Unravelling the proteome of degenerative human mitral valves.
Proteomics
; 15(17): 2934-44, 2015 Sep.
Article
em En
| MEDLINE
| ID: mdl-25914152
ABSTRACT
Degenerative mitral valve disease (DMVD), which includes the syndromes of mitral valve prolapse (MVP) and flail leaflet, is a common valvular condition which can be complicated by mitral regurgitation and adverse cardiovascular outcomes. Although several genetic and other studies of MVP in dog models have provided some information regarding the underlying disease mechanisms, the proteins and molecular events mediating human MVP pathogenesis have not been unraveled. In this study, we report the first large-scale proteome profiling of mitral valve tissue resected from patients with MVP. A total of 1134 proteins were identified, some of which were validated using SWATH-MS and western blotting. GO annotation of these proteins confirmed the validity of this proteome database in various cardiovascular processes. Among the list of proteins, we found several structural and extracellular matrix proteins, such as asporin, biglycan, decorin, lumican, mimecan, prolargin, versican, and vinculin, that have putative roles in the pathophysiology of MVP. These proteins could also be involved in the cardiac remodeling associated with mitral regurgitation. All MS data have been deposited in the ProteomeXchange with identifier PXD000774 (http//proteomecentral.proteomexchange.org/dataset/PXD000774).
Palavras-chave
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Proteoma
/
Bases de Dados de Proteínas
/
Valva Mitral
/
Insuficiência da Valva Mitral
Limite:
Humans
Idioma:
En
Ano de publicação:
2015
Tipo de documento:
Article