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      Genesis and growth of extracellular vesicle-derived microcalcification in atherosclerotic plaques

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          Abstract

          Clinical evidence links arterial calcification and cardiovascular risk. Finite-element modelling of the stress distribution within atherosclerotic plaques has suggested that subcellular microcalcifications in the fibrous cap may promote material failure of the plaque, but that large calcifications can stabilize it. Yet the physicochemical mechanisms underlying such mineral formation and growth in atheromata remain unknown. Here, by using three-dimensional collagen hydrogels that mimic structural features of the atherosclerotic fibrous cap, and high-resolution microscopic and spectroscopic analyses of both the hydrogels and of calcified human plaques, we demonstrate that calcific mineral formation and maturation results from a series of events involving the aggregation of calcifying extracellular vesicles, and the formation of microcalcifications and ultimately large calcification zones. We also show that calcification morphology and the plaque’s collagen content – two determinants of atherosclerotic plaque stability - are interlinked.

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          Most cited references51

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          Heart Disease and Stroke Statistics—2015 Update: A Report From the American Heart Association

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            Critical Evaluation of Nanoparticle Tracking Analysis (NTA) by NanoSight for the Measurement of Nanoparticles and Protein Aggregates

            Purpose To evaluate the nanoparticle tracking analysis (NTA) technique, compare it with dynamic light scattering (DLS) and test its performance in characterizing drug delivery nanoparticles and protein aggregates. Methods Standard polystyrene beads of sizes ranging from 60 to 1,000 nm and physical mixtures thereof were analyzed with NTA and DLS. The influence of different ratios of particle populations was tested. Drug delivery nanoparticles and protein aggregates were analyzed by NTA and DLS. Live monitoring of heat-induced protein aggregation was performed with NTA. Results NTA was shown to accurately analyze the size distribution of monodisperse and polydisperse samples. Sample visualization and individual particle tracking are features that enable a thorough size distribution analysis. The presence of small amounts of large (1,000 nm) particles generally does not compromise the accuracy of NTA measurements, and a broad range of population ratios can easily be detected and accurately sized. NTA proved to be suitable to characterize drug delivery nanoparticles and protein aggregates, complementing DLS. Live monitoring of heat-induced protein aggregation provides information about aggregation kinetics and size of submicron aggregates. Conclusion NTA is a powerful characterization technique that complements DLS and is particularly valuable for analyzing polydisperse nanosized particles and protein aggregates.
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              Measuring the global burden of disease.

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                Author and article information

                Journal
                101155473
                30248
                Nat Mater
                Nat Mater
                Nature materials
                1476-1122
                2 December 2015
                11 January 2016
                March 2016
                11 July 2016
                : 15
                : 3
                : 335-343
                Affiliations
                [1 ]Center for Interdisciplinary Cardiovascular Sciences, Cardiovascular Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA
                [2 ]Department of Medical Physics & Biomedical Engineering, University College London, London, UK
                [3 ]Department of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, The Netherlands
                [4 ]Center for Excellence in Vascular Biology, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA
                [5 ]Department of Biomedical Engineering, City College of New York, New York, NY, USA
                Author notes
                Corresponding author: Elena Aikawa, MD, PhD, 3 Blackfan St, CLSB, CICS, 17 th floor, Brigham and Women’s Hospital, Boston, MA 02115, Phone: 617-730-7755, Fax: 617-730-7791, eaikawa@ 123456partners.org
                Article
                NIHMS741464
                10.1038/nmat4519
                4767675
                26752654
                de141b60-8ef0-48b1-9f61-468dd8557119

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                Materials science
                Materials science

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