Division of Cardiology, Department of Internal Medicine Louisiana State University Health Sciences Centre Shreveport LA USA.
School of Medicine and Population Health University of Sheffield Sheffield UK.
J Am Heart Assoc. 2024 Mar 5;13(5):e032987. doi: 10.1161/JAHA.123.032987. Epub 2024 Feb 23.
Cardiovascular disease remains the leading cause of death worldwide, characterized by atherosclerotic activity within large and medium-sized arteries. Inflammation has been shown to be a primary driver of atherosclerotic plaque formation, with interleukin-1 (IL-1) having a principal role. This review focuses on the current state of knowledge of molecular mechanisms of IL-1 release from cells in atherosclerotic plaques. A more in-depth understanding of the process of IL-1's release into the vascular environment is necessary for the treatment of inflammatory disease processes, as the current selection of medicines being used primarily target IL-1 after it has been released. IL-1 is secreted by several heterogenous mechanisms, some of which are cell type-specific and could provide further specialized targets for therapeutic intervention. A major unmet challenge is to understand the mechanism before and leading to IL-1 release, especially by cells in atherosclerotic plaques, including endothelial cells, vascular smooth muscle cells, and macrophages. Data so far indicate a heterogeneity of IL-1 release mechanisms that vary according to cell type and are stimulus-dependent. Unraveling this complexity may reveal new targets to block excess vascular inflammation.
心血管疾病仍然是全球范围内的主要死亡原因,其特征是大动脉和中动脉内的动脉粥样硬化活性。炎症已被证明是动脉粥样硬化斑块形成的主要驱动因素,白细胞介素-1(IL-1)起着主要作用。本综述重点介绍了目前对细胞在动脉粥样硬化斑块中释放白细胞介素-1的分子机制的认识。为了治疗炎症性疾病过程,深入了解白细胞介素-1释放到血管环境中的过程是必要的,因为目前使用的药物主要是在白细胞介素-1释放后才起作用。白细胞介素-1通过几种异质机制分泌,其中一些机制是细胞类型特异性的,可以为治疗干预提供进一步的专门靶点。一个主要的未满足的挑战是了解在白细胞介素-1释放之前和之后的机制,特别是在动脉粥样硬化斑块中的细胞,包括内皮细胞、血管平滑肌细胞和巨噬细胞。到目前为止的数据表明,白细胞介素-1释放机制存在异质性,根据细胞类型和刺激因素的不同而有所不同。揭示这种复杂性可能会发现新的靶点来阻断过度的血管炎症。