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Impaired Insulin/IGF1 Signaling Extends Life Span by Promoting Mitochondrial L-Proline Catabolism to Induce a Transient ROS Signal
Open accessAbstract
Impaired insulin and IGF-1 signaling (iIIS) in C. elegans daf-2 mutants extends life span more than 2-fold. Constitutively, iIIS increases mitochondrial activity and reduces reactive oxygen species (ROS) levels. By contrast, acute impairment of daf-2 in adult C. elegans reduces glucose uptake and transiently increases ROS. Consistent with the concept of mitohormesis, this ROS signal causes an adaptive response by inducing ROS defense enzymes (SOD, catalase), culminating in ultimately reduced ROS levels despite increased mitochondrial activity. Inhibition of this ROS signal by antioxidants reduces iIIS-mediated longevity by up to 60%. Induction of the ROS signal requires AAK-2 (AMPK), while PMK-1 (p38) and SKN-1 (NRF-2) are needed for the retrograde response. IIIS upregulates mitochondrial L-proline catabolism, and impairment of the latter impairs the life span-extending capacity of iIIS while L-proline supplementation extends C. elegans life span. Taken together, iIIS promotes L-proline metabolism to generate a ROS signal for the adaptive induction of endogenous stress defense to extend life span.
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“Impaired insulin/IGF-1 signaling (IIS) extends lifespan by 2-fold in C. elegans daf-2 mutants, by promoting L-proline catabolism and endogenous stress defense response via a transient ROS signal”
From Benefits of Metformin in Attenuating the Hallmarks of Aging (2020) · cites this paper as Zarse et al. 2012
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“In addition, increased ROS levels induced expression of antioxidant enzymes, followed by a decrease in ROS levels20.”
From Mitochondrial and metabolic dysfunction in ageing and age-related diseases (2022) · cites this paper as [20]
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Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
Benjamini, Y., & Hochberg, Y. (1995) · Journal of the Royal Statistical Society Series B: Statistical Methodology · doi:10.1111/j.2517-6161.1995.tb02031.x · Cited by 109,482
Robinson, M. D., McCarthy, D. J., & Smyth, G. K. (2010) · Bioinformatics · doi:10.1093/bioinformatics/btp616 · Cited by 41,364
Ultrafast and memory-efficient alignment of short DNA sequences to the human genome.
Langmead, B., Trapnell, C., Pop, M., & Salzberg, S. L. (2009) · Genome Biology · doi:10.1186/gb-2009-10-3-r25 · Cited by 21,849
Differential expression analysis for sequence count data
Anders, S., & Huber, W. (2010) · Genome Biology · doi:10.1186/gb-2010-11-10-r106 · Cited by 15,581
Health benefits of physical activity: the evidence
Warburton, D. E. R. (2006) · Canadian Medical Association Journal · doi:10.1503/cmaj.051351 · Cited by 8,007
A C. elegans mutant that lives twice as long as wild type
Kenyon, C., Chang, J., Gensch, E., Rudner, A., & Tabtiang, R. (1993) · Nature · doi:10.1038/366461a0 · Cited by 3,387
Signal transduction by reactive oxygen species
Finkel, T. (2011) · Journal of Cell Biology · doi:10.1083/jcb.201102095 · Cited by 2,322
Genes that act downstream of DAF-16 to influence the lifespan of Caenorhabditis elegans
Murphy, C. T., McCarroll, S. A., Bargmann, C. I., Fraser, A., Kamath, R. S., Ahringer, J., Li, H., & Kenyon, C. (2003) · Nature · doi:10.1038/nature01789 · Cited by 2,280
Kimura, K. D., Tissenbaum, H. A., Liu, Y., & Ruvkun, G. (1997) · Science · doi:10.1126/science.277.5328.942 · Cited by 2,250
IGF-1 receptor regulates lifespan and resistance to oxidative stress in mice
Holzenberger, M., Dupont, J., Ducos, B., Leneuve, P., Géloën, A., Even, P. C., Cervera, P., & Le Bouc, Y. (2003) · Nature · doi:10.1038/nature01298 · Cited by 2,109
