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Metformin Enhances Autophagy and Normalizes Mitochondrial Function to Alleviate Aging-Associated Inflammation
Open accessAbstract
Age is a non-modifiable risk factor for the inflammation that underlies age-associated diseases; thus, anti-inflammaging drugs hold promise for increasing health span. Cytokine profiling and bioinformatic analyses showed that Th17 cytokine production differentiates CD4+ T cells from lean, normoglycemic older and younger subjects, and mimics a diabetes-associated Th17 profile. T cells from older compared to younger subjects also had defects in autophagy and mitochondrial bioenergetics that associate with redox imbalance. Metformin ameliorated the Th17 inflammaging profile by increasing autophagy and improving mitochondrial bioenergetics. By contrast, autophagy-targeting siRNA disrupted redox balance in T cells from young subjects and activated the Th17 profile by activating the Th17 master regulator, STAT3, which in turn bound IL-17A and F promoters. Mitophagy-targeting siRNA failed to activate the Th17 profile. We conclude that metformin improves autophagy and mitochondrial function largely in parallel to ameliorate a newly defined inflammaging profile that echoes inflammation in diabetes.
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“Additionally, metformin, which is widely used to treat T2DM, activates AMPK, improves mitochondrial function, decreases age-associated inflammation and improves hyperglycaemia in people with obesity and prediabetes, as well as in HFD-fed mice238,239.”
From Mitochondrial and metabolic dysfunction in ageing and age-related diseases (2022) · cites this paper as [238]
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Cites
How mitochondria produce reactive oxygen species
Murphy, M. P. (2009) · Biochemical Journal · doi:10.1042/bj20081386 · Cited by 8,207
Mitochondrial Reactive Oxygen Species (ROS) and ROS-Induced ROS Release
Zorov, D. B., Juhaszova, M., & Sollott, S. J. (2014) · Physiological Reviews · doi:10.1152/physrev.00026.2013 · Cited by 5,383
Cillà, S. D., Farruggio, S., Vujosevic, S., Raina, G., Filippini, D. A., Gatti, V., Clemente, N., Mary, D., Vezzola, D., Casini, G., et al. (2017) · Cellular Physiology and Biochemistry · doi:10.1159/000479441 · Cited by 5,154
Methods in Mammalian Autophagy Research
Mizushima, N., Yoshimori, T., & Levine, B. (2010) · Cell · doi:10.1016/j.cell.2010.01.028 · Cited by 4,497
mixOmics: An R package for ‘omics feature selection and multiple data integration
Rohart, F., Gautier, B., Singh, A., & Lê Cao, K.-A. (2017) · PLOS Computational Biology · doi:10.1371/journal.pcbi.1005752 · Cited by 4,056
Autophagy: cellular and molecular mechanisms
Glick, D. R., Barth, S., & Macleod, K. F. (2010) · The Journal of Pathology · doi:10.1002/path.2697 · Cited by 3,995
Chronic Inflammation (Inflammaging) and Its Potential Contribution to Age-Associated Diseases
Franceschi, C., & Campisi, J. (2014) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glu057 · Cited by 3,891
PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1
Geisler, S., Holmström, K. M., Skujat, D., Fiesel, F. C., Rothfuss, O. C., Kahle, P. J., & Springer, W. (2010) · Nature Cell Biology · doi:10.1038/ncb2012 · Cited by 2,835
Cepharanthine potently enhances the sensitivity of anticancer agents in K562 cells
Ikeda, R., Che, X., Yamaguchi, T., Ushiyama, M., Zheng, C., Okumura, H., Takeda, Y., Shibayama, Y., Nakamura, K. T., Jeung, H., et al. (2005) · Cancer Science · doi:10.1111/j.1349-7006.2005.00057.x · Cited by 2,268
The transcription factor Myc controls metabolic reprogramming upon T lymphocyte activation
Wang, R., Dillon, C. P., Shi, L. Z., Milasta, S., Carter, R., Finkelstein, D., McCormick, L. L., Fitzgerald, P., Chi, H., Munger, J., et al. (2011) · Immunity · doi:10.1016/j.immuni.2011.09.021 · Cited by 2,140 · cited 9×
“CD4+ T cells from O compared Y subjects produced less lactate 46 Cell Metabolism 32, 44–55, July 7, 2020 and had lower ECAR (Figures 2A–2D and S2A–S2D).”
