Bioreactor Conditioning of Valve Scaffolds Seeded Internally with Adult Stem Cells.
10.1007/s13770-016-9114-1
- Author:
Allison KENNAMER
1
;
Leslie SIERAD
;
Richard PASCAL
;
Nicholas RIERSON
;
Christopher ALBERS
;
Marius HARPA
;
Ovidiu COTOI
;
Lucian HARCEAGA
;
Peter OLAH
;
Preda TEREZIA
;
Agneta SIMIONESCU
;
Dan SIMIONESCU
Author Information
1. Biocompatibility and Tissue Regeneration Laboratories, Department of Bioengineering, Clemson University, Clemson, SC, USA. dsimion@clemson.edu
- Publication Type:Original Article
- Keywords:
Scaffolds;
Heart valves;
Stem cells;
Bioreactor
- MeSH:
Actins;
Adult Stem Cells*;
Adult*;
Bioreactors*;
Extracellular Matrix;
Heart Valves;
Hemodynamics;
Humans;
Immunohistochemistry;
In Vitro Techniques;
Islands;
Muscle Cells;
Phenotype;
Stem Cells;
Vimentin
- From:
Tissue Engineering and Regenerative Medicine
2016;13(5):507-515
- CountryRepublic of Korea
- Language:English
-
Abstract:
The goal of this study was to test the hypothesis that stem cells, as a response to valve-specific extracellular matrix “niches” and mechanical stimuli, would differentiate into valvular interstitial cells (VICs). Porcine aortic root scaffolds were prepared by decellularization. After verifying that roots exhibited adequate hemodynamics in vitro, we seeded human adipose-derived stem cells (hADSCs) within the interstitium of the cusps and subjected the valves to in vitro pulsatile bioreactor testing in pulmonary pressures and flow conditions. As controls we incubated cell-seeded valves in a rotator device which allowed fluid to flow through the valves ensuring gas and nutrient exchange without subjecting the cusps to significant stress. After 24 days of conditioning, valves were analyzed for cell phenotype using immunohistochemistry for vimentin, alpha-smooth muscle cell actin (SMA) and prolyl-hydroxylase (PHA). Fresh native valves were used as immunohistochemistry controls. Analysis of bioreactor-conditioned valves showed that almost all seeded cells had died and large islands of cell debris were found within each cusp. Remnants of cells were positive for vimentin. Cell seeded controls, which were only rotated slowly to ensure gas and nutrient exchange, maintained about 50% of cells alive; these cells were positive for vimentin and negative for alpha-SMA and PHA, similar to native VICs. These results highlight for the first time the extreme vulnerability of hADSCs to valve-specific mechanical forces and also suggest that careful, progressive mechanical adaptation to valve-specific forces might encourage stem cell differentiation towards the VIC phenotype.
