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Department of Biological Sciences
Phone: ext 4814
Animal lifespans range widely, from several days to over a century, yet the underlying reasons for these vast differences remain poorly understood. Many cell types are terminally differentiated in adult organisms, and in some instances these individual cells may endure for the entire adult lifespan. The goal of my research program is to gain a better understanding of the molecular mechanisms permitting these long-lived cells to maintain their functional integrity throughout the lifespan. Currently, we are using two types of experimental models to explore this. We use mice harbouring gene mutations that confer increases in maximal lifespan of up to 50% (e.g. the Snell dwarf mouse). We also employ a broadly comparative approach, using naturally short- and long-lived animal species to identify characteristics that have been selected during the evolution of increased lifespans.
We hypothesize that longevity is associated with one or more of the following cellular properties: (1) improved reactive oxygen species (ROS) metabolism. ROS are produced by mitochondria during normal respiration and, though ROS have important biological functions, they can initiate reactions leading to cell death. We study differences in the expression of antioxidant enzymes that neutralize the lethal effects of ROS. (2) improved ability to handle proteotoxic stress. Protein damage due to both endogenous and exogenous stressors interrupts normal cellular functions and activities leading, in the worse case scenario, to cell death. We study differences in proteasome activity, protein repair and heat shock protein expression that are associated with longevity. (3) improved ability to handle genotoxic stress. DNA damage from endogenous and exogenous agents threatens cell viability. The enhancement of longevity may be achievable by maintaining robust DNA protection and repair activities. We study DNA base excision repair activities, in the nucleus and mitochondria of animal cells, and how these relate to lifespan. (4) improved capacity for dead cell replacement. We are interested in the role of tissue resident stem cells (progenitor cells) in longevity, as the ability of these cells to replace lost tissue cells may be critical to achieving longer lifespans.
We are also studying the biological activities of phytoestrogens, such as resveratrol. This molecule, found in red wine and a variety of fruit and vegetables, interacts with cellular signaling pathways and enhances cellular stress resistance. We have identified the mitochondrial superoxide dismutase (MnSOD) as an important target of resveratrol and are now studying the detailed molecular mechanisms by which resveratrol elicits the induction of MnSOD and developing ways to enhance resveratrol delivery in vivo.
The Comparative Cellular and Molecular Biology of Longevity Database
Vertebrate species maximum lifespans vary from several years to over two centuries, and this presents an opportunity to investigate the underlying biological traits that have co-evolved with longevity. We maintain a cell and tissue bank with brain, heart, liver, and kidney samples and skeletal muscle myoblasts from over 20 mammalian, avian and reptilian species. These collections provide a means to investigate the expression levels of various putative longevity traits in the context of longevity.
The Comparative Cellular and Molecular Biology of Longevity (CCMBL) database (http://genomics.brocku.ca/ccmbl/) contains the combined datasets from dozens of studies (including ours) in which cellular and molecular traits have been measured in the context of evolved species longevity. The purpose of the CCMBL database is simply to provide a convenient repository that brings together the accumulating wealth of species longevity data that is available but distributed widely in the scientific literature. We hope that this single-source collection of information will promote an integrative appreciation of the cellular and molecular biology of longevity by providing a broad comparative framework into which new data can be inserted as it becomes available.
To suggest inclusion of a dataset, or request tissue samples for new analyses, please email: email@example.com
Stuart, J.A., Editor, Mitochondrial DNA: Methods and Protocols, 2nd edition. Volume 197 In: Methods in Molecular Biology, Human Press, Totowa, New Jersey. 2009.
Page, M.M. and Stuart, J.A. In vitro measurement of mitochondrial DNA base excision repair enzyme activities. In: Mitochondrial DNA: Methods and Protocols, 2nd edition. Methods in Molecular Biology Series, J.M. Walker, Human Press, Totowa, New Jersey. Published online June 2009.
Stuart, J.A. and Page, M.M. DNA oxidative damage and cancer. Oxidative Stress in Aging: From Model Systems to Human Diseases. Humana Press, May 2008.
Robb, E.L., Maddalena,
Page, M.M. and Stuart, J.A., 2011. Activities of DNA base excision repair enzymes in liver and brain correlate with body mass, but not lifespan. Age. In press.
Kronenberg, G., Gertz, K., Overall, R.W., Harms, C., Klein, J., Page, M.M., Stuart, J.A., Endres, M., 2011. Folate deficiency increases mtDNA and D-1 mtDNA deletion in aged brain of mice lacking uracil-DNA glycosylase. Exptl. Neurol. In press.
