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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.
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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]
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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
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Items 901–1,000 of 1,068
Narayanan, S. A., Metzger, C. E., Bloomfield, S. A., & Zawieja, D. C. (2018) · The FASEB Journal · doi:10.1096/fj.201800178r · Cited by 69
Decreased Concentration of Irisin Is Associated with Poor Functional Outcome in Ischemic Stroke
Tu, W., Qiu, H., Cao, J., Liu, Q., Zeng, X., & Zhao, J.-Z. (2018) · Neurotherapeutics · doi:10.1007/s13311-018-0651-2 · Cited by 69
Exercise-Induced Irisin, the Fat Browning Myokine, as a Potential Anticancer Agent
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Ma, E. B., Sahar, N.-E., Jeong, M., & Huh, J. Y. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.01085 · Cited by 69
Functional effects of muscle PGC-1alpha in aged animals
Yang, S., Loro, E., Wada, S., Kim, B., Tseng, W.-J., Li, K., Khurana, T. S., & Arany, Z. (2020) · Skeletal Muscle · doi:10.1186/s13395-020-00231-8 · Cited by 68
Hugues, N., Pellegrino, C., Rivera, C., Berton, É., Pin-Barre, C., & Laurin, J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22063003 · Cited by 68
Scheel, A. K., Espelage, L., & Chadt, A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23094759 · Cited by 68
Mittenbühler, M. J., Jedrychowski, M. P., Vranken, J. G. V., Sprenger, H., Wilensky, S. E., Dumesic, P. A., Sun, Y., Tartaglia, A., Laznik-Bogoslavski, D., Mu, A., et al. (2023) · Cell Metabolism · doi:10.1016/j.cmet.2022.12.014 · Cited by 68
Self-citationAging and homeostasis of the hypodermis in the age-related deterioration of skin function
Liu, M., Lu, F., & Feng, J. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-06818-z · Cited by 71
Emerging Regulation and Function of Betatrophin
Tseng, Y., Yeh, Y., Chen, W.-J., & Lin, K. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms151223640 · Cited by 68
Maternal diet, bioactive molecules, and exercising as reprogramming tools of metabolic programming
Mathias, P. C. D. F., Elmhiri, G., de Oliveira, J. C., Delayre‐Orthez, C., Barella, L. F., Tófolo, L. P., Fabricio, G. S., Chango, A., & Abdennebi‐Najar, L. (2014) · European Journal of Nutrition · doi:10.1007/s00394-014-0654-7 · Cited by 68
BMP7 Drives Human Adipogenic Stem Cells into Metabolically Active Beige Adipocytes
Okla, M., Ha, J., Temel, R. E., & Chung, S. (2014) · Lipids · doi:10.1007/s11745-014-3981-9 · Cited by 68
Chang, C. L., Huang, S. Y., Soong, Y. K., Cheng, P. J., Wang, C., & Liang, I. T. (2014) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2014-1180 · Cited by 68
A Review on the Role of Irisin in Insulin Resistance and Type 2 Diabetes Mellitus.
