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Label-free optical biomarkers detect early calcific aortic valve disease in a wild-type mouse model

BACKGROUND: Calcific aortic valve disease (CAVD) pathophysiology is a complex, multistage process, usually diagnosed at advanced stages after significant anatomical and hemodynamic changes in the valve. Early detection of disease progression is thus pivotal in the development of prevention and mitig...

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Autores principales: Tandon, Ishita, Johns, Shelby, Woessner, Alan, Perez, Jessica, Cross, Delaney, Ozkizilcik, Asya, Muldoon, Timothy J., Vallurupalli, Srikanth, Padala, Muralidhar, Quinn, Kyle P., Balachandran, Kartik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7731510/
https://www.ncbi.nlm.nih.gov/pubmed/33308143
http://dx.doi.org/10.1186/s12872-020-01776-8
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author Tandon, Ishita
Johns, Shelby
Woessner, Alan
Perez, Jessica
Cross, Delaney
Ozkizilcik, Asya
Muldoon, Timothy J.
Vallurupalli, Srikanth
Padala, Muralidhar
Quinn, Kyle P.
Balachandran, Kartik
author_facet Tandon, Ishita
Johns, Shelby
Woessner, Alan
Perez, Jessica
Cross, Delaney
Ozkizilcik, Asya
Muldoon, Timothy J.
Vallurupalli, Srikanth
Padala, Muralidhar
Quinn, Kyle P.
Balachandran, Kartik
author_sort Tandon, Ishita
collection PubMed
description BACKGROUND: Calcific aortic valve disease (CAVD) pathophysiology is a complex, multistage process, usually diagnosed at advanced stages after significant anatomical and hemodynamic changes in the valve. Early detection of disease progression is thus pivotal in the development of prevention and mitigation strategies. In this study, we developed a diet-based, non-genetically modified mouse model for early CAVD progression, and explored the utility of two-photon excited fluorescence (TPEF) microscopy for early detection of CAVD progression. TPEF imaging provides label-free, non-invasive, quantitative metrics with the potential to correlate with multiple stages of CAVD pathophysiology including calcium deposition, collagen remodeling and osteogenic differentiation. METHODS: Twenty-week old C57BL/6J mice were fed either a control or pro-calcific diet for 16 weeks and monitored via echocardiography, histology, immunohistochemistry, and quantitative polarized light imaging. Additionally, TPEF imaging was used to quantify tissue autofluorescence (A) at 755 nm, 810 nm and 860 nm excitation, to calculate TPEF 755–860 ratio (A(860/525)/(A(755/460) + A(860/525))) and TPEF Collagen-Calcium ratio (A(810/525)/(A(810/460) + A(810/525))) in the murine valves. In a separate experiment, animals were fed the above diets till 28 weeks to assess for later-stage calcification. RESULTS: Pro-calcific mice showed evidence of lipid deposition at 4 weeks and calcification at 16 weeks at the valve commissures. The valves of pro-calcific mice also showed positive expression for markers of osteogenic differentiation, myofibroblast activation, proliferation, inflammatory cytokines and collagen remodeling. Pro-calcific mice exhibited lower TPEF autofluorescence ratios, at locations coincident with calcification, that correlated with increased collagen disorganization and positive expression of osteogenic markers. Additionally, locations with lower TPEF autofluorescence ratios at 4 and 16 weeks exhibited increased calcification at later 28-week timepoints. CONCLUSIONS: This study suggests the potential of TPEF autofluorescence metrics to serve as a label-free tool for early detection and monitoring of CAVD pathophysiology.
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spelling pubmed-77315102020-12-15 Label-free optical biomarkers detect early calcific aortic valve disease in a wild-type mouse model Tandon, Ishita Johns, Shelby Woessner, Alan Perez, Jessica Cross, Delaney Ozkizilcik, Asya Muldoon, Timothy J. Vallurupalli, Srikanth Padala, Muralidhar Quinn, Kyle P. Balachandran, Kartik BMC Cardiovasc Disord Research Article BACKGROUND: Calcific aortic valve disease (CAVD) pathophysiology is a complex, multistage process, usually diagnosed at advanced stages after significant anatomical and hemodynamic changes in the valve. Early detection of disease progression is thus pivotal in the development of prevention and mitigation strategies. In this study, we developed a diet-based, non-genetically modified mouse model for early CAVD progression, and explored the utility of two-photon excited fluorescence (TPEF) microscopy for early detection of CAVD progression. TPEF imaging provides label-free, non-invasive, quantitative metrics with the potential to correlate with multiple stages of CAVD pathophysiology including calcium deposition, collagen remodeling and osteogenic differentiation. METHODS: Twenty-week old C57BL/6J mice were fed either a control or pro-calcific diet for 16 weeks and monitored via echocardiography, histology, immunohistochemistry, and quantitative polarized light imaging. Additionally, TPEF imaging was used to quantify tissue autofluorescence (A) at 755 nm, 810 nm and 860 nm excitation, to calculate TPEF 755–860 ratio (A(860/525)/(A(755/460) + A(860/525))) and TPEF Collagen-Calcium ratio (A(810/525)/(A(810/460) + A(810/525))) in the murine valves. In a separate experiment, animals were fed the above diets till 28 weeks to assess for later-stage calcification. RESULTS: Pro-calcific mice showed evidence of lipid deposition at 4 weeks and calcification at 16 weeks at the valve commissures. The valves of pro-calcific mice also showed positive expression for markers of osteogenic differentiation, myofibroblast activation, proliferation, inflammatory cytokines and collagen remodeling. Pro-calcific mice exhibited lower TPEF autofluorescence ratios, at locations coincident with calcification, that correlated with increased collagen disorganization and positive expression of osteogenic markers. Additionally, locations with lower TPEF autofluorescence ratios at 4 and 16 weeks exhibited increased calcification at later 28-week timepoints. CONCLUSIONS: This study suggests the potential of TPEF autofluorescence metrics to serve as a label-free tool for early detection and monitoring of CAVD pathophysiology. BioMed Central 2020-12-11 /pmc/articles/PMC7731510/ /pubmed/33308143 http://dx.doi.org/10.1186/s12872-020-01776-8 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Tandon, Ishita
Johns, Shelby
Woessner, Alan
Perez, Jessica
Cross, Delaney
Ozkizilcik, Asya
Muldoon, Timothy J.
Vallurupalli, Srikanth
Padala, Muralidhar
Quinn, Kyle P.
Balachandran, Kartik
Label-free optical biomarkers detect early calcific aortic valve disease in a wild-type mouse model
title Label-free optical biomarkers detect early calcific aortic valve disease in a wild-type mouse model
title_full Label-free optical biomarkers detect early calcific aortic valve disease in a wild-type mouse model
title_fullStr Label-free optical biomarkers detect early calcific aortic valve disease in a wild-type mouse model
title_full_unstemmed Label-free optical biomarkers detect early calcific aortic valve disease in a wild-type mouse model
title_short Label-free optical biomarkers detect early calcific aortic valve disease in a wild-type mouse model
title_sort label-free optical biomarkers detect early calcific aortic valve disease in a wild-type mouse model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7731510/
https://www.ncbi.nlm.nih.gov/pubmed/33308143
http://dx.doi.org/10.1186/s12872-020-01776-8
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