The DOI matches its Crossref record; 26 of the 26 references it cites were found in a registry or an index.
A PGC1-α-dependent myokine that drives brown-fat-like development of white fat and thermogenesis
Open accessAbstract
Exercise benefits a variety of organ systems in mammals, and some of the best-recognized effects of exercise on muscle are mediated by the transcriptional co-activator PPAR-γ co-activator-1 α (PGC1-α). Here we show in mouse that PGC1-α expression in muscle stimulates an increase in expression of FNDC5, a membrane protein that is cleaved and secreted as a newly identified hormone, irisin. Irisin acts on white adipose cells in culture and in vivo to stimulate UCP1 expression and a broad program of brown-fat-like development. Irisin is induced with exercise in mice and humans, and mildly increased irisin levels in the blood cause an increase in energy expenditure in mice with no changes in movement or food intake. This results in improvements in obesity and glucose homeostasis. Irisin could be therapeutic for human metabolic disease and other disorders that are improved with exercise.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“When originally described, it was found to exert browning of WAT, increase energy expenditure, improve insulin sensitivity, and induce weight loss, through upregulation of UCP1 in exercised mice overexpressing PGC-1α [57].”
From The Role of Exercise in the Interplay between Myokines, Hepatokines, Osteokines, Adipokines, and Modulation of Inflammation for Energy Substrate Redistribution and Fat Mass Loss: A Review (2020) · cites this paper as [57]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“The myokines irisin [57] and BAIBA [104] have been described to directly induce WAT “browning” both in vitro and in vivo, by upregulating genes involved in mitochondrial biogenesis, FAO, oxidative phosphorylation, and thermogenesis (1).”
From The Role of Exercise in the Interplay between Myokines, Hepatokines, Osteokines, Adipokines, and Modulation of Inflammation for Energy Substrate Redistribution and Fat Mass Loss: A Review (2020) · cites this paper as [57]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“FNDC-5 is known to drive development of brown-fat-like cells in WAT, which enhances lipid metabolism/oxidation via mitochondrial uncoupling protein 1 (UCP-1) activity [12].”
From β-hydroxy-β -methylbutyrate supplementation benefits the effects of resistance training on body fat reduction via increased irisin expression in white adipose tissue (2021) · cites this paper as [12]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“However, only the irisin precursor FNDC5 was able to promote the differentiation of stromal vascular cells isolated from WAT from beige mice (browning phenomenon; Bostrom et al., 2012).”
From Physical Exercise-Induced Myokines and Muscle-Adipose Tissue Crosstalk: A Review of Current Knowledge and the Implications for Health and Metabolic Diseases (2018) · cites this paper as Bostrom et al., 2012
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Irisin is a myokine that promotes white adipose tissue browning, originally identified through animal studies [38] and subsequently confirmed in humans [39].”
From Exercise-Induced Myokines in Obesity-Related Metabolic Disorders and Cardiovascular Protection: A Narrative Review (2026) · cites this paper as [38]
The cited source says what the claim attributes to it.
In the citing paper
“which is known to upregulate the WAT browning myokines FNDC5-irisin [57], METRNL [274], and BAIBA [104].”
The cited source says what the claim attributes to it.
In the citing paper
“Irisin is stimulated by ‘Peroxisome proliferator-activated receptor-Gamma Coactivator 1α’ (PGC1α), and mediates beneficial metabolic effects through the beiging of white AT [17,49], thereby activating UCP1 and inducing enhanced thermogenesis within the white AT.”
From Optimised Skeletal Muscle Mass as a Key Strategy for Obesity Management (2025) · cites this paper as [49]
The cited source says what the claim attributes to it.
In the citing paper
“Thus, following the characterization of irisin as a myokine capable of activating adipose tissue browning in rodents in response to exercise (Bostrom et al., 2012) the concept that factors secreted by SkM could signal to other organs has grown and developed.”
From Physical Exercise-Induced Myokines and Muscle-Adipose Tissue Crosstalk: A Review of Current Knowledge and the Implications for Health and Metabolic Diseases (2018) · cites this paper as Bostrom et al., 2012
The cited source says what the claim attributes to it.
In the citing paper
“Irisin, formerly called Iris, is a recently identified myokine, released into the circulation by SkM in an exercise-dependent manner.”
From Physical Exercise-Induced Myokines and Muscle-Adipose Tissue Crosstalk: A Review of Current Knowledge and the Implications for Health and Metabolic Diseases (2018) · cites this paper as Bostrom et al., 2012
The cited source says what the claim attributes to it.
In the citing paper
“It is reported to have the ability to convert WAT to BAT, a phenomenon known as browning; a phenotype set of adaptations that results in increasing total energy expenditure (Bostrom et al., 2012).”
From Physical Exercise-Induced Myokines and Muscle-Adipose Tissue Crosstalk: A Review of Current Knowledge and the Implications for Health and Metabolic Diseases (2018) · cites this paper as Bostrom et al., 2012
The cited source says what the claim attributes to it.
In the citing paper
“Five candidate proteins were found to be mediated by PGC-1α in the muscle: IL-15, Fndc5, VEGFβ, Lrg1, and TIMP4.”
