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Letter
Nature 443, 448-452 (28 September 2006) | doi:10.1038/nature05091; Received 10 April 2006; Accepted 25 July 2006; Published online 6 September 2006
Increasing p16INK4a expression decreases forebrain progenitors and neurogenesis during ageing
Anna V. Molofsky1,4, Shalom G. Slutsky1,4, Nancy M. Joseph1, Shenghui He1, Ricardo Pardal1,3, Janakiraman Krishnamurthy2, Norman E. Sharpless2 & Sean J. Morrison1
- Howard Hughes Medical Institute, Department of Internal Medicine, and Center for Stem Cell Biology, University of Michigan, Ann Arbor, Michigan 48109-2216, USA
- Departments of Medicine and Genetics, The Lineberger Comprehensive Cancer Center, The University of North Carolina School of Medicine, Chapel Hill, North Carolina 27599-7295, USA
- †Present address: Laboratorio de Investigaciones Biomedicas, Hospital Universitario Virgen del Rocio, Universidad de Sevilla, E-41013 Seville, Spain
- *These authors contributed equally to this work
Correspondence to: Sean J. Morrison1 Correspondence and requests for materials should be addressed to S.J.M. (Email: seanjm@umich.edu).
Abstract
Mammalian ageing is associated with reduced regenerative capacity in tissues that contain stem cells1, 2. It has been proposed that this is at least partially caused by the senescence of progenitors with age3, 4; however, it has not yet been tested whether genes associated with senescence functionally contribute to physiological declines in progenitor activity. Here we show that progenitor proliferation in the subventricular zone and neurogenesis in the olfactory bulb, as well as multipotent progenitor frequency and self-renewal potential, all decline with age in the mouse forebrain. These declines in progenitor frequency and function correlate with increased expression of p16INK4a, which encodes a cyclin-dependent kinase inhibitor linked to senescence5. Ageing p16INK4a-deficient mice showed a significantly smaller decline in subventricular zone proliferation, olfactory bulb neurogenesis, and the frequency and self-renewal potential of multipotent progenitors. p16INK4a deficiency did not detectably affect progenitor function in the dentate gyrus or enteric nervous system, indicating regional differences in the response of neural progenitors to increased p16INK4a expression during ageing. Declining subventricular zone progenitor function and olfactory bulb neurogenesis during ageing are thus caused partly by increasing p16INK4a expression.
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