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Stimuli and sensors that initiate skeletal muscle hypertrophy following resistance exercise
Open accessAbstract
One of the most striking adaptations to exercise is the skeletal muscle hypertrophy that occurs in response to resistance exercise. A large body of work shows that a mammalian target of rapamycin complex 1 (mTORC1)-mediated increase of muscle protein synthesis is the key, but not sole, mechanism by which resistance exercise causes muscle hypertrophy. While much of the hypertrophy signaling cascade has been identified, the initiating, resistance exercise-induced and hypertrophy-stimulating stimuli have remained elusive. For the purpose of this review, we define an initiating, resistance exercise-induced and hypertrophy-stimulating signal as "hypertrophy stimulus," and the sensor of such a signal as "hypertrophy sensor." In this review we discuss our current knowledge of specific mechanical stimuli, damage/injury-associated and metabolic stress-associated triggers, as potential hypertrophy stimuli. Mechanical signals are the prime hypertrophy stimuli candidates, and a filamin-C-BAG3-dependent regulation of mTORC1, Hippo, and autophagy signaling is a plausible albeit still incompletely characterized hypertrophy sensor. Other candidate mechanosensing mechanisms are nuclear deformation-initiated signaling or several mechanisms related to costameres, which are the functional equivalents of focal adhesions in other cells. While exercise-induced muscle damage is probably not essential for hypertrophy, it is still unclear whether and how such muscle damage could augment a hypertrophic response. Interventions that combine blood flow restriction and especially low load resistance exercise suggest that resistance exercise-regulated metabolites could be hypertrophy stimuli, but this is based on indirect evidence and metabolite candidates are poorly characterized.
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“Understanding this mechanobiological connection confirms mechanical loading as the primary upstream driver of ribosome biogenesis”
From Ribosome Biogenesis as a Putative Bottleneck to Skeletal Muscle Hypertrophy: Mechanisms, Human Evidence, and Practical Modulators (2026) · cites this paper as [45]
In the citing paper
“The most defensible interpretation is that load intensity probably matters indirectly through its effects on mechanical tension, motor-unit recruitment, and the feasibility of accumulating productive volume [45,145].”
From Ribosome Biogenesis as a Putative Bottleneck to Skeletal Muscle Hypertrophy: Mechanisms, Human Evidence, and Practical Modulators (2026) · cites this paper as [45]
In the citing paper
“The ribosomal literature provides almost no direct basis for claiming that one of these broad categories is inherently superior for stimulating ribosome biogenesis [45].”
From Ribosome Biogenesis as a Putative Bottleneck to Skeletal Muscle Hypertrophy: Mechanisms, Human Evidence, and Practical Modulators (2026) · cites this paper as [45]
In the citing paper
“mTORC1 is also activated by mechanical stimuli, e.g., induced through resistance training [173]”
From Effects of Skeletal Muscle Hypertrophy on Fat Mass and Glucose Homeostasis in Humans and Animals: A Narrative Review with Systematic Literature Search (2025) · cites this paper as [173]
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1 retracted
Cai, X., Zhu, C., Xu, Y., Jing, Y., Yuan, Y., Wang, L., Wang, S., Zhu, X., Gao, P., Zhang, Y., et al. (2016) · Scientific Reports · doi:10.1038/srep26802 · Cited by 54
RetractedRole of YAP/TAZ in mechanotransduction
Dupont, S., Morsut, L., Aragona, M., Enzo, E., Giulitti, S., Cordenonsi, M., Zanconato, F., Le Digabel, J., Forcato, M., Bicciato, S., et al. (2011) · Nature · doi:10.1038/nature10137 · Cited by 5,979
Progression Models in Resistance Training for Healthy Adults
(2009) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0b013e3181915670 · Cited by 4,332
TSC2 Mediates Cellular Energy Response to Control Cell Growth and Survival
Inoki, K., Zhu, T., & Guan, K.-L. (2003) · Cell · doi:10.1016/s0092-8674(03)00929-2 · Cited by 3,914
Bodine, S. C., Stitt, T. N., Gonzalez, M., Kline, W. O., Stover, G. L., Bauerlein, R., Zlotchenko, E., Scrimgeour, A., Lawrence, J. C., Glass, D. J., et al. (2001) · Nature Cell Biology · doi:10.1038/ncb1101-1014 · Cited by 2,752
Skeletal muscle fatigue: cellular mechanisms
Allen, D. G., Lamb, G. D., & Westerblad, H. (2008) · Physiological Reviews · doi:10.1152/physrev.00015.2007 · Cited by 2,495
Mass-spectrometric exploration of proteome structure and function
Aebersold, R., & Mann, M. (2016) · Nature · doi:10.1038/nature19949 · Cited by 2,334
Bidirectional Transport of Amino Acids Regulates mTOR and Autophagy
Nicklin, P., Bergman, P., Zhang, B., Triantafellow, E., Wang, H., Nyfeler, B., Yang, H., Hild, M., Kung, C., Wilson, C., et al. (2009) · Cell · doi:10.1016/j.cell.2008.11.044 · Cited by 1,798
Psychogios, N., Hau, D., Peng, J., Guo, A. C., Mandal, R., Bouatra, S., Sinelnikov, I. V., Krishnamurthy, R., Eisner, R., Gautam, B., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016957 · Cited by 1,779
The underappreciated role of muscle in health and disease
Wolfe, R. R. (2006) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/84.3.475 · Cited by 1,641
