Wu Jingyi, Huang Yifan, Zhou Xiaoyan, Xiang Zujin, Yang Zishu, Meng Di, Wu Di, Zhang Jing, Yang Jian
Department of Cardiology, the First College of Clinical Medical Science, China Three Gorges University, Yichang, China.
Institute of Cardiovascular Disease, China Three Gorges University, Yichang, China.
Cardiovasc Diagn Ther. 2022 Dec;12(6):926-942. doi: 10.21037/cdt-22-206.
Atherosclerosis (AS), is characterized by the subintima lipid accumulation and chronic inflammation inside the arterial wall, causing much mortality and morbidity worldwide. Activating transcription factor 3 (ATF3) is a member of ATF/cAMP-responsive element-binding (CREB) family of transcription factors, which acts as a master regulator of adaptive response. Recent studies have indicated the implicated role of ATF3 in atherogenesis and AS progression due to its impact on metabolic disorder, vascular injury, plaque formation, and stability. In this review, we summarize the current advances in the mechanism of ATF3 activation and the contribution of ATF3 in AS, highlighting vascular intrinsic and extrinsic mechanisms of how ATF3 influences the pathology of AS.
The relevant literature (from origin to March 2022) was retrieved through PubMed research to explore the regulatory mechanism of ATF3 and the specific role of ATF3 in AS. Only English publications were reviewed in this paper.
ATF3 acts as a key regulator of AS progression, which not only directly affects atherosclerotic lesions by regulating vascular homeostasis, but also gets involved in AS through systemic glucolipid metabolism and inflammatory response. The two different promoters, transcript variants, and post-translational modification in distinct cell types partly contribute to the regulatory diversity of ATF3 in AS.
ATF3 is a crucial transcription regulatory factor during atherogenesis and AS progression. Gaining a better understanding of how ATF3 affects vascular, metabolic, and immune homeostasis would advance the progress of ATF3-targeted therapy in AS.
动脉粥样硬化(AS)的特征是动脉壁内膜下脂质堆积和慢性炎症,在全球范围内导致大量死亡和发病。激活转录因子3(ATF3)是ATF/环磷酸腺苷反应元件结合(CREB)转录因子家族的成员,作为适应性反应的主要调节因子发挥作用。最近的研究表明,ATF3因其对代谢紊乱、血管损伤、斑块形成和稳定性的影响,在动脉粥样硬化发生和AS进展中起重要作用。在本综述中,我们总结了ATF3激活机制的当前进展以及ATF3在AS中的作用,强调了ATF3影响AS病理的血管内在和外在机制。
通过PubMed检索相关文献(截至2022年3月),以探讨ATF3的调节机制及其在AS中的具体作用。本文仅综述英文出版物。
ATF3是AS进展的关键调节因子,它不仅通过调节血管稳态直接影响动脉粥样硬化病变,还通过全身糖脂代谢和炎症反应参与AS。不同细胞类型中两种不同的启动子、转录变体和翻译后修饰部分促成了ATF3在AS中的调节多样性。
ATF3是动脉粥样硬化发生和AS进展过程中的关键转录调节因子。更好地了解ATF3如何影响血管、代谢和免疫稳态将推动AS中针对ATF3治疗的进展。