From Physical Exercise-Induced Myokines and Muscle-Adipose Tissue Crosstalk: A Review of Current Knowledge and the Implications for Health and Metabolic Diseases (2018) · cites this paper as Bostrom et al., 2012
The cited source says what the claim attributes to it.
In the citing paper
“Other papers have demonstrated that exercise induces upregulation in skeletal muscle of PGC1α, a transcriptional co-activator of mitochondrial biogenesis and oxidative metabolism in brown adipose tissue and muscle. In muscle, the increase of PGC1α expression stimulates an upregulation of FNDC5, a membrane protein that is cleaved and secreted into the circulation as the myokine irisin [237].”
From Neurotrophic Factor BDNF, Physiological Functions and Therapeutic Potential in Depression, Neurodegeneration and Brain Cancer (2020) · cites this paper as [237]
In the citing paper
“Irisin is a PPARγ-coactivator-1α (PGCα)-dependent myokine that stimulates browning in subcutaneous adipose tissues and induces increased energy expenditure, which improves obesity and IR through the MAPK and ERK pathways [92,93].”
From Sarcopenic obesity, insulin resistance, and their implications in cardiovascular and metabolic consequences (2020) · cites this paper as [92]
In the citing paper
“Irisin is released by skeletal muscles and has been shown to increase thermogenesis and energy expenditure by promoting the browning of subcutaneous adipocytes.”
From Diet and physical exercise as key players to tackle MASLD through improvement of insulin resistance and metabolic flexibility (2024) · cites this paper as [88]
In the citing paper
“Moreover, resistance exercise may improve MASLD through muscle-liver crosstalk mediated by a myokine called irisin (88, 89).”
From Diet and physical exercise as key players to tackle MASLD through improvement of insulin resistance and metabolic flexibility (2024) · cites this paper as [88]
In the citing paper
“It also exhibits regulatory effects on lipid metabolism in hepatocytes (88).”
From Diet and physical exercise as key players to tackle MASLD through improvement of insulin resistance and metabolic flexibility (2024) · cites this paper as [88]
In the citing paper
“The main and well-described function of irisin is to induce WAT browning and thus UCP-1-dependent mitochondrial uncoupling [206].”
From Mitochondrial Uncoupling: A Key Controller of Biological Processes in Physiology and Diseases (2019) · cites this paper as [206]
In the citing paper
“Thus, whether exercise can brown WAT in humans, especially through an irisin-mediated pathway, remains controversial55,83,84,90.”
From Exerkines in health, resilience and disease (2022) · cites this paper as [84]
In the citing paper
“Transgenic mice that overexpress muscle peroxisome proliferator-activated receptor-γ coactivator 1-α (PGClα) have higher circulating levels of irisin and increased WAT browning than control mice84.”
From Exerkines in health, resilience and disease (2022) · cites this paper as [84]
In the citing paper
“In a mouse model, fibronectin type III domain containing 5 is cleaved in the muscle cell and secreted as irisin, which induces WAT browning to increase energy expenditure and consequently reduce obesity84.”
From Exerkines in health, resilience and disease (2022) · cites this paper as [84]
In the citing paper
“The first paper to describe irisin, a PGC1α-dependent myokine, that drives ‘browning’ of WAT in an animal model”
From Exerkines in health, resilience and disease (2022) · cites this paper as [84]
In the citing paper
“FNDC5 induces thermogenesis and elevates mitochondrial gene expression [131], and resilient mice have increased NAc metabolism [132].”
From The molecular and cellular mechanisms of depression: a focus on reward circuitry (2019) · cites this paper as [131]
In the citing paper
“recent studies have identified secreted proteins that stimulate brown adipocyte thermogenesis and recruit brown (or beige) adipocytes to white adipose tissue [60] [61].”
From Regulation of obesity and insulin resistance by nitric oxide (2014) · cites this paper as [61]
In the citing paper
“Interestingly, a moderate increase (threefold) in irisin blood levels in mice enhanced energy expenditure and improved obesity and glucose homeostasis ([12](#B12)).”
From Mitochondrial fatty acid oxidation in obesity (2013) · cites this paper as [12]
In the citing paper
“Recent landmark studies have identified novel secreted proteins, such as liver FGF21 ([72](#B72)), cardiac natriuretic peptides ([11](#B11)), and irisin ([12](#B12)), that stimulate brown adipocyte thermogenesis.”
From Mitochondrial fatty acid oxidation in obesity (2013) · cites this paper as [12]
In the citing paper
“Irisin was shown to trigger WAT remodeling by increasing p38 signaling, UCP1 expression, and therefore browning 115, 116.”