InfluentialThévenot, E., Roux, A., Xu, Y., Ezan, É., & Junot, C. (2015) · Journal of Proteome Research · doi:10.1021/acs.jproteome.5b00354 · Cited by 1,802
The mitochondrial basis of aging
Sun, N., Youle, R. J., & Finkel, T. (2016) · Molecular Cell · doi:10.1016/j.molcel.2016.01.028 · Cited by 1,441
LC3, GABARAP and GATE16 localize to autophagosomal membrane depending on form-II formation
Kabeya, Y., Mizushima, N., Yamamoto, A., Oshitani-Okamoto, S., Ohsumi, Y., & Yoshimori, T. (2004) · Journal of Cell Science · doi:10.1242/jcs.01131 · Cited by 1,394
Yoshimori, T., Yamamoto, A., Moriyama, Y., Futai, M., & Tashiro, Y. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)47429-2 · Cited by 1,334
Generation of reactive oxygen species by the mitochondrial electron transport chain
Liu, Y., Fiskum, G., & Schubert, D. (2002) · Journal of Neurochemistry · doi:10.1046/j.0022-3042.2002.00744.x · Cited by 1,260
Glucose Metabolism Regulates T Cell Activation, Differentiation, and Functions
Palmer, C. S., Ostrowski, M., Balderson, B., Christian, N., & Crowe, S. M. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00001 · Cited by 1,015
Franceschi, C., Garagnani, P., Vitale, G., Capri, M., & Salvioli, S. (2017) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2016.09.005 · Cited by 997
Double-check: validation of diagnostic statistics for PLS-DA models in metabolomics studies
Szymańska, E., Saccenti, E., Smilde, A. K., & Westerhuis, J. A. (2011) · Metabolomics · doi:10.1007/s11306-011-0330-3 · Cited by 913
The origins of age-related proinflammatory state
Ferrucci, L., Corsi, A., Lauretani, F., Bandinelli, S., Bartali, B., Taub, D. D., Guralnik, J. M., & Longo, D. L. (2005) · Blood · doi:10.1182/blood-2004-07-2599 · Cited by 908
Kubli, D. A., & Gustafsson, Å. B. (2012) · Circulation Research · doi:10.1161/circresaha.112.265819 · Cited by 825
Mitochondrial Fission Inhibitors Suppress Endothelin-1-Induced Artery Constriction
Chen, C., Gao, J., Liu, M., Li, S., Xuan, X., Zhang, X., Zhang, X.-Y., Wei, Y., Zhen, C., Jin, J., et al. (2017) · Cellular Physiology and Biochemistry · doi:10.1159/000479536 · Cited by 782
Upregulated NLRP3 Inflammasome Activation in Patients With Type 2 Diabetes
Lee, H., Kim, J.-J., Kim, H. J., Shong, M., Ku, B. J., & Jo, E. (2012) · Diabetes · doi:10.2337/db12-0420 · Cited by 745
Therapeutic Targeting of Mitochondrial Superoxide in Hypertension
Dikalova, A., Bikineyeva, A. T., Budzyn, K., Nazarewicz, R. R., McCann, L. A., Lewis, W., Harrison, D. G., & Dikalov, S. (2010) · Circulation Research · doi:10.1161/circresaha.109.214601 · Cited by 745
Mitochondrial STAT3 Supports Ras-Dependent Oncogenic Transformation
Gough, D. J., Corlett, A., Schlessinger, K., Wegrzyn, J., Larner, A. C., & Levy, D. E. (2009) · Science · doi:10.1126/science.1171721 · Cited by 716
Anti-inflammatory effects of metformin irrespective of diabetes status
Cameron, A. R., Morrison, V. L., Levin, D., Mohan, M., Forteath, C., Beall, C., McNeilly, A. D., Balfour, D. J. K., Savinko, T., Wong, A. K. F., et al. (2016) · Circulation Research · doi:10.1161/circresaha.116.308445 · Cited by 704
IL-21 Is Produced by Th17 Cells and Drives IL-17 Production in a STAT3-dependent Manner
