Exercise induces expression of leukaemia inhibitory factor in human skeletal muscle
Open accessAbstract
The leukaemia inhibitory factor (LIF) belongs to the interleukin (IL)-6 cytokine superfamily and is constitutively expressed in skeletal muscle. We tested the hypothesis that LIF expression in human skeletal muscle is regulated by exercise. Fifteen healthy young male volunteers performed either 3 h of cycle ergometer exercise at approximately 60% of VO2,max(n = 8) or rested (n = 7). Muscle biopsies were obtained from the vastus lateralis prior to exercise, immediately after exercise, and at 1.5, 3, 6 and 24 h post exercise. Control subjects had biopsy samples taken at the same time points as during the exercise trial. Skeletal muscle LIF mRNA increased immediately after the exercise and declined gradually during recovery. However, LIF protein was unchanged at the investigated time points. Moreover, we tested the hypothesis that LIF mRNA and protein expressions are modulated by calcium (Ca(2+)) in primary human skeletal myocytes. Treatment of myocytes with the Ca(2+) ionophore, ionomycin, for 6 h resulted in an increase in both LIF mRNA and LIF protein levels. This finding suggests that Ca(2+) may be involved in the regulation of LIF in endurance-exercised skeletal muscle. In conclusion, primary human skeletal myocytes have the capability to produce LIF in response to ionomycin stimulation and LIF mRNA levels increase in skeletal muscle following concentric exercise. The finding that the increase in LIF mRNA levels is not followed by a similar increase in skeletal muscle LIF protein suggests that other exercise stimuli or repetitive stimuli are necessary in order to induce a detectable accumulation of LIF protein.
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
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?
LIF is secreted from human cultured myotubes when electrically stimulated and stimulates satellite cell proliferation.
“LIF protein has been shown to be secreted from human cultured myotubes; when electrically stimulated (50) LIF stimulates satellite cell proliferation (51).”
From Muscle–Organ Crosstalk: The Emerging Roles of Myokines (2020) · cites this paper as [50]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
1 retracted
THIS ARTICLE HAS BEEN RETRACTED Exercise induces interleukin‐8 expression in human skeletal muscle
Akerstrom, T. C. A., Steensberg, A., Keller, P., Keller, C., Penkowa, M., & Pedersen, B. K. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.077610 · Cited by 128 · see citing works
RetractedInterleukin-6-type cytokine signalling through the gp130/Jak/STAT pathway
HEINRICH, P. C., BEHRMANN, I., MÜLLER-NEWEN, G., SCHAPER, F., & GRAEVE, L. (1998) · Biochemical Journal · doi:10.1042/bj3340297 · Cited by 2,130 · see citing works
Calcium oscillations increase the efficiency and specificity of gene expression
Dolmetsch, R. E., Xu, K., & Lewis, R. S. (1998) · Nature · doi:10.1038/31960 · Cited by 1,896 · see citing works
Myogenic satellite cells: physiology to molecular biology
Hawke, T. J., & Garry, D. J. (2001) · Journal of Applied Physiology · doi:10.1152/jappl.2001.91.2.534 · Cited by 1,646 · see citing works
Functional and clinical significance of skeletal muscle architecture
Lieber, R. L., & n, J. F. (2000) · Muscle & Nerve · doi:10.1002/1097-4598(200011)23:11 · Cited by 1,249 · see citing works
Steensberg, A., van Hall, G., Osada, T., Sacchetti, M., Saltin, B., & Pedersen, B. K. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.00237.x · Cited by 1,095 · see citing works
Muscle‐derived interleukin‐6: mechanisms for activation and possible biological roles
FEBBRAIO, M. A., & PEDERSEN, B. K. (2002) · The FASEB Journal · doi:10.1096/fj.01-0876rev · Cited by 875 · see citing works
Optimizing the exercise protocol for cardiopulmonary assessment
Buchfuhrer, M. J., Hansen, J. E., Robinson, T. E., Sue, D. Y., Wasserman, K., & Whipp, B. J. (1983) · Journal of Applied Physiology · doi:10.1152/jappl.1983.55.5.1558 · Cited by 872 · see citing works
Cell-permeant caged InsP3 ester shows that Ca2+ spike frequency can optimize gene expression
Li, W., Llopis, J. L., Whitney, M. A., Zlokarnik, G., & Tsien, R. Y. (1998) · Nature · doi:10.1038/31965 · Cited by 845 · see citing works
Wernbom, M., Augustsson, J., & Thome??, R. (2007) · Sports Medicine · doi:10.2165/00007256-200737030-00004 · Cited by 583 · see citing works
Searching for the exercise factor: is IL-6 a candidate?