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Items 101–200 of 430
Zhang, J., Shi, R., Li, H., Xiang, Y., Xiao, L., Hu, M., Ma, F., Ma, C. W., & Huang, Z. (2016) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2016.09.031 · Cited by 112
Mitophagy plays a central role in mitochondrial ageing
Diot, A., Morten, K., & Poulton, J. (2016) · Mammalian Genome · doi:10.1007/s00335-016-9651-x · Cited by 112
Segref, A., Kevei, É., Pokrzywa, W., Schmeißer, K., Mansfeld, J., Livnat‐Levanon, N., Ensenauer, R. E., Glickman, M. H., Ristow, M., & Hoppe, T. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.01.016 · Cited by 106
Self-citationProline Metabolism IncreaseskatGExpression and Oxidative Stress Resistance in Escherichia coli
Zhang, L., Alfano, J. R., & Becker, D. (2014) · Journal of Bacteriology · doi:10.1128/jb.02282-14 · Cited by 105
The paradox of mitochondrial dysfunction and extended longevity
Munkácsy, E., & Rea, S. L. (2014) · Experimental Gerontology · doi:10.1016/j.exger.2014.03.016 · Cited by 103
Regulation of Proline Accumulation and Its Molecular and Physiological Functions in Stress Defence
Forlani, G., Trovato, M., Funck, D., & Signorelli, S. (2019) · Springer eBooks · doi:10.1007/978-3-030-27423-8_3 · Cited by 102
Conserved senescence associated genes and pathways in primary human fibroblasts detected by RNA-seq
Marthandan, S., Baumgart, M., Priebe, S., Groth, M., Schaer, J., Kaether, C., Guthke, R., Cellerino, A., Platzer, M., Diekmann, S., et al. (2016) · PLOS ONE · doi:10.1371/journal.pone.0154531 · Cited by 91
“Heatmap plot for Spearman correlation of “overall” gene counts between 8 samples of mouse embryonic fibroblasts (MEF) from the study by [61].”
MethodResultSelf-citationTheurey, P., & Pizzo, P. (2018) · Genes · doi:10.3390/genes9010022 · Cited by 108
Quinlan, C. L., Perevoschikova, I. V., Goncalves, R. L. S., Hey‐Mogensen, M., & Brand, M. D. (2013) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/b978-0-12-405883-5.00012-0 · Cited by 101
Malate and Fumarate Extend Lifespan in Caenorhabditis elegans
Edwards, C., Copes, N., Brito, A. G., Canfield, J., & Bradshaw, P. C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0058345 · Cited by 103
Natural genetic variation drives microbiome selection in the Caenorhabditis elegans gut
Zhang, F., Weckhorst, J. L., Assié, A., Hosea, C. N., Ayoub, C. A., Khodakova, A. S., Cabrera, M. L., Vidal, D., Félix, M., & Samuel, B. S. (2021) · Current Biology · doi:10.1016/j.cub.2021.04.046 · Cited by 92
Redmann, M., Darley-Usmar, V. M., & Zhang, J. (2016) · Aging and Disease · doi:10.14336/ad.2015.0820 · Cited by 93
Comes, S., Gagliardi, M., Laprano, N., Fico, A., Cimmino, A., Palamidessi, A., Cesare, D. D., Falco, S. D., Angelini, C., Scita, G., et al. (2013) · Stem Cell Reports · doi:10.1016/j.stemcr.2013.09.001 · Cited by 90
Proline mediates metabolic communication between retinal pigment epithelial cells and the retina
Yam, M., Engel, A. L., Wang, Y., Zhu, S., Hauer, A., Zhang, R., Lohner, D., Huang, J., Dinterman, M., Zhao, C., et al. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.007983 · Cited by 89
Targeting metabolic pathways for extension of lifespan and healthspan across multiple species
Parkhitko, A. A., Filine, E., Mohr, S. E., Moskalev, A., & Perrimon, N. (2020) · Ageing Research Reviews · doi:10.1016/j.arr.2020.101188 · Cited by 91
Proline dehydrogenase (oxidase) in cancer
Liu, W., & Phang, J. M. (2012) · BioFactors · doi:10.1002/biof.1036 · Cited by 88
Structure, function, and mechanism of proline utilization A (PutA)
Liu, L.-K., Becker, D., & Tanner, J. J. (2017) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2017.07.005 · Cited by 87
Reprogramming of energy metabolism as a driver of aging
Feng, Z., Hanson, R. W., Berger, N. A., & Trubitsyn, A. G. (2016) · Oncotarget · doi:10.18632/oncotarget.7645 · Cited by 84
