IGF-1 has sexually dimorphic, pleiotropic, and time-dependent effects on healthspan, pathology, and lifespan

GeroScience - Tập 39 - Trang 129-145 - 2017
Nicole M. Ashpole1, Sreemathi Logan2, Andriy Yabluchanskiy2, Matthew C. Mitschelen2, Han Yan2, Julie A. Farley2, Erik L. Hodges2, Zoltan Ungvari2, Anna Csiszar2, Sixia Chen3, Constantin Georgescu4, Gene B. Hubbard5,6, Yuji Ikeno5,6, William E. Sonntag2
1Department of BioMolecular Sciences, University of Mississippi, Oxford, USA
2Reynolds Oklahoma Center on Aging, Department of Geriatric Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, USA
3Department of Biostatistics and Epidemiology, University of Oklahoma Health Sciences Center, Oklahoma, USA
4Oklahoma Medical Research Foundation, Oklahoma, USA
5The Barshop Institute for Longevity and Aging Studies and Department of Pathology, The University of Texas Health Science Center at San Antonio, San Antonio, USA
6Research Service, Audie L. Murphy VA Hospital, San Antonio, USA

Tóm tắt

Reduced circulating levels of IGF-1 have been proposed as a conserved anti-aging mechanism that contributes to increased lifespan in diverse experimental models. However, IGF-1 has also been shown to be essential for normal development and the maintenance of tissue function late into the lifespan. These disparate findings suggest that IGF-1 may be a pleiotropic modulator of health and aging, as reductions in IGF-1 may be beneficial for one aspect of aging, but detrimental for another. We postulated that the effects of IGF-1 on tissue health and function in advanced age are dependent on the tissue, the sex of the animal, and the age at which IGF-1 is manipulated. In this study, we examined how alterations in IGF-1 levels at multiple stages of development and aging influence overall lifespan, healthspan, and pathology. Specifically, we investigated the effects of perinatal, post-pubertal, and late-adult onset IGF-1 deficiency using genetic and viral approaches in both male and female igf f/f C57Bl/6 mice. Our results support the concept that IGF-1 levels early during lifespan establish the conditions necessary for subsequent healthspan and pathological changes that contribute to aging. Nevertheless, these changes are specific for each sex and tissue. Importantly, late-life IGF-1 deficiency (a time point relevant for human studies) reduces cancer risk but does not increase lifespan. Overall, our results indicate that the levels of IGF-1 during development influence late-life pathology, suggesting that IGF-1 is a developmental driver of healthspan, pathology, and lifespan.

Tài liệu tham khảo

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