Wei, L., Laurence, A. D. J., Elias, K. M., & O’Shea, J. J. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m705100200 · Cited by 664
Belkina, A. C., Ciccolella, C. O., Anno, R., Halpert, R., Špidlen, J., & Snyder-Cappione, J. E. (2019) · Nature Communications · doi:10.1038/s41467-019-13055-y · Cited by 624
Self-citationFarrés, M., Platikanov, S., Tsakovski, S. L., & Tauler, R. (2015) · Journal of Chemometrics · doi:10.1002/cem.2736 · Cited by 610
Activation of the JAK-STAT pathway by reactive oxygen species
Simon, A. R., Rai, U., Fanburg, B. L., & Cochran, B. (1998) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1998.275.6.c1640 · Cited by 597
Glucose Intolerance and Aging: Evidence for Tissue Insensitivity to Insulin
DeFronzo, R. A. (1979) · Diabetes · doi:10.2337/diab.28.12.1095 · Cited by 595
The role of STAT3 in autophagy
You, L., Wang, Z., Li, H., Shou, J., Jing, Z., Xie, J., Sui, X., Pan, H., & Han, W. (2015) · Autophagy · doi:10.1080/15548627.2015.1017192 · Cited by 515
A clinically meaningful metric of immune age derived from high-dimensional longitudinal monitoring
Alpert, A., Pickman, Y., Leipold, M., Rosenberg-Hasson, Y., Ji, X., Gaujoux, R., Rabani, H., Starosvetsky, E., Kveler, K., Schaffert, S., et al. (2019) · Nature Medicine · doi:10.1038/s41591-019-0381-y · Cited by 513
Glutathione primes t cell metabolism for inflammation
Mak, T. W., Grusdat, M., Duncan, G. S., Dostert, C., Nonnenmacher, Y., Cox, M., Binsfeld, C., Hao, Z., Brüstle, A., Itsumi, M., et al. (2017) · Immunity · doi:10.1016/j.immuni.2017.03.019 · Cited by 511
Menk, A. V., Scharping, N. E., Moreci, R. S., Zeng, X., Guy, C. S., Salvatore, S. R., Bae, H. R., Xie, J., Young, H. A., Wendell, S. G., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.01.040 · Cited by 496
Metabolic pathways in T cell activation and lineage differentiation
Almeida, L., Lochner, M., Berod, L., & Sparwasser, T. D. (2016) · Seminars in Immunology · doi:10.1016/j.smim.2016.10.009 · Cited by 492
Wei, J., Long, L., Yang, K., Guy, C., Shrestha, S., Chen, Z., Wu, C., Vogel, P., Neale, G., Green, D. R., et al. (2016) · Nature Immunology · doi:10.1038/ni.3365 · Cited by 470
Metformin and inflammation: its potential Beyond glucose-lowering effect
Saisho, Y. (2015) · Endocrine, Metabolic & Immune Disorders-Drug Targets · doi:10.2174/1871530315666150316124019 · Cited by 450 · cited 2×
“These data significantly extend demonstrations that metformin alleviates a limited definition of ‘‘inflammation’’ in pre-clinical and clinical studies (Saisho, 2015; Cameron et al., 2016; Lee et al., 2013) by identifying that metformin can act in either of two pathways to exert its…”
BackgroundMetabolic Shifts in Immunity and Inflammation
Kominsky, D. J., Campbell, E. L., & Colgan, S. P. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0903002 · Cited by 422
Monocyte Cytokine Production in an Elderly Population: Effect of Age and Inflammation
Roubenoff, R., Harris, T. B., Abad, L. W., Wilson, P. W. F., Dallal, G. E., & Dinarello, C. A. (1998) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/53a.1.m20 · Cited by 418 · cited 5×
“However, PLSDA showed that the majority of Th17 signature cytokines (IL-17A, IL-17F IL-6, and IL-21; Figure 1F) were not important for distinguishing compendium cytokine profiles from LDH inhibitor-treated Y cells.”