From Inter‐organ communication: a gatekeeper for metabolic health (2019) · cites this paper as [115]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
2 retracted
Wenz, T., Rossi, S. G., Rotundo, R. L., Spiegelman, B. M., & Moraes, C. T. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911570106 · Cited by 600
Self-citationRetractedBoström, P., Andersson, L. K., Vind, B. F., Håversen, L., Rutberg, M., Wickström, Y., Larsson, E. N. V., Jansson, P., Svensson, M. K. E., Brånemark, R., et al. (2010) · Diabetes · doi:10.2337/db09-1503 · Cited by 44
Self-citationRetractedA Cold-Inducible Coactivator of Nuclear Receptors Linked to Adaptive Thermogenesis
Puigserver, P., Wu, Z., Park, C. W., Graves, R., Wright, M., & Spiegelman, B. M. (1998) · Cell · doi:10.1016/s0092-8674(00)81410-5 · Cited by 3,864
Self-citationLocating proteins in the cell using TargetP, SignalP and related tools
Emanuelsson, O., Brunak, S., von HEIJNE, G., & Nielsen, H. (2007) · Nature Protocols · doi:10.1038/nprot.2007.131 · Cited by 3,215
Prdm16 determines the thermogenic program of subcutaneous white adipose tissue in mice
Seale, P., Conroe, H. M., Estall, J. L., Kajimura, S., Frontini, A., Ishibashi, J., Cohen, P., Cinti, S., & Spiegelman, B. M. (2010) · Journal of Clinical Investigation · doi:10.1172/jci44271 · Cited by 1,273
Self-citationNew role of bone morphogenetic protein 7 in brown adipogenesis and energy expenditure
Tseng, Y.-H., Kokkotou, E., Schulz, T. J., Huang, T. L., Winnay, J. N., Taniguchi, C. M., Tran, T. T., Suzuki, R., Espinoza, D. O., Yamamoto, Y., et al. (2008) · Nature · doi:10.1038/nature07221 · Cited by 1,099
The role of exercise and PGC1α in inflammation and chronic disease
Handschin, C., & Spiegelman, B. M. (2008) · Nature · doi:10.1038/nature07206 · Cited by 1,083
Self-citationSandri, M., Lin, J., Handschin, C., Yang, W., Arany, Z. P., Lecker, S. H., Goldberg, A. L., & Spiegelman, B. M. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0607795103 · Cited by 974
Self-citationInitiation of myoblast to brown fat switch by a PRDM16–C/EBP-β transcriptional complex
Kajimura, S., Seale, P., Kubota, K., Lunsford, E., Frangioni, J. V., Gygi, S. P., & Spiegelman, B. M. (2009) · Nature · doi:10.1038/nature08262 · Cited by 703
Self-citationThe SCX/IMAC enrichment approach for global phosphorylation analysis by mass spectrometry
Villén, J., & Gygi, S. P. (2008) · Nature Protocols · doi:10.1038/nprot.2008.150 · Cited by 637
Self-citation
Cited by
Sorted by citations
Items 601–700 of 1,068
Son, J. S., Zhao, L., Chen, Y., Chen, K., Chae, S. A., de Avila, J. M., Wang, H., Zhu, M.-J., Jiang, Z., & Du, M. (2020) · Science Advances · doi:10.1126/sciadv.aaz0359 · Cited by 101
Does PGC1α/FNDC5/BDNF Elicit the Beneficial Effects of Exercise on Neurodegenerative Disorders?
Jodeiri Farshbaf, M., Ghaedi, K., Megraw, T. L., Curtiss, J., Shirani Faradonbeh, M., Vaziri, P., & Nasr-Esfahani, M. H. (2016) · NeuroMolecular Medicine · doi:10.1007/s12017-015-8370-x · Cited by 101
Vargas‐Castillo, A., Fuentes‐Romero, R., Rodríguez-López, L. A., Torres, N., & Tovar, A. R. (2017) · Archives of Medical Research · doi:10.1016/j.arcmed.2017.10.002 · Cited by 101
Kim, G., Lee, S., Jun, J. E., Lee, Y., Ahn, J., Bae, J. C., Jin, S., Hur, K. Y., Jee, J. H., Lee, M., et al. (2018) · Cardiovascular Diabetology · doi:10.1186/s12933-018-0659-2 · Cited by 101
Tang, Y.-J., Zhang, Z., Yan, T., Chen, K., Xu, G.-F., Xiong, S., Wu, D.-Q., Chen, J., José, P. A., Zeng, C., et al. (2024) · Cardiovascular Diabetology · doi:10.1186/s12933-024-02183-5 · Cited by 101
Tiano, J. P., Springer, D., & Rane, S. G. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.617399 · Cited by 101
Shu, L., Hoo, R. L. C., Wu, X., Pan, Y., Lee, I. P. C., Cheong, L. Y., Bornstein, S. R., Rong, X., Guo, J., & Xu, A. (2017) · Nature Communications · doi:10.1038/ncomms14147 · Cited by 101
Matsuo, Y., Gleitsmann, K., Mangner, N., Werner, S., Fischer, T., Bowen, T. S., Kricke, A., Matsumoto, Y., Kurabayashi, M., Schuler, G., et al. (2015) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12006 · Cited by 100
