Cargando…

Integrated Regional Cardiac Hemodynamic Imaging and RNA Sequencing Reveal Corresponding Heterogeneity of Ventricular Wall Shear Stress and Endocardial Transcriptome

BACKGROUND: Unlike arteries, in which regionally distinct hemodynamics are associated with phenotypic heterogeneity, the relationships between endocardial endothelial cell phenotype and intraventricular flow remain largely unexplored. We investigated regional differences in left ventricular wall she...

Descripción completa

Detalles Bibliográficos
Autores principales: McCormick, Margaret E., Manduchi, Elisabetta, Witschey, Walter R. T., Gorman, Robert C., Gorman, Joseph H., Jiang, Yi‐Zhou, Stoeckert, Christian J., Barker, Alex J., Markl, Michael, Davies, Peter F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4859290/
https://www.ncbi.nlm.nih.gov/pubmed/27091183
http://dx.doi.org/10.1161/JAHA.115.003170
_version_ 1782430943744622592
author McCormick, Margaret E.
Manduchi, Elisabetta
Witschey, Walter R. T.
Gorman, Robert C.
Gorman, Joseph H.
Jiang, Yi‐Zhou
Stoeckert, Christian J.
Barker, Alex J.
Markl, Michael
Davies, Peter F.
author_facet McCormick, Margaret E.
Manduchi, Elisabetta
Witschey, Walter R. T.
Gorman, Robert C.
Gorman, Joseph H.
Jiang, Yi‐Zhou
Stoeckert, Christian J.
Barker, Alex J.
Markl, Michael
Davies, Peter F.
author_sort McCormick, Margaret E.
collection PubMed
description BACKGROUND: Unlike arteries, in which regionally distinct hemodynamics are associated with phenotypic heterogeneity, the relationships between endocardial endothelial cell phenotype and intraventricular flow remain largely unexplored. We investigated regional differences in left ventricular wall shear stress and their association with endocardial endothelial cell gene expression. METHODS AND RESULTS: Local wall shear stress was calculated from 4‐dimensional flow magnetic resonance imaging in 3 distinct regions of human (n=8) and pig (n=5) left ventricle: base, adjacent to the outflow tract; midventricle; and apex. In both species, wall shear stress values were significantly lower in the apex and midventricle relative to the base; oscillatory shear index was elevated in the apex. RNA sequencing of the endocardial endothelial cell transcriptome in pig left ventricle (n=8) at a false discovery rate ≤10% identified 1051 genes differentially expressed between the base and the apex and 327 between the base and the midventricle; no differentially expressed genes were detected at this false discovery rate between the apex and the midventricle. Enrichment analyses identified apical upregulation of genes associated with translation initiation including mammalian target of rapamycin, and eukaryotic initiation factor 2 signaling. Genes of mitochondrial dysfunction and oxidative phosphorylation were also consistently upregulated in the left ventricular apex, as were tissue factor pathway inhibitor (mean 50‐fold) and prostacyclin synthase (5‐fold)—genes prominently associated with antithrombotic protection. CONCLUSIONS: We report the first spatiotemporal measurements of wall shear stress within the left ventricle and linked regional hemodynamics to heterogeneity in ventricular endothelial gene expression, most notably to translation initiation and anticoagulation properties in the left ventricular apex, in which oscillatory shear index is increased and wall shear stress is decreased.
format Online
Article
Text
id pubmed-4859290
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-48592902016-05-20 Integrated Regional Cardiac Hemodynamic Imaging and RNA Sequencing Reveal Corresponding Heterogeneity of Ventricular Wall Shear Stress and Endocardial Transcriptome McCormick, Margaret E. Manduchi, Elisabetta Witschey, Walter R. T. Gorman, Robert C. Gorman, Joseph H. Jiang, Yi‐Zhou Stoeckert, Christian J. Barker, Alex J. Markl, Michael Davies, Peter F. J Am Heart Assoc Original Research BACKGROUND: Unlike arteries, in which regionally distinct hemodynamics are associated with phenotypic heterogeneity, the relationships between endocardial endothelial cell phenotype and intraventricular flow remain largely unexplored. We investigated regional differences in left ventricular wall shear stress and their association with endocardial endothelial cell gene expression. METHODS AND RESULTS: Local wall shear stress was calculated from 4‐dimensional flow magnetic resonance imaging in 3 distinct regions of human (n=8) and pig (n=5) left ventricle: base, adjacent to the outflow tract; midventricle; and apex. In both species, wall shear stress values were significantly lower in the apex and midventricle relative to the base; oscillatory shear index was elevated in the apex. RNA sequencing