Title

Reduced activin receptor-like kinase 1 activity promotes cardiac fibrosis in heart failure

Document Type

Article

Abstract

© 2017 Elsevier Inc. Introduction Activin receptor-like kinase 1 (ALK1) mediates signaling via the transforming growth factor beta-1 (TGFβ1), a pro-fibrogenic cytokine. No studies have defined a role for ALK1 in heart failure. Hypothesis We tested the hypothesis that reduced ALK1 expression promotes maladaptive cardiac remodeling in heart failure. Methods and results In patients with advanced heart failure referred for left ventricular (LV) assist device implantation, LV Alk1 mRNA and protein levels were lower than control LV obtained from patients without heart failure. To investigate the role of ALK1 in heart failure, Alk1 haploinsufficient (Alk1+/−) and wild-type (WT) mice were studied 2 weeks after severe transverse aortic constriction (TAC). LV and lung weights were higher in Alk1+/− mice after TAC. Cardiomyocyte area and LV mRNA levels of brain natriuretic peptide and β-myosin heavy chain were increased similarly in Alk1+/− and WT mice after TAC. Alk-1 mice exhibited reduced Smad 1 phosphorylation and signaling compared to WT mice after TAC. Compared to WT, LV fibrosis and Type 1 collagen mRNA and protein levels were higher in Alk1+/− mice. LV fractional shortening was lower in Alk1+/− mice after TAC. Conclusions Reduced expression of ALK1 promotes cardiac fibrosis and impaired LV function in a murine model of heart failure. Further studies examining the role of ALK1 and ALK1 inhibitors on cardiac remodeling are required.

Publication Date

11-1-2017

Publication Title

Cardiovascular Pathology

ISSN

10548807

E-ISSN

18791336

Volume

31

First Page

26

Last Page

33

PubMed ID

28820968

Digital Object Identifier (DOI)

10.1016/j.carpath.2017.07.004

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