Banitalebi, E., Kazemi, A., Faramarzi, M., Nasiri, S., & Haghighi, M. M. (2018) · Life Sciences · doi:10.1016/j.lfs.2018.11.062 · Cited by 100
Jin, Y., Sumsuzzman, D. M., Choi, J., Kang, H., Lee, S., & Hong, Y. (2018) · Molecules · doi:10.3390/molecules23123229 · Cited by 100
Self-citationHousing temperature affects the acute and chronic metabolic adaptations to exercise in mice
McKie, G. L., Medak, K. D., Knuth, C. M., Shamshoum, H., Townsend, L. K., Peppler, W. T., & Wright, D. C. (2019) · The Journal of Physiology · doi:10.1113/jp278221 · Cited by 100
Irisin Levels During Pregnancy and Changes Associated With the Development of Preeclampsia
Garcés, M. F., Franco, J. J. P., Ruíz-Linares, C. E., Lozano, A. R., Poveda, N. E., Torres‐Sierra, A. L., Eslava-Schmalbach, J. H., Álzate, J. P., Sánchez, A. Y., Sánchez, E., et al. (2014) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2013-4127 · Cited by 100
Exercise-Mediated Browning of White Adipose Tissue: Its Significance, Mechanism and Effectiveness
Mu, W.-J., Zhu, J.-Y., Chen, M., & Guo, L. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111512 · Cited by 99
Understanding the brown adipocyte as a contributor to energy homeostasis
Chechi, K., Carpentier, A. C., & Richard, D. (2013) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2013.04.002 · Cited by 99
Placental Regulation of Energy Homeostasis During Human Pregnancy
Armistead, B., Johnson, E., Vanderkamp, R., Kula-Eversole, E., Kadam, L., Drewlo, S., & Kohan‐Ghadr, H. (2020) · Endocrinology · doi:10.1210/endocr/bqaa076 · Cited by 99
Regulatory microRNAs in Brown, Brite and White Adipose Tissue
Gharanei, S., Shabir, K., Brown, J. E. P., Weickert, M. O., Barber, T. M., Kyrou, I., & Randeva, H. S. (2020) · Cells · doi:10.3390/cells9112489 · Cited by 100
How does the skeletal muscle communicate with the brain in health and disease?
Isaac, A. R., Lima‐Filho, R. A. S., & Lourenco, M. V. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108744 · Cited by 99
Bean, C., Audano, M., Varanita, T., Favaretto, F., Medaglia, M., Gerdol, M., Pernas, L. F., Stasi, F., Giacomello, M., Herkenne, S., et al. (2021) · Nature Metabolism · doi:10.1038/s42255-021-00497-2 · Cited by 101
Michalakis, K. G., Goulis, D. G., Vazaiou, A., Mintziori, G., Polymeris, A., & Abrahamian-Michalakis, A. (2013) · Metabolism · doi:10.1016/j.metabol.2013.05.019 · Cited by 99
Crosstalk between nonalcoholic fatty liver disease and cardiometabolic syndrome
Lim, S. K., Taskinen, M., & Borén, J. (2018) · Obesity Reviews · doi:10.1111/obr.12820 · Cited by 99
Brown adipose tissue as an anti‐obesity tissue in humans
Chechi, K., Nedergaard, J., & Richard, D. (2013) · Obesity Reviews · doi:10.1111/obr.12116 · Cited by 98
Lower irisin level in patients with type 2 diabetes mellitus: A case‐control study and meta‐analysis
Zhang, C., Ding, Z., Lv, G., Li, J., Zhou, P., & Zhang, J. (2014) · Journal of Diabetes · doi:10.1111/1753-0407.12256 · Cited by 98
Xiang, L., Xiang, G., Yue, L., Zhang, J., & Zhao, L. (2014) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2014.04.036 · Cited by 98
Irisin: A new potential hormonal target for the treatment of obesity and type 2 diabetes
Sanchis‐Gomar, F., Lippi, G., Mayero, S., Pérez-Quilis, C., & García‐Giménez, J. L. (2012) · Journal of Diabetes · doi:10.1111/j.1753-0407.2012.00194.x · Cited by 98
Drescher, C., Konishi, M., Ebner, N., & Springer, J. (2015) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12082 · Cited by 98
MicroRNA-Regulated Proinflammatory Cytokines in Sarcopenia
Fan, J., Kou, X., Yang, Y., & Chen, N. (2016) · Mediators of Inflammation · doi:10.1155/2016/1438686 · Cited by 98
Côté, S., Gagné‐Ouellet, V., Guay, S., Allard, C., Houde, A.-A., Perron, P., Baillargeon, J., Gaudet, D., Guérin, R., Brisson, D., et al. (2016) · Clinical Epigenetics · doi:10.1186/s13148-016-0239-9 · Cited by 98
Belviranlı, M., & Okudan, N. (2018) · NeuroMolecular Medicine · doi:10.1007/s12017-018-8500-3 · Cited by 98
Brown adipose tissue as a heat-producing thermoeffector
Nedergaard, J., & Cannon, B. (2018) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63912-7.00009-6 · Cited by 99
