Biochemical and histological evidence of deteriorated bioprosthetic valve leaflets: the accumulation of fibrinogen and plasminogen

Author:

Sakaue Tomohisa12ORCID,Nakaoka Hirotomo13,Shikata Fumiaki14ORCID,Aono Jun5ORCID,Kurata Mie67ORCID,Uetani Teruyoshi5ORCID,Hamaguchi Mika5,Kojima Ai1,Uchita Shunji1ORCID,Yasugi Takumi1,Higashi Haruhiko5,Suzuki Jun5ORCID,Ikeda Shuntaro5ORCID,Higaki Jitsuo5,Higashiyama Shigeki28ORCID,Izutani Hironori1ORCID

Affiliation:

1. Department of Cardiovascular and Thoracic Surgery, Ehime University Graduate School of Medicine, Ehime 791-0295, Japan

2. Department of Cell Growth and Tumor Regulation, Proteo-Science Center (PROS), Toon, Ehime 791-0295, Japan

3. Division of Laboratory Animal Research, Advanced Research Support Center (ADRES), Toon, Ehime 791-0295, Japan

4. Department of Cardiothoracic Surgery, St Vincent's Hospital Sydney, NSW 791-0295, Australia

5. Department of Cardiology, Pulmonology, Hypertension, and Nephrology, Ehime University Graduate School of Medicine, Ehime 791-0295, Japan

6. Department of Pathology, Division of Analytical Pathology, Ehime University Graduate School of Medicine, Ehime 791-0295, Japan

7. Department of Pathology, Proteo-Science Center (PROS), Toon, Ehime 791-0295, Japan

8. Department of Biochemistry and Molecular Genetics, Ehime University Graduate School of Medicine, Toon, Ehime 791-0295, Japan

Abstract

ABSTRACT Calcification of bioprosthetic valves (BVs) implanted in aortic position can result in gradual deterioration and necessitate aortic valve replacement. The molecular mechanism of calcium deposition on BV leaflets has been investigated, but remains to be fully elucidated. The present study aimed to identify explanted bioprosthetic valve (eBV)-specific proteins using a proteomics approach and to unveil their biochemical and histological involvements in calcium deposition on BV leaflets. Calcification, fibrosis, and glycosylation of the valves were histologically assessed using Von Kossa, Masson's Trichrome and Alcian Blue staining, as well as immunostaining. Protein expression in the explanted biological valves was analysed using proteomics and western blotting. In a histological evaluation, αSMA-positive myofibroblasts were not observed in eBV, whereas severe fibrosis occurred around calcified areas. SDS-PAGE revealed three major bands with considerably increased intensity in BV leaflets that were identified as plasminogen and fibrinogen gamma chain (100 kDa), and fibrinogen beta chain (50 and 37 kDa) by mass analysis. Immunohistochemistry showed that fibrinogen β-chain was distributed throughout the valve tissue. On the contrary, plasminogen was strongly stained in CD68-positive macrophages, as evidenced by immunofluorescence. The results suggest that two important blood coagulation-related proteins, plasminogen and fibrinogen, might affect the progression of BV degeneration.

Funder

Ministry of Education, Culture, Sports, Science and Technology

Cardiovascular Research Foundation

Takeda Science Foundation

MSD Life Science Foundation

Public Interest Incorporated Foundation

SENSHIN Medical Research Foundation

Publisher

The Company of Biologists

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology

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