Regulation of the Hippo-YAP Pathway by G-Protein-Coupled Receptor Signaling
Yu, F.-X., Zhao, B., Panupinthu, N., Jewell, J. L., Lian, I., Wang, L. H., Zhao, J., Yuan, H., Tumaneng, K., Li, H., et al. (2012) · Cell · doi:10.1016/j.cell.2012.06.037 · Cited by 1,628
Force triggers YAP nuclear entry by regulating transport across nuclear pores
Elosegui-Artola, A., Andreu, I., Beedle, A. E. M., Lezamiz, A., Uroz, M., Kosmalska, A. J., Oria, R., Kechagia, J. Z., Rico-Lastres, P., Le Roux, A.-L., et al. (2017) · Cell · doi:10.1016/j.cell.2017.10.008 · Cited by 1,491
Exercise-Induced Muscle Damage in Humans
Clarkson, P. M., & Hubal, M. J. (2002) · American Journal of Physical Medicine & Rehabilitation · doi:10.1097/00002060-200211001-00007 · Cited by 1,478
The human transcriptome across tissues and individuals
Melé, M., Ferreira, P. G., Reverter, F., DeLuca, D. S., Monlong, J., Sammeth, M., Young, T. R., Goldmann, J. M., Pervouchine, D. D., Sullivan, T. J., et al. (2015) · Science · doi:10.1126/science.aaa0355 · Cited by 1,304
Morton, R. W., Murphy, K. T., McKellar, S. R., Schoenfeld, B. J., Henselmans, M., Helms, E., Aragon, A. A., Devries, M. C., Banfield, L., Krieger, J. W., et al. (2018) · British Journal of Sports Medicine · doi:10.1136/bjsports-2017-097608 · Cited by 1,269
Objectively measured physical capability levels and mortality: systematic review and meta-analysis
Cooper, R., Kuh, D., Hardy, R., Mortality Review Group, & teams, O. B. O. T. F. A. H. S. (2010) · BMJ · doi:10.1136/bmj.c4467 · Cited by 1,166
Mixed muscle protein synthesis and breakdown after resistance exercise in humans
Phillips, S. M., Tipton, K. D., Aarsland, A., Wolf, S. E., & Wolfe, R. R. (1997) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1997.273.1.e99 · Cited by 1,132
Integrin-mediated mechanotransduction
Sun, Z., Guo, S., & Fässler, R. (2016) · The Journal of Cell Biology · doi:10.1083/jcb.201609037 · Cited by 1,128
Interleukin-6 Is an Essential Regulator of Satellite Cell-Mediated Skeletal Muscle Hypertrophy
Serrano, A. L., Baeza-Raja, B., Perdiguero, E., Jardí, M., & Muñoz-Cánoves, P. (2008) · Cell Metabolism · doi:10.1016/j.cmet.2007.11.011 · Cited by 873
Bolster, D. R., Crozier, S. J., Kimball, S. R., & Jefferson, L. S. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.c200171200 · Cited by 851
Schoenfeld, B. J., Grgic, J., Ogborn, D., & Krieger, J. W. (2017) · Journal of Strength and Conditioning Research · doi:10.1519/jsc.0000000000002200 · Cited by 851
Self-citationAppreciating force and shape—the rise of mechanotransduction in cell biology
Iskratsch, T., Wolfenson, H., & Sheetz, M. P. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3903 · Cited by 798
Celis-Morales, C. A., Welsh, P., Lyall, D. M., Steell, L., Petermann, F., Anderson, J., Iliodromiti, S., Sillars, A., Graham, N., Mackay, D. F., et al. (2018) · BMJ · doi:10.1136/bmj.k1651 · Cited by 772
Kumar, V., Selby, A., Rankin, D., Patel, R., Atherton, P., Hildebrandt, W., Williams, J., Smith, K., Seynnes, O., Hiscock, N., et al. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2008.164483 · Cited by 740
Muscle damage and inflammation during recovery from exercise.
Peake, J., Neubauer, O., Gatta, P. D. D., & Nosaka, K. (2016) · Journal of applied physiology · doi:10.1152/japplphysiol.00971.2016 · Cited by 740
Radak, Z. O., Zhao, Z., Koltai, E., Ohno, H., & Atalay, M. (2012) · Antioxidants and Redox Signaling · doi:10.1089/ars.2011.4498 · Cited by 643
Effective fiber hypertrophy in satellite cell-depleted skeletal muscle
McCarthy, J. J., Mula, J., Miyazaki, M., Erfani, R., Garrison, K., Farooqui, A. B., Srikuea, R., Lawson, B. A., Grimes, B., Keller, C., et al. (2011) · Development · doi:10.1242/dev.068858 · Cited by 616
Miller, B. F., Olesen, J. L., Hansen, M., Døssing, S., Crameri, R. M., Welling, R. J., Langberg, H., Flyvbjerg, A., Kjaer, M., Babraj, J. A., et al. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2005.093690 · Cited by 610
Paulsen, G., Mikkelsen, U. R., Raastad, T., & Peake, J. M. (2026) · PubMed · doi:10.22029/eir.2012.1668 · Cited by 572
Chaperone-Assisted Selective Autophagy Is Essential for Muscle Maintenance
Arndt, V., Dick, N., Tawo, R., Dreiseidler, M., Wenzel, D., Hesse, M., Fürst, D. O., Säftig, P., Saint, R. B., Fleischmann, B. K., et al. (2010) · Current Biology · doi:10.1016/j.cub.2009.11.022 · Cited by 572
Comparative Study of Injury Models for Studying Muscle Regeneration in Mice
Hardy, D., Besnard, A., Latil, M., Jouvion, G., Briand, D., Thépenier, C., Pascal, Q., Guguin, A., Gayraud-Morel, B., Cavaillon, J., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0147198 · Cited by 546
Schoenfeld, B. J. (2013) · Sports Medicine · doi:10.1007/s40279-013-0017-1 · Cited by 538
Low intensity blood flow restriction training: a meta-analysis
Loenneke, J. P., Wilson, J. M., Marin, P. J., Zourdos, M. C., & Bemben, M. G. (2011) · European Journal of Applied Physiology · doi:10.1007/s00421-011-2167-x · Cited by 532
Computational prediction of human metabolic pathways from the complete human genome
Romero, P. R., Wagg, J., GREEN, M. L., Kaiser, D., Krummenacker, M., & Karp, P. D. (2004) · Genome biology · doi:10.1186/gb-2004-6-1-r2 · Cited by 512
YAP mediates crosstalk between the Hippo and PI(3)K–TOR pathways by suppressing PTEN via miR-29
