The essential role of FoxO6 phosphorylation in aging and calorie restriction

• Published in: AGE 2014, Vol.36 (4), p.9679-9679, Article 9679
• Main Authors: Kim, Dae Hyun, Park, Min Hi, Chung, Ki Wung, Kim, Min Jo, Jung, Yu Ri, Bae, Ha Ram, Jang, Eun Ji, Lee, Jun Sik, Im, Dong Soon, Yu, Byung Pal, Chung, Hae Young
• Format: Article
• Language: English
• Subjects: Age; Aging; Aging - metabolism; Analysis; Animals; Biomedical and Life Sciences; Blotting, Western; Caloric Restriction - methods; Calories; Cell Biology; Cell cycle; Cells, Cultured; Diet; Disease Models, Animal; Epigenetics; Forkhead Transcription Factors - metabolism; Geriatrics/Gerontology; Homeostasis; Humans; Immunoprecipitation; Insulin; Investigations; Kidneys; Kinases; Life Sciences; Male; Mammals; Metabolism; Molecular Medicine; Mutation; Oxidative stress; Pharmacy; Phosphorylation; Proteins; Rats; Rats, Inbred F344; Roles; Studies; Transcription factors
• ISSN: 0161-9152; 2509-2715; 1574-4647; 2509-2723
• DOI: 10.1007/s11357-014-9679-3

Changes in the activities of FoxOs caused by phosphorylation, acetylation, or ubiquitination induce expressional changes in the genes involved in the modulation of oxidative stress by modifying histones and chromatins and can substantially alter cellular functions during aging and age-related diseases. However, the precise role that FoxO6, a novel member of the FoxO class of transcription factors, plays in the aging kidney has not been determined. The purpose of this study was to determine the role played by FoxO6 in the maintenance of redox homeostasis in HEK293T cells and aged kidney tissues isolated from ad libitum (AL)-fed and 40 % calorie restriction (CR) rats. The results obtained from AL-fed rats showed that diminished FoxO6 activity during aging was caused by FoxO6 phosphorylation, which disabled its transcriptional activity. In contrast, CR rats were found to have significantly higher FoxO6 activities and maintained redox balance. To determine the molecular mechanism responsible for FoxO6 modification by age-related oxidative stress, we examined H 2 O 2 -treated HEK293T cells in which FoxO6 was inactivated by phosphorylation and found that H 2 O 2 -induced oxidative stress promoted FoxO6 phosphorylation via PI3K/Akt signaling. The results of this study show that the protective role of FoxO6 in the aging process may in part be related to its ability to attenuate oxidative stress by upregulating catalase expression, as shown in CR. This delineation of the role of FoxO6 expands understanding of the pathological and physiological mechanisms of aging.