Developmental potential of rat L6 myoblasts in vivo following injection into regenerating muscles

Developmental Biology

Volumn 188, Issue 1, 1997, Pages 147-166

  Pin, Christopher L ^a,b   Merrifield, Peter A ^a  

^a UNIVERSITY OF WESTERN ONTARIO   (Canada)

^b PURDUE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MYOSIN HEAVY CHAIN;

ANIMAL CELL; ANIMAL TISSUE; ANTIBODY SPECIFICITY; ARTICLE; CELL DIFFERENTIATION; EMBRYO; HISTOPATHOLOGY; MUSCLE FIBER MEMBRANE CONDUCTANCE; MUSCLE REGENERATION; MYOBLAST; NEWBORN; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; RAT;

ANIMALIA;

EID: 0031214743     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1006/dbio.1997.8624     Document Type: Article

References (57)

1. Armstrong R., Phelps R. Muscle fiber type composition of the rat hindlimb. Am. J. Anat. 171:1984;259-272.
2. Benoit P., Belt W. D. Destruction and regeneration of skeletal muscle after treatment with a local anaesthetic, bupivicaine (marcaine). J. Anat. 107:1970;547-556.
3. Bischoff R. A satellite cell mitogen from crushed adult muscle. Dev. Biol. 115:1986;140-147.
4. Bouvagnet P., Leger J., Pons F., Dechesne C. Fibre types and myosin types in human atrial and ventricular myocardium. Circ. Res. 55:1984;794-804.
5. Braun T., Arnold H. H. Inactivation of myf-5 genes in mice leads to alterations in skeletal muscle development. Embro J. 14:1995;1176-1186.
6. Buller A., Eccles J., Eccles R. Differentiation of fast and slow muscles in the cat hind limb. J. Physiol. 150:1960;399-416.
7. Butler-Browne G. S., Whalen R. G. Myosin isozyme transitions occurring during the postnatal development of the rat soleus muscle. Dev. Biol. 102:1984;324-334.
8. Campione M., Ausoni S., Guezennec C., Schiaffino S. Myosin and troponin changes in rat soleus muscle after hindlimb suspension. J. Appl. Physiol. 74:1993;1156-1160.
9. Cho M., Hughes S. M., Karsch-Mizrachi I., Travis M., Leinwand L. A., Blau H. M. Fast myosin heavy chains expressed in secondary mammalian muscle fibres at the time of their inception. J. Cell Sci. 107:1994;2361-2371.
10. Clarke E., Nandan D., Brickenden A., Cates G., Ball E., Sanwal B. Glycoprotein glycans may not be necessary for the differentiation of skeletal myoblasts. Exp. Cell Res. 180:1989;178-188.
11. Condon K., Silberstein L., Blau H., Thompson W. Development of muscle fiber type in the prenatal rat hindlimb. Dev. Biol. 138:1990;256-274.
12. Covault J., Merlie J., Goridis C., Sanes J. Molecular forms of N-CAM and its RNA in developing and denervated skeletal muscle. J. Cell Biol. 102:1986;731-739.
13. Covault J., Sanes J. Neural cell adhesion molecule (N-CAM) accumulates in denervated and paralyzed skeletal muscles. Proc. Natl. Acad. Sci. USA. 82:1985;4544-4548.
14. Cox R., Weydert A., Barlow D., Buckingham M. Three linked myosin heavy chain genes clustered within 370 kb of each other show independent transcriptional and post-transcriptional regulation during differentiation of a mouse muscle cell line. Dev. Biol. 143:1991;36-43.
15. Cusella-DeAngelis M., Lyons G., Sonnino C., DeAngelis L., Vivarelli E., Farmer K., Wright W., Molinaro M., Bouche M., Buckingham M., Cossu G. MyoD, myogenin independent differentiation of primordial myoblasts in mouse somites. J. Cell Biol. 116:1992;1243-1255.
16. Dahm L., Landmesser L. The regulation of nerve branching during normal development and following activity blockade. Dev. Biol. 130:1988;621-644.
17. D'Albis A., Couteaux R., Janmot C., Mira J. Myosin isoform transitions in regeneration of fast and slow muscles during postnatal development of the rat. Dev. Biol. 135:1989;320-325.
18. D'Albis A., Couteaux R., Janmot C., Roulet A., Mira J. Regeneration after cardiotoxin injury of innervated and denervated slow and fast muscles of mammals: Myosin isoform analysis. Eur. J. Biochem. 174:1988;103-110.
19. DeNardi C., Ausoni S., Moretti P., Gorza L., Velleca M., Buckingham M., Schiaffino S. Type 2X myosin heavy chain is coded by a muscle fiber type specific and developmentally regulated gene. J. Cell Biol. 123:1993;823-835.
20. DiMario J., Fernyak S., Stockdale F. Myoblasts transferred to the limbs of embryos are committed to specific fibre fates. Nature. 362:1993;165-167.
21. DiMario J., Stockdale F. Differences in the developmental fate of cultured and noncultured myoblasts when transplanted into embryonic limbs. Exp. Cell Res. 216:1995;431-442.
22. Ecob-Prince M., Jenkison M., Butler-Browne G., Whalen R. Neonatal and adult myosin heavy chain isoforms in a nerve-muscle culture system. J. Cell Biol. 103:1986;995-1005.
23. Edom F., Mouly V., Barbet J., Fiszman M., Butler-Browne G. Clones of human satellite cells can expressin vitro. Dev. Biol. 164:1994;219-229.
24. Figarella-Branger D., Pellissier J., Bianco N., Pons F., Leger J., Rougon G. Expression of various NCAM isoforms in human embryonic muscles: Correlation with myosin heavy chain phenotypes. J. Neuropathol. Exp. Neurol. 51:1992;12-23.