Tumaneng, K., Schlegelmilch, K., Russell, R. C., Yimlamai, D., Basnet, H., Mahadevan, N., Fitamant, J., Bardeesy, N., Camargo, F. D., & Guan, K.-L. (2012) · Nature Cell Biology · doi:10.1038/ncb2615 · Cited by 453
Hashimoto, T., Hussien, R., Oommen, S., Gohil, K., & Brooks, G. A. (2007) · The FASEB Journal · doi:10.1096/fj.07-8174com · Cited by 442
Drummond, M. J., Fry, C. S., Glynn, E. L., Dreyer, H. C., Dhanani, S., Timmerman, K. L., Volpi, E., & Rasmussen, B. B. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2008.163816 · Cited by 439
Petrella, J. K., Kim, J.-S., Mayhew, D. L., Cross, J. M., & Bamman, M. M. (2008) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01215.2007 · Cited by 435
Hoffman, N. J., Parker, B. L., Chaudhuri, R., Fisher-Wellman, K. H., Kleinert, M., Humphrey, S. J., Yang, P., Holliday, M., Trefely, S., Fazakerley, D. J., et al. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.09.001 · Cited by 426
Hameed, M., Orrell, R. W., COBBOLD, M., Goldspink, G., & Harridge, S. D. R. (2002) · The Journal of Physiology · doi:10.1111/j.1469-7793.2003.00247.x · Cited by 420
Street, S. F. (1983) · Journal of Cellular Physiology · doi:10.1002/jcp.1041140314 · Cited by 401
Chronic Adaptations to Eccentric Training: A Systematic Review
Douglas, J. M., Pearson, S. N., Ross, A., & McGuigan, M. R. (2016) · Sports Medicine · doi:10.1007/s40279-016-0628-4 · Cited by 385
Characterization of a novel protein‐binding module — the WW domain
Sudol, M., Chen, H. I., Bougeret, C., Einbond, A., & Peer Bork, B. (1995) · FEBS Letters · doi:10.1016/0014-5793(95)00550-s · Cited by 381
Applications of vascular occlusion diminish disuse atrophy of knee extensor muscles
Takarada, Y., Takazawa, H., & Ishii, N. (2000) · Medicine & Science in Sports & Exercise · doi:10.1097/00005768-200012000-00011 · Cited by 377
RAP2 mediates mechanoresponses of the Hippo pathway
Meng, Z., Qiu, Y., Lin, K. C., Kumar, A., Placone, J. K., Fang, C., Wang, K.-C., Lu, S., Pan, M., Hong, A. W., et al. (2018) · Nature · doi:10.1038/s41586-018-0444-0 · Cited by 377
Changes in indicators of inflammation after eccentric exercise of the elbow flexors
Nosaka, K., & Clarkson, P. M. (1996) · Medicine & Science in Sports & Exercise · doi:10.1097/00005768-199608000-00003 · Cited by 365
Muscular Atrophy Following Immobilisation
Appell, H.-J. (1990) · Sports Medicine · doi:10.2165/00007256-199010010-00005 · Cited by 358
Mechanoenzymatics of titin kinase
Puchner, E. M., Alexandrovich, A., Kho, A. L., Hensen, U., Schäfer, L. V., Brandmeier, B., Gräter, F., Grubmüller, H., Gaub, H. E., & Gautel, M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0805034105 · Cited by 347
Lengthening our perspective: Morphological, cellular, and molecular responses to eccentric exercise
Hyldahl, R. D., & Hubal, M. J. (2014) · Muscle and Nerve · doi:10.1002/mus.24077 · Cited by 343
Hameed, M., Orrell, R. W., COBBOLD, M., et al. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2002.032136 · Cited by 337
Paulsen, G., Cumming, K. T., Holden, G., Hallén, J., Rønnestad, B. R., Sveen, O., Skaug, A., Paur, I., Bastani, N. E., Østgaard, H. N., et al. (2014) · The Journal of Physiology · doi:10.1113/jphysiol.2013.267419 · Cited by 333
Skeletal Muscle Hypertrophy After Aerobic Exercise Training
Konopka, A. R., & Harber, M. P. (2014) · Exercise and Sport Sciences Reviews · doi:10.1249/jes.0000000000000007 · Cited by 320
Piazzesi, G., Reconditi, M., Linari, M., Lucii, L., Bianco, P., Brunello, E., Decostre, V., Stewart, A., Gore, D. B., Irving, T. C., et al. (2007) · Cell · doi:10.1016/j.cell.2007.09.045 · Cited by 320
Crameri, R. M., Aagaard, P., Qvortrup, K., Langberg, H., Olesen, J., & Kjær, M. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.128827 · Cited by 319
Alpha‐ketoglutarate: physiological functions and applications
Wu, N., Yang, M., Gaur, U., Xu, H., Yao, Y., & Li, D. (2016) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2015.078 · Cited by 316
Hornberger, T. A., Chu, W. K., Mak, Y. W., Hsiung, J. W., Huang, S. A., & Chien, S. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0600678103 · Cited by 312
The role of skeletal muscle mTOR in the regulation of mechanical load‐induced growth
Goodman, C. A., Frey, J. W., Mabrey, D. M., Jacobs, B. L., Lincoln, H. C., You, J., & Hornberger, T. A. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2011.218255 · Cited by 297
Cellular Mechanotransduction Relies on Tension-Induced and Chaperone-Assisted Autophagy
Ulbricht, A., Eppler, F. J., Tapia, V. E., van der Ven, P. F. M., Hampe, N., Hersch, N., Vakeel, P., Stadel, D., Haas, A., Saftig, P., et al. (2013) · Current Biology · doi:10.1016/j.cub.2013.01.064 · Cited by 288
Muscle fiber necrosis associated with human marathon runners
Hikida, R. S., Staron, R. S., Hagerman, F. C., Sherman, W. M., & Costill, D. L. (1983) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(83)90037-0 · Cited by 276
Regulation of the muscle fiber micro environment by activated satellite cells during hypertrophy
Fry, C. S., Lee, J. D., Jackson, J. R., Kirby, T. J., Stasko, S. A., Liu, H., Dupont‐Versteegden, E. E., McCarthy, J. J., & Peterson, C. A. (2014) · The FASEB Journal · doi:10.1096/fj.13-239426 · Cited by 273
Moore, D. R., Phillips, S. M., Babraj, J. A., Smith, K., & Rennie, M. J. (2005) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00387.2004 · Cited by 268
Changes in satellite cells in human skeletal muscle after a single bout of high intensity exercise.
