2016, Number 1
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Rev Invest Clin 2016; 68 (1)
Biology of Healthy Aging and Longevity
Carmona JJ, Michan S
Language: English
References: 84
Page: 7-16
PDF size: 151.76 Kb.
ABSTRACT
As human life expectancy is prolonged, age-related diseases are thriving. Aging is a complex multifactorial process of
molecular and cellular decline that affects tissue function over time, rendering organisms frail and susceptible to disease and
death. Over the last decades, a growing body of scientific literature across different biological models, ranging from yeast,
worms, flies, and mice to primates, humans and other long-lived animals, has contributed greatly towards identifying conserved
biological mechanisms that ward off structural and functional deterioration within living systems. Collectively, these data offer
powerful insights into healthy aging and longevity. For example, molecular integrity of the genome, telomere length, epigenetic
landscape stability, and protein homeostasis are all features linked to “youthful” states. These molecular hallmarks underlie
cellular functions associated with aging like mitochondrial fitness, nutrient sensing, efficient intercellular communication, stem
cell renewal, and regenerative capacity in tissues. At present, calorie restriction remains the most robust strategy for extending
health and lifespan in most biological models tested. Thus, pathways that mediate the beneficial effects of calorie restriction
by integrating metabolic signals to aging processes have received major attention, such as insulin/insulin growth factor-1,
sirtuins, mammalian target of rapamycin, and 5’ adenosine monophosphate-activated protein kinase. Consequently, smallmolecule
targets of these pathways have emerged in the impetuous search for calorie restriction mimetics, of which resveratrol,
metformin, and rapamycin are the most extensively studied. A comprehensive understanding of the molecular and cellular
mechanisms that underlie age-related deterioration and repair, and how these pathways interconnect, remains a major challenge
for uncovering interventions to slow human aging while extending molecular and physiological youthfulness, vitality, and health.
This review summarizes key molecular mechanisms underlying the biology of healthy aging and longevity.
REFERENCES
López-Otín C, Blasco MA, Partridge L, Serrano M, Kroemer G. The hallmarks of aging. Cell. 2013;153:1194-217.
Pérez VI, Buffenstein R, Masamsetti V, et al. Protein stability and resistance to oxidative stress are determinants of longevity in the longest-living rodent, the naked mole-rat. Proc Natl Acad Sci U S A. 2009;106:3059-64.
Johnson TE, Cypser J, de Castro E, et al. Gerontogenes mediate health and longevity in nematodes through increasing resistance to environmental toxins and stressors. Exp Gerontol. 2000; 35:687-94.
Miller RA, Buehner G, Chang Y, Harper JM, Sigler R, Smith-Wheelock M. Methionine-deficient diet extends mouse lifespan, slows immune and lens aging, alters glucose, T4, IGF-I and insulin levels, and increases hepatocyte MIF levels and stress resistance. Aging Cell. 2005;4:119-25.
Lin Y, Seroude L, Benzer S. Extended life-span and stress resistance in the Drosophila mutant methuselah. Science. 1998;282: 943-6.
Smith ED, Kaeberlein TL, Lydum BT, et al. Age- and calorie-independent life span extension from dietary restriction by bacterial deprivation in Caenorhabditis elegans. BMC Dev Biol. 2008;8:49.
Finley LWS, Haigis MC. The coordination of nuclear and mitochondrial communication during aging and calorie restriction. Ageing Res Rev. 2009;8:173-88.
Johnson T, Lithgow G. The search for the genetic basis of aging: the identification of gerontogenes in the nematode Caenorhabditis elegans. J Am Geriatr Soc. 1992;40:936-45.
Salminen A, Kaarniranta K. Regulation of the aging process by autophagy. Trends Mol Med. 2009;15:217-24.
Villeda SA, Luo J, Mosher KI, et al. The ageing systemic milieu negatively regulates neurogenesis and cognitive function. Nature. 2011;477:90-4.
Egerman MA, Cadena SM, Gilbert JA, et al. GDF11 increases with age and inhibits skeletal muscle regeneration. Cell Metab. 2015; 22:164-74.