Pedersen (2003) · Journal of Muscle Research and Cell Motility · doi:10.1023/a:1026070911202 · Cited by 564 · see citing works
Cullinan, E. B., Abbondanzo, S. J., Anderson, P. S., Pollard, J. W., Lessey, B. A., & Stewart, C. L. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.7.3115 · Cited by 431 · see citing works
Satellite cell activity is required for hypertrophy of overloaded adult rat muscle
Rosenblatt, J. D., Yong, D., & Parry, D. J. (1994) · Muscle & Nerve · doi:10.1002/mus.880170607 · Cited by 356 · see citing works
Nieman, D. C., Davis, J. M., Henson, D. A., Walberg-Rankin, J., Shute, M., Dumke, C. L., Utter, A. C., Vinci, D. M., Carson, J. A., Brown, A., et al. (2003) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01130.2002 · Cited by 353 · see citing works
Nielsen, A. R., Mounier, R., Plomgaard, P., Mortensen, O. H., Penkowa, M., Speerschneider, T., Pilegaard, H., & Pedersen, B. K. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.139618 · Cited by 266 · see citing works
Effects of eccentric and concentric muscle actions in resistance training
Colliander, E. B., & Tesch, P. A. (1990) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1990.tb08973.x · Cited by 221 · see citing works
Negoro, S., Oh, H., Tone, E., Kunisada, K., Fujio, Y., Walsh, K., Kishimoto, T., & Yamauchi‐Takihara, K. (2001) · Circulation · doi:10.1161/01.cir.103.4.555 · Cited by 217 · see citing works
Multiple signaling pathways mediate LIF-induced skeletal muscle satellite cell proliferation
Spangenburg, E. E., & Booth, F. W. (2002) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00574.2001 · Cited by 181 · see citing works
Skeletal troponin I as a marker of exercise-induced muscle damage
Sorichter, S., Mair, J., Koller, A., Gebert, W., Rama, D., Calzolari, C., Artner‐Dworzak, E., & Puschendorf, B. (1997) · Journal of Applied Physiology · doi:10.1152/jappl.1997.83.4.1076 · Cited by 177 · see citing works
Calcineurin signaling and neural control of skeletal muscle fiber type and size
Schiaffino, S., & Serrano, A. (2002) · Trends in Pharmacological Sciences · doi:10.1016/s0165-6147(02)02111-9 · Cited by 165 · see citing works
A muscle precursor cell-dependent pathway contributes to muscle growth after atrophy
Mitchell, P. O., & Pavlath, G. K. (2001) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.2001.281.5.c1706 · Cited by 164 · see citing works
Chan, S. M. H., Carey, A. L., Watt, M. J., & Febbraio, M. A. (2004) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00030.2004 · Cited by 156 · see citing works
Stimulation of myoblast proliferation in culture by leukaemia inhibitory factor and other cytokines
Austin, L., & Burgess, A. W. (1991) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(91)90045-9 · Cited by 152 · see citing works
Impact of three different types of exercise on components of the inflammatory response
Brenner, I., Natale, V. M., Vasiliou, P., Moldoveanu, A., Shek, P. N., & Shephard, R. J. (1999) · European Journal of Applied Physiology and Occupational Physiology · doi:10.1007/s004210050617 · Cited by 145 · see citing works
Barnard, W., Bower, J., Brown, M. A., Murphy, M., & Austin, L. (1994) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(94)90211-9 · Cited by 140 · see citing works
Sakuma, K., Watanabe, K., Sano, M., Uramoto, I., & Totsuka, T. (2000) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/s0167-4889(00)00044-6 · Cited by 120 · see citing works
Exercise induces interleukin‐8 receptor (CXCR2) expression in human skeletal muscle
Frydelund‐Larsen, L., Penkowa, M., Akerstrom, T., Zankari, A., Nielsen, S., & Pedersen, B. K. (2007) · Experimental Physiology · doi:10.1113/expphysiol.2006.034769 · Cited by 106 · see citing works
SECRETION OF IL-6, IL-11 AND LIF BY HUMAN CARDIOMYOCYTES IN PRIMARY CULTURE
Ancey, C., Corbi, P., Froger, J., Delwail, A., Wijdenes, J., Gascan, H., Potreau, D., & Lecron, J. (2002) · Cytokine · doi:10.1006/cyto.2002.1033 · Cited by 99 · see citing works
Interaction between signalling pathways involved in skeletal muscle responses to endurance exercise
Koulmann, N., & Bigard, A. X. (2006) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-005-0030-9 · Cited by 97 · see citing works
