Fine-Tuning Cardiac Insulin-Like Growth Factor 1 Receptor Signaling to Promote Health and Longevity. Issue 25 (26th May 2022)

• Record Type: Journal Article
• Authors: Abdellatif, Mahmoud; Trummer-Herbst, Viktoria; Heberle, Alexander Martin; Humnig, Alina; Pendl, Tobias; Durand, Sylvère; Cerrato, Giulia; Hofer, Sebastian J.; Islam, Moydul; Voglhuber, Julia; Ramos Pittol, José Miguel; Kepp, Oliver; Hoefler, Gerald; Schmidt, Albrecht; Rainer, Peter P.; Scherr, Daniel; von Lewinski, Dirk; Bisping, Egbert; McMullen, Julie R.; Diwan, Abhinav; Eisenberg, Tobias; Madeo, Frank; Thedieck, Kathrin; Kroemer, Guido; Sedej, Simon
• Is Part Of: Circulation. Volume 145:Issue 25(2022)
• Page Start: 1853
• Page End: 1866
• Publication Date: 2022-05-26
• Subjects: aging -- autophagy -- cardiomyopathies -- insulin-like growth factor 1 -- mitochondria -- mouse -- phosphatidylinositol 3-kinases; Blood -- Circulation -- Periodicals; Cardiovascular system -- Periodicals; Cardiology -- Periodicals; Heart -- Diseases -- Periodicals; Blood Circulation; Cardiovascular System; Vascular Diseases; 616.1
• DOI: 10.1161/CIRCULATIONAHA.122.059863
• Languages: English
• ISSNs: 0009-7322

Abstract

Abstract : Background: The insulin-like growth factor 1 (IGF1) pathway is a key regulator of cellular metabolism and aging. Although its inhibition promotes longevity across species, the effect of attenuated IGF1 signaling on cardiac aging remains controversial. Methods: We performed a lifelong study to assess cardiac health and lifespan in 2 cardiomyocyte-specific transgenic mouse models with enhanced versus reduced IGF1 receptor (IGF1R) signaling. Male mice with human IGF1R overexpression or dominant negative phosphoinositide 3-kinase mutation were examined at different life stages by echocardiography, invasive hemodynamics, and treadmill coupled to indirect calorimetry. In vitro assays included cardiac histology, mitochondrial respiration, ATP synthesis, autophagic flux, and targeted metabolome profiling, and immunoblots of key IGF1R downstream targets in mouse and human explanted failing and nonfailing hearts, as well. Results: Young mice with increased IGF1R signaling exhibited superior cardiac function that progressively declined with aging in an accelerated fashion compared with wild-type animals, resulting in heart failure and a reduced lifespan. In contrast, mice with low cardiac IGF1R signaling exhibited inferior cardiac function early in life, but superior cardiac performance during aging, and increased maximum lifespan, as well. Mechanistically, the late-life detrimental effects of IGF1R activation correlated with suppressed autophagic flux and impaired oxidative phosphorylation in the heart. Low IGF1R activity consistently improved myocardial bioenergetics and function of the aging heart in an autophagy-dependent manner. In humans, failing hearts, but not those with compensated hypertrophy, displayed exaggerated IGF1R expression and signaling activity. Conclusions: Our findings indicate that the relationship between IGF1R signaling and cardiac health is not linear, but rather biphasic. Hence, pharmacological inhibitors of the IGF1 pathway, albeit unsuitable for young individuals, might be worth considering in older adults.