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Updated: Sep 4, 2025

Protein Isolation from the Developing Embryonic Mouse Heart Valve Region
Published on: September 23, 2014
Follistatin-like 1 and its paralogs in heart development and cardiovascular disease
Martin Horak1,2, DeLisa Fairweather3, Piia Kokkonen2
1Department of Pathological Physiology, Faculty of Medicine, Masaryk University, Kamenice 5, Brno, 625 00, Czech Republic.
Insights
Follistatin-like 1 (FSTL1) is a heart-released protein associated with cardiovascular diseases (CVDs). Research explores its protective roles and potential as a biomarker for poor outcomes and therapeutic development.
Area of Science:
- Cardiology
- Molecular Biology
- Biochemistry
Background:
- Cardiovascular diseases (CVDs) are a major global cause of death.
- There is a critical need for novel cardiokines to protect the heart.
- Follistatin-like 1 (FSTL1) is a cardiokine expressed in the heart, released into serum after injury, and linked to CVD outcomes.
Purpose of the Study:
- To comprehensively review the literature on FSTL1 and its homologs.
- To understand the role of FSTL1 in normal heart physiology and CVD.
- To evaluate FSTL1's potential as a prognostic biomarker and therapeutic agent.
Main Methods:
- Literature review of FSTL1 research in cardiovascular disease models.
- Analysis of studies on FSTL1's tissue expression and post-translational modifications.
- Synthesis of data on FSTL1's effects, including anti-inflammation, anti-remodeling, anti-fibrosis, angiogenesis, and hypertrophy.
Main Results:
- FSTL1 is implicated in various protective mechanisms in heart disease models.
- Its effects are dependent on tissue source and cell-specific post-translational modifications.
- Extensive animal studies over 15 years highlight FSTL1's predominantly protective role.
Conclusions:
- FSTL1 exhibits significant protective functions in the heart.
- Further understanding of FSTL1 and its homologs is essential.
- FSTL1 holds potential as a biomarker for predicting poor CVD outcomes and as a therapeutic target.
Abstract:
Cardiovascular diseases (CVDs) are a group of disorders affecting the heart and blood vessels and a leading cause of death worldwide. Thus, there is a need to identify new cardiokines that may protect the heart from damage as reported in GBD 2017 Causes of Death Collaborators (2018) (The Lancet 392:1736-1788). Follistatin-like 1 (FSTL1) is a cardiokine that is highly expressed in the heart and released to the serum after cardiac injury where it is associated with CVD and predicts poor outcome. The action of FSTL1 likely depends not only on the tissue source but also post-translation modifications that are target tissue- and cell-specific. Animal studies examining the effect of FSTL1 in various models of heart disease have exploded over the past 15 years and primarily report a protective effect spanning from inhibiting inflammation via transforming growth factor, preventing remodeling and fibrosis to promoting angiogenesis and hypertrophy. A better understanding of FSTL1 and its homologs is needed to determine whether this protein could be a useful novel biomarker to predict poor outcome and death and whether it has therapeutic potential. The aim of this review is to provide a comprehensive description of the literature for this family of proteins in order to better understand their role in normal physiology and CVD.
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