Metabolic syndrome-associated murine aortic wall stiffening is associated with premature elastic fibers aging.

IF 5 2区 生物学 Q2 CELL BIOLOGY American journal of physiology. Cell physiology Pub Date : 2024-09-01 Epub Date: 2024-07-01 DOI:10.1152/ajpcell.00615.2023
Laetitia Vanalderwiert, Auberi Henry, Amandine Wahart, Daniel A Carvajal Berrio, Eva M Brauchle, Lara El Kaakour, Katja Schenke-Layland, Juergen Brinckmann, Heiko Steenbock, Laurent Debelle, Isabelle Six, Gilles Faury, Stéphane Jaisson, Philippe Gillery, Vincent Durlach, Hervé Sartelet, Pascal Maurice, Amar Bennasroune, Laurent Martiny, Laurent Duca, Béatrice Romier, Sébastien Blaise
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Abstract

Type 2 diabetes (T2D) constitutes a major public health problem, and despite prevention efforts, this pandemic disease is one of the deadliest diseases in the world. In 2022, 6.7 million patients with T2D died prematurely from vascular complications. Indeed, diabetes increases the risk of myocardial infarction or stroke eightfold. The identification of the molecular factors involved in the occurrence of cardiovascular complications and their prevention are therefore major axes. Our hypothesis is that factors brought into play during physiological aging appear prematurely with diabetes progression. Our study focused on the aging of the extracellular matrix (ECM), a major element in the maintenance of vascular homeostasis. We characterized the morphological and functional aspects of aorta, with a focus on the collagen and elastic fibers of diabetic mice aged from 6 mo to nondiabetic mice aged 6 mo and 20 mo. The comparison with the two nondiabetic models (young and old) highlighted an exacerbated activity of proteases, which could explain a disturbance in the collagen accumulation and an excessive degradation of elastic fibers. Moreover, the generation of circulating elastin-derived peptides reflects premature aging of the ECM. These extracellular elements contribute to the appearance of vascular rigidity, often the origin of pathologies such as hypertension and atherosclerosis. In conclusion, we show that diabetic mice aged 6 mo present the same characteristics of ECM wear as those observed in mice aged 20 mo. This accelerated aortic wall remodeling could then explain the early onset of cardiovascular diseases and, therefore, the premature death of patients with T2D.NEW & NOTEWORTHY Aortic elastic fibers of young (6-mo old) individuals with diabetes degrade prematurely and exhibit an appearance like that found in aged (20-mo old) nondiabetic mice. Exacerbated elastolysis and elastin-derived peptide production are characteristic elements, contributing to early aortic wall rigidity and hypertension development. Therefore, limiting this early aging could be a judicious therapeutic approach to reduce cardiovascular complications and premature death in patients with diabetes.

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代谢综合征相关的小鼠主动脉壁僵化与弹性纤维过早老化有关。
2 型糖尿病(T2D)是一个重大的公共卫生问题,尽管预防工作做得很好,但这一流行病仍是 "世界上最致命的疾病之一"。2022 年,将有 670 万 2 型糖尿病患者因血管并发症而过早死亡。事实上,糖尿病会使心肌梗死或中风的风险增加八倍。因此,确定参与心血管并发症发生的分子角色以及预防这些并发症的发生是我们的主攻方向。我们的假设是,在生理衰老过程中发挥作用的因素会随着糖尿病的进展而过早出现。我们的研究重点是细胞外基质(ECM)的老化,这是维持血管稳态的主要因素。我们研究了 6 个月糖尿病小鼠与 6 个月和 20 个月非糖尿病小鼠主动脉的形态和功能,重点是胶原蛋白和弹性纤维。与两种非糖尿病模型(年轻和年老)的比较显示,蛋白酶的活性增强,这可能是胶原蛋白堆积紊乱和弹性纤维过度降解的原因。此外,循环中弹性蛋白肽的生成反映了 ECM 的过早老化。这些细胞外元素有助于血管僵化的出现,而血管僵化往往是高血压和动脉粥样硬化等病症的根源。总之,我们发现 6 个月大的糖尿病小鼠与 20 个月大的小鼠具有相同的 ECM 磨损特征。这种加速的主动脉壁重塑可以解释心血管疾病的早期发病,因此也可以解释 DT2 患者的过早死亡。
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来源期刊
CiteScore
9.10
自引率
1.80%
发文量
252
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Cell Physiology is dedicated to innovative approaches to the study of cell and molecular physiology. Contributions that use cellular and molecular approaches to shed light on mechanisms of physiological control at higher levels of organization also appear regularly. Manuscripts dealing with the structure and function of cell membranes, contractile systems, cellular organelles, and membrane channels, transporters, and pumps are encouraged. Studies dealing with integrated regulation of cellular function, including mechanisms of signal transduction, development, gene expression, cell-to-cell interactions, and the cell physiology of pathophysiological states, are also eagerly sought. Interdisciplinary studies that apply the approaches of biochemistry, biophysics, molecular biology, morphology, and immunology to the determination of new principles in cell physiology are especially welcome.
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