InfluentialDavidson, M. B. (1979) · Metabolism · doi:10.1016/0026-0495(79)90024-6 · Cited by 411
Rosa, V. D., Galgani, M., Porcellini, A., Colamatteo, A., Santopaolo, M., Zuchegna, C., Romano, A., Simone, S. D., Procaccini, C., Rocca, C. L., et al. (2015) · Nature Immunology · doi:10.1038/ni.3269 · Cited by 397
Reversal of Mitochondrial Transhydrogenase Causes Oxidative Stress in Heart Failure
Nickel, A. G., von Hardenberg, A., Hohl, M., Löffler, J., Kohlhaas, M., Becker, J., Reil, J., Kazakov, A., Bonnekoh, J., Stadelmaier, M., et al. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.07.008 · Cited by 383
CHEN, M., BERGMAN, R. N., PACINI, G., & PORTE, D. (1985) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-60-1-13 · Cited by 353
Resveratrol attenuates mitochondrial oxidative stress in coronary arterial endothelial cells
Ungvari, Z. I., Labinskyy, N., Mukhopadhyay, P., Pinto, J. T., Bagi, Z. A., Ballabh, P., Zhang, C., Pacher, P., & Csiszár, A. (2009) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00375.2009 · Cited by 348
Greiner, E. F., Guppy, M., & Brand, K. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)31720-4 · Cited by 307
Rana, A., Oliveira, M. P., Khamoui, A. V., Aparicio, R., Rera, M., Rossiter, H. B., & Walker, D. W. (2017) · Nature Communications · doi:10.1038/s41467-017-00525-4 · Cited by 294
Human Aging and Longevity Are Characterized by High Levels of Mitokines
Conte, M., Ostan, R., Fabbri, C., Santoro, A., Guidarelli, G., Vitale, G., Mari, D., Sevini, F., Capri, M., Sandri, M., et al. (2019) · The Journals of Gerontology: Series A · doi:10.1093/gerona/gly153 · Cited by 219
Chakraborty, A., Chowdhury, S., & Bhattacharyya, M. (2010) · Diabetes Research and Clinical Practice · doi:10.1016/j.diabres.2010.11.030 · Cited by 215
The Role of Reactive Oxygen Species in Regulating T Cell-mediated Immunity and Disease
Yarosz, E. L., & Chang, C.-H. (2018) · Immune Network · doi:10.4110/in.2018.18.e14 · Cited by 214
Autophagosome-Lysosome Fusion Depends on the pH in Acidic Compartments in CHO Cells
Kawai, A., Uchiyama, H., Takano, S., Nakamura, N., & Ohkuma, S. (2007) · Autophagy · doi:10.4161/auto.3634 · Cited by 205
Kabat, A. M., Harrison, O. J., Riffelmacher, T., Moghaddam, A. E., Pearson, C. F., Laing, A., Abeler-Dörner, L., Forman, S. P., Grencis, R. K., Sattentau, Q., et al. (2016) · eLife · doi:10.7554/elife.12444 · Cited by 193
Evolutionary theory predicts late-life mortality plateaus
Mueller, L. D., & Rose, M. R. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.26.15249 · Cited by 190
Smooth-muscle BMAL1 participates in blood pressure circadian rhythm regulation
Xie, Z., Su, W., Liu, S., Zhao, G., Esser, K., Schroder, E. A., Lefta, M., Stauss, H. M., Guo, Z., & Gong, M. C. (2015) · Journal of Clinical Investigation · doi:10.1172/jci76881 · Cited by 189
Self-citationMeasuring Bioenergetics in T Cells Using a Seahorse Extracellular Flux Analyzer
van der Windt, G. J. W., Chang, C., & Pearce, E. L. (2016) · Current Protocols in Immunology · doi:10.1002/0471142735.im0316bs113 · Cited by 189
