Cardiomyocyte-specific deletion of TGFB3 exacerbated cardiac dysfunction and fibrosis following pressure overload by enhancing SMAD3 phosphorylation and fibroblast activation.
Human heart failure myocardial specimens and plasma (n=35) (HF group: age ≥18 years, NT-proBNP ≥300 pg/mL, EF <50%; Control group: NT-proBNP <100 pg/mL, EF ≥60%), wild-type mice, and cardiomyocyte-specific TGFB3 knockout mice (Myh6-Cre;TGFB3flox/flox and Myh6-CreER;TGFB3flox/flox) subjected to transverse aortic constriction (TAC) or sham surgery, and primary murine cardiomyocytes and fibroblasts.
Cardiomyocyte-specific deletion of TGFB3 via Cre-lox system, with pressure overload induced by transverse aortic constriction (TAC) for 8 weeks.
Littermate controls (wild-type TGFB3) and sham-operated mice.
Cardiac dysfunction (ejection fraction, fractional shortening) and myocardial fibrosis (interstitial collagen deposition, profibrotic gene expression) at 8 weeks post-TAC.surrogate
Cardiomyocyte-derived TGFB3 acts as an endogenous protective factor against pathological cardiac fibrosis in heart failure by competitively inhibiting TGFB1-mediated Smad3 activation.
Heart failure, the common end-stage of cardiovascular diseases, features cardiac fibrosis. Transforming growth factor-β3 (TGFB3), a key TGFB/SMAD ligand, is upregulated in cardiac disorders, but its cellular source and precise role are debated. This study examined TGFB3 in human and mouse heart failure tissues. Histological and molecular analyses showed its increase mainly from cardiomyocytes, induced by angiotensin II. Circulating TGFB3 in patients positively correlated with plasma proBNP, a heart failure severity marker. A cardiomyocyte-specific TGFB3 knockout mouse model showed its absence worsens cardiac dysfunction and fibrosis under pressure overload. Mechanically, TGFB3 competes with TGFB1 for receptors, reducing Smad3 phosphorylation and profibrotic gene activation. Loss of TGFB3 in cardiomyocytes increased expression of profibrotic mediators such as CTGF and SERPINE1, ultimately accelerating fibrotic remodeling during HF progression. These findings identify cardiomyocyte-derived TGFB3 as a crucial endogenous modulator that protects against pathological cardiac fibrosis and highlight its therapeutic potential in HF.
Building similarity graph...
Analyzing shared references across papers
Loading...
Jizhong Xuan
Henan Provincial People's Hospital
Jiayu Zhou
Shanghai Jiao Tong University
Yuanji Huang
Shanghai Jiao Tong University
Scientific Reports
Shanghai Jiao Tong University
Shanghai Chest Hospital
Henan Provincial People's Hospital
Building similarity graph...
Analyzing shared references across papers
Loading...
Xuan et al. (Mon,) conducted a other in Heart failure (n=35). Cardiomyocyte-specific TGFB3 knockout vs. Wild-type/sham controls was evaluated on Cardiac function (ejection fraction, fractional shortening) and cardiac fibrosis. Cardiomyocyte-specific deletion of TGFB3 exacerbated cardiac dysfunction and fibrosis following pressure overload by enhancing SMAD3 phosphorylation and fibroblast activation.
synapsesocial.com/papers/69a91cbed6127c7a504bfbab — DOI: https://doi.org/10.1038/s41598-026-42367-5