Inducible activation of Akt increases skeletal muscle mass and force without satellite cell activation

A better understanding of the signaling pathways that control muscle growth is required to identify appropriate countermeasures to prevent or reverse the loss of muscle mass and force induced by aging, disuse, or neuromuscular diseases. However, two major issues in this field have not yet been fully addressed. The first concerns the pathways involved in leading to physiological changes in muscle size. Muscle hypertrophy based on perturbations of specific signaling pathways is either characterized by impaired force generation, e.g., myostatin knockout, or incompletely studied from the physiological point of view, e.g., IGF‐1 overexpression. A second issue is whether satellite cell proliferation and incorporation into growing muscle fibers is required for a functional hypertrophy. To address these issues, we used an inducible transgenic model of muscle hypertrophy by short‐term Akt activation in adult skeletal muscle. In this model, Akt activation for 3 wk was followed by marked hypertrophy (̃50% of muscle mass) and by increased force generation, as determined in vivo by ankle plantar flexor stimulation, ex vivo in intact isolated diaphragm strips, and in single‐skinned muscle fibers. No changes in fiber‐type distribution and resistance to fatigue were detectable. Bromodeoxyuridine incorporation experiments showed that Akt‐dependent muscle hypertrophy was accompanied by proliferation of interstitial cells but not by satellite cell activation and new myonuclei incorporation, pointing to an increase in myonuclear domain size. We can conclude that during a fast hyper‐trophic growth myonuclear domain can increase without compromising muscle performance.—Blaauw, B., Canato, M., Agatea, L., Toniolo, L., Mammucari, C., Masiero, E., Abraham, R., Sandri, M., Schiaffino, S., Reggiani, C. Inducible activation of Akt increases skeletal muscle mass and force without satellite cell activation. FASEBJ. 23, 3896‐3905 (2009). www.fasebj.org

[1]  R. Herrick,et al.  Time course adaptations in rat skeletal muscle isomyosins during compensatory growth and regression. , 1987, Journal of applied physiology.

[2]  L. Andersen,et al.  The effects of heavy resistance training and detraining on satellite cells in human skeletal muscles , 2004, The Journal of physiology.

[3]  F. Chrétien,et al.  Human macrophages rescue myoblasts and myotubes from apoptosis through a set of adhesion molecular systems , 2006, Journal of Cell Science.

[4]  D. Mukhopadhyay,et al.  Myogenic Akt Signaling Regulates Blood Vessel Recruitment during Myofiber Growth , 2002, Molecular and Cellular Biology.

[5]  E. Blough,et al.  Enhanced electrophoretic separation and resolution of myosin heavy chains in mammalian and avian skeletal muscles. , 1996, Analytical biochemistry.

[6]  G. Yancopoulos,et al.  The IGF-1/PI3K/Akt pathway prevents expression of muscle atrophy-induced ubiquitin ligases by inhibiting FOXO transcription factors. , 2004, Molecular cell.

[7]  G. D’Antona,et al.  Skeletal muscle hypertrophy and structure and function of skeletal muscle fibres in male body builders , 2006, The Journal of physiology.

[8]  S. Houser,et al.  Nuclear Targeting of Akt Enhances Ventricular Function and Myocyte Contractility , 2005, Circulation research.

[9]  C. P. Leblond,et al.  Satellite cells as the source of nuclei in muscles of growing rats , 1971, The Anatomical record.

[10]  C. Mantilla,et al.  Satellite cell addition is/is not obligatory for skeletal muscle hypertrophy , 2007 .

[11]  D. Hood Plasticity in Skeletal, Cardiac, and Smooth Muscle Invited Review: Contractile activity-induced mitochondrial biogenesis in skeletal muscle , 2001 .

[12]  G. Nader Molecular determinants of skeletal muscle mass: getting the "AKT" together. , 2005, The international journal of biochemistry & cell biology.

[13]  C. Mantilla,et al.  Developmental effects on myonuclear domain size of rat diaphragm fibers. , 2008, Journal of applied physiology.

[14]  C. Reggiani,et al.  Imaging and elasticity measurements of the sarcolemma of fully differentiated skeletal muscle fibres , 2005, Microscopy research and technique.

[15]  D. Maughan,et al.  Swelling of skinned muscle fibers of the frog. Experimental observations. , 1977, Biophysical journal.

[16]  L. Larsson,et al.  Myonuclear domain size and myosin isoform expression in muscle fibres from mammals representing a 100 000‐fold difference in body size , 2009, Experimental physiology.

[17]  C. Reggiani,et al.  Reorganized stores and impaired calcium handling in skeletal muscle of mice lacking calsequestrin‐1 , 2007, The Journal of physiology.

[18]  R. Moss,et al.  Shortening velocity in skinned single muscle fibers. Influence of filament lattice spacing. , 1987, Biophysical journal.

[19]  A. Goldberg,et al.  FoxO3 controls autophagy in skeletal muscle in vivo. , 2007, Cell metabolism.

[20]  D. J. Parry,et al.  Satellite cell activity is required for hypertrophy of overloaded adult rat muscle , 1994, Muscle & nerve.