IL ‐17: overview and role in oral immunity and microbiome
Abusleme, L., & Moutsopoulos, N. M. (2016) · Oral Diseases · doi:10.1111/odi.12598 · Cited by 189
Martínez-López, N., Athonvarangkul, D., & Singh, R. (2015) · Advances in experimental medicine and biology · doi:10.1007/978-1-4939-2404-2_3 · Cited by 185
Mitochondrial degradation and energy metabolism
Melser, S., Lavie, J., & Bénard, G. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2015.05.010 · Cited by 167
Nicholas, D., Proctor, E. A., Agrawal, M., Belkina, A. C., Nostrand, S. C. V., Bharath, L. P., Jones, A. R., Raval, F., Ip, B. C., Zhu, M., et al. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2019.07.004 · Cited by 163
Self-citationVereb, G., Matkó, J., Vámosi, G., Ibrahim, S., Magyar, E., Varga, S., Szöllõsi, J., Jenei, A., Gáspár, R., Waldmann, T. A., et al. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.11.6013 · Cited by 152
Poli, V., & Camporeale, A. (2015) · Frontiers in Oncology · doi:10.3389/fonc.2015.00121 · Cited by 139
Ip, B. C., Cilfone, N. A., Belkina, A. C., DeFuria, J., Jagannathan‐Bogdan, M., Zhu, M., Kuchibhatla, R., McDonnell, M. E., Xiao, Q., Kepler, T. B., et al. (2015) · Obesity · doi:10.1002/oby.21243 · Cited by 132
Self-citationBharath, L. P., Mueller, R., Li, Y., Ruan, T., Kunz, D., Goodrich, R., Mills, T. J., Deeter, L., Sargsyan, A., Babu, P. V. A., et al. (2014) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2014-0017 · Cited by 131
Self-citationCeramide-Initiated Protein Phosphatase 2A Activation Contributes to Arterial Dysfunction In Vivo
Bharath, L. P., Ruan, T., Li, Y., Ravindran, A., Wan, X., Nhan, J. K., Walker, M., Deeter, L., Goodrich, R., Johnson, E., et al. (2015) · Diabetes · doi:10.2337/db15-0244 · Cited by 127
Self-citationNew insights into the roles of Stat5a/b and Stat3 in T cell development and differentiation
Wei, L., Laurence, A. D. J., & O’Shea, J. J. (2008) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2008.07.011 · Cited by 126
Glutathione Primes T Cell Metabolism for Inflammation
Mak, T. W., Grusdat, M., Duncan, G. S., Dostert, C., Nonnenmacher, Y., Cox, M. A., Binsfeld, C., Hao, Z., Brüstle, A., Itsumi, M., et al. (2017) · Immunity · doi:10.1016/j.immuni.2017.06.009 · Cited by 118
Bektas, A., Schurman, S. H., Gonzalez-Freire, M., Dunn, C. A., Singh, A. K., Macian, F., Cuervo, A. M., Sen, R., & Ferrucci, L. (2019) · Aging · doi:10.18632/aging.102438 · Cited by 116
Cytobank: Providing an Analytics Platform for Community Cytometry Data Analysis and Collaboration
Chen, T. J., & Kotecha, N. (2014) · Current topics in microbiology and immunology · doi:10.1007/82_2014_364 · Cited by 108
Stat3 Phosphorylation Mediates Resistance of Primary Human T Cells to Regulatory T Cell Suppression
Goodman, W. A., Young, A. B., McCormick, T. S., Cooper, K. D., & Levine, A. D. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1001455 · Cited by 106
Fidan, E., Ersöz, H. Ö., Yılmaz, M., Yilmaz, H., Koçak, M., Karahan, C., & Erem, C. (2011) · Acta Diabetologica · doi:10.1007/s00592-011-0276-y · Cited by 102