A Metabolomics-driven Elucidation of the Anti-obesity Mechanisms of Xanthohumol
Kirkwood, J. S., Legette, L. L., Miranda, C. L., Jiang, Y., & Stevens, J. F. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.445452 · Cited by 85
Hekimi, S., Wang, Y., & Noë, A. (2016) · Frontiers in Genetics · doi:10.3389/fgene.2016.00161 · Cited by 83
Zhao, Y., Jia, M., Chen, W., & Liu, Z. (2022) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2022.02.021 · Cited by 89
Ewald, C. Y., Hourihan, J. M., Bland, M. S., Obieglo, C., Katic, I., Mazzeo, L. E. M., Alcedo, J., Blackwell, T. K., & Hynes, N. E. (2017) · eLife · doi:10.7554/elife.19493 · Cited by 88
Shanmugam, G., Mohankumar, A., Duraisamy, K., Thiruppathi, G., Nivitha, S., & Sundararaj, P. (2018) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2018.03.128 · Cited by 84
Targeting Oxidative Stress with Polyphenols to Fight Liver Diseases
Machado, I. F., Miranda, R. G., Dorta, D. J., Rolo, A. P., & Palmeira, C. M. (2023) · Antioxidants · doi:10.3390/antiox12061212 · Cited by 89
Impairing L-Threonine Catabolism Promotes Healthspan through Methylglyoxal-Mediated Proteohormesis
Ravichandran, M., Priebe, S., Grigolon, G., Rozanov, L. F., Groth, M., Laube, B., Guthke, R., Platzer, M., Zarse, K., & Ristow, M. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.02.004 · Cited by 79
Self-citationDenzel, M. S., Lapierre, L. R., & Mack, H. I. D. (2018) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2018.08.001 · Cited by 82
Co-regulation of mitochondrial respiration by proline dehydrogenase/oxidase and succinate
Hancock, C. N., Liu, W., Alvord, W. G., & Phang, J. M. (2015) · Amino Acids · doi:10.1007/s00726-015-2134-7 · Cited by 80
TOR Signaling Couples Oxygen Sensing to Lifespan in C. elegans
Schieber, M., & Chandel, N. S. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.08.075 · Cited by 80
Metformin: A Potential Candidate for Targeting Aging Mechanisms
Hu, D., Xie, F., Xiao, Y., Chen, L., Zhong, J., Huang, D., Chen, J., Wei, J., Jiang, Y., & Zhong, T. (2021) · Aging and Disease · doi:10.14336/ad.2020.0702 · Cited by 84
Tian, J., Geiss, C., Zarse, K., Madreiter‐Sokolowski, C. T., & Ristow, M. (2021) · Aging · doi:10.18632/aging.203597 · Cited by 81
Self-citationBrown, J. D., Day, A. M., Taylor, S. R., Tomalin, L. E., Morgan, B. A., & Veal, E. A. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.10.036 · Cited by 77
Reactive oxygen species, ageing and the hormesis police
Ludovico, P., & Burhans, W. C. (2013) · FEMS Yeast Research · doi:10.1111/1567-1364.12070 · Cited by 80
Akhoon, B. A., Pandey, S., Tiwari, S., & Pandey, R. (2016) · Experimental Gerontology · doi:10.1016/j.exger.2016.03.004 · Cited by 78
Gao, A. W., Chatzispyrou, I. A., Kamble, R., Liu, Y. J., Herzog, K., Smith, R. L., van Lenthe, H., Vervaart, M. A. T., van Cruchten, A., Luyf, A. C., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-02539-w · Cited by 77
Singh, H., Arentson, B. W., Becker, D., & Tanner, J. J. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1321621111 · Cited by 76
Hexokinase is a key regulator of energy metabolism and ROS activity in insect lifespan extension
Lin, X.-W., & Xu, W. (2016) · Aging · doi:10.18632/aging.100885 · Cited by 75
Mitochondria: multifaceted regulators of aging
Son, J. M., & Lee, C. D. (2019) · BMB Reports · doi:10.5483/bmbrep.2019.52.1.300 · Cited by 76
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Teoh, S. T., & Lunt, S. Y. (2017) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.1406 · Cited by 77
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Detienne, G., Haes, W. D., Mergan, L., Edwards, S. L., Temmerman, L., & Bael, S. V. (2018) · Ageing Research Reviews · doi:10.1016/j.arr.2018.03.005 · Cited by 77
