Models and Techniques to Study Aortic Valve Calcification in Vitro, ex Vivo and in Vivo. An Overview

Aortic valve stenosis secondary to aortic valve calcification is the most common valve disease in the Western world. Calcification is a result of pathological proliferation and osteogenic differentiation of resident valve interstitial cells. To develop non-surgical treatments, the molecular and cell...

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Main Authors: Maria Bogdanova, Arsenii Zabirnyk, Anna Malashicheva, Daria Semenova, John-Peder Escobar Kvitting, Mari-Liis Kaljusto, Maria del Mar Perez, Anna Kostareva, Kåre-Olav Stensløkken, Gareth J Sullivan, Arkady Rutkovskiy, Jarle Vaage
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-06-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphar.2022.835825/full
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author Maria Bogdanova
Arsenii Zabirnyk
Arsenii Zabirnyk
Anna Malashicheva
Daria Semenova
John-Peder Escobar Kvitting
Mari-Liis Kaljusto
Maria del Mar Perez
Anna Kostareva
Anna Kostareva
Kåre-Olav Stensløkken
Gareth J Sullivan
Gareth J Sullivan
Gareth J Sullivan
Gareth J Sullivan
Gareth J Sullivan
Arkady Rutkovskiy
Arkady Rutkovskiy
Jarle Vaage
Jarle Vaage
Jarle Vaage
author_facet Maria Bogdanova
Arsenii Zabirnyk
Arsenii Zabirnyk
Anna Malashicheva
Daria Semenova
John-Peder Escobar Kvitting
Mari-Liis Kaljusto
Maria del Mar Perez
Anna Kostareva
Anna Kostareva
Kåre-Olav Stensløkken
Gareth J Sullivan
Gareth J Sullivan
Gareth J Sullivan
Gareth J Sullivan
Gareth J Sullivan
Arkady Rutkovskiy
Arkady Rutkovskiy
Jarle Vaage
Jarle Vaage
Jarle Vaage
author_sort Maria Bogdanova
collection DOAJ
description Aortic valve stenosis secondary to aortic valve calcification is the most common valve disease in the Western world. Calcification is a result of pathological proliferation and osteogenic differentiation of resident valve interstitial cells. To develop non-surgical treatments, the molecular and cellular mechanisms of pathological calcification must be revealed. In the current overview, we present methods for evaluation of calcification in different ex vivo, in vitro and in vivo situations including imaging in patients. The latter include echocardiography, scanning with computed tomography and magnetic resonance imaging. Particular emphasis is on translational studies of calcific aortic valve stenosis with a special focus on cell culture using human primary cell cultures. Such models are widely used and suitable for screening of drugs against calcification. Animal models are presented, but there is no animal model that faithfully mimics human calcific aortic valve disease. A model of experimentally induced calcification in whole porcine aortic valve leaflets ex vivo is also included. Finally, miscellaneous methods and aspects of aortic valve calcification, such as, for instance, biomarkers are presented.
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spelling doaj.art-bee968d2f14e495b851a83949d91c8bb2022-12-22T02:27:02ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122022-06-011310.3389/fphar.2022.835825835825Models and Techniques to Study Aortic Valve Calcification in Vitro, ex Vivo and in Vivo. An OverviewMaria Bogdanova0Arsenii Zabirnyk1Arsenii Zabirnyk2Anna Malashicheva3Daria Semenova4John-Peder Escobar Kvitting5Mari-Liis Kaljusto6Maria del Mar Perez7Anna Kostareva8Anna Kostareva9Kåre-Olav Stensløkken10Gareth J Sullivan11Gareth J Sullivan12Gareth J Sullivan13Gareth J Sullivan14Gareth J Sullivan15Arkady Rutkovskiy16Arkady Rutkovskiy17Jarle Vaage18Jarle Vaage19Jarle Vaage20Department of Molecular Medicine, Institute of Basic Medical Sciences, University of Oslo, Oslo, NorwayDepartment of Molecular Medicine, Institute of Basic Medical Sciences, University of Oslo, Oslo, NorwayDepartment of Research and Development, Division of Emergencies and Critical Care, Oslo University Hospital, Oslo, NorwayInstitute of Cytology, Russian Academy of Sciences, Saint Petersburg, RussiaInstitute of Cytology, Russian Academy of Sciences, Saint Petersburg, RussiaDepartment of Cardiothoracic Surgery, Oslo University Hospital, Oslo, NorwayDepartment of