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Efficacy of myonuclear addition may explain differential myofiber growth among resistance-trained young and older men and women

Petrella, John K., Kim, Jeong-su, Cross, James M., Kosek, David J., Bamman, Marcas M.·2006·American Journal of Physiology-Endocrinology and Metabolism

DOI 10.1152/ajpendo.00190.2006

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Abstract

Skeletal muscle stem (satellite) cells supporting growth/regeneration are thought to be activated and incorporated into growing myofibers by both endocrine and locally expressed autocrine/paracrine growth factors, the latter being load sensitive. We recently found that myofiber hypertrophy with resistance training is superior in young men (YM) vs. young women and older adults (Kosek DJ, Kim JS, Petrella JK, Cross JM, and Bamman MM. J Appl Physiol 101: 531-544, 2006). We hypothesized that the advanced myofiber hypertrophy in YM is facilitated by myonuclear addition in response to a milieu promoting stem cell activation. Twenty-six young (27.0 +/- 1 yr, 50% women) and 26 older (63.7 +/- 1 yr, 50% women) adults completed 16 wk of knee extensor resistance training. Vastus lateralis biopsies were obtained at baseline, 24 h after one bout, and after 16 wk. Muscle stem cells were identified immunohistochemically with anti-neural cell adhesion molecule (NCAM+). Muscle transcript levels of IGF-I and mechanogrowth factor (MGF) were determined by RT-PCR. Serum IGF-I, IGF-binding protein (IGFBP)-3, IGFBP-1, total and free testosterone, sex hormone-binding globulin (SHBG), and androstenedione were assessed by radioimmunoassay. Myofiber hypertrophy was twofold greater in YM vs. others, and only YM increased NCAM+ cells per 100 myofibers (49%) and myonuclei per fiber (19%) (P < 0.05). IGF-IEa mRNA was higher in young and increased acutely (29%) with summation by 16 wk (96%) (P < 0.05). MGF mRNA increased only in young after one bout (81%) and by 16 wk (85%) (P < 0.001). Circulating IGF-I was twofold higher in young, whereas IGFBP-1 was lowest in YM (P < 0.05). Among men, free testosterone was 59% higher in YM (P < 0.01). Myonuclear addition was most effectively accomplished in YM, which likely drove the superior growth.