Loffredo FS, Steinhauser ML, Jay SM, et al. Growth differentiation factor 11 is a circulating factor that reverses age-related cardiac hypertrophy. Cell. 2013;153:828-39.
Bouchard J, Villeda SA. Aging and brain rejuvenation as systemic events. J Neurochem. 2015;132:5-19.
Keane M, Semeiks J, Webb AE, et al. Insights into the evolution of longevity from the bowhead whale genome. Cell Rep. 2015; 10:112-22.
Treaster SB, Ridgway ID, Richardson CA, Gaspar MB, Chaudhuri AR, Austad SN. Superior proteome stability in the longest lived animal. Age (Omaha). 2013;36:1009-17.
Wu Z, Song L, Liu SQQ, Huang D. A high throughput screening assay for determination of chronological lifespan of yeast. Exp Gerontol. 2011;11:915-22.
Ford D, Ions LJ, Alatawi F, Wakeling LA. The potential role of epigenetic responses to diet in ageing. Proc Nutr Soc. 2011; 70:374-84.
Fontana L, Partridge L. Promoting health and longevity through diet: from model organisms to humans. Cell. 2015;161:106-18.
McCay C, Crowell M, Maynakd L. The effect of retarded growth upon the length of life span and upon the ultimate body size. J Nutr. 1935;10:63-79.
Weindruch R. Calorie restriction and aging. Sci Am. 1996;274: 46-52.
Mattison JA, Roth GS, Beasley TM, et al. Impact of caloric restriction on health and survival in rhesus monkeys from the NIA study. Nature. 2012;489:318-21.
Colman RJ, Anderson RM, Johnson SC, et al. Caloric restriction delays disease onset and mortality in rhesus monkeys. Science. 2009;325:201-4.
Michan S. Calorie restriction and NAD+/sirtuin counteract the hallmarks of aging. Front Biosci. 2014;19:1300-19.
Valdez G, Tapia JC, Kang H, et al. Attenuation of age-related changes in mouse neuromuscular synapses by caloric restriction and exercise. Proc Natl Acad Sci U S A. 2010;107:14863-8.
Longo VD, Fontana L. Calorie restriction and cancer prevention: metabolic and molecular mechanisms. Trends Pharmacol Sci. 2010;31:89-98.
Cantó C, Auwerx J. Calorie restriction: is AMPK a key sensor and effector? Physiology (Bethesda). 2011;26:214-24.
Brandhorst S, Choi IY, Wei M, et al. A periodic diet that mimics fasting promotes multi-system regeneration, enhanced cognitive performance, and healthspan. Cell Metab. 2015;22: 86-99.
Lane MA, Roth GS, Ingram DK. Caloric restriction mimetics: a novel approach for biogerontology. Methods Mol Biol. 2007; 371:143-9
Venter JC, Adams MD, Myers EW, et al. The sequence of the human genome. Science. 2001;291:1304-51.
Hoeijmakers JH. DNA damage, aging, and cancer. N Engl J Med. 2009;361:1475-85.
Lu T, Pan Y, Kao S-Y, et al. Gene regulation and DNA damage in the ageing human brain. Nature. 2004;429:883-91.
Trifunovic A, Wredenberg A, Falkenberg M, et al. Premature ageing in mice expressing defective mitochondrial DNA polymerase. Nature. 2004;429:417-23.
Lin J, Epel E, Blackburn E. Telomeres and lifestyle factors: roles in cellular aging. Mutat Res. 2012;730:85-9.
Armanios M, Blackburn EH. The telomere syndromes. Nat Rev Genet. 2012;13:693-704.
Vera E, Bernardes de Jesus B, Foronda M, Flores JM, Blasco MA. Telomerase reverse transcriptase synergizes with calorie restriction to increase health span and extend mouse longevity. PLoS One. 2013;8:e53760.
Vukmirovic OG, Tilghman SM. Exploring genome space. Nature. 2000;405:820-2.
Kim EB, Fang X, Fushan AA, et al. Genome sequencing reveals insights into physiology and longevity of the naked mole rat. Nature. 2011;479:223-7.