Crameri, R. M., Langberg, H., Magnusson, P., Jensen, C. H., Schrøder, H. D., Olesen, J. L., Suetta, C., Teisner, B., & Kjaer, M. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.061846 · Cited by 262
Muscle metabolism during intense, heavy-resistance exercise
Tesch, P. A., Colliander, E. B., & Kaiser, P. (1986) · European Journal of Applied Physiology and Occupational Physiology · doi:10.1007/bf00422734 · Cited by 259
Does Exercise-Induced Muscle Damage Play a Role in Skeletal Muscle Hypertrophy?
Schoenfeld, B. J. (2012) · The Journal of Strength and Conditioning Research · doi:10.1519/jsc.0b013e31824f207e · Cited by 258
Damas, F., Libardi, C. A., & Ugrinowitsch, C. (2018) · European Journal of Applied Physiology · doi:10.1007/s00421-017-3792-9 · Cited by 254
Intramuscular metabolism during low-intensity resistance exercise with blood flow restriction
Suga, T., Okita, K., Morita, N., Yokota, T., Hirabayashi, K., Horiuchi, M., Takada, S., Takahashi, T., Omokawa, M., Kinugawa, S., et al. (2009) · Journal of Applied Physiology · doi:10.1152/japplphysiol.90368.2008 · Cited by 253
BAG3 Deficiency Results in Fulminant Myopathy and Early Lethality
Homma, S., Iwasaki, M., Shelton, G. D., Engvall, E., Reed, J. C., & Takayama, S. (2006) · The American Journal of Pathology · doi:10.2353/ajpath.2006.060250 · Cited by 243
The sarcomeric Z-disc: a nodal point in signalling and disease
Frank, D., Kuhn, C., Katus, H. A., & Frey, N. (2006) · Journal of Molecular Medicine · doi:10.1007/s00109-005-0033-1 · Cited by 235
O’Neil, T. K., Duffy, L. R., Frey, J. W., & Hornberger, T. A. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2009.173609 · Cited by 230
3 The Metabolic Effects of Exercise-Induced Muscle Damage
Evans, W. J., & Cannon, J. G. (1991) · Exercise and Sport Sciences Reviews · doi:10.1249/00003677-199101000-00003 · Cited by 230
Satellite cell depletion prevents fiber hypertrophy in skeletal muscle
Egner, I. M., Bruusgaard, J. C., & Gundersen, K. (2016) · Development · doi:10.1242/dev.134411 · Cited by 216
Hansen, C. G., Ng, Y. L. D., Lam, W.-L. M., Plouffe, S. W., & Guan, K.-L. (2015) · Cell Research · doi:10.1038/cr.2015.140 · Cited by 212
Suga, T., Okita, K., Takada, S., Omokawa, M., Kadoguchi, T., Yokota, T., Hirabayashi, K., Takahashi, M., Morita, N., Horiuchi, M., et al. (2012) · European Journal of Applied Physiology · doi:10.1007/s00421-012-2377-x · Cited by 207
Effect of range of motion in heavy load squatting on muscle and tendon adaptations
Bloomquist, K., Langberg, H., Karlsen, S. F., Madsgaard, S., Boesen, M., & Raastad, T. (2013) · European Journal of Applied Physiology · doi:10.1007/s00421-013-2642-7 · Cited by 204
Selcen, D. (2011) · Neuromuscular Disorders · doi:10.1016/j.nmd.2010.12.007 · Cited by 202
Manimmanakorn, A., Hamlin, M. J., Ross, J. J., Taylor, R., & Manimmanakorn, N. (2012) · Journal of science and medicine in sport · doi:10.1016/j.jsams.2012.08.009 · Cited by 196
Lee, M. N., Ha, S. H., Kim, J. J., Koh, A., Lee, C. S., Kim, J. H., Jeon, H., Kim, D., Suh, P., & Ryu, S. H. (2009) · Molecular and Cellular Biology · doi:10.1128/mcb.00165-09 · Cited by 196
Farup, J., de Paoli, F., Bjerg, K., Riis, S., Ringgard, S., & Vissing, K. (2015) · Scandinavian Journal of Medicine & Science in Sports · doi:10.1111/sms.12396 · Cited by 195
Macnaughton, L. S., Wardle, S. L., Witard, O. C., McGlory, C., Hamilton, D. L., Jeromson, S., Lawrence, C. E., Wallis, G. A., & Tipton, K. D. (2016) · Physiological Reports · doi:10.14814/phy2.12893 · Cited by 191
The muscle satellite cell at 50: the formative years
Scharner, J., & Zammit, P. S. (2011) · Skeletal Muscle · doi:10.1186/2044-5040-1-28 · Cited by 180
Lasevicius, T., Ugrinowitsch, C., Schoenfeld, B. J., Roschel, H., Tavares, L. D., De Souza, E. O., Laurentino, G., & Tricoli, V. (2018) · European Journal of Sport Science · doi:10.1080/17461391.2018.1450898 · Cited by 180
