Cyclophilin A in Arrhythmogenic Cardiomyopathy Cardiac Remodeling.
Adipogenesis
/ physiology
Adipose Tissue
/ pathology
Arrhythmias, Cardiac
/ metabolism
Cardiomyopathies
/ metabolism
Cell Differentiation
Cyclophilin A
/ genetics
Death, Sudden, Cardiac
/ pathology
Fibrosis
Gene Expression
Heart Ventricles
/ metabolism
Humans
Inflammation
Mesenchymal Stem Cells
/ pathology
Myocardium
Ventricular Remodeling
adipogenesis
arrhythmogenic cardiomyopathy
cardiac mesenchymal stromal cells
cyclophilin A
fibrosis
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
15 May 2019
15 May 2019
Historique:
received:
15
04
2019
revised:
07
05
2019
accepted:
12
05
2019
entrez:
18
5
2019
pubmed:
18
5
2019
medline:
30
10
2019
Statut:
epublish
Résumé
Arrhythmogenic cardiomyopathy (ACM) is a genetic disorder characterized by the progressive substitution of functional myocardium with noncontractile fibro-fatty tissue contributing to ventricular arrhythmias and sudden cardiac death. Cyclophilin A (CyPA) is a ubiquitous protein involved in several pathological mechanisms, which also characterize ACM (i.e., fibrosis, inflammation, and adipogenesis). Nevertheless, the involvement of CyPA in ACM cardiac remodeling has not been investigated yet. Thus, we first evaluated CyPA expression levels in the right ventricle (RV) tissue specimens obtained from ACM patients and healthy controls (HC) by immunohistochemistry. Then, we took advantage of ACM- and HC-derived cardiac mesenchymal stromal cells (C-MSC) to assess CyPA modulation during adipogenic differentiation. Interestingly, CyPA was more expressed in the RV sections obtained from ACM vs. HC subjects and positively correlated with the adipose replacement extent. Moreover, CyPA was upregulated at early stages of C-MSC adipogenic differentiation and was secreted at higher level over time in ACM- derived C-MSC. Our study provides novel ex vivo and in vitro information on CyPA expression in ACM remodeling paving the way for future C-MSC-based mechanistic and therapeutic investigations.
Identifiants
pubmed: 31096574
pii: ijms20102403
doi: 10.3390/ijms20102403
pmc: PMC6566687
pii:
doi:
Substances chimiques
Cyclophilin A
EC 5.2.1.-
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Ministero della Salute
ID : RC 2016-2017
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