Biological Progression from Adult Bone Marrow to Mononucleate Muscle Stem Cell to Multinucleate Muscle Fiber in Response to Injury

Adult bone marrow-derived cells (BMDC) are shown to contribute to muscle tissue in a step-wise biological progression. Following irradiation-induced damage, transplanted GFP-labeled BMDC become satellite cells: membrane-ensheathed mononucleate muscle stem cells. Following a subsequent exercise-induced damage, GFP-labeled multinucleate myofibers are detected. Isolated GFP-labeled satellite cells are heritably myogenic. They express three characteristic muscle markers, are karyotypically diploid, and form clones that can fuse into multinucleate cells in culture or into myofibers after injection into mouse muscles. These results suggest that two temporally distinct injury-related signals first induce BMDC to occupy the muscle stem cell niche and then to help regenerate mature muscle fibers. The stress-induced progression of BMDC to muscle satellite cell to muscle fiber results in a contribution to as many as 3.5% of muscle fibers and is due to developmental plasticity in response to environmental cues.

[1]  R. Goyer,et al.  Taurine and creatine excretion after x-irradiation and plasmocid-induced muscle necrosis in the rat. , 1967, Radiation research.

[2]  David M. Bodine,et al.  Bone marrow cells regenerate infarcted myocardium , 2001, Nature.

[3]  C. Bader,et al.  Identification of self-renewing myoblasts in the progeny of single human muscle satellite cells. , 1996, Differentiation; research in biological diversity.

[4]  T. Partridge,et al.  Patterns of repair of dystrophic mouse muscle: Studies on isolated fibers , 1999, Developmental dynamics : an official publication of the American Association of Anatomists.

[5]  G Cossu,et al.  Muscle regeneration by bone marrow-derived myogenic progenitors. , 1998, Science.

[6]  A. Horwitz,et al.  Alpha 7 beta 1 integrin is a component of the myotendinous junction on skeletal muscle. , 1993, Journal of cell science.

[7]  R. Mulligan,et al.  Dystrophin expression in the mdx mouse restored by stem cell transplantation , 1999, Nature.

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

[9]  Fred H. Gage,et al.  Can stem cells cross lineage boundaries? , 2001, Nature Medicine.

[10]  A. Ruifrok,et al.  Hepatocytes and epithelial cells of donor origin in recipients of peripheral-blood stem cells. , 2002, The New England journal of medicine.

[11]  M. Grounds Age‐associated Changes in the Response of Skeletal Muscle Cells to Exercise and Regeneration a , 1998, Annals of the New York Academy of Sciences.

[12]  Neil D. Theise,et al.  Multi-Organ, Multi-Lineage Engraftment by a Single Bone Marrow-Derived Stem Cell , 2001, Cell.

[13]  Sunil Badve,et al.  Derivation of hepatocytes from bone marrow cells in mice after radiation‐induced myeloablation , 2000, Hepatology.

[14]  A. K. Gulati The effect of X-irradiation on skeletal muscle regeneration in the adult rat , 1987, Journal of the Neurological Sciences.

[15]  J. Morgan,et al.  Evidence for a myogenic stem cell that is exhausted in dystrophic muscle. , 2000, Journal of cell science.

[16]  C. Robertson,et al.  Failure of bone marrow cells to transdifferentiate into neural cells in vivo. , 2002, Science.

[17]  H. Blau,et al.  From marrow to brain: expression of neuronal phenotypes in adult mice. , 2000, Science.

[18]  P. Zammit,et al.  The skeletal muscle satellite cell: stem cell or son of stem cell? , 2001, Differentiation; research in biological diversity.

[19]  S. Warren Effects of radiation on normal tissues , 1980 .

[20]  F M Watt,et al.  Out of Eden: stem cells and their niches. , 2000, Science.

[21]  M. Grompe,et al.  Kinetics of liver repopulation after bone marrow transplantation. , 2002, The American journal of pathology.

[22]  Qi-Long Ying,et al.  Changing potency by spontaneous fusion , 2002, Nature.