of the endocardial endothelial cell transcriptome in pig left ventricle (n=8) at a false discovery rate ≤10% identified 1051 genes differentially expressed between the base and the apex and 327 between the base and the midventricle; no differentially expressed genes were detected at this false discovery rate between the apex and the midventricle. Enrichment analyses identified apical upregulation of genes associated with translation initiation including mammalian target of rapamycin, and eukaryotic initiation factor 2 signaling. Genes of mitochondrial dysfunction and oxidative phosphorylation were also consistently upregulated in the left ventricular apex, as were tissue factor pathway inhibitor (mean 50‐fold) and prostacyclin synthase (5‐fold)—genes prominently associated with antithrombotic protection. CONCLUSIONS: We report the first spatiotemporal measurements of wall shear stress within the left ventricle and linked regional hemodynamics to heterogeneity in ventricular endothelial gene expression, most notably to translation initiation and anticoagulation properties in the left ventricular apex, in which oscillatory shear index is increased and wall shear stress is decreased. John Wiley and Sons Inc. 2016-04-18 /pmc/articles/PMC4859290/ /pubmed/27091183 http://dx.doi.org/10.1161/JAHA.115.003170 Text en © 2016 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley Blackwell. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Research
McCormick, Margaret E.
Manduchi, Elisabetta
Witschey, Walter R. T.
Gorman, Robert C.
Gorman, Joseph H.
Jiang, Yi‐Zhou
Stoeckert, Christian J.
Barker, Alex J.
Markl, Michael
Davies, Peter F.
Integrated Regional Cardiac Hemodynamic Imaging and RNA Sequencing Reveal Corresponding Heterogeneity of Ventricular Wall Shear Stress and Endocardial Transcriptome
title Integrated Regional Cardiac Hemodynamic Imaging and RNA Sequencing Reveal Corresponding Heterogeneity of Ventricular Wall Shear Stress and Endocardial Transcriptome
title_full Integrated Regional Cardiac Hemodynamic Imaging and RNA Sequencing Reveal Corresponding Heterogeneity of Ventricular Wall Shear Stress and Endocardial Transcriptome
title_fullStr Integrated Regional Cardiac Hemodynamic Imaging and RNA Sequencing Reveal Corresponding Heterogeneity of Ventricular Wall Shear Stress and Endocardial Transcriptome
title_full_unstemmed Integrated Regional Cardiac Hemodynamic Imaging and RNA Sequencing Reveal Corresponding Heterogeneity of Ventricular Wall Shear Stress and Endocardial Transcriptome
title_short Integrated Regional Cardiac Hemodynamic Imaging and RNA Sequencing Reveal Corresponding Heterogeneity of Ventricular Wall Shear Stress and Endocardial Transcriptome
title_sort integrated regional cardiac hemodynamic imaging and rna sequencing reveal corresponding heterogeneity of ventricular wall shear stress and endocardial transcriptome
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4859290/
https://www.ncbi.nlm.nih.gov/pubmed/27091183
http://dx.doi.org/10.1161/JAHA.115.003170
work_keys_str_mv AT mccormickmargarete integratedregionalcardiachemodynamicimagingandrnasequencingrevealcorrespondingheterogeneityofventricularwallshearstressandendocardialtranscriptome
AT manduchielisabetta integratedregionalcardiachemodynamicimagingandrnasequencingrevealcorrespondingheterogeneityofventricularwallshearstressandendocardialtranscriptome
AT witscheywalterrt integratedregionalcardiachemodynamicimagingandrnasequencingrevealcorrespondingheterogeneityofventricularwallshearstressandendocardialtranscriptome
AT gormanrobertc integratedregionalcardiachemodynamicimagingandrnasequencingrevealcorrespondingheterogeneityofventricularwallshearstressandendocardialtranscriptome
AT gormanjosephh integratedregionalcardiachemodynamicimagingandrnasequencingrevealcorrespondingheterogeneityofventricularwallshearstressandendocardialtranscriptome
AT jiangyizhou integratedregionalcardiachemodynamicimagingandrnasequencingrevealcorrespondingheterogeneityofventricularwallshearstressandendocardialtranscriptome
AT stoeckertchristianj integratedregionalcardiachemodynamicimagingandrnasequencingrevealcorrespondingheterogeneityofventricularwallshearstressandendocardialtranscriptome
AT barkeralexj integratedregionalcardiachemodynamicimagingandrnasequencingrevealcorrespondingheterogeneityofventricularwallshearstressandendocardialtranscriptome
AT marklmichael integratedregionalcardiachemodynamicimagingandrnasequencingrevealcorrespondingheterogeneityofventricularwallshearstressandendocardialtranscriptome
AT daviespeterf integratedregionalcardiachemodynamicimagingandrnasequencingrevealcorrespondingheterogeneityofventricularwallshearstressandendocardialtranscriptome