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Inhibition of Myocardin-related Transcription Factor A Ameliorates Pathological Remodeling of the Pressure-loaded Right Ventricle

delete2025-02-01
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PRE
AI
M
Mark F Rzepka *
S
Sonja Raschzok
X
Xavier Lee
K
Kana Yazaki
J
John D. Dauz
M
Mei Sun
T
Théo A Meister
G
Golam Kabir
J
Jean‐François Desjardins
W
Wolfgang M. Kuebler
A
András Kapùs
K
Kim A. Connelly
M
Mark K. Friedberg
DOI:10.1165/rcmb.2023-0465OCdelete
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Abstract

Abstract

En 中文
Right ventricular (RV) fibrosis is associated with RV dysfunction in a variety of RV pressure-loading conditions in which RV mechanical stress is increased, but the underlying mechanisms driving RV fibrosis are incompletely understood. In pulmonary and cardiovascular diseases characterized by elevated mechanical stress and transforming growth factor-(31 signaling, myocardinrelated transcription factor A (MRTF-A) is a mechanosensitive protein critical to driving myofibroblast transition and fibrosis. In this study, we investigated whether MRTF-A inhibition improves RV profibrotic remodeling and function in response to a pulmonary artery banding (PAB) model of RV pressure loading. Rats were assigned into either sham or PAB groups. MRTF-A inhibitor CCG-1423 was administered daily at 0.75 mg/kg in a subset of PAB animals. Echocardiography and pressure-volume hemodynamics were obtained at a terminal experiment 6 weeks later. RV myocardial samples were analyzed for fibrosis, cardiomyocyte hypertrophy, and profibrotic signaling. MRTF-A inhibition slightly reduced systolic dysfunction in PAB rats reflected by increased lateral tricuspid annulus peak systolic velocity, whereas diastolic function parameters were not significantly improved. RV remodeling was attenuated in PAB rats with MRTF-A inhibition, displaying reduced fibrosis. This was accompanied with a reduction in PAB-induced upregulation of Yes-associated protein (YAP) and its paralog transcriptional coactivator with PDZ-binding motif (TAZ). We also confirmed, using a second-generation MRTF-A inhibitor CCG-203971, that MRTF-A is critical in driving RV fibroblast expression of TAZ and markers of myofibroblast transition in response to transforming growth factor-(31 stress and RhoA activation. These studies identify RhoA, MRTF-A, and YAP/TAZ as interconnected regulators of profibrotic signaling in RV pressure loading and as potential targets to improve RV profibrotic remodeling.
Keywords:
right ventricle
fibrosis
myocardin-related transcription factor A
mechanotransduction
transforming growth factor-(31

Journal

American Journal of Respiratory Cell and Molecular Biology cover
American Journal of Respiratory Cell and Molecular Biology
IF:
5.3
Papers:
5.5K
Citations:
1.2W

Organization

S
saint michaels hospital toronto
Scholars:
5.9K
Papers: 5.0K
Citations: 12
U
university of toronto
Scholars:
14.5W
Papers: 11.9W
Citations: 165
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