Skeletal muscle response to tenotomy
Jamali, A. A., Afshar, P., Abrams, R. A., & Lieber, R. L. (2000) · Muscle & Nerve · doi:10.1002/(sici)1097-4598(200006)23:6 · Cited by 97 · see citing works
Elevated Levels of IL-18 in Plasma and Skeletal Muscle in Chronic Obstructive Pulmonary Disease
Petersen, A. M. W., Penkowa, M., Iversen, M., Frydelund-Larsen, L., Andersen, J. L., Mortensen, J., Lange, P., & Pedersen, B. K. (2007) · Lung · doi:10.1007/s00408-007-9000-7 · Cited by 83 · see citing works
Spangenburg, E. E., & Booth, F. W. (2006) · Cytokine · doi:10.1016/j.cyto.2006.05.001 · Cited by 73 · see citing works
Angelini, C. I., Fanin, M., Menegazzo, E., Freda, M. P., Duggan, D. J., & Hoffman, E. P. (1998) · Muscle & Nerve · doi:10.1002/(sici)1097-4598(199806)21:6 · Cited by 71 · see citing works
Sakuma, K., Watanabe, K., Totsuka, T., Uramoto, I., Sano, M., & Sakamoto, K. (1998) · Acta Neuropathologica · doi:10.1007/s004010050775 · Cited by 34 · see citing works
Roques, M., & Vidal, H. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.48.34005 · Cited by 29 · see citing works
Regulation of the Human Leukemia Inhibitory Factor Gene by ets Transcription Factors
Bamberger, A., Jenatschke, S., Schulte, H. M., Ellebrecht, I., Beil, F. U., & Bamberger, C. M. (2003) · NeuroImmunoModulation · doi:10.1159/000072964 · Cited by 15 · see citing works
Immunolocalization of leukemia inhibitory factor in normal and denervated human muscle
Schoser, B. G. H., Storjohann, S., & Kunze, K. (1998) · Neuroreport · doi:10.1097/00001756-199808240-00029 · Cited by 14 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Muscles, exercise and obesity: skeletal muscle as a secretory organ
Pedersen, B. K., & Febbraio, M. A. (2012) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2012.49 · Cited by 2,909 · see citing works
Muscle–Organ Crosstalk: The Emerging Roles of Myokines
Severinsen, M. C. K., & Pedersen, B. K. (2020) · Endocrine Reviews · doi:10.1210/endrev/bnaa016 · Cited by 1,226 · see citing works
“LIF protein has been shown to be secreted from human cultured myotubes; when electrically stimulated (50) LIF stimulates satellite cell proliferation (51).”
BackgroundExercise is the real polypill.
Fiuza-Luces, C., Garatachea, N., Berger, N. A., & Lucia, A. (2013) · Physiology · doi:10.1152/physiol.00019.2013 · Cited by 791 · see citing works
The diseasome of physical inactivity – and the role of myokines in muscle–fat cross talk
Pedersen, B. K. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2009.179515 · Cited by 631 · see citing works
Role of Inflammation in Muscle Homeostasis and Myogenesis
Costamagna, D., Costelli, P., Sampaolesi, M., & Penna, F. (2015) · Mediators of Inflammation · doi:10.1155/2015/805172 · Cited by 390 · see citing works
Pedersen, B. K. (2013) · Comprehensive physiology · doi:10.1002/cphy.c120033 · Cited by 516 · see citing works
Muscle, Bone, and Fat Crosstalk: The Biological Role of Myokines, Osteokines, and Adipokines
Kirk, B., Feehan, J., Lombardi, G., & Duque, G. (2020) · Current Osteoporosis Reports · doi:10.1007/s11914-020-00599-y · Cited by 510 · see citing works
AMPK in skeletal muscle function and metabolism
Kjøbsted, R., Hingst, J. R., Fentz, J., Foretz, M., Sanz, M.-N., Pehmøller, C. K., Shum, M., Marette, A., Mounier, R., Treebak, J. T., et al. (2017) · The FASEB Journal · doi:10.1096/fj.201700442r · Cited by 496 · see citing works
Exercise-induced immune system response: Anti-inflammatory status on peripheral and central organs
Scheffer, D. D. L., & Latini, A. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2020.165823 · Cited by 509 · see citing works
The Role of Exercise-Induced Myokines in Muscle Homeostasis and the Defense against Chronic Diseases
Brandt, C., & Pedersen, B. K. (2010) · BioMed Research International · doi:10.1155/2010/520258 · Cited by 426 · see citing works
Muscle and bone, two interconnected tissues
Tagliaferri, C., Wittrant, Y., Davicco, M.-J., Walrand, S., & Coxam, V. (2015) · Ageing Research Reviews · doi:10.1016/j.arr.2015.03.002 · Cited by 394 · see citing works
Skeletal Muscle as an Endocrine Organ: The Role of Myokines in Exercise Adaptations
Hoffmann, C., & Weigert, C. (2017) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a029793 · Cited by 393 · see citing works
