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Label-free metabolic biomarkers for assessing valve interstitial cell calcific progression
Calcific aortic valve disease (CAVD) is the most common form of valve disease where the only available treatment strategy is surgical valve replacement. Technologies for the early detection of CAVD would benefit the development of prevention, mitigation and alternate therapeutic strategies. Two-phot...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7316720/ https://www.ncbi.nlm.nih.gov/pubmed/32587322 http://dx.doi.org/10.1038/s41598-020-66960-4 |
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author | Tandon, Ishita Kolenc, Olivia I. Cross, Delaney Vargas, Isaac Johns, Shelby Quinn, Kyle P. Balachandran, Kartik |
author_facet | Tandon, Ishita Kolenc, Olivia I. Cross, Delaney Vargas, Isaac Johns, Shelby Quinn, Kyle P. Balachandran, Kartik |
author_sort | Tandon, Ishita |
collection | PubMed |
description | Calcific aortic valve disease (CAVD) is the most common form of valve disease where the only available treatment strategy is surgical valve replacement. Technologies for the early detection of CAVD would benefit the development of prevention, mitigation and alternate therapeutic strategies. Two-photon excited fluorescence (TPEF) microscopy is a label-free, non-destructive imaging technique that has been shown to correlate with multiple markers for cellular differentiation and phenotypic changes in cancer and wound healing. Here we show how specific TPEF markers, namely, the optical redox ratio and mitochondrial fractal dimension, correlate with structural, functional and phenotypic changes occurring in the aortic valve interstitial cells (VICs) during osteogenic differentiation. The optical redox ratio, and fractal dimension of mitochondria were assessed and correlated with gene expression and nuclear morphology of VICs. The optical redox ratio decreased for VICs during early osteogenic differentiation and correlated with biological markers for CAVD progression. Fractal dimension correlated with structural and osteogenic markers as well as measures of nuclear morphology. Our study suggests that TPEF imaging markers, specifically the optical redox ratio and mitochondrial fractal dimension, can be potentially used as a tool for assessing early CAVD progression in vitro. |
format | Online Article Text |
id | pubmed-7316720 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73167202020-06-26 Label-free metabolic biomarkers for assessing valve interstitial cell calcific progression Tandon, Ishita Kolenc, Olivia I. Cross, Delaney Vargas, Isaac Johns, Shelby Quinn, Kyle P. Balachandran, Kartik Sci Rep Article Calcific aortic valve disease (CAVD) is the most common form of valve disease where the only available treatment strategy is surgical valve replacement. Technologies for the early detection of CAVD would benefit the development of prevention, mitigation and alternate therapeutic strategies. Two-photon excited fluorescence (TPEF) microscopy is a label-free, non-destructive imaging technique that has been shown to correlate with multiple markers for cellular differentiation and phenotypic changes in cancer and wound healing. Here we show how specific TPEF markers, namely, the optical redox ratio and mitochondrial fractal dimension, correlate with structural, functional and phenotypic changes occurring in the aortic valve interstitial cells (VICs) during osteogenic differentiation. The optical redox ratio, and fractal dimension of mitochondria were assessed and correlated with gene expression and nuclear morphology of VICs. The optical redox ratio decreased for VICs during early osteogenic differentiation and correlated with biological markers for CAVD progression. Fractal dimension correlated with structural and osteogenic markers as well as measures of nuclear morphology. Our study suggests that TPEF imaging markers, specifically the optical redox ratio and mitochondrial fractal dimension, can be potentially used as a tool for assessing early CAVD progression in vitro. Nature Publishing Group UK 2020-06-25 /pmc/articles/PMC7316720/ /pubmed/32587322 http://dx.doi.org/10.1038/s41598-020-66960-4 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Tandon, Ishita Kolenc, Olivia I. Cross, Delaney Vargas, Isaac Johns, Shelby Quinn, Kyle P. Balachandran, Kartik Label-free metabolic biomarkers for assessing valve interstitial cell calcific progression |
title | Label-free metabolic biomarkers for assessing valve interstitial cell calcific progression |
title_full | Label-free metabolic biomarkers for assessing valve interstitial cell calcific progression |
title_fullStr | Label-free metabolic biomarkers for assessing valve interstitial cell calcific progression |
title_full_unstemmed | Label-free metabolic biomarkers for assessing valve interstitial cell calcific progression |
title_short | Label-free metabolic biomarkers for assessing valve interstitial cell calcific progression |
title_sort | label-free metabolic biomarkers for assessing valve interstitial cell calcific progression |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7316720/ https://www.ncbi.nlm.nih.gov/pubmed/32587322 http://dx.doi.org/10.1038/s41598-020-66960-4 |
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