Patterson Ashley J Scott, Patil Vaidehi A, Figueroa-Rios Lysmarie, Borelli Alexandra N, Masters Kristyn S
Medical Scientist Training Program, University of Wisconsin-Madison, Madison, WI, 53705, USA.
Cellular and Molecular Biology Program, University of Wisconsin-Madison, Madison, WI, 53705, USA.
J Heart Valve Soc. 2024 Oct-Dec;1(1). doi: 10.1177/30494826241296675. Epub 2024 Dec 26.
The extracellular matrix (ECM) of the aortic valve plays a pivotal role in maintaining valve function and becomes profoundly altered during the progression of calcific stenosis of the native aortic valve (CAS). CAS involves fibrocalcific ECM remodeling characterized by increased proteoglycans and glycosaminoglycans, enhanced collagen deposition, and fragmentation of elastic fibers, all of which contribute to valve thickening, fibrosis, and calcification. In this brief review, we provide an overview of these ECM changes and discuss the relationship between aberrant ECM remodeling and other pathological features of CAS - namely, differentiation of the resident valve cell types, inflammatory activity, lipid deposition, and relative hypoxia. Sexual dimorphism in ECM dynamics and the creation of disease-inspired scaffold environments to mimic CAS fibrosis are also discussed. Overall, understanding the complex interplay between cell phenotypes and ECM remodeling is crucial for elucidating the pathophysiology of CAS and developing novel treatment strategies.
主动脉瓣的细胞外基质(ECM)在维持瓣膜功能方面起着关键作用,并且在天然主动脉瓣钙化性狭窄(CAS)的进展过程中会发生深刻变化。CAS涉及纤维钙化性ECM重塑,其特征是蛋白聚糖和糖胺聚糖增加、胶原沉积增强以及弹性纤维断裂,所有这些都导致瓣膜增厚、纤维化和钙化。在这篇简短的综述中,我们概述了这些ECM变化,并讨论了异常ECM重塑与CAS的其他病理特征之间的关系,即驻留瓣膜细胞类型的分化、炎症活性、脂质沉积和相对缺氧。还讨论了ECM动态中的性别差异以及创建受疾病启发的支架环境以模拟CAS纤维化。总体而言,了解细胞表型与ECM重塑之间的复杂相互作用对于阐明CAS的病理生理学和开发新的治疗策略至关重要。