Organism-wide, cell-type-specific secretome mapping of exercise training in mice
Wei, W., Riley, N. M., Lyu, X., Shen, X., Guo, J., Raun, S. H., Zhao, M., Moya-Garzón, M. D., Basu, H., Tung, A. S.-H., et al. (2023) · Cell Metabolism · doi:10.1016/j.cmet.2023.04.011 · Cited by 101
Self-citationCentral and Peripheral Irisin Differentially Regulate Blood Pressure
Zhang, W., Chang, L., Zhang, C., Zhang, R., Li, Z., Chai, B., Li, J., Chen, E., & Mulholland, M. T. (2015) · Cardiovascular Drugs and Therapy · doi:10.1007/s10557-015-6580-y · Cited by 98
Liu, P., Zou, D., Yi, L., Chen, M., Gao, Y., Zhou, R., Zhang, Q., Zhou, Y. G., Zhu, J., Chen, K., et al. (2015) · Restorative Neurology and Neuroscience · doi:10.3233/rnn-140446 · Cited by 98
Lee, M. J., Lee, S. A., Nam, B. Y., Park, S., Lee, S., Ryu, H. J., Kwon, Y. E., Kim, Y. L., Park, K. S., Oh, H. J., et al. (2015) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2015.08.002 · Cited by 98
Gao, Y., Guo, M., Wang, D., Zhao, D., & Wang, M. (2022) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2022.11.099 · Cited by 97
Eicosanoids in Metabolic Syndrome
Hardwick, J. P., Eckman, K., Lee, Y., Abdelmegeed, M. A., Esterle, A. R., Chilian, W. M., Chiang, J. Y. L., & Song, B. (2013) · Advances in pharmacology · doi:10.1016/b978-0-12-404717-4.00005-6 · Cited by 97
Can exercise affect the course of inflammatory bowel disease? Experimental and clinical evidence
Bilski, J., Mazur-Biały, A. I., Brzozowski, B., Magierowski, M., Zahradnik-Bilska, J., Wójcik-Grzybek, D., Magierowska, K., Kwiecień, S., Mach, T., & Brzozowski, T. (2016) · Pharmacological Reports · doi:10.1016/j.pharep.2016.04.009 · Cited by 97
Kong, G., Jiang, Y., Sun, X., Cao, Z., Zhang, G., Zhao, Z., Zhao, Y. B., Qian, Y., & Cheng, G. (2017) · Oncology Reports · doi:10.3892/or.2017.5973 · Cited by 97
Guo, B., Zhang, Z.-K., Liang, C., Li, J., Liu, J., Lu, A., Zhang, B.-T., & Zhang, G. (2017) · Calcified Tissue International · doi:10.1007/s00223-016-0209-4 · Cited by 96
Xie, C., Zhang, Y., Tran, T. D. N., Wang, H., Li, S., George, E. V., Zhuang, H., Zhang, P., Kandel, A., Lai, Y., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0136816 · Cited by 96
Qiu, S., Cai, X., Yin, H., Zügel, M., Sun, Z., Steinacker, J. M., & Schümann, U. (2016) · Metabolism · doi:10.1016/j.metabol.2016.02.006 · Cited by 96
Khalafi, M., Mohebbi, H., Symonds, M. E., Karimi, P., Akbari, A. M., Tabari, E., Faridnia, M., & Moghaddami, K. (2020) · Nutrients · doi:10.3390/nu12040925 · Cited by 96
Los colores del tejido adiposo
Frigolet, M. E., & Gutiérrez‐Aguilar, R. (2020) · Gaceta Médica de México · doi:10.24875/gmm.20005541 · Cited by 96
Childhood Obesity, Diabetes, and Cardiovascular Disease Risk
Salama, M., Balagopal, B., Fennoy, I., & Kumar, S. (2023) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgad361 · Cited by 96
Peri-adipocyte ECM remodeling in obesity and adipose tissue fibrosis
Chun, T. (2012) · Adipocyte · doi:10.4161/adip.19752 · Cited by 96
Assessment of brown adipose tissue function
Virtue, S., & Vidal‐Puig, A. (2013) · Frontiers in Physiology · doi:10.3389/fphys.2013.00128 · Cited by 96
Palacios‐González, B., Vadillo‐Ortega, F., Polo‐Oteyza, E., Sánchez, T. S., Ancira‐Moreno, M., Romero‐Hidalgo, S., Meraz‐Cruz, N., & Antuna-Puente, B. (2015) · Obesity · doi:10.1002/oby.21029 · Cited by 96
Leal‐Díaz, A. M., Noriega, L. G., Torre-Villalvazo, I., Torres, N., Alemán, G., López‐Romero, P., Sánchez‐Tapia, M., Aguilar‐López, M., Furuzawa‐Carballeda, J., Velázquez‐Villegas, L. A., et al. (2016) · Scientific Reports · doi:10.1038/srep34242 · Cited by 96
Wu, F., Song, H., Zhang, Y., Zhang, Y., Mu, Q., Jiang, M., Wang, F., Zhang, W., Li, L., Li, H., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0134662 · Cited by 95
Thermogenic brown and beige/brite adipogenesis in humans
Cereijo, R., Giralt, M., & Villarroya, F. (2014) · Annals of Medicine · doi:10.3109/07853890.2014.952328 · Cited by 95
Hu, P., Yin, L., Aggabao, P. C., Perkins, T. G., Chia, J. M., & Gilsanz, V. (2013) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.24053 · Cited by 95