Lactate as a Signaling Molecule That Regulates Exercise-Induced Adaptations
Nalbandian, M., & Takeda, M. (2016) · Biology · doi:10.3390/biology5040038 · Cited by 174
Mechanotransduction and the regulation of mTORC1 signaling in skeletal muscle
Hornberger, T. A. (2011) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2011.05.007 · Cited by 170
Ulbricht, A., Gehlert, S., Leciejewski, B., Schiffer, T., Bloch, W., & Höhfeld, J. (2015) · Autophagy · doi:10.1080/15548627.2015.1017186 · Cited by 169
Increasing Role of Titin Mutations in Neuromuscular Disorders
Savarese, M., Sarparanta, J., Vihola, A., Udd, B., & Hackman, P. (2016) · Journal of Neuromuscular Diseases · doi:10.3233/jnd-160158 · Cited by 168
The Hippo pathway effector YAP is a critical regulator of skeletal muscle fibre size
Watt, K. I., Turner, B. J., Hagg, A., Zhang, X., Davey, J. R., Qian, H., Beyer, C., Winbanks, C. E., Harvey, K. F., & Gregorevic, P. (2015) · Nature Communications · doi:10.1038/ncomms7048 · Cited by 164
Eliasson, J., Brink-Elfegoun, T., Nilsson, J. E., Köhnke, R., Ekblom, B. T., & Blomstrand, E. (2006) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00141.2006 · Cited by 163
You, J.-S., Lincoln, H. C., Kim, C.-R., Frey, J. W., Goodman, C. A., Zhong, X.-P., & Hornberger, T. A. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.531392 · Cited by 163
Androgen Receptor Nuclear Translocation Is Facilitated by the f-Actin Cross-Linking Protein Filamin
Ozanne, D. M., Brady, M. E., Cook, S., Gaughan, L., Neal, D. E., & Robson, C. N. (2000) · Molecular Endocrinology · doi:10.1210/mend.14.10.0541 · Cited by 162
Mechanotransduction in skeletal muscle
Thomas, J. F. (2006) · Frontiers in bioscience · doi:10.2741/2057 · Cited by 159
Dynamic force sensing of filamin revealed in single-molecule experiments
Rognoni, L., Stigler, J., Pelz, B., Ylänne, J., & Rief, M. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1211274109 · Cited by 159
Murach, K. A., White, S. H., Wen, Y., Ho, A., Dupont-Versteegden, E. E., McCarthy, J. J., & Peterson, C. A. (2017) · Skeletal Muscle · doi:10.1186/s13395-017-0132-z · Cited by 156
Finni, T. J., Ikegawa, S., Lepola, V., & Komi, P. V. (2003) · Acta Physiologica Scandinavica · doi:10.1046/j.1365-201x.2003.01069.x · Cited by 152
Assessing the role of muscle protein breakdown in response to nutrition and exercise in humans.
Tipton, K. D., Hamilton, D. L., & Gallagher, I. J. (2018) · Sports Medicine · doi:10.1007/s40279-017-0845-5 · Cited by 152
Self-citationMR measurements of muscle damage and adaptation after eccentric exercise
Foley, J. M., Jayaraman, R. C., Prior, B. M., Pivarnik, J. M., & Meyer, R. A. (1999) · Journal of Applied Physiology · doi:10.1152/jappl.1999.87.6.2311 · Cited by 149
Single muscle fiber adaptations with marathon training
Trappe, S. W., Harber, M. P., Creer, A., Gallagher, P. M., Slivka, D. R., Minchev, K., & Whitsett, D. A. (2006) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01595.2005 · Cited by 146
Tatsumi, R. (2009) · Animal Science Journal · doi:10.1111/j.1740-0929.2009.00712.x · Cited by 143
Hypoxia Increases Muscle Hypertrophy Induced by Resistance Training
Nishimura, A., Sugita, M., Kato, K., Fukuda, A., Sudo, A., & Uchida, A. (2010) · International Journal of Sports Physiology and Performance · doi:10.1123/ijspp.5.4.497 · Cited by 138
Using Molecular Biology to Maximize Concurrent Training
Baar, K. (2014) · Sports Medicine · doi:10.1007/s40279-014-0252-0 · Cited by 135
Important role for AMPKαl in limiting skeletal muscle cell hypertrophy
Mounier, R., Lantier, L., Leclerc, J., Sotiropoulos, A., Pende, M., Daegelen, D., Sakamoto, K., Foretz, M., & Viollet, B. (2009) · The FASEB Journal · doi:10.1096/fj.08-119057 · Cited by 133
Muscle damage and muscle remodeling: no pain, no gain?