[21]  C. Reggiani,et al.  Akt activation prevents the force drop induced by eccentric contractions in dystrophin-deficient skeletal muscle. , 2008, Human molecular genetics.

[22]  B. Sacchetti,et al.  Pericytes of human skeletal muscle are myogenic precursors distinct from satellite cells , 2007, Nature Cell Biology.

[23]  H. Sweeney,et al.  Contribution of satellite cells to IGF-I induced hypertrophy of skeletal muscle. , 1999, Acta physiologica Scandinavica.

[24]  A. Brack,et al.  Muscle hypertrophy induced by the Ski protein: cyto-architecture and ultrastructure. , 2005, Acta physiologica Scandinavica.

[25]  Marco Sandri,et al.  Foxo Transcription Factors Induce the Atrophy-Related Ubiquitin Ligase Atrogin-1 and Cause Skeletal Muscle Atrophy , 2004, Cell.

[26]  K. Esser,et al.  Counterpoint: Satellite cell addition is not obligatory for skeletal muscle hypertrophy. , 2007, Journal of applied physiology.

[27]  Antonio Musarò,et al.  Localized Igf-1 transgene expression sustains hypertrophy and regeneration in senescent skeletal muscle , 2001, Nature Genetics.

[28]  G. Yancopoulos,et al.  Conditional Activation of Akt in Adult Skeletal Muscle Induces Rapid Hypertrophy , 2004, Molecular and Cellular Biology.

[29]  J. Haspel,et al.  Selective expression of Cre recombinase in skeletal muscle fibers , 2000, Genesis.

[30]  L. Goodyear,et al.  Contraction Regulation of Akt in Rat Skeletal Muscle* , 2002, The Journal of Biological Chemistry.

[31]  P. Couture,et al.  Thy-1 expression by cardiac fibroblasts: lack of association with myofibroblast contractile markers. , 2007, Journal of molecular and cellular cardiology.

[32]  E. Calabria,et al.  A protein kinase B-dependent and rapamycin-sensitive pathway controls skeletal muscle growth but not fiber type specification , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[33]  G. Pavlath,et al.  Point:Counterpoint: Satellite cell addition is/is not obligatory for skeletal muscle hypertrophy. , 2007, Journal of applied physiology.

[34]  Thomas N. Sato,et al.  Versatile inducible activation system of Akt/PKB signaling pathway in mice , 2003, Genesis.

[35]  K. Esser,et al.  Last Word on Point:Counterpoint: Satellite cell addition is/is not obligatory for skeletal muscle hypertrophy. , 2007, Journal of applied physiology.

[36]  D. Lowe,et al.  Stretch-induced myogenin, MyoD, and MRF4 expression and acute hypertrophy in quail slow-tonic muscle are not dependent upon satellite cell proliferation , 1999, Cell and Tissue Research.

[37]  V R Edgerton,et al.  Modulation of myonuclear number in functionally overloaded and exercised rat plantaris fibers. , 1999, Journal of applied physiology.

[38]  K. Herbst,et al.  Testosterone action on skeletal muscle , 2004, Current opinion in clinical nutrition and metabolic care.

[39]  F. Haddad,et al.  Cellular and molecular responses to increased skeletal muscle loading after irradiation. , 2002, American journal of physiology. Cell physiology.

[40]  D. Lowe In response to Point:Counterpoint: "Satellite cell addition is/is not obligatory for skeletal muscle hypertrophy". , 2007, Journal of applied physiology.

[41]  A. Seligman,et al.  CYTOCHEMICAL DEMONSTRATION OF SUCCINIC DEHYDROGENASE BY THE USE OF A NEW p-NITROPHENYL SUBSTITUTED DITETRAZOLE , 1957, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[42]  C. Rehfeldt In response to Point:Counterpoint: "Satellite cell addition is/is not obligatory for skeletal muscle hypertrophy". , 2007, Journal of applied physiology.

[43]  Susan C. Brown,et al.  Lack of myostatin results in excessive muscle growth but impaired force generation , 2007, Proceedings of the National Academy of Sciences.

[44]  S. Schiaffino,et al.  The fate of newly formed satellite cells during compensatory muscle hypertrophy , 1976, Virchows Archiv. B, Cell pathology.

[45]  J. Rosenblatt,et al.  Gamma irradiation prevents compensatory hypertrophy of overloaded mouse extensor digitorum longus muscle. , 1992, Journal of applied physiology.

[46]  H. Blau,et al.  Localization of muscle gene products in nuclear domains , 1989, Nature.

[47]  C. Reggiani,et al.  Force‐velocity properties of human skeletal muscle fibres: myosin heavy chain isoform and temperature dependence. , 1996, The Journal of physiology.

[48]  N. LeBrasseur,et al.  Fast/Glycolytic muscle fiber growth reduces fat mass and improves metabolic parameters in obese mice. , 2008, Cell metabolism.

[49]  C. Croce,et al.  Mechanism of Enhanced Cardiac Function in Mice with Hypertrophy Induced by Overexpressed Akt* , 2003, Journal of Biological Chemistry.

[50]  K. Patel,et al.  Muscle hypertrophy driven by myostatin blockade does not require stem/precursor-cell activity , 2009, Proceedings of the National Academy of Sciences.