4.7 Article Proceedings Paper

AMP-activated Protein Kinase and FoxO Transcription Factors in Dietary Restriction-induced Longevity

期刊

INTERNATIONAL SYMPOSIUM ON OLFACTION AND TASTE
卷 1170, 期 -, 页码 688-692

出版社

WILEY-BLACKWELL
DOI: 10.1111/j.1749-6632.2009.04019.x

关键词

AMPK; FoxO; dietary restriction; caloric restriction; longevity; aging

资金

  1. NIH/NIA [R01 AG02664-8-01, 1F31AG032837-01]
  2. Institute for Cancer Research
  3. American Association for Aging Research
  4. NIH/NCI [5T32CA09302-28]
  5. NSF
  6. Stanford Graduate Fellowship
  7. NATIONAL CANCER INSTITUTE [T32CA009302] Funding Source: NIH RePORTER
  8. NATIONAL INSTITUTE ON AGING [R01AG031198, F31AG032837, R01AG026648] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Aging is regulated by modifications in single genes and by simple changes in the environment. The signaling pathway connecting insulin to FoxO transcription factors integrates environmental stimuli to regulate lifespan. FoxO transcription factors are directly phosphorylated in response to insulin/growth factor signaling by the protein kinase Akt, thereby causing their sequestration in the cytoplasm. In the absence of insulin/growth factors, FoxO factors translocate to the nucleus where they trigger a range of cellular responses, including resistance to oxidative stress-a phenotype highly coupled with lifespan extension. Our recent results indicate that FoxO transcription factors are also regulated in response to nutrient deprivation by the AMP-activated protein kinase (AMPK) pathway. The energy-sensing AMPK directly phosphorylates FoxO transcription factors at six regulatory sites. AMPK phosphorylation enhances FoxO transcriptional activity, leading to the expression of specific target genes involved in stress resistance and changes in energy metabolism. The AMPK-FoxO pathway plays a crucial role in the ability of a dietary restriction regimen to extend lifespan in Caenorhabditis elegans. Understanding the intricate signaling networks that translate environmental conditions like dietary restriction into changes in gene expression that extend lifespan will be of critical importance to identify ways to delay the onset of aging and age-dependent diseases.

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