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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...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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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. |
format | Online Article Text |
id | pubmed-4767675 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
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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