Exercise-induced myokines and their role in chronic diseases
Pedersen, B. K. (2011) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2011.02.010 · Cited by 358 · see citing works
Adipo-myokines: two sides of the same coin–mediators of inflammation and mediators of exercise
Raschke, S., & Eckel, J. (2013) · Mediators of Inflammation · doi:10.1155/2013/320724 · Cited by 296 · see citing works
Acute Exercise Induces FGF21 Expression in Mice and in Healthy Humans
Kim, K. H., Kim, S. H., Min, Y.-K., Yang, H.-M., Lee, J.-B., & Lee, M.-S. (2013) · PLoS ONE · doi:10.1371/journal.pone.0063517 · Cited by 290 · see citing works
Myokines: The endocrine coupling of skeletal muscle and bone
Gomarasca, M., Banfi, G., & Lombardi, G. (2019) · Advances in clinical chemistry · doi:10.1016/bs.acc.2019.07.010 · Cited by 274 · see citing works
The role of exercise-induced myokines in regulating metabolism
Huh, J. Y. (2018) · Archives of Pharmacal Research · doi:10.1007/s12272-017-0994-y · Cited by 242 · see citing works
Irisin, a Novel Myokine, Regulates Glucose Uptake in Skeletal Muscle Cells via AMPK
Lee, H. J., Lee, J. O., Kim, N., Kim, J. K., Kim, H. I., Lee, Y. W., Kim, S. J., Choi, J., Oh, Y., Kim, J. H., et al. (2015) · Molecular Endocrinology · doi:10.1210/me.2014-1353 · Cited by 219 · see citing works
Edward F. Adolph Distinguished Lecture: Muscle as an endocrine organ: IL-6 and other myokines
Pedersen, B. K. (2009) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00734.2009 · Cited by 214 · see citing works
Metabolic adaptation in obesity and type ii diabetes: myokines, adipokines and hepatokines
Oh, K.-J., Lee, D., Kim, W., Han, B., Lee, S., & Bae, K.-H. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms18010008 · Cited by 210 · see citing works
Hansen, J., Brandt, C., Nielsen, A. R., Hojman, P., Whitham, M., Febbraio, M. A., Pedersen, B. K., & Plomgaard, P. (2011) · Endocrinology · doi:10.1210/en.2010-0868 · Cited by 200 · see citing works
Raschke, S., Eckardt, K., Bjørklund Holven, K., Jensen, J., & Eckel, J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062008 · Cited by 199 · see citing works
Exercise-Induced Myokines With Therapeutic Potential for Muscle Wasting
Piccirillo, R. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00287 · Cited by 190 · see citing works
Crosstalk between adipokines and myokines in fat browning
Rodrı́guez, A., Becerril, S., Ezquerro, S., Méndez-Giménez, L., & Frühbeck, G. (2016) · Acta Physiologica · doi:10.1111/apha.12686 · Cited by 192 · see citing works
Exercise and regulation of adipokine and myokine production
(2015) · Progress in Molecular Biology and Translational Science · doi:10.1016/bs.pmbts.2015.07.002 · Cited by 168 · see citing works
ROS and myokines promote muscle adaptation to exercise
Schéele, C., Nielsen, S. J., & Pedersen, B. K. (2009) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2008.12.002 · Cited by 164 · see citing works
Eckardt, K., Taube, A., & Eckel, J. (2011) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-011-9168-2 · Cited by 157 · see citing works
LIF is a contraction-induced myokine stimulating human myocyte proliferation
Broholm, C., Laye, M. J., Brandt, C., Vadalasetty, R., Pilegaard, H., Pedersen, B. K., & Scheele, C. C. (2011) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01399.2010 · Cited by 155 · see citing works
Sarcopenia and Cognitive Function: Role of Myokines in Muscle Brain Cross-Talk
Scisciola, L., Fontanella, R. A., Surina, S., Cataldo, V., Paolisso, G., & Barbieri, M. (2021) · Life · doi:10.3390/life11020173 · Cited by 143 · see citing works
The search for exercise factors in humans
Catoire, M., & Kersten, S. (2015) · The FASEB Journal · doi:10.1096/fj.14-263699 · Cited by 137 · see citing works
Exercise-induced myokines in health and metabolic diseases
So, B., Kim, H., Kim, J., & Song, W. J. (2014) · Integrative Medicine Research · doi:10.1016/j.imr.2014.09.007 · Cited by 133 · see citing works
Regulation of myokine expression: Role of exercise and cellular stress
Ost, M., Coleman, V., Kasch, J., & Klaus, S. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.02.018 · Cited by 131 · see citing works
