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

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 c...

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Autores principales: Hutcheson, Joshua D., Goettsch, Claudia, Bertazzo, Sergio, Maldonado, Natalia, Ruiz, Jessica L., Goh, Wilson, Yabusaki, Katsumi, Faits, Tyler, Bouten, Carlijn, Franck, Gregory, Quillard, Thibaut, Libby, Peter, Aikawa, Masanori, Weinbaum, Sheldon, Aikawa, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4767675/
https://www.ncbi.nlm.nih.gov/pubmed/26752654
http://dx.doi.org/10.1038/nmat4519
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author Hutcheson, Joshua D.
Goettsch, Claudia
Bertazzo, Sergio
Maldonado, Natalia
Ruiz, Jessica L.
Goh, Wilson
Yabusaki, Katsumi
Faits, Tyler
Bouten, Carlijn
Franck, Gregory
Quillard, Thibaut
Libby, Peter
Aikawa, Masanori
Weinbaum, Sheldon
Aikawa, Elena
author_facet Hutcheson, Joshua D.
Goettsch, Claudia
Bertazzo, Sergio
Maldonado, Natalia
Ruiz, Jessica L.
Goh, Wilson
Yabusaki, Katsumi
Faits, Tyler
Bouten, Carlijn
Franck, Gregory
Quillard, Thibaut
Libby, Peter
Aikawa, Masanori
Weinbaum, Sheldon
Aikawa, Elena
author_sort Hutcheson, Joshua D.
collection PubMed
description 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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spelling pubmed-47676752016-07-11 Genesis and growth of extracellular vesicle-derived microcalcification in atherosclerotic plaques Hutcheson, Joshua D. Goettsch, Claudia Bertazzo, Sergio Maldonado, Natalia Ruiz, Jessica L. Goh, Wilson Yabusaki, Katsumi Faits, Tyler Bouten, Carlijn Franck, Gregory Quillard, Thibaut Libby, Peter Aikawa, Masanori Weinbaum, Sheldon Aikawa, Elena Nat Mater Article 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. 2016-01-11 2016-03 /pmc/articles/PMC4767675/ /pubmed/26752654 http://dx.doi.org/10.1038/nmat4519 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Hutcheson, Joshua D.
Goettsch, Claudia
Bertazzo, Sergio
Maldonado, Natalia
Ruiz, Jessica L.
Goh, Wilson
Yabusaki, Katsumi
Faits, Tyler
Bouten, Carlijn
Franck, Gregory
Quillard, Thibaut
Libby, Peter
Aikawa, Masanori
Weinbaum, Sheldon
Aikawa, Elena
Genesis and growth of extracellular vesicle-derived microcalcification in atherosclerotic plaques
title Genesis and growth of extracellular vesicle-derived microcalcification in atherosclerotic plaques
title_full Genesis and growth of extracellular vesicle-derived microcalcification in atherosclerotic plaques
title_fullStr Genesis and growth of extracellular vesicle-derived microcalcification in atherosclerotic plaques
title_full_unstemmed Genesis and growth of extracellular vesicle-derived microcalcification in atherosclerotic plaques
title_short Genesis and growth of extracellular vesicle-derived microcalcification in atherosclerotic plaques
title_sort genesis and growth of extracellular vesicle-derived microcalcification in atherosclerotic plaques
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4767675/
https://www.ncbi.nlm.nih.gov/pubmed/26752654
http://dx.doi.org/10.1038/nmat4519
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