Hong, Z., Kutty, S., Tóth, P. T., Marsboom, G., Hammel, J. M., Chamberlain, C., Ryan, J. J., Zhang, H. J., Sharp, W. W., Morrow, E., et al. (2013) · Circulation Research · doi:10.1161/circresaha.111.300285 · Cited by 100
Bharath, L. P., Cho, J. M., Park, S.-K., Ruan, T., Li, Y., Mueller, R., Bean, T., Reese, V. R., Richardson, R. S., Cai, J., et al. (2017) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.117.309510 · Cited by 98
Self-citationLiang, Z., Ustyugova, I. V., Chen, X., Zhang, Q., & Wu, M. X. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1200528 · Cited by 84
Nicholas, D., Proctor, E. A., Raval, F., Ip, B. C., Habib, C., Ritou, E., Grammatopoulos, T. N., Steenkamp, D., Dooms, H., Apovian, C. M., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0170975 · Cited by 80
Self-citationProhibitin 1 Modulates Mitochondrial Stress-Related Autophagy in Human Colonic Epithelial Cells
Kathiria, A. S., Butcher, L. D., Feagins, L. A., Souza, R. F., Boland, C. R., & Theiss, A. L. (2012) · PLoS ONE · doi:10.1371/journal.pone.0031231 · Cited by 74
Priyadharshini, B., Loschi, M. L., Newton, R. H., Zhang, J.-W., Finn, K. K., Gerriets, V. A., Huynh, A., Rathmell, J. C., Blazar, B. R., & Turka, L. A. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1800311 · Cited by 73
Zapała, B., Kaczyński, Ł., Kieć‐Wilk, B., Staszel, T., Knapp, A., Thoresen, G. H., Wybrańska, I., & Dembinska-Kiec, A. (2010) · Pharmacological Reports · doi:10.1016/s1734-1140(10)70337-6 · Cited by 70
Age Associated Oxidative Damage in Lymphocytes
Gautam, N., Das, S., Mahapatra, S. K., Chakraborty, S. P., Kundu, P. K., & Roy, S. (2010) · Oxidative Medicine and Cellular Longevity · doi:10.4161/oxim.3.4.12860 · Cited by 67
Inflammaging: Age and Systemic, Cellular, and Nuclear Inflammatory Biology in Older Adults
Piber, D., Olmstead, R., Cho, J. H.-J., Witarama, T., Perez, C., Dietz, N., Seeman, T. E., Breen, E. C., Cole, S. W., & Irwin, M. R. (2019) · The Journals of Gerontology: Series A · doi:10.1093/gerona/glz130 · Cited by 62
Autophagy-dependent regulatory T cells are critical for the control of graft-versus-host disease
Texier, L. L., Lineburg, K. E., Cao, B., McDonald-Hyman, C. S., Leveque, L., Nicholls, J., Melino, M., Nalkurthi, B. C., Alexander, K. A., Teal, B. E., et al. (2016) · JCI Insight · doi:10.1172/jci.insight.86850 · Cited by 58
A New Perspective: Mitochondrial Stat3 as a Regulator for Lymphocyte Function
Rincón, M., & Pereira, F. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19061656 · Cited by 57
TNF-α, leptin, and lymphocyte function in human aging
Brüünsgaard, H., Pedersen, B. K., Schroll, M., Skinhøj, P., & Pedersen, B. K. (2000) · Life Sciences · doi:10.1016/s0024-3205(00)00851-1 · Cited by 50
YFP photoconversion revisited: confirmation of the CFP-like species
Kirber, M. T., Chen, K., & Keaney, J. F. (2007) · Nature Methods · doi:10.1038/nmeth1007-767 · Cited by 49
Smith, L. M., Yao‐Borengasser, A., Starks, T., Tripputi, M., Kern, P. A., & Rasouli, N. (2010) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2010-0017 · Cited by 41