Sims, N. A. (2016) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2016.08.003 · Cited by 125 · see citing works
Cytokine response of primary human myotubes in an in vitro exercise model
Scheler, M., Irmler, M., Lehr, S., Hartwig, S., Staiger, H., Al-Hasani, H., Beckers, J., Hrabé de Angelis, M., Häring, H.-U., & Weigert, C. (2013) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00043.2013 · Cited by 123 · see citing works
Egan, B., O’Connor, P. L., Zierath, J. R., & O’Gorman, D. J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0074098 · Cited by 120 · see citing works
Kwon, J. H., Moon, K. M., & Min, K.-W. (2020) · Healthcare · doi:10.3390/healthcare8040378 · Cited by 116 · see citing works
Implications of exercise-induced adipo-myokines in bone metabolism
Lombardi, G., Sanchis‐Gomar, F., Perego, S., Sansoni, V., & Banfi, G. (2015) · Endocrine · doi:10.1007/s12020-015-0834-0 · Cited by 117 · see citing works
Nikolić, N., Görgens, S. W., Thoresen, G. H., Aas, V., Eckel, J., & Eckardt, K. (2016) · Acta Physiologica · doi:10.1111/apha.12830 · Cited by 110 · see citing works
Endurance training enhances skeletal muscle interleukin-15 in human male subjects
Rinnov, A., Yfanti, C., Nielsen, S., Åkerström, T. C. A., Peijs, L., Zankari, A., Fischer, C. P., & Pedersen, B. K. (2014) · Endocrine · doi:10.1007/s12020-013-9969-z · Cited by 103 · see citing works
Philippou, A., Maridaki, M., Theos, A., & Koutsilieris, M. (2012) · Advances in Clinical Chemistry · doi:10.1016/b978-0-12-394383-5.00010-2 · Cited by 91 · see citing works
Irisin, a Link among Fatty Liver Disease, Physical Inactivity and Insulin Resistance
Arias, M., Ranchal, I., Romero‐Gómez, M., & Crespo, J. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms151223163 · Cited by 87 · see citing works
Sarcopenic obesity: Myokines as potential diagnostic biomarkers and therapeutic targets?
Guo, A., Li, K., & Xiao, Q. (2020) · Experimental Gerontology · doi:10.1016/j.exger.2020.111022 · Cited by 83 · see citing works
Lombardi, G., Ziemann, E., & Banfi, G. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00060 · Cited by 88 · see citing works
Influence of Physical Exercise on Neuroimmunological Functioning and Health: Aging and Stress
Archer, T., Fredriksson, A., Schϋtz, E., & Kostrzewa, R. M. (2010) · Neurotoxicity Research · doi:10.1007/s12640-010-9224-9 · Cited by 81 · see citing works
Physical Exercise-Induced Myokines in Neurodegenerative Diseases
Lee, B., Shin, M., Park, Y., Won, S.-Y., & Cho, K. S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22115795 · Cited by 79 · see citing works
Muscle Irisin Response to Aerobic vs HIIT in Overweight Female Adolescents
Archundia-Herrera, C., Macias-Cervantes, M., Ruiz-Muñoz, B., Vargas-Ortiz, K., Kornhauser, C., & Perez-Vazquez, V. (2017) · Diabetology & Metabolic Syndrome · doi:10.1186/s13098-017-0302-5 · Cited by 72 · see citing works
Metabolic Health—The Role of Adipo-Myokines
Gräf, C., & Ferrari, N. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20246159 · Cited by 67 · see citing works
Jia, D., Cai, M., Xi, Y., Du, S., & Tian, Z. (2017) · Life Sciences · doi:10.1016/j.lfs.2017.12.009 · Cited by 64 · see citing works
Pedersen, B. K. (2013) · Comprehensive physiology · doi:10.1002/j.2040-4603.2013.tb00522.x · Cited by 59 · see citing works
Johnson, R. W., White, J. D., Walker, E. C., Martin, T. J., & Sims, N. A. (2014) · Bone · doi:10.1016/j.bone.2014.03.053 · Cited by 59 · see citing works
Current evidence that exercise can increase the number of adult stem cells
Macaluso, F., & Myburgh, K. H. (2012) · Journal of Muscle Research and Cell Motility · doi:10.1007/s10974-012-9302-0 · Cited by 55 · see citing works
Ringleb, M., Javelle, F., Haunhorst, S., Bloch, W., Fennen, L., Baumgart, S., Drube, S., Reuken, P. A., Pletz, M. W., Wagner, H., et al. (2024) · The FASEB Journal · doi:10.1096/fj.202301619r · Cited by 68 · see citing works
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 59 · see citing works
Carter, S., & Solomon, T. P. J. (2018) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-018-2210-4 · Cited by 54 · see citing works
