Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2810339 | Trends in Endocrinology & Metabolism | 2014 | 10 Pages |
•Insulin-like growth factor 1 (IGF-1) has pleotropic actions in the heart.•Deficiency in IGF-1 may drive cardiovascular disease.•IGF-1 activates canonical and noncanonical signaling pathways in the heart.•Local IGF-1 and progenitor cell therapies prevent heart injuries in experimental models.
Insulin-like growth factor 1 (IGF-1) signaling regulates contractility, metabolism, hypertrophy, autophagy, senescence, and apoptosis in the heart. IGF-1 deficiency is associated with an increased risk of cardiovascular disease, whereas cardiac activation of IGF-1 receptor (IGF-1R) protects from the detrimental effects of a high-fat diet and myocardial infarction. IGF-1R activates multiple pathways through its intrinsic tyrosine kinase activity and through coupling to heterotrimeric G protein. These pathways involve classic second messengers, phosphorylation cascades, lipid signaling, Ca2+ transients, and gene expression. In addition, IGF-1R triggers signaling in different subcellular locations including the plasma membrane, perinuclear T tubules, and also in internalized vesicles. In this review, we provide a fresh and updated view of the complex IGF-1 scenario in the heart, including a critical focus on therapeutic strategies.