STAT3 expression is reduced in cardiac pericytes in HFpEF and its loss reduces cellular adhesion and induces pericyte senescence
1 June 2025·,,,,,
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Leah Rebecca Vanicek
Ariane Fischer
Mariano Ruz Jurado
Anita Tamiato
Tara Procida-Kowalski
Jochen Wilhelm
Dennis Hecker
Maximilian Merten
Felicitas Escher
Badder Kattih
Valentina Puntmann
David John
Marcel H. Schulz
Eike Nagel
Stefanie Dimmeler
Guillermo Luxán
Abstract
Heart failure with preserved ejection fraction (HFpEF) accounts for half of heart failure cases and is characterised by reduced pericyte coverage. While the contributions of other cardiac cell types to HFpEF are well-studied, the role of pericytes remains less understood. Using murine single-nucleus RNA-sequencing to study cardiac pericytes in HFpEF, we identified reduced STAT3 expression as a hallmark of HFpEF pericytes. Mechanistic studies in vitro revealed that STAT3 deletion induces cellular senescence and impairs pericyte adhesion, recapitulating HFpEF-like characteristics. These findings suggest that STAT3 is crucial for maintaining pericyte homeostasis and highlight its reduction as a potential driver of pericyte loss, a defining feature of HFpEF.
Type
Publication
FEBS letters

Authors
Dennis Hecker
(he/him)
Postdoc
I am a biologist by training that turned into a bioinformatician for the PhD. Since starting in the SchulzLab, I have been working on analysing a variety of data and their integration with a focus on the epignome, specifically interactions between regulatory regions and genes. I also have a love-hate relationship with chromatin contact data. What keeps me going is the variety of research questions that we work on to know more about human biology and its use in medicine. I am a big fan of Python and coffee.