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Mauro, A. (1961) · The Journal of Cell Biology · doi:10.1083/jcb.9.2.493 · Cited by 3,683
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Conboy, I. M., Conboy, M. J., Wagers, A. J., Girma, E. R., Weissman, I. L., & Rando, T. A. (2005) · Nature · doi:10.1038/nature03260 · Cited by 2,287
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Hawke, T. J., & Garry, D. J. (2001) · Journal of Applied Physiology · doi:10.1152/jappl.2001.91.2.534 · Cited by 1,646
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Conboy, I. M., Conboy, M. J., Smythe, G. M., & Rando, T. A. (2003) · Science · doi:10.1126/science.1087573 · Cited by 1,121
Calculation of free and bound fractions of testosterone and estradiol-17β to human plasma proteins at body temperature
Södergard, R., Bäckström, T., Shanbhag, V., & Carstensen, H. (1982) · Journal of Steroid Biochemistry · doi:10.1016/0022-4731(82)90038-3 · Cited by 1,080
The Endocrinology of Aging
Lamberts, S. W. J., van den Beld, A. W., & van der Lely, A.-J. (1997) · Science · doi:10.1126/science.278.5337.419 · Cited by 980
Prevalence of sarcopenia and predictors of skeletal muscle mass in healthy, older men and women
Iannuzzi-Sucich, M., Prestwood, K. M., & Kenny, A. M. (2002) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/57.12.m772 · Cited by 890 · cited 1×
“A number of studies have associated age-related declines in circulating anabolic factors, including IGF-I and testosterone, with the muscle atrophy of aging (10, 32, 41), suggesting that these serum factors are important for the constitutive maintenance of muscle mass.”
Background
Predictors of skeletal muscle mass in elderly men and women
Baumgartner, R. N., Waters, D. L., Gallagher, D., Morley, J. E., & Garry, P. J. (1999) · Mechanisms of Ageing and Development · doi:10.1016/s0047-6374(98)00130-4 · Cited by 809 · cited 1×
“A number of studies have associated age-related declines in circulating anabolic factors, including IGF-I and testosterone, with the muscle atrophy of aging (10, 32, 41), suggesting that these serum factors are important for the constitutive maintenance of muscle mass.”
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Suction applied to a muscle biopsy maximizes sample size
Evans, W. J., Phinney, S. D., & Young, V. R. (1982) · Medicine & Science in Sports & Exercise · doi:10.1249/00005768-198201000-00018 · Cited by 525
Efficacy of 3 days/wk resistance training on myofiber hypertrophy and myogenic mechanisms in young vs. older adults
Kosek, D. J., Kim, J.-S., Petrella, J. K., Cross, J. M., & Bamman, M. M. (2006) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01474.2005 · Cited by 503
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Roberts, B. M., Lavin, K. M., Many, G. M., Thalacker‐Mercer, A. E., Merritt, E. K., Bickel, C. S., Mayhew, D. L., Tuggle, S. C., Cross, J. M., Kosek, D. J., et al. (2018) · Experimental Gerontology · doi:10.1016/j.exger.2018.02.023 · Cited by 111
Self-citation
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Goh, Q., Song, T., Petrany, M. J., Cramer, A., Sun, C., Sadayappan, S., Lee, S., & Millay, D. P. (2019) · eLife · doi:10.7554/elife.44876 · Cited by 111
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Roberts, M. D., Haun, C. T., Mobley, C. B., Mumford, P. W., Romero, M. A., Roberson, P. A., Vann, C. G., & McCarthy, J. J. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00834 · Cited by 107
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Snijders, T., Verdijk, L. B., Smeets, J. S. J., McKay, B. R., Senden, J. M., Hartgens, F., Parise, G., Greenhaff, P. L., & van Loon, L. J. C. (2014) · AGE · doi:10.1007/s11357-014-9699-z · Cited by 112
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Ratkevičius, A., Joyson, A., Selmer, I.-S., Dhanani, T., Grierson, C., Tommasi, A. M., DeVries, A., Rauchhaus, P., Crowther, D. J., Alesci, S., et al. (2011) · The Journals of Gerontology Series A · doi:10.1093/gerona/glr025 · Cited by 108
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Mobley, C., Haun, C., Roberson, P., Mumford, P., Romero, M., Kephart, W., Anderson, R., Vann, C., Osburn, S., Pledge, C., et al. (2017) · Nutrients · doi:10.3390/nu9090972 · Cited by 103
Aging alters gene expression of growth and remodeling factors in human skeletal muscle both at rest and in response to acute resistance exercise
Dennis, R. A., PRZYBYLA, B. D., Gurley, C. M., KORTEBEIN, P. M., Simpson, P. M., Sullivan, D. H., & Peterson, C. A. (2007) · Physiological Genomics · doi:10.1152/physiolgenomics.00191.2007 · Cited by 101
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Blocquiaux, S., Gorski, T., Roie, E. V., Ramaekers, M., Thienen, R. V., Nielens, H., Delecluse, C., Bock, K. D., & Thomis, M. A. (2020) · Experimental Gerontology · doi:10.1016/j.exger.2020.110860 · Cited by 107
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Kim, J.-S., Petrella, J. K., Cross, J. M., & Bamman, M. M. (2007) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01194.2006 · Cited by 99
Self-citation
Molecular Regulation of Exercise-Induced Muscle Fiber HypertrophyPreprint
Bamman, M. M., Roberts, B. M., & Adams, G. R. (2017) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a029751 · Cited by 98
Self-citation
Myonuclear Domain Flexibility Challenges Rigid Assumptions on Satellite Cell Contribution to Skeletal Muscle Fiber Hypertrophy
Murach, K. A., Englund, D. A., Dupont‐Versteegden, E. E., McCarthy, J. J., & Peterson, C. A. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00635 · Cited by 96
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Snijders, T., Aussieker, T., Holwerda, A. M., Parise, G., van Loon, L. J. C., & Verdijk, L. B. (2020) · Acta Physiologica · doi:10.1111/apha.13465 · Cited by 96
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Stec, M. J., Thalacker-Mercer, A., Mayhew, D. L., Kelly, N. A., Tuggle, S. C., Merritt, E. K., Brown, C. J., Windham, S. T., Dell'Italia, L. J., Bickel, C. S., et al. (2017) · Experimental Gerontology · doi:10.1016/j.exger.2017.09.018 · Cited by 95
Self-citation
Effects of training, detraining, and retraining on strength, hypertrophy, and myonuclear number in human skeletal muscle
Psilander, N., Eftestøl, E., Cumming, K. T., Juvkam, I., Ekblom, M. M., Sunding, K., Wernbom, M., Holmberg, H.-C., Ekblom, B., Bruusgaard, J. C., et al. (2019) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00917.2018 · Cited by 95
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Murach, K. A., Vechetti, I. J., Van Pelt, D. W., Crow, S. E., Dungan, C. M., Figueiredo, V. C., Kosmac, K., Fu, X., Richards, C. I., Fry, C. S., et al. (2020) · Function · doi:10.1093/function/zqaa009 · Cited by 94
Recent advances in understanding resistance exercise training-induced skeletal muscle hypertrophy in humans
Joanisse, S., Lim, C., McKendry, J., Mcleod, J. C., Stokes, T., & Phillips, S. M. (2020) · F1000Research · doi:10.12688/f1000research.21588.1 · Cited by 90
Activation of mTOR signalling in young and old human skeletal muscle in response to combined resistance exercise and whey protein ingestion
Farnfield, M. M., Breen, L., Carey, K. A., Garnham, A., & Cameron-Smith, D. (2012) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/h11-132 · Cited by 89
Resistance exercise training promotes fiber type-specific myonuclear adaptations in older adults
Moro, T., Brightwell, C. R., Volpi, E., Rasmussen, B. B., & Fry, C. S. (2020) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00723.2019 · Cited by 85
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Horwath, O., Envall, H., Röja, J., Emanuelsson, E. B., Sanz, G., Ekblom, B., Apró, W., & Moberg, M. (2021) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00053.2021 · Cited by 87
ACL injury reduces satellite cell abundance and promotes fibrogenic cell expansion within skeletal muscle
Fry, C. S., Johnson, D. L., Ireland, M. L., & Noehren, B. W. (2016) · Journal of Orthopaedic Research® · doi:10.1002/jor.23502 · Cited by 85
Fidelity of muscle fibre reinnervation modulates ageing muscle impact in elderly women
Sonjak, V., Jacob, K. J., Morais, J. A., Rivera-Zengotita, M. L., Spendiff, S., Spake, C. S. L., Taivassalo, T., Chevalier, S., & Hepple, R. T. (2019) · The Journal of Physiology · doi:10.1113/jp278261 · Cited by 88
Skeletal muscle adaptations to testosterone and resistance training in men with COPD
Lewis, M. I., Fournier, M., Storer, T. W., Bhasin, S., Pórszász, J., Ren, S.-G., Da, X., & Casaburi, R. H. (2007) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00150.2007 · Cited by 86
Evidence for the contribution of muscle stem cells to nonhypertrophic skeletal muscle remodeling in humans
Joanisse, S., Gillen, J. B., Bellamy, L. M., McKay, B. R., Tarnopolsky, M. A., Gibala, M. J., & Parise, G. (2013) · The FASEB Journal · doi:10.1096/fj.13-229799 · Cited by 82
MicroRNA expression profiling in skeletal muscle reveals different regulatory patterns in high and low responders to resistance training
Ogasawara, R., Akimoto, T., Umeno, T., Sawada, S., Hamaoka, T., & Fujita, S. (2016) · Physiological Genomics · doi:10.1152/physiolgenomics.00124.2015 · Cited by 81
The effects of age and resistance loading on skeletal muscle ribosome biogenesis
Stec, M. J., Mayhew, D. L., & Bamman, M. M. (2015) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00489.2015 · Cited by 80
Self-citation
Myeloid Cell-Derived Tumor Necrosis Factor-Alpha Promotes Sarcopenia and Regulates Muscle Cell Fusion with Aging Muscle Fibers
Wang, Y., Welc, S. S., Wehling‐Henricks, M., & Tidball, J. G. (2018) · Aging Cell · doi:10.1111/acel.12828 · Cited by 80
Is the myonuclear domain size fixed?
van der Meer, S. F. T., Jaspers, R. T., & Degens, H. (2011) · PubMed · Cited by 78

