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Physiol. Rev. 84: 209-238, 2004; doi:10.1152/physrev.00019.2003
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Cellular and Molecular Regulation of Muscle Regeneration

SOPHIE B. P. CHARGÉ and MICHAEL A. RUDNICKI

Ottawa Health Research Institute, Ottawa, Canada

Chargé, Sophie B. P., and Michael A. Rudnicki. Cellular and Molecular Regulation of Muscle Regeneration. Physiol Rev 84: 209–238, 2004; 10.1152/physrev.00019.2003.—Under normal circumstances, mammalian adult skeletal muscle is a stable tissue with very little turnover of nuclei. However, upon injury, skeletal muscle has the remarkable ability to initiate a rapid and extensive repair process preventing the loss of muscle mass. Skeletal muscle repair is a highly synchronized process involving the activation of various cellular responses. The initial phase of muscle repair is characterized by necrosis of the damaged tissue and activation of an inflammatory response. This phase is rapidly followed by activation of myogenic cells to proliferate, differentiate, and fuse leading to new myofiber formation and reconstitution of a functional contractile apparatus. Activation of adult muscle satellite cells is a key element in this process. Muscle satellite cell activation resembles embryonic myogenesis in several ways including the de novo induction of the myogenic regulatory factors. Signaling factors released during the regenerating process have been identified, but their functions remain to be fully defined. In addition, recent evidence supports the possible contribution of adult stem cells in the muscle regeneration process. In particular, bone marrow-derived and muscle-derived stem cells contribute to new myofiber formation and to the satellite cell pool after injury.


Address for reprint requests and other correspondence: M. A. Rudnicki, Ottawa Health Research Institute, 501 Smyth Rd., Ottawa, Ontario K1H 8L6, Canada (E-mail: mrudnicki{at}ohri.ca).




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JCBHome page
T. Yokoyama, K. Takano, A. Yoshida, F. Katada, P. Sun, T. Takenawa, T. Andoh, and T. Endo
DA-Raf1, a competent intrinsic dominant-negative antagonist of the Ras-ERK pathway, is required for myogenic differentiation
J. Cell Biol., June 21, 2007; 177(5): 781 - 793.
[Abstract] [Full Text] [PDF]


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Am. J. Respir. Crit. Care Med.Home page
C. A. C. Ottenheijm, L. M. A. Heunks, and P. N. R. Dekhuijzen
Diaphragm Muscle Fiber Dysfunction in Chronic Obstructive Pulmonary Disease: Toward a Pathophysiological Concept
Am. J. Respir. Crit. Care Med., June 15, 2007; 175(12): 1233 - 1240.
[Abstract] [Full Text] [PDF]


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BioinformaticsHome page
D. M. Kemp, N. R. Nirmala, and J. D. Szustakowski
Extending the pathway analysis framework with a test for transcriptional variance implicates novel pathway modulation during myogenic differentiation
Bioinformatics, June 1, 2007; 23(11): 1356 - 1362.
[Abstract] [Full Text] [PDF]


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Proc. Natl. Acad. Sci. USAHome page
C. E. Gleason, D. N. Gross, and M. J. Birnbaum
When the usual insulin is just not enough
PNAS, May 22, 2007; 104(21): 8681 - 8682.
[Full Text] [PDF]


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JCBHome page
H. Sun, L. Li, C. Vercherat, N. T. Gulbagci, S. Acharjee, J. Li, T.-K. Chung, T. H. Thin, and R. Taneja
Stra13 regulates satellite cell activation by antagonizing Notch signaling
J. Cell Biol., May 21, 2007; 177(4): 647 - 657.
[Abstract] [Full Text] [PDF]


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J. Biol. Chem.Home page
C. Dogra, S. L. Hall, N. Wedhas, T. A. Linkhart, and A. Kumar
Fibroblast Growth Factor Inducible 14 (Fn14) Is Required for the Expression of Myogenic Regulatory Factors and Differentiation of Myoblasts into Myotubes: EVIDENCE FOR TWEAK-INDEPENDENT FUNCTIONS OF Fn14 DURING MYOGENESIS
J. Biol. Chem., May 18, 2007; 282(20): 15000 - 15010.
[Abstract] [Full Text] [PDF]