Flann, K. L., LaStayo, P. C., McClain, D. A., Hazel, M., & Lindstedt, S. L. (2011) · Journal of Experimental Biology · doi:10.1242/jeb.050112 · Cited by 133
Muscle wasting and interleukin-6-induced atrogin-I expression in the cachectic Apc Min/+ mouse
Baltgalvis, K. A., Berger, F. G., Peña, M. M. O., Davis, J. M., White, J. P., & Carson, J. A. (2008) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-008-0574-6 · Cited by 129
Abe, T., Loenneke, J. P., Fahs, C. A., Rossow, L. M., Thiebaud, R. S., & Bemben, M. G. (2012) · Clinical Physiology and Functional Imaging · doi:10.1111/j.1475-097x.2012.01126.x · Cited by 127
Christie, G. R., Hajduch, E., Hundal, H. S., Proud, C. G., & Taylor, P. M. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m107694200 · Cited by 125
The Molecular Basis for Load-Induced Skeletal Muscle Hypertrophy
Marcotte, G. R., West, D. W. D., & Baar, K. (2014) · Calcified Tissue International · doi:10.1007/s00223-014-9925-9 · Cited by 123
Focal adhesion kinase and its role in skeletal muscle
Graham, Z., Gallagher, P. M., & Cardozo, C. P. (2015) · Journal of Muscle Research and Cell Motility · doi:10.1007/s10974-015-9415-3 · Cited by 122
Schoenfeld, B. J., Ogborn, D. I., Vigotsky, A. D., Franchi, M. V., & Krieger, J. W. (2017) · Journal of Strength and Conditioning Research · doi:10.1519/jsc.0000000000001983 · Cited by 122
Self-citationGoodman, C. A., Dietz, J. M., Jacobs, B. L., McNally, R. M., You, J.-S., & Hornberger, T. A. (2015) · FEBS Letters · doi:10.1016/j.febslet.2015.04.047 · Cited by 121
Prevention of Muscle Aging by Myofiber-Associated Satellite Cell Transplantation
Hall, J. K., Banks, G. B., Chamberlain, J. S., & Olwin, B. B. (2010) · Science Translational Medicine · doi:10.1126/scitranslmed.3001081 · Cited by 121
A new paradigm for muscle contraction
Herzog, W., Powers, K. L., Johnston, K., & Duvall, M. (2015) · Frontiers in Physiology · doi:10.3389/fphys.2015.00174 · Cited by 116
Type 1 Muscle Fiber Hypertrophy after Blood Flow-restricted Training in Powerlifters
BJØRNSEN, T., WERNBOM, M., KIRKETEIG, A., PAULSEN, G., SAMNØY, L., BÆKKEN, L., CAMERON-SMITH, D., BERNTSEN, S., & RAASTAD, T. (2019) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000001775 · Cited by 115
Krüger, M., & Kötter, S. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2016.00076 · Cited by 113
A metabolic link to skeletal muscle wasting and regeneration
Koopman, R., Ly, C., & Ryall, J. G. (2014) · Frontiers in Physiology · doi:10.3389/fphys.2014.00032 · Cited by 112
Androgen receptor antagonist suppresses exercise-induced hypertrophy of skeletal muscle
Inoue, K., Yamasaki, S., Fushiki, T., Okada, Y., & Sugimoto, E. (1994) · European Journal of Applied Physiology · doi:10.1007/bf00867933 · Cited by 111
Do metabolites that are produced during resistance exercise enhance muscle hypertrophy?
Dankel, S. J., Mattocks, K. T., Jessee, M. B., Buckner, S. L., Mouser, J. G., & Loenneke, J. P. (2017) · European Journal of Applied Physiology · doi:10.1007/s00421-017-3690-1 · Cited by 111
Bjørnsen, T., Salvesen, S., Berntsen, S., Hetlelid, K. J., Stea, T. H., Lohne‐Seiler, H., Rohde, G. E., Haraldstad, K., Raastad, T., Köpp, U. M. S., et al. (2015) · Scandinavian Journal of Medicine and Science in Sports · doi:10.1111/sms.12506 · Cited by 110
Lactate increases myotube diameter via activation of MEK/ERK pathway in C2C12 cells
Ohno, Y., Oyama, A., Kaneko, H., Egawa, T., YOKOYAMA, S., Sugiura, T., Ohira, Y., Yoshioka, T., & Goto, K. (2018) · Acta Physiologica · doi:10.1111/apha.13042 · Cited by 109
Blood vessels and desmin control the positioning of nuclei in skeletal muscle fibers
Ralston, E., Lu, Z., Biscocho, N., Soumaka, E., Mavroidis, M., Prats, C., Lømo, T., Capetanaki, Y., & Ploug, T. (2006) · Journal of Cellular Physiology · doi:10.1002/jcp.20780 · Cited by 100
Time course of gene expression during mouse skeletal muscle hypertrophy
Chaillou, T., Lee, J. D., England, J. H., Esser, K. A., & McCarthy, J. J. (2013) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00611.2013 · Cited by 99
Spangenburg, E. E., & McBride, T. A. (2005) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00619.2005 · Cited by 96
Crossland, H., Kazi, A. A., Lang, C. H., Timmons, J. A., Pierre, P., Wilkinson, D. J., Smith, K., Szewczyk, N. J., & Atherton, P. J. (2013) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00541.2012 · Cited by 95
mVps34 is activated following high‐resistance contractions
MacKenzie, M. G., Hamilton, D. L., Murray, J. T., Taylor, P. M., & Baar, K. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2008.159830 · Cited by 94
The Hippo signal transduction network in skeletal and cardiac muscle
Wackerhage, H., Del Re, D. P., Judson, R. N., Sudol, M., & Sadoshima, J. (2014) · Science Signaling · doi:10.1126/scisignal.2005096 · Cited by 92
Self-citationOishi, Y., Tsukamoto, H., Yokokawa, T., Hirotsu, K., Shimazu, M., Uchida, K., Tomi, H., Higashida, K., Iwanaka, N., & Hashimoto, T. (2015) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00054.2014 · Cited by 90