DeBusk FL. The Hutchinson-Gilford progeria syndrome. J Pediatr. 1972;80:697-724.
Ding S-LL, Shen C-YY. Model of human aging: recent findings on Werner’s and Hutchinson-Gilford progeria syndromes. Clin Interv Aging. 2008;3:431-44.
Guarente L, Kenyon C. Genetic pathways that regulate ageing in model organisms. Nature. 2000;408:255-62.
Tan Q, Christiansen L, von Bornemann Hjelmborg J, Christensen K. Twin methodology in epigenetic studies. J Exp Biol. 2015;218: 134-9.
Carmona JJ, Sofer T, Hutchinson J, et al. Short-term airborne particulate matter exposure alters the epigenetic landscape of human genes associated with the mitogen-activated protein kinase network: a cross-sectional study. Environ Health. 2014; 13:94.
Benayoun BA, Pollina EA, Brunet A. Epigenetic regulation of ageing: linking environmental inputs to genomic stability. Nat Rev Mol Cell Biol. 2015;16:593-610.
Godfrey KM, Costello PM, Lillycrop KA. The developmental environment, epigenetic biomarkers and long-term health. J Dev Orig Health Dis. 2015;6:399-406.
Lu T, Pan Y, Kao S-Y, et al. Gene regulation and DNA damage in the ageing human brain. Nature. 2004;429:883-91.
Peters MJ, Joehanes R, Pilling LC, et al. The transcriptional landscape of age in human peripheral blood. Nat Commun. 2015;6:8570.
Ng JW, Barrett LM, Wong A, Kuh D, Smith GD, Relton CL. The role of longitudinal cohort studies in epigenetic epidemiology: challenges and opportunities. Genome Biol. 2012;13.
Horvath S. DNA methylation age of human tissues and cell types. Genome Biol. 2013;14:R115.
Marioni RE, Shah S, McRae AF, et al. DNA methylation age of blood predicts all-cause mortality in later life. Genome Biol. 2015;16-25.
Taylor RC, Dillin A. Aging as an event of proteostasis collapse. Cold Spring Harb Perspect Biol. 2011;3:a00444
Morimoto RI. The heat shock response: systems biology of proteotoxic stress in aging and disease. Cold Spring Harb Symp Quant Biol. 2011;76:91-9.
Dokladny K, Zuhl MN, Mandell M, et al. Regulatory coordination between two major intracellular homeostatic systems: heat shock response and autophagy. J Biol Chem. 2013;288:14959-72.
Hipp MS, Park S-H, Hartl FU. Proteostasis impairment in proteinmisfolding and -aggregation diseases. Trends Cell Biol. 2014;24: 506-14.
Ori A, Toyama BH, Harris MS, et al. Integrated transcriptome and proteome analyses reveal organ-specific proteome deterioration in old rats. Cell Syst. 2015;1:224-37.
Michan S. Acetylome regulation by sirtuins in the brain: from normal physiology to aging and pathology. Curr Pharm Des. 2013;19:6823-38.
Schwer B, Eckersdorff M, Li Y, et al. Calorie restriction alters mitochondrial protein acetylation. Aging Cell. 2009;8:604-6.
Nowotny K, Jung T, Grune T, Höhn A. Accumulation of modified proteins and aggregate formation in aging. Exp Gerontol. 2014; 57:122-31.
Palacios OM, Carmona JJ, Michan S, et al. Diet and exercise signals regulate SIRT3 and activate AMPK and PGC-1alpha in skeletal muscle. Aging (Albany NY). 2009;1:771-83.
Yang H, Yang T, Baur JA, et al. Nutrient-sensitive mitochondrial NAD+ levels dictate cell survival. Cell. 2007;130:1095-107.
Burkewitz K, Zhang Y, Mair WB. AMPK at the nexus of energetics and aging. Cell Metab. 2014;20:10-25.
Johnson SC, Rabinovitch PS, Kaeberlein M. mTOR is a key modulator of ageing and age-related disease. Nature. 2013;493:338-45.
van Heemst D, Beekman M, Mooijaart SP, et al. Reduced insulin/ IGF-1 signalling and human longevity. Aging Cell. 2005;4:79-85.