Scialò, F., Mallikarjun, V., Stefanatos, R. K. A., & Sanz, A. (2012) · Antioxidants and Redox Signaling · doi:10.1089/ars.2012.4900 · Cited by 70
Wodrich, A. P. K., Scott, A. W., Shukla, A. K., Harris, B. T., & Giniger, E. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.831116 · Cited by 73
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Phang, J. M., Liu, W., & Hancock, C. N. (2013) · Epigenetics · doi:10.4161/epi.24042 · Cited by 71
Iron promotes protein insolubility and aging in C. elegans
Klang, I. M., Schilling, B., Sorensen, D. J., Sahu, A. K., Kapahi, P., Andersen, J. K., Swoboda, P., Killilea, D. W., Gibson, B. W., & Lithgow, G. J. (2014) · Aging · doi:10.18632/aging.100689 · Cited by 69
Insulin/IGF-1 Signaling Regulates Proteasome Activity through the Deubiquitinating Enzyme UBH-4
Matilainen, O., Arpalahti, L., Rantanen, V., Hautaniemi, S., & Holmberg, C. I. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.05.012 · Cited by 70
Context of action of Proline Dehydrogenase (ProDH) in the Hypersensitive Response of Arabidopsis
Monteoliva, M. I., Rizzi, Y. S., Cecchini, N. M., Hajirezaei, M., & Álvarez, M. E. (2014) · BMC Plant Biology · doi:10.1186/1471-2229-14-21 · Cited by 69
Lettieri‐Barbato, D., Aquilano, K., Baldelli, S., Cannata, S. M., Bernardini, S., Rotilio, G., & Ciriolo, M. R. (2013) · Cell Death and Differentiation · doi:10.1038/cdd.2013.137 · Cited by 70
Mitochondrial maintenance failure in aging and role of sexual dimorphism
Tower, J. (2014) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2014.10.008 · Cited by 68
Campos, J. C., Wu, Z., Rudich, P. D., Soo, S. K., Mistry, M., Ferreira, J. C. B., Blackwell, T. K., & Raamsdonk, J. M. V. (2021) · EMBO Reports · doi:10.15252/embr.202152964 · Cited by 69
Bennett, C. F., Kwon, J. J., Chen, C., Russell, J., Acosta, K., Burnaevskiy, N., Crane, M. M., Bitto, A., Wende, H. V., Simko, M., et al. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1006695 · Cited by 66
Oláhová, M., & Veal, E. A. (2015) · Aging Cell · doi:10.1111/acel.12321 · Cited by 66
Promotion of behavior and neuronal function by reactive oxygen species in C. elegans
Li, G., Gong, J., Lei, H., Liu, J., & Xu, X. Z. S. (2016) · Nature Communications · doi:10.1038/ncomms13234 · Cited by 67
Bennett, C. F., & Kaeberlein, M. R. (2014) · Experimental Gerontology · doi:10.1016/j.exger.2014.02.002 · Cited by 61
Proline Catabolism Modulates Innate Immunity in Caenorhabditis elegans
Tang, H., & Pang, S. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.11.038 · Cited by 61
Ren, J., Yuan, L., Wang, W., Zhang, M., Wang, Q., Li, S., Zhang, L., & Hu, K. (2019) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2019.114617 · Cited by 63
Ginsenoside extract from ginseng extends lifespan and health span in Caenorhabditis elegans
Wang, H., Zhang, S., Zhai, L., Sun, L., Zhao, D., Wang, Z., & Li, X. (2021) · Food & Function · doi:10.1039/d1fo00576f · Cited by 66
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Riemer, J., Schwarzländer, M., Conrad, M., & Herrmann, J. M. (2015) · Biological Chemistry · doi:10.1515/hsz-2014-0293 · Cited by 58
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Penkov, S., Raghuraman, B. K., Erkut, C., Oertel, J., Galli, R., Ackerman, E. J. M., Vorkel, D., Verbavatz, J., Koch, E., Fahmy, K., et al. (2020) · BMC Biology · doi:10.1186/s12915-020-0760-3 · Cited by 60
The interplay between mitochondria and autophagy and its role in the aging process
Schiavi, A., & Ventura, N. (2014) · Experimental Gerontology · doi:10.1016/j.exger.2014.02.015 · Cited by 61
Proline dehydrogenase promotes senescence through the generation of reactive oxygen species
Nagano, T., Nakashima, A., Onishi, K., Kawai, K., Awai, Y., Kinugasa, M., Iwasaki, T., Kikkawa, U., & Kamada, S. (2017) · Journal of Cell Science · doi:10.1242/jcs.196469 · Cited by 58