Gizaw, M., Anandakumar, P., & Tolessa, D. (2017) · Europe PMC (PubMed Central) · doi:10.3831/kpi.2017.20.029 · Cited by 68
RetractedRuiz, J. R., Martínez‐Téllez, B., Sánchez‐Delgado, G., Osuna‐Prieto, F. J., Rensen, P. C. N., & Boon, M. R. (2018) · Progress in Cardiovascular Diseases · doi:10.1016/j.pcad.2018.07.002 · Cited by 68
Preventive and Therapeutic Potential of Physical Exercise in Neurodegenerative Diseases
Marques‐Aleixo, I., Beleza, J., Sampaio, A., Stevanović, J., Coxito, P. M., Gonçalves, I. O., Ascensão, A. A. M. R., & Magalhães, J. (2020) · Antioxidants and Redox Signaling · doi:10.1089/ars.2020.8075 · Cited by 68
Shortcuts to a functional adipose tissue: The role of small non-coding RNAs
Brandão, B. B., Guerra, B. A., & Mori, M. A. (2017) · Redox Biology · doi:10.1016/j.redox.2017.01.020 · Cited by 67
Adipose mTORC1 Suppresses Prostaglandin Signaling and Beige Adipogenesis via the CRTC2-COX-2 Pathway
Zhang, X., Luo, Y., Wang, C., Ding, X., Yang, X., Wu, D., Silva, F. D., Yang, Z., Zhou, Q., Wang, L., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.08.055 · Cited by 67
The Effect of Irisin as a Metabolic Regulator and Its Therapeutic Potential for Obesity
Li, H., Wang, F., Mu, Y., Sun, J., Zhao, Y. C., & Tang, D. (2021) · International Journal of Endocrinology · doi:10.1155/2021/6572342 · Cited by 67
Fndc5 overexpression facilitated neural differentiation of mouse embryonic stem cells
Forouzanfar, M., Rabiee, F., Ghaedi, K., Beheshti, S., Tanhaei, S., Nejati, A. S., Farshbaf, M. J., Baharvand, H., & Nasr‐Esfahani, M. H. (2015) · Cell Biology International · doi:10.1002/cbin.10427 · Cited by 67
Increased levels of irisin in people with long‐standing Type 1 diabetes
Espes, D., Lau, J., & Carlsson, P. (2015) · Diabetic Medicine · doi:10.1111/dme.12731 · Cited by 67
Influencing Factors of Thermogenic Adipose Tissue Activity
Zhang, G., Sun, Q., & Liu, C. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2016.00029 · Cited by 68
Myostatin signals through miR-34a to regulate Fndc5 expression and browning of white adipocytes
Ge, X., Sathiakumar, D., Lua, B.-N., Kukreti, H., Lee, M., & McFarlane, C. (2016) · International Journal of Obesity · doi:10.1038/ijo.2016.110 · Cited by 67
Activation and recruitment of brown adipose tissue by cold exposure and food ingredients in humans
Saito, M., Yoneshiro, T., & Matsushita, M. (2016) · Best Practice & Research Clinical Endocrinology & Metabolism · doi:10.1016/j.beem.2016.08.003 · Cited by 67
Brown and Beige Adipose Tissue
Mulya, A., & Kirwan, J. P. (2016) · Endocrinology and Metabolism Clinics of North America · doi:10.1016/j.ecl.2016.04.010 · Cited by 68
Non‐shivering thermogenesis as a mechanism to facilitate sustainable weight loss
Palmer, B. F., & Clegg, D. J. (2017) · Obesity Reviews · doi:10.1111/obr.12563 · Cited by 67
Plasma irisin is elevated in type 2 diabetes and is associated with increased E-selectin levels
Rana, K. S., Pararasa, C., Afzal, I., Nagel, D. A., Hill, E. J., Bailey, C. J., Griffiths, H. R., Kyrou, I., Randeva, H. S., Bellary, S., et al. (2017) · Cardiovascular Diabetology · doi:10.1186/s12933-017-0627-2 · Cited by 67
Do skeletal muscle-secreted factors influence the function of pancreatic β-cells?
Barlow, J. P., & Solomon, T. P. J. (2017) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00353.2017 · Cited by 67
Adipose tissue inflammation and metabolic dysfunction: role of exercise.