The expanding problem of adipose depot remodeling and postnatal adipocyte progenitor recruitment
Hepler, C., & Gupta, R. K. (2016) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2016.10.011 · Cited by 95
Garneau, L., & Aguer, C. (2019) · Diabetes & Metabolism · doi:10.1016/j.diabet.2019.02.006 · Cited by 95
The Role of Exercise, Diet, and Cytokines in Preventing Obesity and Improving Adipose Tissue
ATAKAN, M. M., Koşar, Ş. N., Güzel, Y., Tin, H. T., & Yan, X. (2021) · Nutrients · doi:10.3390/nu13051459 · Cited by 96
Irisin exhibits neuroprotection by preventing mitochondrial damage in Parkinson’s disease
Zhang, X., Xu, S., Hu, Y. H., Liu, Q., Liu, C., Chai, H., Luo, Y., Jin, L., & Li, S. (2023) · npj Parkinson s Disease · doi:10.1038/s41531-023-00453-9 · Cited by 97
Distinct functions ofUlk1andUlk2in the regulation of lipid metabolism in adipocytes
Ro, S.-H., Jung, C. H., Hahn, W. S., Xu, X., Kim, Y.-M., Yun, Y. S., Park, J.-M., Kim, K. H., Seo, M., Ha, T.-Y., et al. (2013) · Autophagy · doi:10.4161/auto.26563 · Cited by 93
Is irisin the new player in exercise-induced adaptations or not? A 2017 update
Fatouros, I. G. (2017) · Clinical Chemistry and Laboratory Medicine (CCLM) · doi:10.1515/cclm-2017-0674 · Cited by 95
The p38–PGC-1α–irisin–betatrophin axis
Sanchis‐Gomar, F., & Pérez-Quilis, C. (2013) · Adipocyte · doi:10.4161/adip.27370 · Cited by 95
Activation and recruitment of brown adipose tissue as anti-obesity regimens in humans
Yoneshiro, T., & Saito, M. (2014) · Annals of Medicine · doi:10.3109/07853890.2014.911595 · Cited by 94
Irisin exerts a therapeutic effect against myocardial infarction via promoting angiogenesis
Liao, Q., Qu, S., Tang, L., Li, L.-P., He, D., Zeng, C., & Wang, W. E. (2019) · Acta Pharmacologica Sinica · doi:10.1038/s41401-019-0230-z · Cited by 94
Harnessing Muscle–Liver Crosstalk to Treat Nonalcoholic Steatohepatitis
Chakravarthy, M. V., Siddiqui, M. S., Forsgren, M. F., & Sanyal, A. J. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.592373 · Cited by 96
Hu, X., Wang, Z., Wang, W., Cui, P., Kong, C., Chen, X., & Lu, S. (2023) · Journal of Advanced Research · doi:10.1016/j.jare.2023.09.001 · Cited by 94
Molecular insights of exercise therapy in disease prevention and treatment
Walzik, D., Chirino, T. Y. W., Zimmer, P., & Joisten, N. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01841-0 · Cited by 95
Greulich, T., Nell, C., Koepke, J., Fechtel, J., Franke, M., Schmeck, B., Haid, D., Apelt, S., Filipovic, S., Kenn, K., et al. (2014) · BMC Pulmonary Medicine · doi:10.1186/1471-2466-14-60 · Cited by 94
Gong, X.-M., Li, Y., Luo, J., Wang, J., Wei, J. N., Wang, J.-Q., Xiao, T., Xie, C., Hong, J., Ning, G., et al. (2019) · Nature Metabolism · doi:10.1038/s42255-019-0065-4 · Cited by 93
Albrecht, E., Schering, L., Buck, F., Vlach, K., Schober, H., Drevon, C. A., & Maak, S. (2020) · Molecular Metabolism · doi:10.1016/j.molmet.2020.01.016 · Cited by 93
Muscle Directs Diurnal Energy Homeostasis through a Myokine-Dependent Hormone Module in Drosophila
Zhao, X. L., & Karpac, J. (2017) · Current Biology · doi:10.1016/j.cub.2017.06.004 · Cited by 93
Bai, Z., Chai, X., Yoon, M. J., Kim, H.-J., Lo, K. A., Zhang, Z., Xu, D., Siang, D. T. C., Arcinas, C., Xu, S., et al. (2017) · PLoS Biology · doi:10.1371/journal.pbio.2002176 · Cited by 93
Housing temperature influences exercise training adaptations in mice
Raun, S. H., Henríquez‐Olguín, C., Karavaeva, I. E., Ali, M. S., Møller, L. L. V., Kot, W., Castro-Mejía, J. L., Nielsen, D. S., Gerhart‐Hines, Z., Richter, E. A., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-15311-y · Cited by 93
Yuan, Y., Xu, P., Jiang, Q., Cai, X., Wang, T., Peng, W., Sun, J., Zhu, C., Zhang, C., Yue, D., et al. (2020) · The EMBO Journal · doi:10.15252/embj.2019103304 · Cited by 88
“Many myokines secreted in response to exercise improve glucose homeostasis and protect against obesity, such as irisin (Bostrom et al , 2012), interleukin-15 (IL-15) (Barra et al , 2014), and Mete-orin-like (METRNL) (Rao et al , 2014).”