Self-citationWang, J., Feng, X., Zeng, Y., Fan, J., Wu, J., Li, Z., Liu, X., Huang, R., Huang, F., Yu, X., et al. (2013) · BMC Microbiology · doi:10.1186/1471-2180-13-255 · Cited by 35
Jiang, K., Yang, Z., Cheng, L., Wang, S., Ning, K., Zhou, L., Lin, J., Zhong, H., Wang, L., Yang, L., et al. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.467837 · Cited by 32
Self-citationMalínská, H., Oliyarnyk, O., Škop, V., Šilhavý, J., Landa, V., Zı́dek, V., Mlejnek, P., Šimáková, M., Strnad, H., Kazdová, L., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0150924 · Cited by 22
Adaptive Immunity and Metabolic Health: Harmony Becomes Dissonant in Obesity and Aging
Bharath, L. P., Ip, B. C., & Nikolajczyk, B. S. (2017) · Comprehensive physiology · doi:10.1002/cphy.c160042 · Cited by 21
Self-citationMcCormick, J., VanDusseldorp, T., Ulrich, C., Lanphere, R., Dokładny, K., Mosely, P., & Mermier, C. (2018) · Physiology International · doi:10.1556/2060.105.2018.3.20 · Cited by 19
Tyrosine 705 Phosphorylation of STAT3 Is Associated with Phenotype Severity in TGFβ1 Transgenic Mice
Guadagnin, E., Narola, J., Bonnemann, C., & Chen, Y.-W. (2015) · BioMed Research International · doi:10.1155/2015/843743 · Cited by 16
Author Correction: Metformin inhibits gluconeogenesis via a redox-dependent mechanism in vivo
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Metadata
- Authors
- Bharath, L. P., Agrawal, M., McCambridge, G., Nicholas, D. A., Hasturk, H., Liu, J., Jiang, K., Liu, R., Guo, Z., Deeney, J., Apovian, C. M., Snyder-Cappione, J., Hawk, G. S., Fleeman, R. M., Pihl, R. M. F., Thompson, K., Belkina, A. C., Cui, L., Proctor, E. A., Kern, P. A., & Nikolajczyk, B. S.
- Affiliations
- Merrimack College (US)
- University of Kentucky (US)
- University of California San Diego (US)
- Boston University (US)
- Pennsylvania State University (US)
- Corresponding author
- Nikolajczyk, Barbara S.
- ORCID
- Venue
- Cell Metabolism
- Publisher
- Elsevier BV
- Published
- 2020-07
- Volume
- 32
- Issue
- 1
- Pages
- 44-55.e6
- ISSN
- 1550-4131 (ISSN-L)
- PMC
- PMC7217133
- OpenAlex
- W3024177706
- Cited by
- 614
- References
- 90
- Citations by year
- 2026: 66 · 2025: 123 · 2024: 110 · 2023: 120 · 2022: 83 · 2021: 81 · 2020: 29
- FWCI
- 56.30
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell Metabolism (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- UKnowledge (University of Kentucky) (submittedVersion)
- Digital Commons-TMC (Texas Medical Center) (submittedVersion)
- Funders
- National Institutes of Health
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- metformin, autophagy, mitochondrial function, inflammaging, Th17 cells, CD4+ T cells, aging, STAT3, IL-17A, redox imbalance, mitophagy, healthspan
- MeSH terms
- Adult, Aging, Autophagy, Humans, Hypoglycemic Agents, Inflammation, Metformin, Middle Aged, Mitochondria
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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