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J. Virol.Home page
T. E. Morrison, R. J. Fraser, P. N. Smith, S. Mahalingam, and M. T. Heise
Complement Contributes to Inflammatory Tissue Destruction in a Mouse Model of Ross River Virus-Induced Disease
J. Virol., May 15, 2007; 81(10): 5132 - 5143.
[Abstract] [Full Text] [PDF]


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Am. J. Physiol. Cell Physiol.Home page
H. Shi, C. Zeng, A. Ricome, K. M. Hannon, A. L. Grant, and D. E. Gerrard
Extracellular signal-regulated kinase pathway is differentially involved in beta-agonist-induced hypertrophy in slow and fast muscles
Am J Physiol Cell Physiol, May 1, 2007; 292(5): C1681 - C1689.
[Abstract] [Full Text] [PDF]


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Am. J. Physiol. Cell Physiol.Home page
S.-E. Chen, B. Jin, and Y.-P. Li
TNF-{alpha} regulates myogenesis and muscle regeneration by activating p38 MAPK
Am J Physiol Cell Physiol, May 1, 2007; 292(5): C1660 - C1671.
[Abstract] [Full Text] [PDF]


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Am. J. Physiol. Endocrinol. Metab.Home page
S. Reppe, L. Stilgren, B. Abrahamsen, O. K. Olstad, F. Cero, K. Brixen, L. S. Nissen-Meyer, and K. M. Gautvik
Abnormal muscle and hematopoietic gene expression may be important for clinical morbidity in primary hyperparathyroidism
Am J Physiol Endocrinol Metab, May 1, 2007; 292(5): E1465 - E1473.
[Abstract] [Full Text] [PDF]


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RadiologyHome page
A. M. Heemskerk, G. J. Strijkers, M. R. Drost, G. S. van Bochove, and K. Nicolay
Skeletal Muscle Degeneration and Regeneration after Femoral Artery Ligation in Mice: Monitoring with Diffusion MR Imaging
Radiology, May 1, 2007; 243(2): 413 - 421.
[Abstract] [Full Text] [PDF]


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Stem CellsHome page
A. Schaffler and C. Buchler
Concise Review: Adipose Tissue-Derived Stromal Cells--Basic and Clinical Implications for Novel Cell-Based Therapies
Stem Cells, April 1, 2007; 25(4): 818 - 827.
[Abstract] [Full Text] [PDF]


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J. Leukoc. Biol.Home page
P. K. Shireman, V. Contreras-Shannon, O. Ochoa, B. P. Karia, J. E. Michalek, and L. M. McManus
MCP-1 deficiency causes altered inflammation with impaired skeletal muscle regeneration
J. Leukoc. Biol., March 1, 2007; 81(3): 775 - 785.
[Abstract] [Full Text] [PDF]


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Am. J. Physiol. Cell Physiol.Home page
V. Contreras-Shannon, O. Ochoa, S. M. Reyes-Reyna, D. Sun, J. E. Michalek, W. A. Kuziel, L. M. McManus, and P. K. Shireman
Fat accumulation with altered inflammation and regeneration in skeletal muscle of CCR2-/- mice following ischemic injury
Am J Physiol Cell Physiol, February 1, 2007; 292(2): C953 - C967.
[Abstract] [Full Text] [PDF]


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J. Physiol.Home page
T. Kvorning, M. Andersen, K. Brixen, P. Schjerling, C. Suetta, and K. Madsen
Suppression of testosterone does not blunt mRNA expression of myoD, myogenin, IGF, myostatin or androgen receptor post strength training in humans
J. Physiol., January 15, 2007; 578(2): 579 - 593.
[Abstract] [Full Text] [PDF]


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J. Leukoc. Biol.Home page
A. Germani, F. Limana, and M. C. Capogrossi
Pivotal Advances: High-mobility group box 1 protein--a cytokine with a role in cardiac repair
J. Leukoc. Biol., January 1, 2007; 81(1): 41 - 45.
[Abstract] [Full Text] [PDF]


