scholarly journals In-vivo heterogeneous functional and residual strains in human aortic valve leaflets

2016 ◽  
Vol 49 (12) ◽  
pp. 2481-2490 ◽  
Author(s):  
Ankush Aggarwal ◽  
Alison M. Pouch ◽  
Eric Lai ◽  
John Lesicko ◽  
Paul A. Yushkevich ◽  
...  
2014 ◽  
Vol 97 (4) ◽  
pp. 1255-1258 ◽  
Author(s):  
Arminder S. Jassar ◽  
Melissa M. Levack ◽  
Ricardo D. Solorzano ◽  
Alison M. Pouch ◽  
Giovanni Ferrari ◽  
...  

2021 ◽  
Vol 10 (2) ◽  
pp. 16-24
Author(s):  
T. V. Glushkova ◽  
A. E. Kostyunin

Highlights. The morphology and elemental composition of calcium deposits formed in the tissues of epoxytreated aortic and mitral bioprostheses do not differ from those in the mineralized matrix of stenotic human aortic valve leaflets. Despite similar elemental composition of mineral deposits in the KemCor and UniLine bioprostheses, the morphology of these calcifications differs between bioprosthetic heart valve substitutes and, apparently, is associated with the specific structure of the fibrous matrix of the biological tissues that are used for their manufacturing.Aim. To analyze the morphology and elemental composition of mineral deposits formed in epoxy-treated aortic and mitral bioprosthetic heart valves made from xenoaortic or xenopericardial material and to compare the obtained findings with the data on calcified human aortic valve.Methods. Leaflets of the mitral and aortic bioprosthetic heart valves KemCor and UniLine (NeoKor, L Russia, Kemerovo) that were explanted due to their failure, as well as leaflets of the calcified native aortic valve were evaluated. The morphology of calcifications was studied by scanning electron microscopy using an S-3400N microscope (Hitachi, Japan). The elemental composition of calcium deposits was studied by electron probe microanalysis using Hitachi S-3400N microscope with energy dispersive spectrometer Bruker XFlash 4010 (Bruker, Germany).Results. Large calcifications located at the internal layers of samples were surrounded by collagen fibers commonly with evident signs of the onset of mineralization. Calcium deposits in the native aortic valve and xenoartic bioprostheses KemCor were located mainly at the spongy layer and had a loose structure, while dense lamellar deposits were found at the leaflets of pericardial bioprostheses UniLine. The elemental composition of calcium deposits showed the presence of Ca, P, O, Mg, and Na in the mineralized regions and the presence of S in the regions of low electron density. The calcium to phosphorus ratio (Ca:P) in the calcifications of the aortic valve leaflets was 1.81 (1.79-1.84; min - 1.48; max - 2.05), whereas the Ca:P ratios in the UniLine and KemCor bioprostheses were 1.78 (1.75-1.86; min - 1.52; max - 2.03) and 1.82 (1.81-1.88; min - 1.71; max - 2.06), respectively. There were no significant differences in the Ca:P ratios between calcifications in the study groups (p>0.05).Conclusion. Calcium deposits detected in epoxy-treated bioprostheses and human aortic valve appeared to be formed under dystrophic calcification. The morphology of calcifications in bioprostheses depended on the type of biological tissue. None correlations between the morphological structure of calcifications and the implantation position were found in bioprosthetic leaflets. The elemental composition of mineral deposits was similar in all study samples.


2019 ◽  
Vol 73 (9) ◽  
pp. 1043-1054 ◽  
Author(s):  
Marion Morvan ◽  
Dimitri Arangalage ◽  
Grégory Franck ◽  
Fanny Perez ◽  
Léa Cattan-Levy ◽  
...  

2021 ◽  
Vol 7 (2) ◽  
pp. 45-48
Author(s):  
Maximilian Winkelkotte ◽  
Florian Schmieder ◽  
Stephan Behrens ◽  
Dominic Salminger ◽  
Anett Jannasch ◽  
...  