Gogh, I. J. A. E., Alex, S., Stienstra, R., Brenkman, A. B., Kersten, S., & Kalkhoven, E. (2015) · Scientific Reports · doi:10.1038/srep10944 · Cited by 54 · see citing works
Redox Signaling in Widespread Health Benefits of Exercise
Louzada, R. A. N., Bouvière, J., Matta, L., Werneck‐de‐Castro, J. P., Dupuy, C., de Carvalho, D. P., & Fortunato, R. S. (2020) · Antioxidants and Redox Signaling · doi:10.1089/ars.2019.7949 · Cited by 47 · see citing works
Peck, B. D., Murach, K. A., Walton, R. G., Simmons, A. J., Long, D. E., Kosmac, K., Dungan, C. M., Kern, P. A., Bamman, M. M., & Peterson, C. A. (2022) · The FASEB Journal · doi:10.1096/fj.202100182rr · Cited by 45 · see citing works
Thomas, A. C. Q., Stead, C. A., Burniston, J. G., & Phillips, S. M. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2024.08.010 · Cited by 52 · see citing works
Modulatory Effect of Myokines on Reactive Oxygen Species in Ischemia/Reperfusion
Szabó, M. R., Pipicz, M., Csont, T., & Csonka, C. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21249382 · Cited by 45 · see citing works
Cornish, S. M., Bugera, E. M., Duhamel, T. A., Peeler, J. D., & Anderson, J. E. (2020) · European Journal of Applied Physiology · doi:10.1007/s00421-020-04337-1 · Cited by 43 · see citing works
Leukemia inhibitory factor increases glucose uptake in mouse skeletal muscle
Brandt, N., O’Neill, H. M., Kleinert, M., Schjerling, P., Vernet, E., Steinberg, G. R., Richter, E. A., & Jørgensen, S. B. (2015) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00313.2014 · Cited by 35 · see citing works
Du, J., Yang, J., He, Z., Cui, J., Yang, Y., Xu, M., Qu, X., Zhao, N., Yan, M., Li, H., et al. (2020) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2020.585056 · Cited by 34 · see citing works
The regulatory role of dietary factors in skeletal muscle development, regeneration and function
Wang, L., Xu, Z., Ling, D., Li, J., Wang, Y., & Shan, T. (2020) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2020.1828812 · Cited by 33 · see citing works
Adipose tissue and skeletal muscle plasticity modulates metabolic health
Ukropec, J., Ukropcová, B., Kurdiová, T., Gašperíková, D., & Klimeś, I. (2008) · Archives of Physiology and Biochemistry · doi:10.1080/13813450802535812 · Cited by 33 · see citing works
Goh, J., Niksirat, N., & Campbell, K. L. (2014) · Europe PMC (PubMed Central) · Cited by 32 · see citing works
Discordant skeletal muscle gene and protein responses to exercise
Bishop, D. J., Hoffman, N. J., Taylor, D. F., Saner, N. J., Lee, M. J.-C., & Hawley, J. A. (2023) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2023.08.005 · Cited by 32 · see citing works
Hunt, L., & White, J. (2016) · Advances in Experimental Medicine and Biology · doi:10.1007/978-3-319-27511-6_3 · Cited by 31 · see citing works
Ahsan, M., Garneau, L., & Aguer, C. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.1040809 · Cited by 30 · see citing works
Lee, H. J., Lee, J. O., Lee, Y. W., Kim, S. A., Park, S. H., & Kim, H. S. (2016) · Cellular Signalling · doi:10.1016/j.cellsig.2016.10.013 · Cited by 28 · see citing works
Bimodal impact of skeletal muscle on pancreatic β‐cell function in health and disease
Plomgaard, P., Halban, P. A., & Bouzakri, K. (2012) · Diabetes Obesity and Metabolism · doi:10.1111/j.1463-1326.2012.01641.x · Cited by 28 · see citing works
Exercise, Neuroprotective Exerkines, and Parkinson’s Disease: A Narrative Review
Mitchell, A. K., Bliss, R. R., & Church, F. (2024) · Biomolecules · doi:10.3390/biom14101241 · Cited by 32 · see citing works
Decline of regenerative potential of old muscle stem cells: contribution to muscle aging
Sahinyan, K., Lazure, F., Blackburn, D. M., & Soleimani, V. D. (2022) · FEBS Journal · doi:10.1111/febs.16352 · Cited by 25 · see citing works
Капилевич, Л. В., Кироненко, Т. А., Zakharova, A. N., Kotelevtsev, Y. V., Dulin, N. O., & Orlov, S. N. (2015) · Genes & Diseases · doi:10.1016/j.gendis.2015.10.001 · Cited by 23 · see citing works
Legaard, G. E., & Pedersen, B. K. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-814593-7.00013-x · Cited by 24 · see citing works
Effects of Padel Competition on Brain Health-Related Myokines
de la Fuente, F. P., Gallardo, M. P. C., Nestares, T., Martínez-Díaz, I. C., & Páez, L. C. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph18116042 · Cited by 23 · see citing works
