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Review
. 2021 Aug 26:8:738031.
doi: 10.3389/fcvm.2021.738031. eCollection 2021.

Exosomes and Atherogenesis

Affiliations
Review

Exosomes and Atherogenesis

Bingbing Lin et al. Front Cardiovasc Med. .

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.

Keywords: atherosclerosis; exosome; immunocyte; inflammation; vascular injury.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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References

    1. Zhao D, Liu J, Wang M, Zhang X, Zhou M.Epidemiology of cardiovascular disease in china: Current features and implications. Nat Rev Cardiol. (2019) 16:203–12. 10.1038/s41569-018-0119-4 - DOI - PubMed
    1. Galkina E, Ley K.Immune and inflammatory mechanisms of atherosclerosis (*). Annu Rev Immunol. (2009) 27:165–97. 10.1146/annurev.immunol.021908.132620 - DOI - PMC - PubMed
    1. Freigang S, Ampenberger F, Weiss A, Kanneganti TD, Iwakura Y, Hersberger M, et al. . Fatty acid-induced mitochondrial uncoupling elicits inflammasome-independent il-1alpha and sterile vascular inflammation in atherosclerosis. Nat Immunol. (2013) 14:1045–53. 10.1038/ni.2704 - DOI - PubMed
    1. Witztum JL, Lichtman AH.The influence of innate and adaptive immune responses on atherosclerosis. Annu Rev Pathol. (2014) 9:73–102. 10.1146/annurev-pathol-020712-163936 - DOI - PMC - PubMed
    1. Hansson GK, Robertson AK, Soderberg-Naucler C.Inflammation and atherosclerosis. Annu Rev Pathol. (2006) 1:297–329. 10.1146/annurev.pathol.1.110304.100100 - DOI - PubMed

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