Lilja, M. R., Mandić, M., Apró, W., Melin, M., Olsson, K., Rosenborg, S., Gustafsson, T. P., & Lundberg, T. R. (2017) · Acta Physiologica · doi:10.1111/apha.12948 · Cited by 90
A longitudinal MRI study of muscle atrophy during lower leg immobilization following ankle fracture
Psatha, M., Wu, Z., Gammie, F. M., Ratkevičius, A., Wackerhage, H., Lee, J. H., Redpath, T. W., Gilbert, F. J., Ashcroft, G. P., Meakin, J. R., et al. (2011) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.22864 · Cited by 89
Glover, E. I., Oates, B. R., Tang, J. E., Moore, D. R., Tarnopolsky, M. A., & Phillips, S. M. (2008) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00097.2008 · Cited by 87
Effects of resistance training under hypoxic conditions on muscle hypertrophy and strength
Kurobe, K., Huang, Z., Nishiwaki, M., Yamamoto, M., Kanehisa, H., & Ogita, F. (2014) · Clinical Physiology and Functional Imaging · doi:10.1111/cpf.12147 · Cited by 85
Franchi, M. V., Ruoss, S., Valdivieso, P., Mitchell, K. W., Smith, K., Atherton, P. J., Narici, M. V., & Flück, M. (2018) · Acta Physiologica · doi:10.1111/apha.13056 · Cited by 83
A map of the phosphoproteomic alterations that occur after a bout of maximal‐intensity contractions
Potts, G. K., McNally, R. M., Blanco, R., You, J., Hebert, A. S., Westphall, M. S., Coon, J. J., & Hornberger, T. A. (2017) · The Journal of Physiology · doi:10.1113/jp273904 · Cited by 81
The Hippo Signaling Pathway in the Regulation of Skeletal Muscle Mass and Function
Watt, K. I., Goodman, C. A., Hornberger, T. A., & Gregorevic, P. (2018) · Exercise and Sport Sciences Reviews · doi:10.1249/jes.0000000000000142 · Cited by 80
The α7β1-integrin increases muscle hypertrophy following multiple bouts of eccentric exercise
Zou, K., Meador, B. M., Johnson, B., Huntsman, H. D., Mahmassani, Z. S., Valero, M. C., Huey, K. A., & Boppart, M. D. (2011) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00081.2011 · Cited by 79
Muscle intermediate filaments form a stress-transmitting and stress- signaling network in muscle
Palmisano, M. G., Bremner, S. N., Hornberger, T. A., Meyer, G. A., Domenighetti, A. A., Shah, S. B., Kiss, B., Kellermayer, M., Ryan, A. F., & Lieber, R. L. (2014) · Journal of Cell Science · doi:10.1242/jcs.142463 · Cited by 75
Mechanotransduction via the nuclear envelope: a distant reflection of the cell surface
Aureille, J., Belaadi, N., & Guilluy, C. (2016) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2016.10.003 · Cited by 72
Simplified data access on human skeletal muscle transcriptome responses to differentiated exercise
Vissing, K., & Schjerling, P. (2014) · Scientific Data · doi:10.1038/sdata.2014.41 · Cited by 70
Kathage, B., Gehlert, S., Ulbricht, A., Lüdecke, L., Tapia, V., Orfanos, Z., Wenzel, D., Bloch, W., Volkmer, R., Fleischmann, B. K., et al. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2016.10.007 · Cited by 68
Neural and morphological changes in response to a 20-day intense eccentric training protocol
Krentz, J. R., & Farthing, J. P. (2010) · European Journal of Applied Physiology · doi:10.1007/s00421-010-1513-8 · Cited by 66
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Gilbert, P. M., & Weaver, V. M. (2016) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2016.09.004 · Cited by 65
Relationship between force and size in human single muscle fibres
Krivickas, L. S., Dorer, D. J., Ochala, J., & Frontera, W. R. (2011) · Experimental Physiology · doi:10.1113/expphysiol.2010.055269 · Cited by 64
Noorkõiv, M., Nosaka, K., & Blazevich, A. J. (2015) · Journal of Sports Sciences · doi:10.1080/02640414.2015.1020843 · Cited by 60
Muscle Fiber Hypertrophy and Myonuclei Addition: A Systematic Review and Meta-analysis
Conceição, M. S., VECHIN, F. C., Lixandrão, M. E., Damas, F., Libardi, C. A., Tricoli, V., Roschel, H., CAMERA, D. M., & Ugrinowitsch, C. (2018) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000001593 · Cited by 60
Yu, J., Liu, J., Carlsson, L. M. S., Thornell, L., & Stål, P. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062056 · Cited by 59
Ulbricht, A., & Höhfeld, J. (2013) · Autophagy · doi:10.4161/auto.24213 · Cited by 58
Costamere proteins and their involvement in myopathic processes
Jaka, O., Casas-Fraile, L., de Munaín, A. L., & Sáenz, A. (2015) · Expert Reviews in Molecular Medicine · doi:10.1017/erm.2015.9 · Cited by 56
Verbrugge, S. A. J., Schönfelder, M., Becker, L., Yaghoob Nezhad, F., Hrabě de Angelis, M., & Wackerhage, H. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00553 · Cited by 56
Self-citationDamas, F., Libardi, C. A., Ugrinowitsch, C., VECHIN, F. C., Lixandrão, M. E., Snijders, T., Nederveen, J. P., Bacurau, A. V. N., Brum, P. C., Tricoli, V., et al. (2018) · PLoS ONE · doi:10.1371/journal.pone.0191039 · Cited by 54
McMahon, G. E., Morse, C. I., Burden, A., Winwood, K. L., & Onambélé-Pearson, G. L. (2013) · Muscle & Nerve · doi:10.1002/mus.23884 · Cited by 52
Kappenstein, J., Ferrauti, A., Runkel, B., Fernández-Fernández, J., Müller, K., & Zange, J. (2013) · European Journal of Applied Physiology · doi:10.1007/s00421-013-2712-x · Cited by 50