(2014) · Europe PMC (PubMed Central) · Cited by 67
Re Cecconi, A. D., Forti, M., Chiappa, M., Zhu, Z., Zingman, L. V., Cervo, L., Beltrame, L., Marchini, S., & Piccirillo, R. (2019) · Cancers · doi:10.3390/cancers11101541 · Cited by 66
de la Iglesia, R., Lopez‐Legarrea, P., Crujeiras, A. B., Pardo, M., Casanueva, F. F., Zulet, M. Á., & Martínez, J. A. (2013) · Clinical Endocrinology · doi:10.1111/cen.12383 · Cited by 66
Tao, L., Wang, J., Wang, K., Liu, Q., Li, H., Xu, S., Gu, C., & Zhu, Y. (2024) · Aging Cell · doi:10.1111/acel.14181 · Cited by 66
Li, D., Huang, F., Lu, W., Jiang, G. ‐., Deng, Y., & Shen, F. (2014) · Acta Physiologica · doi:10.1111/apha.12421 · Cited by 66
Human adipose dynamics and metabolic health
Feng, B., Zhang, T., & Xu, H. (2013) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12009 · Cited by 66
Serum irisin concentration in women with gestational diabetes
Kuźmicki, M., Telejko, B., Lipińska, D., Pliszka, J., Szamatowicz, M., Wilk, J., Zbucka-Krętowska, M., Laudański, P., Kretowski, A. J., Górska, M., et al. (2014) · Gynecological Endocrinology · doi:10.3109/09513590.2014.920006 · Cited by 66
Peripheral signalling involved in energy homeostasis control
Lancha, A., Frühbeck, G., & Gómez‐Ambrosi, J. (2012) · Nutrition Research Reviews · doi:10.1017/s0954422412000145 · Cited by 66
Jiang, C., Cano-Vega, M. A., Yue, F., Kuang, L., Narayanan, N., Uzunallı, G., Merkel, M. P., Kuang, S., & Deng, M. (2017) · Molecular Therapy · doi:10.1016/j.ymthe.2017.05.020 · Cited by 66
Effect of resveratrol on expression of genes involved thermogenesis in mice and humans
Andrade, J. M. O., Barcala-Jorge, A. S., Batista-Jorge, G. C., Paraíso, A. F., de Freitas, K. M., Lelis, D. D. F., Guimarães, A. L. S., de Paula, A. M. B., & Santos, S. H. S. (2019) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2019.108634 · Cited by 66
Exercise–Linked Irisin: Consequences on Mental and Cardiovascular Health in Type 2 Diabetes
Sousa, R. A. L. D., Caria, A. C. I., & Souza, B. S. D. F. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22042199 · Cited by 66
Interplay of adipokines and myokines in cancer pathophysiology: Emerging therapeutic implications
Dalamaga, Μ. (2013) · World Journal of Experimental Medicine · doi:10.5493/wjem.v3.i3.26 · Cited by 66
Sharma, N., Castorena, C. M., & Cartee, G. D. (2012) · Nutrition & Metabolism · doi:10.1186/1743-7075-9-90 · Cited by 65
Irisin ameliorates angiotensin II‐induced cardiomyocyte apoptosis through autophagy
Li, R., Wang, X., Wu, S., Yao, W., Chen, H., Xin, J., Li, H., Lan, J., Xue, K., Li, X., et al. (2019) · Journal of Cellular Physiology · doi:10.1002/jcp.28382 · Cited by 65
Lu, J., Han, S., Lv, X., Li, X., Zhang, Z., Kuang, H., Chen, Z., Lv, C.-A., Peng, W., Yang, Z., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-39710-z · Cited by 67
Crooks, D. R., Natarajan, T. G., Jeong, S. Y., Chen, C., Park, S. Y., Huang, H., Ghosh, M. C., Tong, W.-H., Haller, R. G., Wu, C. H., et al. (2013) · Human Molecular Genetics · doi:10.1093/hmg/ddt393 · Cited by 65
Vamvini, M. T., Aronis, K. N., Panagiotou, G., Huh, J. Y., Chamberland, J. P., Brinkoetter, M. T., Petrou, M., Christophi, C. A., Kales, S. N., Christiani, D. C., et al. (2013) · European Journal of Endocrinology · doi:10.1530/eje-13-0276 · Cited by 65
Zhang, M., Chen, P., Chen, S., Sun, Q., Qc, Z., Jy, C., Yx, L., Xh, C., Ren, M., & Wang, J.-K. (2014) · PubMed · Cited by 65
Boa, B. C. S., Yudkin, J. S., van Hinsbergh, V. W. M., Bouskela, E., & Eringa, E. C. (2017) · British Journal of Pharmacology · doi:10.1111/bph.13732 · Cited by 65
Ursolic acid and mechanisms of actions on adipose and muscle tissue: a systematic review
Katashima, C. K., Silva, V. R. R., Gomes, T. L. N., Pichard, C., & Pimentel, G. D. (2017) · Obesity Reviews · doi:10.1111/obr.12523 · Cited by 65
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Mazur-Biały, A. I. (2017) · Life Sciences · doi:10.1016/j.lfs.2017.03.011 · Cited by 65
