provide innovative directions for future progress in the understanding and therapy of atherosclerosis and its associated cardiovascular diseases.

摘要

克隆扩增是一个可以驱动人类疾病发病机制的过程,动脉粥样硬化就是一个突出的例子。尽管人们对动脉粥样硬化的病因学有了更多的了解,但血管细胞的克隆性研究仍处于早期阶段。最近,一些具有开创性的临床前研究已经确定了血管中祖细胞对动脉粥样硬化的克隆扩增。本综述概述了动脉粥样硬化进展中的细胞克隆性,特别关注平滑肌细胞和巨噬细胞。我们讨论了最新研究中的关键发现,这些发现深入了解了血管细胞克隆扩增对疾病病理学的作用机制。进一步探究这些机制将为理解和治疗动脉粥样硬化及其相关心血管疾病的未来进展提供创新性方向。