Suppr超能文献

外泌体与动脉粥样硬化的发生

Exosomes and Atherogenesis.

作者信息

Lin Bingbing, Yang Juan, Song Yuwei, Dang Guohui, Feng Juan

机构信息

Key Laboratory of Molecular Cardiovascular Science, Ministry of Education, Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University, Beijing, China.

Department of Integration of Chinese and Western Medicine, School of Basic Medical Sciences, Peking University, Beijing, China.

出版信息

Front Cardiovasc Med. 2021 Aug 26;8:738031. doi: 10.3389/fcvm.2021.738031. eCollection 2021.

Abstract

Myocardial infarction and ischemic stroke are the leading causes of mortality worldwide. Atherosclerosis is their common pathological foundation. It is known that atherosclerosis is characterized by endothelial activation/injury, accumulation of inflammatory immune cells and lipid-rich foam cells, followed by the development of atherosclerotic plaque. Either from arterial vessel wall or blood circulation, endothelial cells, smooth muscle cells, macrophages, T-lymphocytes, B-lymphocytes, foam cells, and platelets have been considered to contribute to the pathogenesis of atherosclerosis. Exosomes, as natural nano-carriers and intercellular messengers, play a significant role in modulation of cell-to-cell communication. Under physiological or pathological conditions, exosomes can deliver their cargos including donor cell-specific proteins, lipids, and nucleic acids to target cells, which in turn affect the function of the target cells. In this review, we will describe the pathophysiological significance of various exosomes derived from different cell types associated with atherosclerosis, and the potential applications of exosome in clinical diagnosis and treatment.

摘要

心肌梗死和缺血性中风是全球范围内主要的死亡原因。动脉粥样硬化是它们共同的病理基础。众所周知,动脉粥样硬化的特征是内皮激活/损伤、炎性免疫细胞和富含脂质的泡沫细胞的积聚,随后形成动脉粥样硬化斑块。无论是来自动脉血管壁还是血液循环,内皮细胞、平滑肌细胞、巨噬细胞、T淋巴细胞、B淋巴细胞、泡沫细胞和血小板都被认为与动脉粥样硬化的发病机制有关。外泌体作为天然的纳米载体和细胞间信使,在调节细胞间通讯中发挥着重要作用。在生理或病理条件下,外泌体可以将其包括供体细胞特异性蛋白质、脂质和核酸在内的货物递送至靶细胞,进而影响靶细胞的功能。在这篇综述中,我们将描述源自与动脉粥样硬化相关的不同细胞类型的各种外泌体的病理生理意义,以及外泌体在临床诊断和治疗中的潜在应用。

相似文献

1
Exosomes and Atherogenesis.
Front Cardiovasc Med. 2021 Aug 26;8:738031. doi: 10.3389/fcvm.2021.738031. eCollection 2021.
2
Exosomes in Atherosclerosis: Role in the Pathogenesis and Targets for Therapy.
Curr Med Chem. 2024 May 3. doi: 10.2174/0109298673302220240430173404.
3
Exosomes: Multifaceted Messengers in Atherosclerosis.
Curr Atheroscler Rep. 2020 Aug 9;22(10):57. doi: 10.1007/s11883-020-00871-7.
4
Exosomes in Cholesterol Metabolism and Atherosclerosis.
Cardiovasc Hematol Disord Drug Targets. 2017;17(3):185-194. doi: 10.2174/1871529X18666180103124443.
5
CD40 signaling in vascular cells: a key role in atherosclerosis?
Atherosclerosis. 1998 Apr;137 Suppl:S89-95. doi: 10.1016/s0021-9150(97)00309-2.
7
Exosomes: An emerging factor in atherosclerosis.
Biomed Pharmacother. 2019 Jul;115:108951. doi: 10.1016/j.biopha.2019.108951. Epub 2019 May 8.
8
Stem cell-derived exosomes: Role in the pathogenesis and treatment of atherosclerosis.
Int J Biochem Cell Biol. 2021 Jan;130:105884. doi: 10.1016/j.biocel.2020.105884. Epub 2020 Nov 20.
9
Exosomes: Versatile Nano Mediators of Immune Regulation.
Cancers (Basel). 2019 Oct 14;11(10):1557. doi: 10.3390/cancers11101557.
10
Platelet-Derived Exosomes in Atherosclerosis.
Int J Mol Sci. 2022 Oct 19;23(20):12546. doi: 10.3390/ijms232012546.

引用本文的文献

1
Engineered exosomes: a promising drug delivery platform with therapeutic potential.
Front Mol Biosci. 2025 May 9;12:1583992. doi: 10.3389/fmolb.2025.1583992. eCollection 2025.
3
The Role of Macrophages in Atherosclerosis: Participants and Therapists.
Cardiovasc Drugs Ther. 2025 Apr;39(2):459-472. doi: 10.1007/s10557-023-07513-5. Epub 2023 Oct 21.
6
Progression in the Relationship between Exosome Production and Atherosclerosis.
Curr Pharm Biotechnol. 2024;25(9):1099-1111. doi: 10.2174/1389201024666230726114920.
7
miR-186-5p Dysregulation in Serum Exosomes from Patients with AMI Aggravates Atherosclerosis via Targeting LOX-1.
Int J Nanomedicine. 2022 Dec 13;17:6301-6316. doi: 10.2147/IJN.S383904. eCollection 2022.
8
Macrophage-derived exosomal miR-4532 promotes endothelial cells injury by targeting SP1 and NF-κB P65 signalling activation.
J Cell Mol Med. 2022 Oct;26(20):5165-5180. doi: 10.1111/jcmm.17541. Epub 2022 Sep 7.

本文引用的文献

2
Exosome-based gene therapy for familial hypercholesterolemia in a mouse model.
Theranostics. 2021 Jan 1;11(6):2953-2965. doi: 10.7150/thno.49874. eCollection 2021.
3
Mesenchymal stem-cell-derived exosomal miR-145 inhibits atherosclerosis by targeting JAM-A.
Mol Ther Nucleic Acids. 2020 Nov 4;23:119-131. doi: 10.1016/j.omtn.2020.10.037. eCollection 2021 Mar 5.
4
Progress, opportunity, and perspective on exosome isolation - efforts for efficient exosome-based theranostics.
Theranostics. 2020 Feb 19;10(8):3684-3707. doi: 10.7150/thno.41580. eCollection 2020.
8
Molecularly Engineered Macrophage-Derived Exosomes with Inflammation Tropism and Intrinsic Heme Biosynthesis for Atherosclerosis Treatment.
Angew Chem Int Ed Engl. 2020 Mar 2;59(10):4068-4074. doi: 10.1002/anie.201913700. Epub 2020 Jan 23.
10
Exosome-encapsulated miR-505 from ox-LDL-treated vascular endothelial cells aggravates atherosclerosis by inducing NET formation.
Acta Biochim Biophys Sin (Shanghai). 2019 Dec 13;51(12):1233-1241. doi: 10.1093/abbs/gmz123.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验