Department of Biochemistry, College of Medicine, Dongguk University, Gyeongju 38066, Republic of Korea.
Int J Mol Sci. 2024 Mar 8;25(6):3136. doi: 10.3390/ijms25063136.
Vascular smooth muscle cells (VSMCs) are crucial components of the arterial wall, controlling blood flow and pressure by contracting and relaxing the artery walls. VSMCs can switch from a contractile to a synthetic state, leading to increased proliferation and migratory potential. Epigenetic pathways, including DNA methylation, play a crucial role in regulating VSMC differentiation and phenotypic flexibility. DNA methylation involves attaching a methyl group to the 5' carbon of a cytosine base, which regulates gene expression by interacting with transcription factors. Understanding the key factors influencing VSMC plasticity may help to identify new target molecules for the development of innovative drugs to treat various vascular diseases. This review focuses on DNA methylation pathways in VSMCs, summarizing mechanisms involved in controlling vascular remodeling, which can significantly enhance our understanding of related mechanisms and provide promising therapeutic approaches for complex and multifactorial diseases.
血管平滑肌细胞(VSMCs)是动脉壁的重要组成部分,通过收缩和舒张动脉壁来控制血流和血压。VSMCs 可以从收缩状态转变为合成状态,导致增殖和迁移潜能增加。表观遗传途径,包括 DNA 甲基化,在调节 VSMC 分化和表型灵活性方面起着至关重要的作用。DNA 甲基化涉及将一个甲基基团附加到胞嘧啶碱基的 5' 碳上,通过与转录因子相互作用来调节基因表达。了解影响 VSMC 可塑性的关键因素可能有助于确定用于治疗各种血管疾病的创新药物的新靶标分子。本综述重点介绍 VSMCs 中的 DNA 甲基化途径,总结了控制血管重塑的相关机制,这可以显著增强我们对相关机制的理解,并为复杂和多因素疾病提供有前途的治疗方法。