New Dawn for Atherosclerosis: Vascular Endothelial Cell Senescence and Death
- PMID: 37894840
- PMCID: PMC10606899
- DOI: 10.3390/ijms242015160
New Dawn for Atherosclerosis: Vascular Endothelial Cell Senescence and Death
Abstract
Endothelial cells (ECs) form the inner linings of blood vessels, and are directly exposed to endogenous hazard signals and metabolites in the circulatory system. The senescence and death of ECs are not only adverse outcomes, but also causal contributors to endothelial dysfunction, an early risk marker of atherosclerosis. The pathophysiological process of EC senescence involves both structural and functional changes and has been linked to various factors, including oxidative stress, dysregulated cell cycle, hyperuricemia, vascular inflammation, and aberrant metabolite sensing and signaling. Multiple forms of EC death have been documented in atherosclerosis, including autophagic cell death, apoptosis, pyroptosis, NETosis, necroptosis, and ferroptosis. Despite this, the molecular mechanisms underlying EC senescence or death in atherogenesis are not fully understood. To provide a comprehensive update on the subject, this review examines the historic and latest findings on the molecular mechanisms and functional alterations associated with EC senescence and death in different stages of atherosclerosis.
Keywords: atherosclerosis; endothelial cell; endothelial cell death; endothelial cell senescence.
Conflict of interest statement
The authors declare no conflict of interest.
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References
-
- Rossman M.J., Kaplon R.E., Hill S.D., McNamara M.N., Santos-Parker J.R., Pierce G.L., Seals D.R., Donato A.J. Endothelial cell senescence with aging in healthy humans: Prevention by habitual exercise and relation to vascular endothelial function. Am. J. Physiol. Heart Circ. Physiol. 2017;313:H890–H895. doi: 10.1152/ajpheart.00416.2017. - DOI - PMC - PubMed
-
- Lesniewski L.A., Connell M.L., Durrant J.R., Folian B.J., Anderson M.C., Donato A.J., Seals D.R. B6D2F1 Mice are a suitable model of oxidative stress-mediated impaired endothelium-dependent dilation with aging. J. Gerontol. Ser. A Biol. Sci. Med. Sci. 2009;64:9–20. doi: 10.1093/gerona/gln049. - DOI - PMC - PubMed
-
- Yamamoto K., Takeshita K., Shimokawa T., Yi H., Isobe K., Loskutoff D.J., Saito H. Plasminogen activator inhibitor-1 is a major stress-regulated gene: Implications for stress-induced thrombosis in aged individuals. Proc. Natl. Acad. Sci. USA. 2002;99:890–895. doi: 10.1073/pnas.022608799. - DOI - PMC - PubMed
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