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Zhang, X., Wang, X., Yin, H., Zhang, L., Feng, A., Zhang, Q.-X., Yan, L., Bao, B., Hernandez, L. L., Shi, G., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.06.044 · Cited by 65
Sato, H., Taketomi, Y., Miki, Y., Murase, R., Yamamoto, K., & Murakami, M. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107579 · Cited by 65
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Rodrı́guez, A., Becerril, S., Hernández‐Pardos, A. W., & Frühbeck, G. (2020) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2020.04.003 · Cited by 65
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Colaianni, G., Storlino, G., Sanesi, L., Colucci, S. C., & Grano, M. (2020) · Current Osteoporosis Reports · doi:10.1007/s11914-020-00600-8 · Cited by 65
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Senesi, P., Luzi, L., & Terruzzi, I. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21218372 · Cited by 65
Long-Term Effect of Exercise on Irisin Blood Levels—Systematic Review and Meta-Analysis
Jandova, T., Buendía‐Romero, Á., Polanská, H., Hola, V., Říhova, M., Větrovský, T., Courel‐Ibáñez, J., & Šteffl, M. (2021) · Healthcare · doi:10.3390/healthcare9111438 · Cited by 65
Peterson, J. M., Mart, R., & Bond, C. E. (2014) · PeerJ · doi:10.7717/peerj.605 · Cited by 64
The glucose-sensing transcription factor MLX promotes myogenesis via myokine signaling
Hunt, L. C., Xu, B., Finkelstein, D., Fan, Y., Carroll, P. A., Cheng, P.-F., Eisenman, R. N., & Demontis, F. (2015) · Genes & Development · doi:10.1101/gad.267419.115 · Cited by 64
Exercise, Physical Activity, and Cardiometabolic Health
Belanger, M. J., Rao, P., & Robbins, J. (2021) · Cardiology in Review · doi:10.1097/crd.0000000000000417 · Cited by 64
Farì, G., Lunetti, P., Pignatelli, G., Raele, M. V., Cera, A., Mintrone, G., Ranieri, M., Megna, M., & Capobianco, L. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111632 · Cited by 64
Parasitic helminths and their beneficial impact on type 1 and type 2 diabetes
Berbudi, A., Ajendra, J., Wardani, A. P. F., Hoerauf, A. M., & Hübner, M. P. (2015) · Diabetes/Metabolism Research and Reviews · doi:10.1002/dmrr.2673 · Cited by 65
Balaskó, M., Soós, S., Székely, M., & Pétervári, E. (2014) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2014.08.006 · Cited by 64
Dulian, K., Laskowski, R., Grzywacz, T., Kujach, S., Flis, D. J., Smaruj, M., & Ziemann, E. (2015) · Cryobiology · doi:10.1016/j.cryobiol.2015.10.143 · Cited by 64
Ohyama, K., Nogusa, Y., Suzuki, K., Shinoda, K., Kajimura, S., & Bannai, M. (2014) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00354.2014 · Cited by 65
Self-citationMazur-Biały, A. I., Bilski, J., Wójcik-Grzybek, D., Brzozowski, B., Surmiak, M., Hubalewska‐Mazgaj, M., Chmura, A., Magierowski, M., Magierowska, K., Mach, T., et al. (2017) · Nutrients · doi:10.3390/nu9040410 · Cited by 64
Qiu, S., Bosnyák, E., Treff, G., Steinacker, J. M., Niess, A. M., Krüger, K., Mooren, F. C., Zügel, M., & Schümann, U. (2018) · European Journal of Sport Science · doi:10.1080/17461391.2018.1478452 · Cited by 64
Fndc5 loss‐of‐function attenuates exercise‐induced browning of white adipose tissue in mice
Xiong, Y., Wu, Z., Zhang, B., Wang, C., Mao, F., Liu, X., Hu, K., Sun, X., Jin, W. L., & Kuang, S. (2019) · The FASEB Journal · doi:10.1096/fj.201801754rr · Cited by 64
The Impact of Single-Cell Genomics on Adipose Tissue Research
Deutsch, A., Feng, D., Pessin, J. E., & Shinoda, K. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21134773 · Cited by 64
The role of exercise-induced myokines in promoting angiogenesis
Qi, C., Song, X., Wang, H., Yan, Y., & Liu, B. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.981577 · Cited by 63
“Irisin is derived from fibronectin III domain protein 5, which is regulated by the transcription factor PGC1α (Bostrom et al., 2012).”