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J. Cell Sci.Home page
R. S. O'Connor, S. T. Mills, K. A. Jones, S. N. Ho, and G. K. Pavlath
A combinatorial role for NFAT5 in both myoblast migration and differentiation during skeletal muscle myogenesis
J. Cell Sci., January 1, 2007; 120(1): 149 - 159.
[Abstract] [Full Text] [PDF]


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J. Cell Sci.Home page
C. Sciorati, B. G. Galvez, S. Brunelli, E. Tagliafico, S. Ferrari, G. Cossu, and E. Clementi
Ex vivo treatment with nitric oxide increases mesoangioblast therapeutic efficacy in muscular dystrophy
J. Cell Sci., December 15, 2006; 119(24): 5114 - 5123.
[Abstract] [Full Text] [PDF]


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Genes Dev.Home page
M. Schwarzkopf, D. Coletti, D. Sassoon, and G. Marazzi
Muscle cachexia is regulated by a p53-PW1/Peg3-dependent pathway
Genes & Dev., December 15, 2006; 20(24): 3440 - 3452.
[Abstract] [Full Text] [PDF]


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Genes Dev.Home page
T. Fukushige, T. M. Brodigan, L. A. Schriefer, R. H. Waterston, and M. Krause
Defining the transcriptional redundancy of early bodywall muscle development in C. elegans: evidence for a unified theory of animal muscle development
Genes & Dev., December 15, 2006; 20(24): 3395 - 3406.
[Abstract] [Full Text] [PDF]


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J. Appl. Physiol.Home page
M. I. Lewis
Mechanisms underlying myogenesis: complex and likely to become more so!
J Appl Physiol, December 1, 2006; 101(6): 1539 - 1540.
[Full Text] [PDF]


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Mol. Cell. ProteomicsHome page
L. G. Puente, S. Voisin, R. E. C. Lee, and L. A. Megeney
Reconstructing the Regulatory Kinase Pathways of Myogenesis from Phosphopeptide Data
Mol. Cell. Proteomics, December 1, 2006; 5(12): 2244 - 2251.
[Abstract] [Full Text] [PDF]


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J. Histochem. Cytochem.Home page
P. S. Zammit, T. A. Partridge, and Z. Yablonka-Reuveni
The Skeletal Muscle Satellite Cell: The Stem Cell That Came in From the Cold
J. Histochem. Cytochem., November 1, 2006; 54(11): 1177 - 1191.
[Abstract] [Full Text] [PDF]


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J. Biol. Chem.Home page
E. M. Wilson and P. Rotwein
Control of MyoD Function during Initiation of Muscle Differentiation by an Autocrine Signaling Pathway Activated by Insulin-like Growth Factor-II
J. Biol. Chem., October 6, 2006; 281(40): 29962 - 29971.
[Abstract] [Full Text] [PDF]


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Proc. Natl. Acad. Sci. USAHome page
R. N. Kanadia, J. Shin, Y. Yuan, S. G. Beattie, T. M. Wheeler, C. A. Thornton, and M. S. Swanson
Reversal of RNA missplicing and myotonia after muscleblind overexpression in a mouse poly(CUG) model for myotonic dystrophy
PNAS, August 1, 2006; 103(31): 11748 - 11753.
[Abstract] [Full Text] [PDF]


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JCBHome page
Y. Nagata, T. A. Partridge, R. Matsuda, and P. S. Zammit
Entry of muscle satellite cells into the cell cycle requires sphingolipid signaling
J. Cell Biol., July 17, 2006; 174(2): 245 - 253.
[Abstract] [Full Text] [PDF]


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Am. J. Pathol.Home page
Y.-H. Choi, C. Stamm, P. E. Hammer, K. F. Kwaku, J. J. Marler, I. Friehs, M. Jones, C. M. Rader, N. Roy, M.-T. Eddy, et al.
Cardiac Conduction through Engineered Tissue
Am. J. Pathol., July 1, 2006; 169(1): 72 - 85.
[Abstract] [Full Text] [PDF]


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DevelopmentHome page
Y. Chen, G. Lin, and J. M. W. Slack
Control of muscle regeneration in the Xenopus tadpole tail by Pax7
Development, June 15, 2006; 133(12): 2303 - 2313.
[Abstract] [Full Text] [PDF]




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