主动脉瓣钙化中的淀粉样蛋白和胶原蛋白模板。

IF 12.8 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Trends in molecular medicine Pub Date : 2024-11-01 Epub Date: 2024-06-05 DOI:10.1016/j.molmed.2024.04.015
Shobini Jayaraman, Navneet Narula, Jagat Narula, Olga Gursky
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引用次数: 0

摘要

主动脉瓣钙化病(CAVD)是一种广泛流行的心脏疾病,需要药物干预。主动脉瓣的钙化区通常含有淀粉样纤维,可促进体外钙化。这篇论文认为,淀粉样蛋白有助于CAVD的发展;淀粉样蛋白辅助成核可加速羟基磷灰石在胶原基质上的沉积。值得注意的是,淀粉样蛋白中的酸性阵列与无定形羟基磷灰石前体中的钙-钙间距相匹配,而振荡的血流动力学扰动会促进淀粉样蛋白在瓣膜中的沉积。脂蛋白(a)是心血管疾病的遗传风险因素,它通过几种机制促进钙化,其中脂蛋白(a)相关酶水解氧化磷脂(oxPLs)有助于生成正磷酸盐,而脂蛋白(a)则会阻止浆蛋白诱导的纤维降解。目前对溶液中和纤维状复合物中淀粉样蛋白-钙-胶原蛋白相互作用的研究有助于深入了解淀粉样蛋白在钙化中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Amyloid and collagen templates in aortic valve calcification.

Calcific aortic valve disease (CAVD) is a widely prevalent heart disorder in need of pharmacological interventions. Calcified areas in aortic valves often contain amyloid fibrils that promote calcification in vitro. This opinion paper suggests that amyloid contributes to CAVD development; amyloid-assisted nucleation can accelerate hydroxyapatite deposition onto collagen matrix. Notably, acidic arrays in amyloid match calcium-calcium spacing in the amorphous hydroxyapatite precursor, while oscillating hemodynamic perturbations promote amyloid deposition in the valve. Lipoprotein(a), a genetic risk factor for CAVD, augments calcification via several mechanisms, wherein hydrolysis of oxidized phospholipids (oxPLs) by Lp(a)-associated enzymes helps generate orthophosphate, and apolipoprotein(a) blocks plasmin-induced fibril degradation. Current studies of amyloid-calcium-collagen interactions in solution and in fibrillar complexes allow deeper insight into the role of amyloid in calcification.

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来源期刊
Trends in molecular medicine
Trends in molecular medicine 医学-生化与分子生物学
CiteScore
24.60
自引率
0.00%
发文量
142
审稿时长
6-12 weeks
期刊介绍: Trends in Molecular Medicine (TMM) aims to offer concise and contextualized perspectives on the latest research advancing biomedical science toward better diagnosis, treatment, and prevention of human diseases. It focuses on research at the intersection of basic biology and clinical research, covering new concepts in human biology and pathology with clear implications for diagnostics and therapy. TMM reviews bridge the gap between bench and bedside, discussing research from preclinical studies to patient-enrolled trials. The major themes include disease mechanisms, tools and technologies, diagnostics, and therapeutics, with a preference for articles relevant to multiple themes. TMM serves as a platform for discussion, pushing traditional boundaries and fostering collaboration between scientists and clinicians. The journal seeks to publish provocative and authoritative articles that are also accessible to a broad audience, inspiring new directions in molecular medicine to enhance human health.
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