Boucher, J., Charalambous, M., Zarse, K., Mori, M. A., Kleinridders, A., Ristow, M., Ferguson‐Smith, A. C., & Kahn, C. R. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1415475111 · Cited by 58
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Lettieri‐Barbato, D., & Aquilano, K. (2018) · Frontiers in Oncology · doi:10.3389/fonc.2018.00148 · Cited by 58
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Wei, Y., Zhang, Y., Cai, Y., & Xu, M. (2015) · Biological Reviews · doi:10.1111/brv.12103 · Cited by 56
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Choudhury, D., Rong, N., Kumar, H. V. S., Swedick, S., Samuel, R. Z., Mehrotra, P., Toftegaard, J., Rajabian, N., Thiyagarajan, R., Podder, A. K., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.113738 · Cited by 58
Takagi, H. (2021) · Bioscience Biotechnology and Biochemistry · doi:10.1093/bbb/zbab022 · Cited by 55
Lionaki, E., Gkikas, I., Daskalaki, I., Ioannidi, M.-K., Klapa, M. I., & Tavernarakis, N. (2022) · Nature Communications · doi:10.1038/s41467-022-28272-1 · Cited by 56
The biochemistry and cell biology of aging: metabolic regulation through mitochondrial signaling
Long, Y. C., Tan, T. M. C., Inoue, T., & Tang, B. L. (2014) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00665.2013 · Cited by 57
Pro- and antitumor effects of mitochondrial reactive oxygen species
Payen, V. L., Zampieri, L. X., Porporato, P. E., & Sonveaux, P. (2019) · Cancer and Metastasis Reviews · doi:10.1007/s10555-019-09789-2 · Cited by 56
Oh, G. G. K., O’Leary, B. M., Signorelli, S., & Millar, A. H. (2021) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiab578 · Cited by 53
Wan, Q.-L., Fu, X., Meng, X., Luo, Z., Dai, W., Yang, J., Wang, C., Wang, H., & Zhou, Q. (2019) · Food & Function · doi:10.1039/c9fo02000d · Cited by 54
Soo, S. K., Rudich, Z. D., Ko, B., Moldakozhayev, A., AlOkda, A., & Raamsdonk, J. M. V. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.101941 · Cited by 58
Structural Biology of Proline Catabolic Enzymes
Tanner, J. J. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7374 · Cited by 51
Sengupta, S., Yang, G., O’Donnell, J. C., Hinson, M. D., McCormack, S. E., Falk, M. J., La, P., Robinson, M. B., Williams, M., Yohannes, M. T., et al. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.02.004 · Cited by 50
SenGupta, T., Palikaras, K., Esbensen, Y., Konstantinidis, G., Naranjo-Galindo, F. J., Achanta, K., Kassahun, H., Stavgiannoudaki, I., Bohr, V. A., Akbari, M., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109668 · Cited by 55
Effector and regulator: Diverse functions of C. elegans C-type lectin-like domain proteins
Pees, B., Yang, W., Kloock, A., Petersen, C., Peters, L., Li, F., Friedrichsen, M., Butze, S., Zárate-Potes, A., Schulenburg, H., et al. (2021) · PLoS Pathogens · doi:10.1371/journal.ppat.1009454 · Cited by 48
FGT-1 is the major glucose transporter in C. elegans and is central to aging pathways
Feng, Y., Williams, B. G., Koumanov, F., Wolstenholme, A. J., & Holman, G. D. (2013) · Biochemical Journal · doi:10.1042/bj20131101 · Cited by 46
Liang, X., Dickman, M. B., & Becker, D. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.562827 · Cited by 46
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Natarajan, S. K., Muthukrishnan, E., Khalimonchuk, O., Mott, J. L., & Becker, D. (2016) · Journal of Cellular Biochemistry · doi:10.1002/jcb.25825 · Cited by 47
A proteomic atlas of insulin signalling reveals tissue‐specific mechanisms of longevity assurance
Tain, L. S., Sehlke, R., Jain, C., Chokkalingam, M., Nagaraj, N., Essers, P., Rassner, M., Grönke, S., Froelich, J., Dieterich, C., et al. (2017) · Molecular Systems Biology · doi:10.15252/msb.20177663 · Cited by 44