BackgroundThe Inflammatory Profile of Obesity and the Role on Pulmonary Bacterial and Viral Infections
Hornung, F., Rogal, J., Loskill, P., Löffler, B., & Deinhardt‐Emmer, S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22073456 · Cited by 63
Solagna, F., Tezze, C., Lindenmeyer, M. T., Lu, S. Y., Wu, G., Liu, S., Zhao, Y., Mitchell, R., Meyer, C., Omairi, S., et al. (2021) · Journal of Clinical Investigation · doi:10.1172/jci135821 · Cited by 66
The Role of Adipokines in the Pathogenesis of Psoriasis
Kiełbowski, K., Bakinowska, E., Ostrowski, P., Pala, B., Gromowska, E., Gurazda, K., Dec, P., Modrzejewski, A., & Pawlik, A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076390 · Cited by 63
Regulatory mechanisms of macrophage polarization in adipose tissue
Pan, D., Guo, L., Jiang, C., Hu, J., & Hu, X. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1149366 · Cited by 64
Myokine-mediated muscle-organ interactions: Molecular mechanisms and clinical significance
Yi, J., Chen, J., Yao, X., Zhao, Z., Niu, X., Li, X., Sun, J., Ji, Y., Shang, T., Gong, L., et al. (2025) · Biochemical Pharmacology · doi:10.1016/j.bcp.2025.117326 · Cited by 68
MECHANISMS IN ENDOCRINOLOGY: Pathogenesis of type 2 diabetes in South Asians
Bakker, L. E. H., Sleddering, M. A., Schoones, J. W., Meinders, A. E., & Jazet, I. M. (2013) · European Journal of Endocrinology · doi:10.1530/eje-13-0307 · Cited by 63
Brown adipose tissue during puberty and with aging
Rogers, N. H. (2014) · Annals of Medicine · doi:10.3109/07853890.2014.914807 · Cited by 63
Association of irisin concentrations with the presence of diabetic nephropathy and retinopathy
Hu, W., Wang, R., Li, J., Zhang, J., & Wang, W. (2015) · Annals of Clinical Biochemistry International Journal of Laboratory Medicine · doi:10.1177/0004563215582072 · Cited by 63
Quercetin Impacts Expression of Metabolism- and Obesity-Associated Genes in SGBS Adipocytes
Leiherer, A., Stoemmer, K., Muendlein, A., Saely, C. H., Kinz, E., Brandtner, E. M., Fraunberger, P., & Drexel, H. (2016) · Nutrients · doi:10.3390/nu8050282 · Cited by 63
Gao, S., Li, F., Li, H., Yi, H., Liu, Y., & Chen, Y. (2016) · PLoS ONE · doi:10.1371/journal.pone.0147480 · Cited by 63
Association of Serum Irisin Concentrations with Presence and Severity of Coronary Artery Disease
Deng, W. (2016) · Medical Science Monitor · doi:10.12659/msm.897376 · Cited by 63
Benedini, S., Dozio, E., Invernizzi, P. L., Vianello, E., Banfi, G., Terruzzi, I., Luzi, L., & Romanelli, M. M. C. (2017) · Journal of Diabetes Research · doi:10.1155/2017/1039161 · Cited by 63
Glucose Homeostasis: Regulation by Peripheral Circadian Clocks in Rodents and Humans
Gachon, F., Loizides‐Mangold, U., Petrenko, V., & Dibner, C. (2017) · Endocrinology · doi:10.1210/en.2017-00218 · Cited by 63
Meneck, F. D., de Souza, L. V., Oliveira, V., & Franco, M. D. C. (2018) · Nutrition Metabolism and Cardiovascular Diseases · doi:10.1016/j.numecd.2018.04.009 · Cited by 63
Suppression of Endothelial AGO1 Promotes Adipose Tissue Browning and Improves Metabolic Dysfunction
Tang, X., Miao, Y., Luo, Y., Sriram, K., Qi, Z., Lin, F., Gu, Y., Lai, C., Hsu, C., Peterson, K. L., et al. (2020) · Circulation · doi:10.1161/circulationaha.119.041231 · Cited by 63