Cardiothoracic Surgery, Oslo University Hospital, Oslo, NorwaySanifit Therapeutics, Palma de Mallorca, SpainAlmazov National Medical Research Centre, Saint Petersburg, RussiaDepartment of Woman and Children Health, Karolinska Institute, Stockholm, SwedenDepartment of Molecular Medicine, Institute of Basic Medical Sciences, University of Oslo, Oslo, NorwayDepartment of Molecular Medicine, Institute of Basic Medical Sciences, University of Oslo, Oslo, NorwayNorwegian Center for Stem Cell Research, Oslo University Hospital and University of Oslo, Oslo, NorwayInstitute of Immunology, Oslo University Hospital, Oslo, Norway0Hybrid Technology Hub - Centre of Excellence, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway1Department of Pediatric Research, Oslo University Hospital, Oslo, NorwayDepartment of Molecular Medicine, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway2Department of Pulmonary Diseases, Oslo University Hospital, Oslo, NorwayDepartment of Molecular Medicine, Institute of Basic Medical Sciences, University of Oslo, Oslo, NorwayDepartment of Research and Development, Division of Emergencies and Critical Care, Oslo University Hospital, Oslo, Norway3Institute of Clinical Medicine, University of Oslo, Oslo, NorwayAortic valve stenosis secondary to aortic valve calcification is the most common valve disease in the Western world. Calcification is a result of pathological proliferation and osteogenic differentiation of resident valve interstitial cells. To develop non-surgical treatments, the molecular and cellular mechanisms of pathological calcification must be revealed. In the current overview, we present methods for evaluation of calcification in different ex vivo, in vitro and in vivo situations including imaging in patients. The latter include echocardiography, scanning with computed tomography and magnetic resonance imaging. Particular emphasis is on translational studies of calcific aortic valve stenosis with a special focus on cell culture using human primary cell cultures. Such models are widely used and suitable for screening of drugs against calcification. Animal models are presented, but there is no animal model that faithfully mimics human calcific aortic valve disease. A model of experimentally induced calcification in whole porcine aortic valve leaflets ex vivo is also included. Finally, miscellaneous methods and aspects of aortic valve calcification, such as, for instance, biomarkers are presented.https://www.frontiersin.org/articles/10.3389/fphar.2022.835825/fullaortic valveinterstitial cellsendothelial cellscalcificationanimal modelscalcified aortic valve disease
spellingShingle Maria Bogdanova
Arsenii Zabirnyk
Arsenii Zabirnyk
Anna Malashicheva
Daria Semenova
John-Peder Escobar Kvitting
Mari-Liis Kaljusto
Maria del Mar Perez
Anna Kostareva
Anna Kostareva
Kåre-Olav Stensløkken
Gareth J Sullivan
Gareth J Sullivan
Gareth J Sullivan
Gareth J Sullivan
Gareth J Sullivan
Arkady Rutkovskiy
Arkady Rutkovskiy
Jarle Vaage
Jarle Vaage
Jarle Vaage
Models and Techniques to Study Aortic Valve Calcification in Vitro, ex Vivo and in Vivo. An Overview
Frontiers in Pharmacology
aortic valve
interstitial cells
endothelial cells
calcification
animal models
calcified aortic valve disease
title Models and Techniques to Study Aortic Valve Calcification in Vitro, ex Vivo and in Vivo. An Overview
title_full Models and Techniques to Study Aortic Valve Calcification in Vitro, ex Vivo and in Vivo. An Overview
title_fullStr Models and Techniques to Study Aortic Valve Calcification in Vitro, ex Vivo and in Vivo. An Overview
title_full_unstemmed Models and Techniques to Study Aortic Valve Calcification in Vitro, ex Vivo and in Vivo. An Overview
title_short Models and Techniques to Study Aortic Valve Calcification in Vitro, ex Vivo and in Vivo. An Overview
title_sort models and techniques to study aortic valve calcification in vitro ex vivo and in vivo an overview
topic aortic valve
interstitial cells
endothelial cells
calcification
animal models
calcified aortic valve disease
url https://www.frontiersin.org/articles/10.3389/fphar.2022.835825/full
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