Myokines in Appetite Control and Energy Balance
Grannell, A., Kokkinos, A. D., & le Roux, C. W. (2022) · Muscles · doi:10.3390/muscles1010003 · Cited by 23 · see citing works
Liu, W., Zhou, F., Wang, Y., Wang, T., Xing, J. ‐., Zhang, S., Sang, L.-X., Gu, S., & Wang, H. ‐. (2015) · Acta Physiologica · doi:10.1111/apha.12534 · Cited by 23 · see citing works
Hunt, L. C., Coles, C. A., Gorman, C., Tudor, E. M., Smythe, G. M., & White, J. D. (2011) · PLoS Currents · doi:10.1371/currents.rrn1277 · Cited by 22 · see citing works
Glucose ingestion during endurance training in men attenuates expression of myokine receptor
Akerstrom, T. C. A., Krogh‐Madsen, R., Petersen, A. M. W., & Pedersen, B. K. (2009) · Experimental Physiology · doi:10.1113/expphysiol.2009.048983 · Cited by 21 · see citing works
Influence of Nutritional Status and Physical Exercise on Immune Response in Metabolic Syndrome
Lombardo, M., Feraco, A., Bellia, C., Prisco, L., D’Ippolito, I., Padua, E., Storz, M. A., Lauro, D., Caprio, M., & Bellia, A. (2022) · Nutrients · doi:10.3390/nu14102054 · Cited by 21 · see citing works
Interleukin-15 and Other Myokines in Chronic Alcoholics
González‐Reimers, E., Fernández-Rodríguez, C. M., Santolaria-Fernández, F. J., de la Vega-Prieto, M. J., Martín‐González, C., Gómez-Rodrı́guez, M. A., Valls, M. R. A., & Rodrı́guez-Gaspar, M. (2011) · Alcohol and Alcoholism · doi:10.1093/alcalc/agr064 · Cited by 21 · see citing works
Dubé, C., Aguer, C., Adamo, K. B., & Bainbridge, S. A. (2017) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2016-0446 · Cited by 19 · see citing works
Physical Activity, Obesity and Weight Loss Maintenance
Brandt, C., & Pedersen, B. K. (2022) · Handbook of experimental pharmacology · doi:10.1007/164_2021_575 · Cited by 18 · see citing works
Brown, J. C., Spielmann, G., Yang, S., Compton, S. L. E., Jones, L. W., Irwin, M. L., Ligibel, J. A., & Meyerhardt, J. A. (2024) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.13509 · Cited by 18 · see citing works
Identification of CCL5/RANTES as a novel contraction-reducible myokine in mouse skeletal muscle
Ishiuchi, Y., Sato, H., Komatsu, N., Kawaguchi, H., Matsuwaki, T., Yamanouchi, K., Nishihara, M., & Nedachi, T. (2018) · Cytokine · doi:10.1016/j.cyto.2018.03.012 · Cited by 17 · see citing works
Cordingley, D. M., Anderson, J. E., & Cornish, S. M. (2022) · Journal of Science in Sport and Exercise · doi:10.1007/s42978-022-00164-2 · Cited by 15 · see citing works
Komori, T., & Morikawa, Y. (2022) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2022.102686 · Cited by 15 · see citing works
Role of leukemia inhibitory factor in the nervous system and its pathology
Ostašov, P., Houdek, Z., Cendelín, J., & Králíčková, M. (2015) · Reviews in the Neurosciences · doi:10.1515/revneuro-2014-0086 · Cited by 14 · see citing works
Skeletal muscle: a novel and intriguing characteristics as a secretory organ
Aoi, W., & Sakuma, K. (2013) · Biodiscovery · doi:10.7750/biodiscovery.2013.7.2 · Cited by 13 · see citing works
Zakharova, A. N., Кироненко, Т. А., Милованова, К. Г., Орлова, А. А., Dyakova, E. Y., Kalinnikova, J. G., Kabachkova, A. V., Chibalin, A., & Капилевич, Л. В. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.709039 · Cited by 8 · see citing works
Lutosławska, G. (2013) · Human Movement · doi:10.2478/v10038-012-0045-y · Cited by 8 · see citing works
Function of Membrane-Associated Proteoglycans in the Regulation of Satellite Cell Growth
Song, Y. Y. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-27511-6_4 · Cited by 8 · see citing works
Ringleb, M., Javelle, F., Haunhorst, S., Bloch, W., Fennen, L., Baumgart, S., Drube, S., Reuken, P. A., Pletz, M. W., Wagner, H., et al. (2023) · medRxiv · doi:10.1101/2023.05.10.23289790 · Cited by 8 · see citing works
Diagnostic and predictive abilities of myokines in patients with heart failure
Berezin, O. O., Berezina, T. A., Hoppe, U. C., Lichtenauer, M., & Berezin, A. Е. (2024) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2023.12.021 · Cited by 7 · see citing works
Health benefits of physical activity: What role does skeletal muscle-organ crosstalk play?
