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Temporal and spatial changes in wall shear stress during atherosclerotic plaque progression in mice

Wall shear stress (WSS) is involved in atherosclerotic plaque initiation, yet its role in plaque progression remains unclear. We aimed to study (i) the temporal and spatial changes in WSS over a growing plaque and (ii) the correlation between WSS and plaque composition, using animal-specific data in...

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Autores principales: Xing, R., Moerman, A. M., Ridwan, Y., Daemen, M. J., van der Steen, A. F. W., Gijsen, F. J. H., van der Heiden, K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882682/
https://www.ncbi.nlm.nih.gov/pubmed/29657758
http://dx.doi.org/10.1098/rsos.171447
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author Xing, R.
Moerman, A. M.
Ridwan, Y.
Daemen, M. J.
van der Steen, A. F. W.
Gijsen, F. J. H.
van der Heiden, K.
author_facet Xing, R.
Moerman, A. M.
Ridwan, Y.
Daemen, M. J.
van der Steen, A. F. W.
Gijsen, F. J. H.
van der Heiden, K.
author_sort Xing, R.
collection PubMed
description Wall shear stress (WSS) is involved in atherosclerotic plaque initiation, yet its role in plaque progression remains unclear. We aimed to study (i) the temporal and spatial changes in WSS over a growing plaque and (ii) the correlation between WSS and plaque composition, using animal-specific data in an atherosclerotic mouse model. Tapered casts were placed around the right common carotid arteries (RCCA) of ApoE(−/−) mice. At 5, 7 and 9 weeks after cast placement, RCCA geometry was reconstructed using contrast-enhanced micro-CT. Lumen narrowing was observed in all mice, indicating the progression of a lumen intruding plaque. Next, we determined the flow rate in the RCCA of each mouse using Doppler Ultrasound and computed WSS at all time points. Over time, as the plaque developed and further intruded into the lumen, absolute WSS significantly decreased. Finally at week 9, plaque composition was histologically characterized. The proximal part of the plaque was small and eccentric, exposed to relatively lower WSS. Close to the cast a larger and concentric plaque was present, exposed to relatively higher WSS. Lower WSS was significantly correlated to the accumulation of macrophages in the eccentric plaque. When pooling data of all animals, correlation between WSS and plaque composition was weak and no longer statistically significant. In conclusion, our data showed that in our mouse model absolute WSS strikingly decreased during disease progression, which was significantly correlated to plaque area and macrophage content. Besides, our study demonstrates the necessity to analyse individual animals and plaques when studying correlations between WSS and plaque composition.
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spelling pubmed-58826822018-04-13 Temporal and spatial changes in wall shear stress during atherosclerotic plaque progression in mice Xing, R. Moerman, A. M. Ridwan, Y. Daemen, M. J. van der Steen, A. F. W. Gijsen, F. J. H. van der Heiden, K. R Soc Open Sci Biochemistry and Biophysics Wall shear stress (WSS) is involved in atherosclerotic plaque initiation, yet its role in plaque progression remains unclear. We aimed to study (i) the temporal and spatial changes in WSS over a growing plaque and (ii) the correlation between WSS and plaque composition, using animal-specific data in an atherosclerotic mouse model. Tapered casts were placed around the right common carotid arteries (RCCA) of ApoE(−/−) mice. At 5, 7 and 9 weeks after cast placement, RCCA geometry was reconstructed using contrast-enhanced micro-CT. Lumen narrowing was observed in all mice, indicating the progression of a lumen intruding plaque. Next, we determined the flow rate in the RCCA of each mouse using Doppler Ultrasound and computed WSS at all time points. Over time, as the plaque developed and further intruded into the lumen, absolute WSS significantly decreased. Finally at week 9, plaque composition was histologically characterized. The proximal part of the plaque was small and eccentric, exposed to relatively lower WSS. Close to the cast a larger and concentric plaque was present, exposed to relatively higher WSS. Lower WSS was significantly correlated to the accumulation of macrophages in the eccentric plaque. When pooling data of all animals, correlation between WSS and plaque composition was weak and no longer statistically significant. In conclusion, our data showed that in our mouse model absolute WSS strikingly decreased during disease progression, which was significantly correlated to plaque area and macrophage content. Besides, our study demonstrates the necessity to analyse individual animals and plaques when studying correlations between WSS and plaque composition. The Royal Society Publishing 2018-03-14 /pmc/articles/PMC5882682/ /pubmed/29657758 http://dx.doi.org/10.1098/rsos.171447 Text en © 2018 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Biochemistry and Biophysics
Xing, R.
Moerman, A. M.
Ridwan, Y.
Daemen, M. J.
van der Steen, A. F. W.
Gijsen, F. J. H.
van der Heiden, K.
Temporal and spatial changes in wall shear stress during atherosclerotic plaque progression in mice
title Temporal and spatial changes in wall shear stress during atherosclerotic plaque progression in mice
title_full Temporal and spatial changes in wall shear stress during atherosclerotic plaque progression in mice
title_fullStr Temporal and spatial changes in wall shear stress during atherosclerotic plaque progression in mice
title_full_unstemmed Temporal and spatial changes in wall shear stress during atherosclerotic plaque progression in mice
title_short Temporal and spatial changes in wall shear stress during atherosclerotic plaque progression in mice
title_sort temporal and spatial changes in wall shear stress during atherosclerotic plaque progression in mice
topic Biochemistry and Biophysics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882682/
https://www.ncbi.nlm.nih.gov/pubmed/29657758
http://dx.doi.org/10.1098/rsos.171447
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