Hentilä, J., Ahtiainen, J. P., Paulsen, G., Raastad, T., Häkkinen, K., Mero, A. A., & Hulmi, J. J. (2018) · Acta Physiologica · doi:10.1111/apha.13069 · Cited by 50
The Hippo signal transduction network for exercise physiologists
Gabriel, B. M., Hamilton, D. L., Tremblay, A. M., & Wackerhage, H. (2016) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01076.2015 · Cited by 48
Agergaard, J., Bülow, J., Jensen, J. K., Reitelseder, S., Drummond, M. J., Schjerling, P., Scheike, T., Serena, A., & Holm, L. (2016) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00164.2016 · Cited by 47
Rindom, E., & Vissing, K. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2016.00547 · Cited by 44
Boudriau, S., Vincent, M., Côt́e, C. H., & Rogers, P. A. W. (1993) · Journal of Histochemistry & Cytochemistry · doi:10.1177/41.7.8515044 · Cited by 41
Frey, J. W., Farley, E. E., O’Neil, T. K., Burkholder, T. J., & Hornberger, T. A. (2009) · Biophysical Journal · doi:10.1016/j.bpj.2009.04.025 · Cited by 37
Wax, B., Kavazis, A. N., Webb, H. E., & Brown, S. P. (2012) · Journal of the International Society of Sports Nutrition · doi:10.1186/1550-2783-9-17 · Cited by 35
The mechanistic and ergogenic effects of phosphatidic acid in skeletal muscle
Shad, B. J., Smeuninx, B., Atherton, P. J., & Breen, L. (2015) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2015-0350 · Cited by 33
Low, S. Y., & Taylor, P. M. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.481be.x · Cited by 32
Baroni, B., Pompermayer, M. G., Cini, A., Peruzzolo, A., Radaelli, R., Brusco, C., & Pinto, R. (2017) · Journal of Strength and Conditioning Research · doi:10.1519/jsc.0000000000001562 · Cited by 32
Kubica, N., Kimball, S. R., Jefferson, L. S., & Farrell, P. A. (2004) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00962.2003 · Cited by 28
Komulainen, J., & Vihko, V. (1994) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf00724517 · Cited by 24
Pereira, M. G., Dyar, K. A., Nogara, L., Solagna, F., Marabita, M., Baraldo, M., Chemello, F., Germinario, E., Romanello, V., Nolte, H., et al. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00968 · Cited by 24
Gibala, M. J. (2000) · Canadian Journal of Applied Physiology · doi:10.1139/h00-034 · Cited by 20
Contractile cell forces exerted on rigid substrates
Köser, J., Gaiser, S., & Müller, B. (2011) · European Cells and Materials · doi:10.22203/ecm.v021a36 · Cited by 20
Wackerhage, H., Mueller, K., Hoffmann, U., Leyk, D., Eßfeld, D., & Zange, J. (1996) · Magnetic Resonance Materials in Physics Biology and Medicine · doi:10.1007/bf01772002 · Cited by 15
Flagged first, then by citations
Research works printed but not linked: 5
- Goldberg AL, 1975, Med Sci Sports, 7, 185
- Hamilton DL, 2009, Muscle plasticity. Advances in Biochemical and Physiological Research, 45
- Hirvonen J, 1992, Can J Sport Sci, 17, 141
- Paulsen G, 2012, Exerc Immunol Rev, 18, 42
- Schoenfeld BJ, 2014, Strength Condit J, 36, 5
Cited by
Sorted by citations
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Egan, B., & Sharples, A. P. (2023) · Physiological Reviews · doi:10.1152/physrev.00054.2021 · Cited by 278
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Metadata
- Authors
- Wackerhage, H., Schoenfeld, B. J., Hamilton, D. L., Lehti, M., & Hulmi, J. J.
- Affiliations
- Technical University of Munich (DE)
- Lehman College (US)
- Deakin University (AU)
- LIKES – Foundation for Sport and Health Sciences (FI)
- University of Jyväskylä (FI)
- Corresponding author
- Wackerhage, Henning
- Venue
- Journal of Applied Physiology
- Publisher
- American Physiological Society
- Published
- 2019-01-01
- Volume
- 126
- Issue
- 1
- Pages
- 30-43
- ISSN
- 0161-7567 (ISSN-L)
- 8750-7587
- 1522-1601
- OpenAlex
- W2897539462
- Cited by
- 357
- References
- 163
- Citations by year
- 2026: 46 · 2025: 48 · 2024: 41 · 2023: 57 · 2022: 73 · 2021: 43 · 2020: 33 · 2019: 16
- FWCI
- 2.25
- Type
- journal article
- Language
- en
- Open access
- green
- urn.fi
- Locations
- Journal of Applied Physiology (publishedVersion)
- PubMed (publishedVersion)
- Jyväskylä University Digital Archive (University of Jyväskylä) (submittedVersion)
- Own your potential (DEAKIN) (submittedVersion)
- Figshare (submittedVersion, cc-by)
- mediaTUM (Technical University of Munich) (submittedVersion, other-oa)
- Funders
- Foundation for Public Health and Physical Activity LIKES
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Nursing › Nutrition and Dietetics › Muscle metabolism and nutrition
- Health Sciences › Medicine › Physiology (medical) › Cardiovascular and exercise physiology
- Keywords
- skeletal muscle hypertrophy, resistance training, mTORC1 signaling, muscle protein synthesis, mechanical stress, exercise-induced muscle damage, metabolic stress, mechanosensing, filamin C, BAG3, Hippo signaling pathway, autophagy, costameres, blood flow restriction, low-load resistance training
- MeSH terms
- Animals, Humans, Hypertrophy, Stress, Physiological, Weight-Bearing, Muscle, Skeletal, Mechanotransduction, Cellular, Resistance Training
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