Shor B, Gibbons JJ, Abraham RT, Yu K. Targeting mTOR globally in cancer: thinking beyond rapamycin. Cell Cycle. 2009;8:3831-7.
Anisimov VN, Bartke A. The key role of growth hormone-insulin- IGF-1 signaling in aging and cancer. Crit Rev Oncol Hematol. 2013;87:201-23.
Michán S, Sinclair D. Sirtuins in mammals: insights into their biological function. Biochem J. 2007;404:1-13.
Kenyon C, Chang J, Gensch E, Rudner A, Tabtiang R. A C. elegans mutant that lives twice as long as wild type. Nature. 1993; 366:461-4.
Laplante M, Sabatini DM. mTOR signaling in growth control and disease. Cell. 2012;149:274-93.
Harrison DE, Strong R, Sharp ZD, et al. Rapamycin fed late in life extends lifespan in genetically heterogeneous mice. Nature. 2009;460:392-5.
McCormick MA, Tsai SY, Kennedy BK. TOR and ageing: a complex pathway for a complex process. Philos Trans R Soc Lond B Biol Sci. 2011;366:17-27.
Wu JJ, Liu J, Chen EB, et al. Increased mammalian lifespan and a segmental and tissue-specific slowing of aging after genetic reduction of mTOR expression. Cell Rep. 2013;4:913-20.
Canto C, Auwerx J. Calorie Restriction: Is AMPK a key sensor and effector? Physiology. 2011;26:214-24.
Greer EL, Dowlatshahi D, Banko MR, et al. An AMPK-FOXO pathway mediates longevity induced by a novel method of dietary restriction in C. elegans. Curr Biol. 2007;17:1646-56.
Kaeberlein M, McVey M, Guarente L. The SIR2/3/4 complex and SIR2 alone promote longevity in Saccharomyces cerevisiae by two different mechanisms. Genes Dev. 1999;13:2570-80.
Michan S, Li Y, Chou MM, et al. SIRT1 is essential for normal cognitive function and synaptic plasticity. J Neurosci. 2010;30: 9695-707.
Firestein R, Blander G, Michan S, et al. The SIRT1 deacetylase suppresses intestinal tumorigenesis and colon cancer growth. PLoS One. 2008;3:e2020.
North BJ, Rosenberg MA, Jeganathan KB, et al. SIRT2 induces the checkpoint kinase BubR1 to increase lifespan. EMBO J. 2014; 33:1438-53.
Kanfi Y, Naiman S, Amir G, et al. The sirtuin SIRT6 regulates lifespan in male mice. Nature. 2012;483:218-21.
Donmez G, Outeiro TF. SIRT1 and SIRT2: emerging targets in neurodegeneration. EMBO Mol Med. 2013;5:344-52.
Zhang W-GG, Bai X-JJ, Chen X-MM. SIRT1 variants are associated with aging in a healthy Han Chinese population. Clin Chim Acta. 2010;411:1679-83.
Albani D, Ateri E, Mazzuco S, et al. Modulation of human longevity by SIRT3 single nucleotide polymorphisms in the prospective study “Treviso Longeva (TRELONG)”. Age. 2014;36:469-78.
Polito L, Kehoe PG, Davin A, et al. The SIRT2 polymorphism rs10410544 and risk of Alzheimer’s disease in two Caucasian case-control cohorts. Alzheimers Dement. 2013;4:392-9.
Lagouge M, Argmann C, Gerhart-Hines Z, et al. Resveratrol improves mitochondrial function and protects against metabolic disease by activating SIRT1 and PGC-1alpha. Cell. 2006;127: 1109-22.
Hubbard BP, Gomes AP, Dai H, et al. Evidence for a common mechanism of SIRT1 regulation by allosteric activators. Science. 2013;339:1216-9.
Baur JA, Pearson KJ, Price NL, et al. Resveratrol improves health and survival of mice on a high-calorie diet. Nature. 2006;444: 337-42.