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Isolation and Characterization of Primary Rat Valve Interstitial Cells: A New Model to Study Aortic Valve Calcification
Published on: November 20, 2017
Cell Sources for Tissue Engineering Strategies to Treat Calcific Valve Disease
Eva Jover1, Marco Fagnano1, Gianni Angelini1
1Bristol Medical School (Translational Health Sciences), Bristol Heart Institute, University of Bristol, Bristol, United Kingdom.
Insights
Calcific aortic valve stenosis, a common cause of heart valve disease (VHD) in the elderly, involves complex bone-like formation. Tissue engineering of heart valves (TEHV) offers a promising alternative to current treatments.
Area of Science:
- Cardiovascular Biology
- Biomaterials Science
- Regenerative Medicine
Background:
- Cardiovascular calcification, particularly calcific aortic valve stenosis (VHD), is a significant independent risk factor for adverse cardiovascular events in the elderly.
- Aortic valve stenosis affects 2% of individuals over 65, leading to left ventricle outflow obstruction and mortality.
- Current treatments like surgical valve replacement have limitations, including the need for anticoagulation or prosthesis reintervention.
Purpose of the Study:
- To critically review current knowledge on calcific VHD.
- To discuss the advantages and disadvantages of various cell sources for tissue engineering of heart valves (TEHV).
Main Methods:
- Literature review of studies on calcific VHD.
- Analysis of research addressing *in vitro* TEHV using different cell sources.
Main Results:
- Calcific VHD is an active, multifactorial process involving matrix remodeling, osteogenesis, and angiogenesis.
- TEHV is an emerging alternative to address limitations of current VHD treatments.
- Cell source selection is crucial for TEHV efficacy and requires careful consideration.
Conclusions:
- Understanding the complex mechanisms of calcific VHD is essential for developing effective treatments.
- TEHV holds significant promise for definitive VHD management, potentially overcoming limitations of current prostheses.
- Further research into optimal cell sources is critical for advancing TEHV from bench to bedside.
Abstract:
Cardiovascular calcification is an independent risk factor and an established predictor of adverse cardiovascular events. Despite concomitant factors leading to atherosclerosis and heart valve disease (VHD), the latter has been identified as an independent pathological entity. Calcific aortic valve stenosis is the most common form of VDH resulting of either congenital malformations or senile "degeneration." About 2% of the population over 65 years is affected by aortic valve stenosis which represents a major cause of morbidity and mortality in the elderly. A multifactorial, complex and active heterotopic bone-like formation process, including extracellular matrix remodeling, osteogenesis and angiogenesis, drives heart valve "degeneration" and calcification, finally causing left ventricle outflow obstruction. Surgical heart valve replacement is the current therapeutic option for those patients diagnosed with severe VHD representing more than 20% of all cardiac surgeries nowadays. Tissue Engineering of Heart Valves (TEHV) is emerging as a valuable alternative for definitive treatment of VHD and promises to overcome either the chronic oral anticoagulation or the time-dependent deterioration and reintervention of current mechanical or biological prosthesis, respectively. Among the plethora of approaches and stablished techniques for TEHV, utilization of different cell sources may confer of additional properties, desirable and not, which need to be considered before moving from the bench to the bedside. This review aims to provide a critical appraisal of current knowledge about calcific VHD and to discuss the pros and cons of the main cell sources tested in studies addressing in vitro TEHV.
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