Salway, K.D., Gallagher, E.J. and Stuart, J.A., 2011. Longer-lived mammals and birds have higher levels of heat shock proteins. Mech. Age. Devel. In press.
Skandalis, D.A., Stuart, J.A. and Tattersall, G.J., 2011. Responses of Drosophila melanogaster to atypical oxygen atmospheres. J. Insect Physiol. In press.
Robb, E.L. and Stuart, J.A., 2011. Resveratrol interacts with estrogen receptor-β to inhibit cell replicative growth and enhance stress resistance by upregulating mitochondrial superoxide dismutase. Free Radic. Biol. Med. In press.
Stuart, J.A. and Page, M.M., 2010. Plasma [IGF-1] is negatively correlated with body mass in a comparison of 36 mammalian species. Mech. Age. Devel. 131, 591-598.
Salway, K.D. and Stuart, J.A., 2010. Antioxidant enzymes and oxidative damage biomarkers in heart and selected other tissues of estivating and arousing land snails (Achatina fulica). Comp. Biochem. Physiol. 157, 229-36.
Salway, K.D., Page, M. M., Faure, P.A., Burness, G. and Stuart, J.A., 2010. Enhanced protein repair and recycling are not correlated with longevity in 15 vertebrate endotherm species. AGE. Published online Jun 22.
Robb. E.L. and Stuart, J.A., 2010. trans-Resveratrol as a neuroprotectant. Molecules 15, 1196-1212.
Page, M.M., Robb, E.L., Salway, K.D., and Stuart, J.A., 2010. Mitochondrial redox metabolism: aging, longevity and dietary effects. Mech. Ageing and Devel. 131, 242-252.
Page, M.M., Salway, K.D., Ip, Y.K., Chew, S.F., Warren, S.A., Ballantyne, J.S. and Stuart, J.A., 2010. Upregulation of intracellular antioxidant enzymes in brain and heart during estivation in the African lungfish Protopterus dolloi. J. Comp. Physiol. B 180, 361-369.
Page, M.M, Salmon, A.B., Leiser, S.F., Robb, E.L., Brown, M.F., Miller, R.A. and Stuart, J.A. 2009. Mechanisms of stress resistance in Snell dwarf mouse fibroblasts: enhanced antioxidant and DNA base excision repair capacity, but no differences in mitochondrial metabolism. Free Radic. Biol. Med. 46, 1109-1118.
Robb, E.L., Page, M.M. and Stuart, J.A., 2009. Mitochondria, cellular stress resistance, somatic cell depletion and lifespan. Current Aging Science 1, 12-27.
Page, M.M., Peters, C.W., Staples, J.F. and Stuart, J.A., 2009. Intracellular superoxide dismutases are not altered during hibernation in the 13-lined ground squirrel Spermophilus tridecemlineatus. Comp Biochem Physiol A Mol Integr Physiol. 152,115-22.
Robb, E.L., Winkelmolen, L., Visanji, N., Brotchie, J., Stuart, J.A., 2008. Dietary resveratrol administration increases MnSOD expression and activity in mouse brain. Biochem. Biophys. Res. Commun. 372, 254-9.
Robb, E.L., Page, M.M., Wiens, B.E. and Stuart, J.A., 2008. A specific, progressive and profound induction of mitochondrial superoxide dismutase in human cells exposed to trans-resveratrol. Biochem. Biophys. Res. Commun. 367, 406-412.
Brown, M.F. and Stuart, J.A., 2007. Correlation of mitochondrial superoxide dismutase and DNA polymerase β in mammalian dermal fibroblasts with species maximal lifespan. Mech. Age. Dev. 128, 696-705.
Brown, M.F., Gratton, T.P. and Stuart, J.A., 2007. Metabolic Rate does not scale with body mass in cultured mammalian cells. Am. J. Physiol. 292, R2115-2121.
Stuart, J.A. and M.F. Brown, 2006. Mitochondrial DNA maintenance and bioenergetics. Biochim. Biophys. Acta 1757, 79-89.
Stuart, J.A. and M.F. Brown, 2006. Energy, quiescence and the cellular basis of animal life spans. Comp. Biochem. Physiol. A 143, 12-23.
Stuart, J.A., B.M.
Stuart, J.A., S. Mayard, K.
Hashiguchi, K., Stuart, J.A.,
Stuart, J.A., K. Hashiguchi, D.M. WilsonIII, W.C.
Stuart, J.A., B. Karahalil, B.A.