Cell Composition of the Human Pulmonary Valve: a Comparative Study with the Aortic Valve--the VESALIO Project. Vitalitate Exornatum Succedaneum Aorticum Labore Ingegnoso Obtinebitur
Overview
Pulmonary Medicine
Affiliations
Background: Cell populations present in human semilunar valves have not been investigated thoroughly. The aim of this study was to characterize the cell phenotypes in pulmonary valve leaflets (PVL) in comparison with aortic (AVL) valve leaflets.
Methods: AVL and PVL were dissected from hearts (n = 4) harvested from transplanted patients. Leaflets were processed for immunocytochemistry analysis and Western blotting procedures using a panel of monoclonal antibodies specific for cytoskeletal/contractile antigens.
Results: The fibrosa and the ventricularis layers of AVL had a higher cellularity than PVL. In PVL and AVL most cells were reactive for vimentin and nonmuscle (NM) myosin, though vimentin-positive cells were more abundant in AVL than in PVL. Sparse cells positive to anti-smooth muscle (SM) alpha-actin, calponin, and anti-SM myosin antibodies were found only at the outer edge of fibrosa. In Western blotting, AVL and PVL extracts were shown to be equally reactive for vimentin, SM alpha-actin, and NM myosin, whereas both valves were negative for SM myosin and SM22.
Conclusions: Three distinct cell phenotypes have been identified in both valves: fibroblasts, myofibroblasts, and fetal-type SM cells whose distribution is specifically related to the valve layers. Although PVL and AVL cell populations differ quantitatively, some minor qualitative differences exist for vimentin and NM myosin distribution. These data are essential for studies aimed at repopulating valve scaffolds by using tissue engineering technology.
West T, Howsmon D, Massidda M, Vo H, Janobas A, Baker A APL Bioeng. 2023; 7(2):026101.
PMID: 37035541 PMC: 10076067. DOI: 10.1063/5.0138030.
Carbon Nanotubes Substrates Alleviate Pro-Calcific Evolution in Porcine Valve Interstitial Cells.
Ulloa L, Perissinotto F, Rago I, Goldoni A, Santoro R, Pesce M Nanomaterials (Basel). 2021; 11(10).
PMID: 34685165 PMC: 8538037. DOI: 10.3390/nano11102724.
Role of p38 MAPK in Atherosclerosis and Aortic Valve Sclerosis.
Reustle A, Torzewski M Int J Mol Sci. 2018; 19(12).
PMID: 30486366 PMC: 6321637. DOI: 10.3390/ijms19123761.
Dekker S, van Geemen D, van den Bogaerdt A, Driessen-Mol A, Aikawa E, Smits A Front Cardiovasc Med. 2018; 5:105.
PMID: 30159315 PMC: 6104173. DOI: 10.3389/fcvm.2018.00105.
Recellularization of decellularized heart valves: Progress toward the tissue-engineered heart valve.
VeDepo M, Detamore M, Hopkins R, Converse G J Tissue Eng. 2017; 8:2041731417726327.
PMID: 28890780 PMC: 5574480. DOI: 10.1177/2041731417726327.