Circ Res. 2011 Mar 4;108(5):528-30. doi: 10.1161/CIRCRESAHA.111.240861.
The progression of aortic aneurysms involves complex changes in wall structure and results from the interplay of multiple cell types including endothelial cells, SMCs, macrophages and adventitial cells. It is important to realize that these pathogenic steps play out on different response backgrounds in the ascending thoracic aorta compared to the abdominal aorta. Much like genetic modifiers at work in different inbred strains of mice that can sometimes produce dramatically different phenotypic manifestations of the same mutation on different genetic backgrounds, the SMC lineage diversity intrinsic to different aortic segments may play important modifier roles in the origins and progression of aneurysms in thoracic versus abdominal aortic segments in the same individual. Future work will focus on identification of factors produced by endothelial cells exposed to chronic infusions of AngII that initiate response cascades in SMCs and macrophages leading to aneurysm formation. It will also bring into greater focus the ways that advances in understanding basic pathways of vascular development provide important insights into mechanisms of disease pathogenesis in the adult vascular system.
主动脉瘤的进展涉及到壁结构的复杂变化,是多种细胞类型相互作用的结果,包括内皮细胞、平滑肌细胞、巨噬细胞和外膜细胞。重要的是要认识到,与腹主动脉相比,这些致病步骤在胸主动脉上升段的不同反应背景下发生。就像在不同近交系小鼠中起作用的遗传修饰因子一样,有时在不同的遗传背景下,同一突变会产生截然不同的表型表现,不同主动脉段固有平滑肌谱系的多样性可能在同一个体的胸主动脉和腹主动脉段动脉瘤的起源和进展中发挥重要的修饰作用。未来的工作将集中于鉴定内皮细胞在受到慢性血管紧张素 II 输注时产生的因子,这些因子在平滑肌细胞和巨噬细胞中引发反应级联,导致动脉瘤形成。它还将更深入地关注理解血管发育基本途径的进展如何为成人血管系统疾病发病机制提供重要见解。