Reprogramming Therapy Reverses Signs of Aging in Mouse Progeria Model

Animals with progeria show many signs of aging including DNA damage, organ dysfunction, and dramatically shortened lifespan.

To nullify the cancer threat, the investigators decided to induce partial reprogramming by short-term cyclic expression of the OSKM or Yamanaka reprogramming factors: Oct4 (octamer-binding transcription factor 4), Sox2 (SRY (sex determining region Y)-box 2), Klf4 (Kruppel-like factor 4), and c-Myc.

The investigators reported in the December 15, 2016, online edition of the journal Cell that partial reprogramming by short-term cyclic expression of the OSKM factors ameliorated cellular and physiological hallmarks of aging and prolonged lifespan by about 30% in the mouse progeria model. Similarly, expression of OSKM in vivo improved recovery from metabolic disease and muscle injury in older wild-type mice.

"Our study shows that aging may not have to proceed in one single direction," said senior author Dr. Juan Carlos Izpisua Belmonte, a professor in the gene expression laboratory at the Salk Institute for Biological Studies. "It has plasticity and, with careful modulation, aging might be reversed. Obviously, mice are not humans and we know it will be much more complex to rejuvenate a person. But this study shows that aging is a very dynamic and plastic process, and therefore will be more amenable to therapeutic interventions than what we previously thought."

The investigators warned that due to the complexity of aging in humans, potential anti-aging therapies based on these studies in mice may take up to 10 years to reach clinical trials.

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Salk Institute for Biological Studies