Age related extracellular matrix and interstitial cell phenotype in pulmonary valves

Abstract Heart valve disease is a common manifestation of cardiovascular disease and is a significant cause of cardiovascular morbidity and mortality worldwide. The pulmonary valve (PV) is of primary concern because of its involvement in common congenital heart defects, and the PV is usually the sit...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Shaohua Wu, Vikas Kumar, Peng Xiao, Mitchell Kuss, Jung Yul Lim, Chittibabu Guda, Jonathan Butcher, Bin Duan
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2020
Materias:
R
Q
Acceso en línea:https://doaj.org/article/8eb60de4a12b4d4e81af67d3af811050
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:8eb60de4a12b4d4e81af67d3af811050
record_format dspace
spelling oai:doaj.org-article:8eb60de4a12b4d4e81af67d3af8110502021-12-02T15:10:18ZAge related extracellular matrix and interstitial cell phenotype in pulmonary valves10.1038/s41598-020-78507-82045-2322https://doaj.org/article/8eb60de4a12b4d4e81af67d3af8110502020-12-01T00:00:00Zhttps://doi.org/10.1038/s41598-020-78507-8https://doaj.org/toc/2045-2322Abstract Heart valve disease is a common manifestation of cardiovascular disease and is a significant cause of cardiovascular morbidity and mortality worldwide. The pulmonary valve (PV) is of primary concern because of its involvement in common congenital heart defects, and the PV is usually the site for prosthetic replacement following a Ross operation. Although effects of age on valve matrix components and mechanical properties for aortic and mitral valves have been studied, very little is known about the age-related alterations that occur in the PV. In this study, we isolated PV leaflets from porcine hearts in different age groups (~ 4–6 months, denoted as young versus ~ 2 years, denoted as adult) and studied the effects of age on PV leaflet thickness, extracellular matrix components, and mechanical properties. We also conducted proteomics and RNA sequencing to investigate the global changes of PV leaflets and passage zero PV interstitial cells in their protein and gene levels. We found that the size, thickness, elastic modulus, and ultimate stress in both the radial and circumferential directions and the collagen of PV leaflets increased from young to adult age, while the ultimate strain and amount of glycosaminoglycans decreased when age increased. Young and adult PV had both similar and distinct protein and gene expression patterns that are related to their inherent physiological properties. These findings are important for us to better understand the physiological microenvironments of PV leaflet and valve cells for correctively engineering age-specific heart valve tissues.Shaohua WuVikas KumarPeng XiaoMitchell KussJung Yul LimChittibabu GudaJonathan ButcherBin DuanNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Shaohua Wu
Vikas Kumar
Peng Xiao
Mitchell Kuss
Jung Yul Lim
Chittibabu Guda
Jonathan Butcher
Bin Duan
Age related extracellular matrix and interstitial cell phenotype in pulmonary valves
description Abstract Heart valve disease is a common manifestation of cardiovascular disease and is a significant cause of cardiovascular morbidity and mortality worldwide. The pulmonary valve (PV) is of primary concern because of its involvement in common congenital heart defects, and the PV is usually the site for prosthetic replacement following a Ross operation. Although effects of age on valve matrix components and mechanical properties for aortic and mitral valves have been studied, very little is known about the age-related alterations that occur in the PV. In this study, we isolated PV leaflets from porcine hearts in different age groups (~ 4–6 months, denoted as young versus ~ 2 years, denoted as adult) and studied the effects of age on PV leaflet thickness, extracellular matrix components, and mechanical properties. We also conducted proteomics and RNA sequencing to investigate the global changes of PV leaflets and passage zero PV interstitial cells in their protein and gene levels. We found that the size, thickness, elastic modulus, and ultimate stress in both the radial and circumferential directions and the collagen of PV leaflets increased from young to adult age, while the ultimate strain and amount of glycosaminoglycans decreased when age increased. Young and adult PV had both similar and distinct protein and gene expression patterns that are related to their inherent physiological properties. These findings are important for us to better understand the physiological microenvironments of PV leaflet and valve cells for correctively engineering age-specific heart valve tissues.
format article
author Shaohua Wu
Vikas Kumar
Peng Xiao
Mitchell Kuss
Jung Yul Lim
Chittibabu Guda
Jonathan Butcher
Bin Duan
author_facet Shaohua Wu
Vikas Kumar
Peng Xiao
Mitchell Kuss
Jung Yul Lim
Chittibabu Guda
Jonathan Butcher
Bin Duan
author_sort Shaohua Wu
title Age related extracellular matrix and interstitial cell phenotype in pulmonary valves
title_short Age related extracellular matrix and interstitial cell phenotype in pulmonary valves
title_full Age related extracellular matrix and interstitial cell phenotype in pulmonary valves
title_fullStr Age related extracellular matrix and interstitial cell phenotype in pulmonary valves
title_full_unstemmed Age related extracellular matrix and interstitial cell phenotype in pulmonary valves
title_sort age related extracellular matrix and interstitial cell phenotype in pulmonary valves
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/8eb60de4a12b4d4e81af67d3af811050
work_keys_str_mv AT shaohuawu agerelatedextracellularmatrixandinterstitialcellphenotypeinpulmonaryvalves
AT vikaskumar agerelatedextracellularmatrixandinterstitialcellphenotypeinpulmonaryvalves
AT pengxiao agerelatedextracellularmatrixandinterstitialcellphenotypeinpulmonaryvalves
AT mitchellkuss agerelatedextracellularmatrixandinterstitialcellphenotypeinpulmonaryvalves
AT jungyullim agerelatedextracellularmatrixandinterstitialcellphenotypeinpulmonaryvalves
AT chittibabuguda agerelatedextracellularmatrixandinterstitialcellphenotypeinpulmonaryvalves
AT jonathanbutcher agerelatedextracellularmatrixandinterstitialcellphenotypeinpulmonaryvalves
AT binduan agerelatedextracellularmatrixandinterstitialcellphenotypeinpulmonaryvalves
_version_ 1718387704823021568