Powers, S. K., Goldstein, E. R., Lategan-Potgieter, R., Schrager, M. A., Skelton, M., & Demirel, H. A. (2025) · Sports Medicine and Health Science · doi:10.1016/j.smhs.2025.02.010 · Cited by 7 · see citing works
Molecular and Cellular Mechanism of Muscle Regeneration
Sakuma, K., & Yamaguchi, A. (2012) · InTech eBooks · doi:10.5772/48229 · Cited by 4 · see citing works
10 km running race induces an elevation in the plasma myokine level of nonprofessional runners
Marcucci-Barbosa, L. S., Júnior, F. D. A. D. M., Lobo, L. F., Morais, M. G., Moreira, J. M., Vieira, É. L. M., & Nunes-Silva, A. (2019) · Sport Sciences for Health · doi:10.1007/s11332-019-00608-3 · Cited by 7 · see citing works
Skeletal Muscle as Endocrine Organ
Ma, M., Zhang, Z., Hai, B., & Zhang, Y. (2025) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-88361-3_22 · Cited by 6 · see citing works
Halle, J. L., Counts, B. R., Zhang, Q., James, K. M., Puppa, M., Alway, S. E., & Carson, J. A. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1283674 · Cited by 6 · see citing works
Martinelli, A., Andreo, L., Alves, A. N., Terena, S. M. L., Malavazzi, T. C. D. S., Bussadori, S. K., Fernandes, K. P. S., & Mesquita‐Ferrari, R. A. (2020) · Lasers in Medical Science · doi:10.1007/s10103-020-03095-y · Cited by 6 · see citing works
- Authors
- Broholm, C., Mortensen, O. H., Nielsen, S., Akerstrom, T., Zankari, A., Dahl, B., & Pedersen, B. K.
- Affiliations
- Rigshospitalet (DK)
- University of Copenhagen (DK)
- Venue
- The Journal of Physiology
- Publisher
- Wiley
- Published
- 2008-04-14
- Volume
- 586
- Issue
- 8
- Pages
- 2195-2201
- ISSN
- 0022-3751 (ISSN-L)
- 1469-7793
- PMC
- PMC2465206
- OpenAlex
- W1940563701
- Cited by
- 132
- References
- 37
- Citations by year
- 2026: 7 · 2025: 5 · 2024: 10 · 2023: 6 · 2022: 9 · 2021: 5 · 2020: 11 · 2019: 5 · 2018: 5 · 2017: 6 · 2016: 9 · 2015: 14 · 2014: 4 · 2013: 12 · 2012: 9
- FWCI
- 4.99
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- The Journal of Physiology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Research at the University of Copenhagen (University of Copenhagen) (submittedVersion)
- Topics
- Health Sciences › Medicine › Rehabilitation › Exercise and Physiological Responses
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Medicine › Complementary and alternative medicine › Cardiovascular and exercise physiology
- Keywords
- leukemia inhibitory factor, skeletal muscle, physical activity, endurance exercise, calcium signaling, ionomycin, skeletal myocytes, vastus lateralis, muscle biopsy, post-exercise recovery
- MeSH terms
- Adult, Cells, Cultured, Physical Exertion, Gene Expression Regulation, Humans, Male, Muscle Contraction, Physical Endurance, Muscle, Skeletal, Muscle Fibers, Skeletal, Leukemia Inhibitory Factor
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