Key result
Nrf2 signaling regulates vascular smooth muscle cell function to alleviate atherosclerosis progression.
Why the study?
Nrf2 is a key transcription factor regulating vascular smooth muscle cell function in atherosclerosis, but its specific regulatory mechanisms need clarification.
Nrf2 is a key transcription factor regulating vascular smooth muscle cell function in atherosclerosis, representing a potential therapeutic target.
Should not alter atherosclerosis management; extends mechanistic evidence and leaves open clinical translation of Nrf2 targeting.
Atherosclerosis is a common pathological change in cardiovascular disease. Vascular smooth muscle cell is the main source of plaque cell and extracellular matrix, and nuclear factor-erythroid 2-related factor 2 (Nrf2) is a key transcription factor regulating the function of vascular smooth muscle cell. In the process of atherosclerosis, Nrf2 signaling pathway has the following regulatory effects on vascular smooth muscle cell: regulating the phenotype of vascular smooth muscle cell to change to the direction conducive to the alleviation of disease progression; inhibiting the proliferation and migration of vascular smooth muscle cell; mitigating the level of blood lipid; alleviating vascular smooth muscle cell calcification, aging and apoptosis process. This article reviews the specific mechanisms of Nrf2 regulating atherosclerosis, such as phenotypic transformation, proliferation and migration, lipid metabolism, calcification, aging and apoptosis in atherosclerosis, in order to provide a basis for understanding the molecular mechanism of atherosclerosis development and finding therapeutic targets.
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Zhuang et al. (2021) conducted a review in Atherosclerosis. Nrf2 signaling pathway was evaluated. The Nrf2 signaling pathway regulates vascular smooth muscle cell phenotype, proliferation, migration, lipid metabolism, calcification, aging, and apoptosis to alleviate atherosclerosis progression.
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