[23]  Erwin Hauser,et al.  Recruitment of bone-marrow-derived cells by skeletal and cardiac muscle in adult dystrophic mdx mice , 1999, Anatomy and Embryology.

[24]  Owen M. Fiss Out of Eden , 1985 .

[25]  B. Wold,et al.  Single-cell analysis of regulatory gene expression in quiescent and activated mouse skeletal muscle satellite cells. , 1997, Developmental biology.

[26]  P. Rakic,et al.  Cell Proliferation Without Neurogenesis in Adult Primate Neocortex , 2001, Science.

[27]  H. Blau,et al.  Primary mouse myoblast purification, characterization, and transplantation for cell-mediated gene therapy , 1994, The Journal of cell biology.

[28]  M. Fukuda,et al.  [Studies on the haematopoietic stem cells in primary myelofibrosis--in vitro colony forming capacity of the peripheral blood, the spleen, the splenic arterial and venous blood (author's transl)]. , 1978, [Rinsho ketsueki] The Japanese journal of clinical hematology.

[29]  A. Wernig,et al.  Expression of Cd34 and Myf5 Defines the Majority of Quiescent Adult Skeletal Muscle Satellite Cells , 2000, The Journal of cell biology.

[30]  F. Mavilio,et al.  Bone-marrow transplantation: Failure to correct murine muscular dystrophy , 2001, Nature.

[31]  F. Kadi,et al.  Concomitant increases in myonuclear and satellite cell content in female trapezius muscle following strength training , 2000, Histochemistry and Cell Biology.

[32]  P. Anversa,et al.  Chimerism of the transplanted heart. , 2002, The New England journal of medicine.

[33]  Hiroshi Yamamoto,et al.  Muscle regeneration by reconstitution with bone marrow or fetal liver cells from green fluorescent protein-gene transgenic mice. , 2002, Journal of cell science.

[34]  T. Partridge,et al.  Dynamics of Myoblast Transplantation Reveal a Discrete Minority of Precursors with Stem Cell–like Properties as the Myogenic Source , 1999, The Journal of cell biology.

[35]  I. Weissman,et al.  Little Evidence for Developmental Plasticity of Adult Hematopoietic Stem Cells , 2002, Science.

[36]  G. Cossu,et al.  How is myogenesis initiated in the embryo? , 1996, Trends in genetics : TIG.

[37]  R. Bischoff Proliferation of muscle satellite cells on intact myofibers in culture. , 1986, Developmental biology.

[38]  M. Entman,et al.  Regeneration of ischemic cardiac muscle and vascular endothelium by adult stem cells. , 2001, The Journal of clinical investigation.

[39]  H. Blau,et al.  Migration of myoblasts across basal lamina during skeletal muscle development , 1990, Nature.

[40]  C. Hillyer Turning blood into brain: Cells bearing neuronal antigens generated in vivo from bone marrow , 2001 .

[41]  Xin Wang,et al.  Purified hematopoietic stem cells can differentiate into hepatocytes in vivo , 2000, Nature Medicine.

[42]  H. Blau,et al.  Purification of mouse primary myoblasts based on alpha 7 integrin expression. , 2001, Experimental cell research.

[43]  Tomoko Nakanishi,et al.  ‘Green mice’ as a source of ubiquitous green cells , 1997, FEBS letters.

[44]  R. Schofield The relationship between the spleen colony-forming cell and the haemopoietic stem cell. , 1978, Blood cells.

[45]  A. Mauro SATELLITE CELL OF SKELETAL MUSCLE FIBERS , 1961, The Journal of biophysical and biochemical cytology.

[46]  A. Spradling,et al.  Stem cells find their niche , 2001, Nature.

[47]  E. Scott,et al.  Bone marrow cells adopt the phenotype of other cells by spontaneous cell fusion , 2002, Nature.

[48]  M. Grounds Muscle regeneration: molecular aspects and therapeutic implications. , 1999, Current opinion in neurology.