Chamoli, M., Goyala, A., Tabrez, S. S., Siddiqui, A. A., Singh, A., Antebi, A., Lithgow, G. J., Watts, J. L., & Mukhopadhyay, A. (2020) · Nature Communications · doi:10.1038/s41467-020-18690-4 · Cited by 47
Haynes, C. M., & Hekimi, S. (2022) · Genetics · doi:10.1093/genetics/iyac160 · Cited by 45
Resilience to diabetic retinopathy
Serikbaeva, A., Li, Y., Ma, S., Yi, D., & Kazlauskas, A. (2024) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2024.101271 · Cited by 50
Sasakura, H., Moribe, H., Nakano, M., Ikemoto, K., Takeuchi, K., & Mori, I. (2017) · Journal of Cell Science · doi:10.1242/jcs.202119 · Cited by 46
Emerging roles of mitochondrial functions and epigenetic changes in the modulation of stem cell fate
Zhang, C., Meng, Y., & Han, J. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-023-05070-6 · Cited by 51
Mitochondrial form, function and signalling in aging
Amigo, I., da Cunha, F. M., Forni, M. F., Garcia-Neto, W., Kakimoto, P. A., Luévano‐Martínez, L. A., Macedo, F. P., Menezes‐Filho, S. L., Peloggia, J., & Kowaltowski, A. J. (2016) · Biochemical Journal · doi:10.1042/bcj20160451 · Cited by 42
Wang, Z., Li, S., Ren, R., Li, J., & Cui, X. (2015) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.5b02644 · Cited by 42
Labuschagne, C. F., Stigter, E. C. A., Hendriks, M. M. W. B., Berger, R., Rokach, J., Korswagen, H. C., & Brenkman, A. B. (2012) · Aging Cell · doi:10.1111/acel.12043 · Cited by 43
The Energy Maintenance Theory of Aging: Maintaining Energy Metabolism to Allow Longevity
Chaudhari, S. N., & Kipreos, E. T. (2018) · BioEssays · doi:10.1002/bies.201800005 · Cited by 42
Kim, J. Y., Le, T. A. N., Lee, S. Y., Song, D., Hong, S.-C., Hyun, K., Lee, J. W., Pan, C., & Kang, K. (2019) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.9b03039 · Cited by 42
Cai, H. “., Han, B., Hu, Y., Zhao, X., He, Z., Chen, X., Sun, H., Yuan, J., Li, Y., Yang, X., et al. (2020) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2020.4453 · Cited by 43
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Metadata
- Authors
- Zarse, K., Schmeisser, S., Groth, M., Priebe, S., Beuster, G., Kuhlow, D., Guthke, R., Platzer, M., Kahn, C. R., & Ristow, M.
- Affiliations
- Joslin Diabetes Center (US)
- Leibniz Institute on Aging - Fritz Lipmann Institute (FLI) (DE)
- Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e. V. - Hans-Knöll-Institut (HKI) (DE)
- Friedrich Schiller University Jena (DE)
- German Institute of Human Nutrition (DE)
- Corresponding author
- Ristow, Michael
- Venue
- Cell Metabolism
- Publisher
- Elsevier BV
- Published
- 2012-04
- Volume
- 15
- Issue
- 4
- Pages
- 451-465
- ISSN
- 1550-4131 (ISSN-L)
- PMC
- PMC4844853
- OpenAlex
- W2027977649
- Cited by
- 430
- References
- 73
- Citations by year
- 2026: 13 · 2025: 20 · 2024: 28 · 2023: 17 · 2022: 28 · 2021: 36 · 2020: 26 · 2019: 31 · 2018: 27 · 2017: 31 · 2016: 40 · 2015: 41 · 2014: 50 · 2013: 28 · 2012: 12
- FWCI
- 13.58
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 472 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Cell Metabolism (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Center for Research Resources
- University of Minnesota
- Deutsche Forschungsgemeinschaft (RI 1976/3-1)
- Bundesministerium für Bildung und Forschung (0315581, DK31036, DK33201)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- insulin/IGF-1 signaling, lifespan extension, reactive oxygen species, mitohormesis, daf-2, AMPK, p38 MAPK, SKN-1, antioxidant defense, antioxidants, glucose uptake, Caenorhabditis elegans, longevity
- MeSH terms
- Animals, Antioxidants, Glucose, Insulin, Insulin-Like Growth Factor I, Longevity, Mitochondria, Proline, Stress, Physiological, Signal Transduction, Caenorhabditis elegans, Reactive Oxygen Species, Gene Expression Profiling, Models, Animal, Caenorhabditis elegans Proteins, Mice, Transcriptome
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