Li, D.-J., Fu, H., Zhao, T., Ni, M., & Shen, F.-M. (2016) · Metabolism · doi:10.1016/j.metabol.2016.02.009 · Cited by 92
Effects of exercise on brown and beige adipocytes
Dewal, R. S., & Stanford, K. I. (2019) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2018.04.013 · Cited by 92
García-Ruiz, E., Reynés, B., Díaz‐Rúa, R., Ceresi, E., Oliver, P., & Palou, A. (2015) · International Journal of Obesity · doi:10.1038/ijo.2015.112 · Cited by 92
Serum Irisin Levels, Precocious Myocardial Infarction, and Healthy Exceptional Longevity
Emanuele, E., Minoretti, P., Pareja-Galeano, H., Sanchis‐Gomar, F., Garatachea, N., & Lucía, A. (2014) · The American Journal of Medicine · doi:10.1016/j.amjmed.2014.04.025 · Cited by 92
The clinical potential of adipogenesis and obesity-related microRNAs
Zaiou, M., Amri, H. E., & Bakillah, A. (2017) · Nutrition Metabolism and Cardiovascular Diseases · doi:10.1016/j.numecd.2017.10.015 · Cited by 92
Lombardi, G., Ziemann, E., & Banfi, G. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00060 · Cited by 92
Diet quality is associated with circulating C-reactive protein but not irisin levels in humans
Park, K., Zaichenko, L., Peter, P. R., Davis, C. R., Crowell, J. A., & Mantzoros, C. S. (2013) · Metabolism · doi:10.1016/j.metabol.2013.10.011 · Cited by 92
The fat cell senescence hypothesis
Newsholme, P., & de Bittencourt, P. I. H. (2014) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0000000000000077 · Cited by 92
Erythropoietin, a Novel Versatile Player Regulating Energy Metabolism beyond the Erythroid System
Wang, L., Di, L., & Noguchi, C. T. (2014) · International Journal of Biological Sciences · doi:10.7150/ijbs.9518 · Cited by 91
The Role of Irisin in Alzheimer’s Disease
Kim, O. Y., & Song, J. (2018) · Journal of Clinical Medicine · doi:10.3390/jcm7110407 · Cited by 91
Wang, P., Pang, Q., Zhou, T., Song, X., Pan, Y., Jia, L., & Zhang, A.-H. (2022) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2022.02.007 · Cited by 91
Mitochondria and endocrine function of adipose tissue
Medina‐Gómez, G. (2012) · Best Practice & Research Clinical Endocrinology & Metabolism · doi:10.1016/j.beem.2012.06.002 · Cited by 92
Ellefsen, S., Vikmoen, O., Slettaløkken, G., Whist, J. E., Nygaard, H., Hollan, I., Rauk, I., Vegge, G., Strand, T. A., Raastad, T., et al. (2014) · European Journal of Applied Physiology · doi:10.1007/s00421-014-2922-x · Cited by 91
Stier, A., Bize, P., Habold, C., Bouillaud, F., Massemin, S., & Criscuolo, F. (2013) · Journal of Experimental Biology · doi:10.1242/jeb.092700 · Cited by 91
Parr, E. B., CAMERA, D. M., Burke, L. M., Phillips, S. M., Coffey, V. G., & Hawley, J. A. (2016) · PLoS ONE · doi:10.1371/journal.pone.0152545 · Cited by 91
Novel Browning Agents, Mechanisms, and Therapeutic Potentials of Brown Adipose Tissue
Wankhade, U. D., Shen, M., Yadav, H., & Thakali, K. M. (2016) · BioMed Research International · doi:10.1155/2016/2365609 · Cited by 91
Metabolic regulation and the anti-obesity perspectives of human brown fat
Schéele, C., & Nielsen, S. J. (2017) · Redox Biology · doi:10.1016/j.redox.2017.04.011 · Cited by 92
Molecular mechanisms of FOXO1 in adipocyte differentiation
Chen, J., Lü, Y., Tian, M., & Huang, Q. (2019) · Journal of Molecular Endocrinology · doi:10.1530/jme-18-0178 · Cited by 91
Single cell approaches to address adipose tissue stromal cell heterogeneity
Rondini, E. A., & Granneman, J. G. (2020) · Biochemical Journal · doi:10.1042/bcj20190467 · Cited by 90
Searching for the link between inflammaging and sarcopenia
Wang, T. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101611 · Cited by 90
Zhou, W., Shi, Y., Wang, H., Chen, L., Yu, C., Zhang, X., Yang, L., Zhang, X., & Wu, A. (2022) · Experimental & Molecular Medicine · doi:10.1038/s12276-022-00811-2 · Cited by 90
Moon, H., & Mantzoros, C. S. (2013) · Metabolism · doi:10.1016/j.metabol.2013.10.005 · Cited by 90
Moreno, M., Moreno‐Navarrete, J. M., Serrano, M., Ortega, F. J., Delgado, E., Sánchez-Ragnarsson, C., Valdés, S., Botas, P., Ricart, W., & Fernández‐Real, J. M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0124100 · Cited by 90
Adipose Tissue Biology and Cardiomyopathy
Turer, A. T., Hill, J. A., Elmquist, J. K., & Scherer, P. E. (2012) · Circulation Research · doi:10.1161/circresaha.111.262493 · Cited by 91
Irisin immunohistochemistry in gastrointestinal system cancers
