SIRT1 transgenic mice show phenotypes resembling calorie restriction

Aging Cell - Tập 6 Số 6 - Trang 759-767 - 2007
Laura Bordone1,2, David S. Cohen2, Ashley Robinson2,3, Maria Carla Motta2, J. Edward Van Veen2, Agnieszka Czopik2, Andrew D. Steele2,4, Hayley Crowe5, Stephen Marmor5, Jianyuan Luo6, Wei Gu6, Leonard Guarente2
1.Present address: Novartis Institutes for BioMedical Research, Diabetes and Metabolism Disease Area, Cambridge, MA 02139, USA
2Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139 USA
3Present address: Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, CA 94143-0448, USA.
4The Whitehead Institute, Cambridge, MA 02142, USA
5Diabetes and Metabolism Disease Area, Novartis Institutes for BioMedical Research, Inc., Cambridge, MA 02139, USA
6Institute of Cancer Genetics and Department of Pathology, College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA

Tóm tắt

Summary

We generated mice that overexpress the sirtuin, SIRT1. Transgenic mice have been generated by knocking in SIRT1 cDNA into the β‐actin locus. Mice that are hemizygous for this transgene express normal levels of β‐actin and higher levels of SIRT1 protein in several tissues. Transgenic mice display some phenotypes similar to mice on a calorie‐restricted diet: they are leaner than littermate controls; are more metabolically active; display reductions in blood cholesterol, adipokines, insulin and fasted glucose; and are more glucose tolerant. Furthermore, transgenic mice perform better on a rotarod challenge and also show a delay in reproduction. Our findings suggest that increased expression of SIRT1 in mice elicits beneficial phenotypes that may be relevant to human health and longevity.

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