4.7 Review

Medial Arterial Calcification: An Overlooked Player in Peripheral Arterial Disease

期刊

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/ATVBAHA.116.306717

关键词

aging; calcification; DNA damage; neuropathy; nuclear lamina

资金

  1. BHF Programme [RG/11/14/29056]
  2. British Heart Foundation [RG/11/14/29056] Funding Source: researchfish

向作者/读者索取更多资源

Peripheral arterial disease (PAD) is a global health issue that is becoming more prevalent in an aging world population. Diabetes mellitus and chronic kidney disease are also on the increase, and both are associated with accelerated vascular calcification and an unfavorable prognosis in PAD. These data challenge the traditional athero-centric view of PAD, instead pointing toward a disease process complicated by medial arterial calcification. Like atherosclerosis, aging is a potent risk factor for medial arterial calcification, and accelerated vascular aging may underpin the devastating manifestations of PAD, particularly in patients prone to calcification. Consequently, this review will attempt to dissect the relationship between medial arterial calcification and atherosclerosis in PAD and identify common as well as novel risk factors that may contribute to and accelerate progression of PAD. In this context, we focus on the complex interplay between oxidative stress, DNA damage, and vascular aging, as well as the unexplored role of neuropathy.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Review Biochemistry & Molecular Biology

Nesprin-1/2: roles in nuclear envelope organisation, myogenesis and muscle disease

Can Zhou, Li Rao, Catherine M. Shanahan, Qiuping Zhang

BIOCHEMICAL SOCIETY TRANSACTIONS (2018)

Review Cardiac & Cardiovascular Systems

Role of smooth muscle cells in vascular calcification: implications in atherosclerosis and arterial stiffness

Andrew L. Durham, Mei Y. Speer, Marta Scatena, Cecilia M. Giachelli, Catherine M. Shanahan

CARDIOVASCULAR RESEARCH (2018)

Editorial Material Cell Biology

Muscle tensions merge to cause a DNA replication crisis

Daniel Brayson, Chin Yee Ho, Catherine M. Shanahan

JOURNAL OF CELL BIOLOGY (2018)

Article Cardiac & Cardiovascular Systems

Calcium phosphate particles stimulate interleukin-1β release from human vascular smooth muscle cells: A role for spleen tyrosine kinase and exosome release

Yana Dautova, Alexander N. Kapustin, Kevin Pappert, Matthias Epple, Hanneke Okkenhaug, Simon J. Cook, Catherine M. Shanahan, Martin D. Bootman, Diane Proudfoot

JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2018)

Editorial Material Urology & Nephrology

Not all vascular smooth muscle cell exosomes calcify equally in chronic kidney disease

Adriana Dusso, Maria Isabel Colombo, Catherine M. Shanahan

KIDNEY INTERNATIONAL (2018)

Article Multidisciplinary Sciences

Magnesium prevents vascular calcification in vitro by inhibition of hydroxyapatite crystal formation

Anique D. ter Braake, Paul T. Tinneman, Catherine M. Shanahan, Joost G. J. Hoenderop, Jeroen H. F. de Baaij

SCIENTIFIC REPORTS (2018)

Article Cardiac & Cardiovascular Systems

Extracellular Matrix Proteomics Reveals Interplay of Aggrecan and Aggrecanases in Vascular Remodeling of Stented Coronary Arteries

Gonca Suna, Wojciech Wojakowski, Marc Lynch, Javier Barallobre-Barreiro, Xiaoke Yin, Ursula Mayr, Ferheen Baig, Ruifang Lu, Marika Fava, Robert Hayward, Chris Molenaar, Stephen J. White, Tomasz Roleder, Krzysztof P. Milewski, Pawel Gasior, Piotr P. Buszman, Pawel Buszman, Marjan Jahangiri, Catherine M. Shanahan, Jonathan Hill, Manuel Mayr

CIRCULATION (2018)

Article Hematology

Endoplasmic Reticulum Stress Mediates Vascular Smooth Muscle Cell Calcification via Increased Release of Grp78 (Glucose-Regulated Protein, 78 kDa)-Loaded Extracellular Vesicles

Malgorzata Furmanik, Rick van Gorp, Meredith Whitehead, Sadia Ahmad, Jayanta Bordoloi, Alexander Kapustin, Leon J. Schurgers, Catherine M. Shanahan

Summary: This study reveals that ER stress induces vascular calcification by increasing release of Grp78-loaded EVs, and for the first time links warfarin to promoting calcification by increasing EV release. The results of the study provide a novel mechanism of action for warfarin and the role of ER stress in cargo loading of EVs.

ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2021)

Article Hematology

Runx2 (Runt-Related Transcription Factor 2) Links the DNA Damage Response to Osteogenic Reprogramming and Apoptosis of Vascular Smooth Muscle Cells

Andrew M. Cobb, Syabira Yusoff, Robert Hayward, Sadia Ahmad, Mengxi Sun, Anja Verhulst, Patrick C. D'Haese, Catherine M. Shanahan

Summary: The study found that DNA damage stimulates Runx2 accumulation and enhances its activation of osteogenic target genes, leading to increased calcification. Runx2 also participates in DNA repair and its PARylation in response to genotoxic stress affects its localization at DNA lesions.

ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2021)

Editorial Material Cardiac & Cardiovascular Systems

Circulating uromodulin: a cytokine trap for osteoinductive inflammatory mediators in chronic kidney disease?

Meredith Whitehead, Catherine M. Shanahan

CARDIOVASCULAR RESEARCH (2021)

Review Engineering, Biomedical

Design considerations for engineering 3D models to study vascular pathologies in vitro

Suzette T. Lust, Catherine M. Shanahan, Rebecca J. Shipley, Pablo Lamata, Eileen Gentleman

Summary: Cardiovascular diseases are often the result of pathological remodelling of blood vessels, driven by changes in vascular cell behaviors and abnormalities in ECM proteins. In vitro models of blood vessels can be useful for studying disease progression, with a focus on maintaining normal cell phenotypes, mimicking cell-ECM interactions, and promoting intercellular communication. By combining advancements in materials science, cell biology, fluidics, and modeling, it may be possible to create patient-specific blood vessel models for developing and testing therapies.

ACTA BIOMATERIALIA (2021)

Editorial Material Cardiac & Cardiovascular Systems

Targeting Cell Stiffness A Paradigm Shift in the Treatment of Aortic Stiffness

Marina Cecelja, Catherine M. Shanahan

CIRCULATION RESEARCH (2021)

Review Cardiac & Cardiovascular Systems

Diseases of the Aorta and Kidney Disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference

Pantelis Sarafidis, Sven Martens, Athanasios Saratzis, Daniella Kadian-Dodov, Patrick T. Murray, Catherine M. Shanahan, Allen D. Hamdan, Daniel T. Engelman, Ulf Teichgraber, Charles A. Herzog, Michael Cheung, Michel Jadoul, Wolfgang C. Winkelmayer, Holger Reinecke, Kirsten Johansen

Summary: Chronic kidney disease is an independent risk factor for abdominal aortic aneurysm, cardiovascular events, and all-cause mortality after AAA or thoracic aortic dissection surgery. Acute kidney injury (AKI) after aortic surgery occurs at a high rate and is linked to future cardiovascular events and mortality. The development of AKI and long-term kidney function differ based on the type of AAA intervention. Knowledge about AAA in the general population may not be applicable to CKD patients, who have higher co-morbidity prevalence and perioperative complication risks. This review summarizes the epidemiology, pathophysiology, diagnosis, and treatment of Aortic Diseases in CKD, highlighting knowledge gaps and areas of controversy for future research.

CARDIOVASCULAR RESEARCH (2022)

Article Multidisciplinary Sciences

Pressure and stiffness sensing together regulate vascular smooth muscle cell phenotype switching

Pamela Swiatlowska, Brian Sit, Zhen Feng, Emilie Marhuenda, Ioannis Xanthis, Simona Zingaro, Matthew Ward, Xinmiao Zhou, Qingzhong Xiao, Cathy Shanahan, Gareth E. Jones, Cheng-han Yu, Thomas Iskratsch

Summary: The study shows that vascular smooth muscle cells (VSMCs) undergo a phenotypic switch when exposed to a combination of hypertensive pressure and matrix compliance, which are prevalent during atherosclerosis. The molecular mechanism involves the regulation of the actin cytoskeleton through cofilin via distinct pathways.

SCIENCE ADVANCES (2022)

Review Hematology

Molecular Mechanisms of Vascular Health: Insights From Vascular Aging and Calcification

Nadia R. Sutton, Rajeev Malhotra, Cynthia St. Hilaire, Elena Aikawa, Roger S. Blumenthal, Grace Gackenbach, Parag Goyal, Adam Johnson, Sagar U. Nigwekar, Catherine M. Shanahan, Dwight A. Towler, Brooke N. Wolford, Yabing Chen

Summary: Cardiovascular disease is the leading cause of death globally, particularly in individuals over the age of 65, with myocardial infarction and stroke being the primary contributors. The development of vascular aging and vascular calcification with aging is not fully understood, but is believed to be influenced by genetic risk, environmental factors, and the ability of vascular smooth muscle cells to acquire an osteogenic phenotype. Understanding the molecular mechanisms behind age-associated vascular pathology may lead to strategies for promoting healthy vascular aging. This article provides a summary of current knowledge on age-associated vascular disease, with a focus on vascular calcification.

ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2023)

暂无数据