Aydın, S., Kuloğlu, T., Özercan, M. R., Albayrak, S., Aydın, S., Bakal, Ü., Yılmaz, M., Kalaycı, M. Z., Yardım, M., Saraç, M., et al. (2016) · Biotechnic & Histochemistry · doi:10.3109/10520295.2015.1136988 · Cited by 90
Tu, Y., Liu, J., Kong, D., Guo, X., Li, J., Long, Z., Peng, J., Wang, Z., Wu, H., Liu, P., et al. (2023) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2023.03.014 · Cited by 89
Gerhard, G. S., Styer, A. M., Strodel, W. E., Roesch, S. L., Yavorek, A., Carey, D. J., Wood, G. C., Petrick, A. T., Gabrielsen, J. D., Ibele, A. R., et al. (2013) · International Journal of Obesity · doi:10.1038/ijo.2013.152 · Cited by 89
Circulating Irisin Concentrations in Rat Models of Thyroid Dysfunction — Effect of Exercise
Samy, D. M., Ismail, C. A., & Nassra, R. A. (2015) · Metabolism · doi:10.1016/j.metabol.2015.01.001 · Cited by 89
HDAC3 is a molecular brake of the metabolic switch supporting white adipose tissue browning
Ferrari, A., Longo, R., Fiorino, E., Silva, R., Mitro, N., Cermenati, G., Gilardi, F., Desvergne, B., Andolfo, A., Magagnotti, C., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-00182-7 · Cited by 89
Exercise, redox system and neurodegenerative diseases
Quan, H., Koltai, E., Suzuki, K., Aguiar, A. S., Pinho, R. A., Boldogh, I. R., Berkes, I., & Radak, Z. O. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2020.165778 · Cited by 89
Bi, J., Zhang, J., Ren, Y., Du, Z., Zhang, Y., Liu, C., Wang, Y., Zhang, L., Shi, Z., Wu, Z., et al. (2020) · JCI Insight · doi:10.1172/jci.insight.136277 · Cited by 89
Metadata
- Authors
- Boström, P., Wu, J., Jedrychowski, M. P., Korde, A., Ye, L., Lo, J. C., Rasbach, K. A., Boström, E. A., Choi, J. H., Long, J. Z., Kajimura, S., Zingaretti, M. C., Vind, B. F., Tu, H., Cinti, S., Højlund, K., Gygi, S. P., & Spiegelman, B. M.
- Affiliations
- Harvard University (US)
- Brigham and Women's Hospital (US)
- University of California, San Francisco (US)
- Marche Polytechnic University (IT)
- Odense University Hospital (DK)
- LakePharma (United States) (US)
- Corresponding author
- Spiegelman, Bruce M.
- ORCID
- Venue
- Nature
- Published
- 2012-01
- Volume
- 481
- Issue
- 7382
- Pages
- 463-468
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC3522098
- OpenAlex
- W2085397620
- Cited by
- 4,810
- References
- 26
- Citations by year
- 2026: 309 · 2025: 347 · 2024: 361 · 2023: 392 · 2022: 453 · 2021: 408 · 2020: 393 · 2019: 331 · 2018: 318 · 2017: 294 · 2016: 275 · 2015: 292 · 2014: 283 · 2013: 229 · 2012: 120
- FWCI
- 198.16
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- University of Southern Denmark Research Portal (University of Southern Denmark) (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion, cc-by)
- RePEc: Research Papers in Economics (submittedVersion)
- Università Politecnica delle Marche (Università Politecnica delle Marche) (submittedVersion)
- Scholarworks@UNIST (Ulsan National Institute of Science and Technology) (submittedVersion)
- Funders
- National Institute of Diabetes and Digestive and Kidney Diseases (K99DK087853, DK54477, R56DK054477, R01DK031405, DK-31405, R01DK061562, R01DK054477, R37DK031405)
- Topics
- Health Sciences › Medicine › Physiology (medical) › Adipose Tissue and Metabolism
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adipokines, Inflammation, and Metabolic Diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Peroxisome Proliferator-Activated Receptors
- Keywords
- irisin, FNDC5, PGC-1α, myokines, brown adipose tissue browning, white adipose tissue, thermogenesis, UCP1, physical activity, energy expenditure, obesity, glucose homeostasis, type 2 diabetes, metabolic disease treatment
- MeSH terms
- Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha, Uncoupling Protein 1, Animals, Adipose Tissue, Brown, Cells, Cultured, Energy Metabolism, Gene Expression Regulation, Hormones, Humans, Insulin Resistance, Ion Channels, Mice, Inbred BALB C, Mice, Transgenic, Obesity, Physical Conditioning, Animal, Plasma, Transcription Factors, Exercise, Trans-Activators, Culture Media, Conditioned, Adipocytes, Cell Respiration, Thermogenesis, Models, Animal, Mitochondrial Proteins, Muscle Cells, Intracellular Signaling Peptides and Proteins, Subcutaneous Fat, Mice, Adipose Tissue, White
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.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review