Lang, X., Zhao, N., He, Q., Li, X., Li, X., Sun, C., & Zhang, X. (2020) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2020.09.015 · Cited by 63
Adipose–Muscle Crosstalk in Age-Related Metabolic Disorders: The Emerging Roles of Adipo-Myokines
Fang, P., She, Y., Yu, M., Min, W., Shang, W., & Zhang, Z. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101829 · Cited by 62
Adipose tissue insulin action and IL-6 signaling after exercise in obese mice
MACPHERSON, R. E. K., HUBER, J. S., FRENDO-CUMBO, S., SIMPSON, J. A., & WRIGHT, D. C. (2015) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000000660 · Cited by 62
Central inhibitory effects on feeding induced by the adipo-myokine irisin
Ferrante, C., Orlando, G., Recinella, L., Leone, S., Chiavaroli, A., Di Nisio, C., Shohreh, R., Manippa, F., Ricciuti, A., Vacca, M., et al. (2016) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2016.09.011 · Cited by 62
Sun, W., Xing, C., Zhao, L., Zhao, P., Yang, G., & Yuan, L. (2020) · Molecular Therapy Nucleic Acids · doi:10.1016/j.omtn.2020.03.016 · Cited by 62
Geng, Z., Fan, W., Zhou, B. R., Ye, C., Tong, Y., Zhou, Y., & Xiong, X. (2019) · Journal of Translational Medicine · doi:10.1186/s12967-019-1857-8 · Cited by 62
Colaianni, G., Sanesi, L., Storlino, G., Brunetti, G., Colucci, S. C., & Grano, M. (2019) · Cells · doi:10.3390/cells8050451 · Cited by 63
Colucci, S. C., Colaianni, G., Brunetti, G., Ferranti, F., Mascetti, G., Mori, G., & Grano, M. (2020) · The FASEB Journal · doi:10.1096/fj.202000216r · Cited by 62
The Role of Irisin in Cancer Disease
Pinkowska, A., Podhorska‐Okołów, M., Dzięgiel, P., & Nowińska, K. (2021) · Cells · doi:10.3390/cells10061479 · Cited by 62
Exercise mimetics: a novel strategy to combat neuroinflammation and Alzheimer’s disease
Zhao, R. (2024) · Journal of Neuroinflammation · doi:10.1186/s12974-024-03031-9 · Cited by 64
Irisin: A true, circulating hormone
Pοlyzos, S. A., Mathew, H., & Mantzoros, C. S. (2015) · Metabolism · doi:10.1016/j.metabol.2015.09.001 · Cited by 62
Free androgen index and Irisin in polycystic ovary syndrome
Li, H., Xu, X., Wang, X., Liao, X., Li, L., Yang, G., & Gao, L. (2015) · Journal of Endocrinological Investigation · doi:10.1007/s40618-015-0403-7 · Cited by 62
Oh, C., Jeon, B. H., Reid Storm, S. N., Jho, S., & No, J.-K. (2017) · Nutrition · doi:10.1016/j.nut.2016.06.004 · Cited by 60
Fuller, O. K., Whitham, M., Mathivanan, S., & Febbraio, M. A. (2020) · Cells · doi:10.3390/cells9102182 · Cited by 60
Irisin promotes fracture healing by improving osteogenesis and angiogenesis
Kan, T., He, Z., Du, J., Xu, M., Cui, J., Han, X., Tong, D., Li, H., Yan, M., & Yu, Z. (2022) · Journal of Orthopaedic Translation · doi:10.1016/j.jot.2022.07.006 · Cited by 60
Myokines as possible therapeutic targets in cancer cachexia
Manole, E., Ceafalan, L. C., Popescu, B. O., Dumitru, C., & Bastian, A. E. (2018) · Journal of Immunology Research · doi:10.1155/2018/8260742 · Cited by 60
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
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