Authors: Petrella, J. K., Kim, J.-S., Cross, J. M., Kosek, D. J., & Bamman, M. M.
Affiliations: University of Alabama at Birmingham (US)
ORCID: Cross, James M.
Bamman, Marcas M.
Venue: American Journal of Physiology-Endocrinology and Metabolism
Publisher: American Physiological Society
Published: 2006-11
Volume: 291
Issue: 5
Pages: E937-E946
ISSN: 0193-1849 (ISSN-L)
1522-1555
DOI: 10.1152/ajpendo.00190.2006
OpenAlex: W2154326737
Cited by: 356
References: 61
Citations by year: 2026: 4 · 2025: 5 · 2024: 8 · 2023: 15 · 2022: 24 · 2021: 15 · 2020: 18 · 2019: 22 · 2018: 24 · 2017: 17 · 2016: 28 · 2015: 22 · 2014: 20 · 2013: 16 · 2012: 25
FWCI: 6.65
Type: journal article
Language: en
Open access: closed
Locations: American Journal of Physiology-Endocrinology and Metabolism (publishedVersion)
PubMed (publishedVersion)
Funders: U.S. Department of Veterans Affairs
University of Alabama at Birmingham
National Institute on Aging (R01AG017896, R01 AG17896)
National Center for Research Resources (M01RR00032, M01RR000032)
NIH Clinical Center
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 › Orthopedics and Sports Medicine › Sports Performance and Training
Keywords: muscle fiber hypertrophy, resistance training, skeletal muscle stem cells, satellite cells, insulin-like growth factor I, IGFBP-1, IGFBP-3, free testosterone, sex differences, aging, vastus lateralis, CD56, androstenedione, sex hormone-binding globulin
MeSH terms: Adult, Aged, Aging, Androstenedione, Cell Nucleus, Female, Humans, Insulin-Like Growth Factor I, Male, Middle Aged, RNA, Messenger, Sex Characteristics, Sex Hormone-Binding Globulin, Testosterone, Exercise, Muscle, Skeletal, Insulin-Like Growth Factor Binding Protein 1, Insulin-Like Growth Factor Binding Protein 3, Neural Cell Adhesion Molecules, Satellite Cells, Skeletal Muscle, Cell Size

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Efficacy of myonuclear addition may explain differential myofiber growth among resistance-trained young and older men and women

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