Abstract Aortic valve (AV) stenosis is characterized by tissue fibrosis and calcification. Fibrous thickening can result in reduced tissue oxygen supply leading to pathological valvular interstitial cell (VIC) differentiation and calcification. Static 2D VIC cultures and animal models are limited in the ability to reflect human AV calcification. Culturing of VICs in micro-physiological-systems (MPS) in a pulsatile flow and the establishment of a modular AV tissue incubation chamber (TIC) are new approaches to evaluate pathophysiological processes of AV disease. Therefore, a MPS able to adjust hypoxic conditions was applied for VIC culture. A significant increase of mRNA-expression of EGLN1 and HIF1α- regulated LDHA and HIF1α nuclear localisation were proven under hypoxia. AV tissue culture was established within a TIC and viability was monitored by Resazurin-reduction in the incubation medium and visualized by LDH-activity in tissue cryosections. Viability was compared between fluid and static incubated tissues revealing an advantageous effect of the fluidic assay condition. Consecutively, the application of MPS in AV research allows i) the investigation of VIC cultures with efficient oxygen regulation and ii) the culture of porcine or human AV tissues preserving viability and specifically reflecting in vivo parameters. These methods open up new possibilities beyond static 2D culture and facilitate a reduction of animal experiments in AV research.


1983 ◽  
Vol 18 (4) ◽  
pp. 474-478
Author(s):  
V. A. Kas'yanov ◽  
D. D. Mungalov ◽  
V. M. Vitin'sh ◽  
D. �. Pablak

1980 ◽  
Vol 47 (5) ◽  
pp. 792-800 ◽  
Author(s):  
M Thubrikar ◽  
W C Piepgrass ◽  
L P Bosher ◽  
S P Nolan

1976 ◽  
Vol 1 (1) ◽  
pp. 33-36 ◽  
Author(s):  
Phillip L. Gould ◽  
Altay Cataloglu ◽  
Richard E. Clark

1973 ◽  
Vol 1 (2) ◽  
pp. 307-321 ◽  
Author(s):  
Ken P. Chong ◽  
David W. Wieting ◽  
Ned H. C. Hwang ◽  
John H. Kennedy

2008 ◽  
Vol 294 (1) ◽  
pp. C29-C35 ◽  
Author(s):  
Xianzhong Meng ◽  
Lihua Ao ◽  
Yong Song ◽  
Ashok Babu ◽  
Xiaoping Yang ◽  
...  

Calcific aortic valve stenosis is the most common indication for surgical valve replacement. Inflammation appears to be one of the mechanisms involved in aortic valve calcification, and valve interstitial cells seem to contribute to that process. Although Toll-like receptors (TLRs) play an important role in the cellular inflammatory response, it is unknown whether human aortic valve interstitial cells (HAVICs) express functional TLRs. We examined the expression of TLR2 and TLR4 in human aortic valve leaflets and in isolated HAVICs and analyzed the response of cultured HAVICs to the TLR2 and TLR4 agonists peptidoglycan (PGN) and LPS. Abundant TLR2 and TLR4 proteins were found in human aortic valve leaflets and in isolated HAVICs, and both receptors were detected in the membrane and cytoplasm of cultured HAVICs. Stimulation by either PGN or LPS resulted in the activation of the NF-κB signaling pathway and the production of multiple proinflammatory mediators, including IL-6, IL-8, and ICAM-1. In addition, stimulation by either PGN or LPS upregulated the expression of bone morphogenetic protein-2 (BMP-2) and Runx2, factors associated with osteogenesis. This study demonstrates for the first time that HAVICs express TLR2 and TLR4 and that stimulation of HAVICs by PGN or LPS induces the expression of proinflammatory mediators and the upregulation of osteogenesis-associated factors. These results suggest that TLR2 and TLR4 may play a role in aortic valve inflammation and stenosis.


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