25. Gauthier G. Skeletal muscle fiber types. Myology. 1986;McGraw-Hill, New York. p. 255-283.
26. Hinterberger T., Sassoon D., Rhodes S., Konieczny S. Expression of the muscle regulatory factor MRF4 during somite and skeletal myofiber development. Dev. Biol. 147:1991;144-156.
27. Hughes S., Blau H. Muscle fiber pattern is independent of cell lineage in postnatal rodent development. Cell. 68:1992;659-671.
28. Hughes S., Cho M., Karsch-Mizrachi I., Travis M., Silberstein L., Leinwand L., Blau H. Three slow myosin heavy chains sequentially expressed in developing mammalian skeletal muscle. Dev. Biol. 158:1993;183-199.
29. Hughes S., Taylor J., Tapscott S., Gurley C., Carter W., Peterson C. Selective accumulation of MyoD and myogenin mRNAs in fast and slow adult skeletal muscle is controlled by innervation and hormones. Development. 118:1993;1137-1147.
30. MacIntyre N., Merrifield P. Fibre-type potential of mouse myoblast cell lines culturedin vitro. Differentiation. 1997.
31. Miller J., Crow M., Stockdale F. Slow and fast myosin heavy chain content defines three types of myotubes in early muscle cell cultures. J. Cell Biol. 101:1985;1643-1650.
32. Oppenheim R., Prevette D., Haverkamp L., Houenou L., Yin Q., McManaman J. Biological studies of a putative avian muscle-derived neurotrophic factor that prevents naturally occurring motoneuron death in vivo. J. Neurobiol. 24(8:1993;1065-1079.
33. Patapoutian A., Yoon J., Miner J., Wang S., Stark K., Wold B. Disruption of the mouse MRF4 gene identifies multiple waves of myogenesis in the myotome. Development. 121:1995;3347-3358.
34. Pavlath G., Rich K., Webster S., Blau H. Localization of muscle gene products in nuclear domains. Nature. 337:1989;570-573.
35. Pette D., Vrbova G. Adaptation of mammalian skeletal muscle fibers to chronic electrical stimulation. Rev. Physiol. Biochem. Pharmacol. 120:1992;115-202.
36. Pin C., Merrifield P. Embryonic and fetal rat myoblasts express different phenotypes following differentiationin vitro. Dev. Genet. 14:1993;356-368.
37. Pin C., Merrifield P. Regionalized expression of myosin isoforms in heterotypic myotubes formed from embryonic and fetal myoblastsin vitro. Devel. Dynamics. 208:1997;420-431.
38. Pin C., Merrifield P. Rat L6 myoblasts represent a IIX fibre type-specific myogenic lineage. Devel. Dynamics. 1997.
39. Price J., Turner D., Cepko C. Lineage analysis in the vertebrate nervous system by retrovirus-mediated gene transfer. Proc. Natl. Acad. Sci. USA. 84:1987;156-160.
40. Roberts P., McGeachie J., Grounds M., Smith E. Initiation and duration of myogenic precursor cell replication in transplants of intact skeletal muscles: An autoradiographic study in mice. Anat. Rec. 224:1989;1-6.
41. Robertson T., Papadimitriou J., Grounds M. Fusion between a myogenic cell in the satellite cell position and undamaged adult myofibre segments. Experientia. 48:1992;394-395.
42. Ross J., Duxson M., Harris A. Formation of primary and secondary myotubes in rat lumbrical muscles. Development. 100:1987;383-394.
43. Rougon G., Marshak D. Structural and immunological characterization of the Amino-terminal domain of mammalian neural cell adhesion molecule. J. Biol. Chem. 261:1986;3396-3401.
44. Rudnicki M., Jaenisch R. The MyoD family of transcription factors and skeletal myogenesis. BioEssays. 17:1995;203-209.
45. Salviati G., Biasia E., Aloisi M. Synthesis of fast myosin induced by fast ectopic innervation of rat soleus muscle is restricted to the ectopic endplate region. Nature. 322:1986;637-639.
46. Sanes J., Johnson Y., Kotzbauer P., Mudd J., Hanley T., Martinou J., Merlie J. Selective expression of an acetylcholine receptor-lacZ transgene in synaptic nuclei of adult muscle fibers. Development. 113:1991;1181-1191.
47. Schiaffino S., Reggiani C. Molecular diversity of myofibrillar proteins: Gene regulation and functional significance. Physiol. Rev. 76:1996;371-423.
48. Shimohama S., Rosenberg M., Fagan A., Wolff J., Short M., Breakefield X., Friedmann T., Gage F. Grafting genetically modified cells into the rat brain: Characteristics of E. coli galactosidase as a reporter gene. Mol. Brain Res. 5:1989;271-278.
49. Simon A., Hoppe P., Burden S. Spatial restriction of AChR gene expression to subsynaptic nuclei. Development. 114:1992;545-553.
50. Smith T., Miller J. Distinct myogenic programs of embryonic and fetal mouse myoblasts cells: expression of the perinatal myosin heavy chain isoform in vitro. Dev. Biol. 149:1992;16-26.
51. Smith T., Block N., Rhodes S., Konieczny S., Miller J. A unique pattern of expression of the four muscle regulatory factor proteins distinguishes somitic from embryonic, fetal and newborn mouse myogenic cells. Development. 117:1993;1125-1133.
52. Vivarelli E., Brown W., Whalen R., Cossu G. The expression of slow myosin during mammalian somitogenesis and limb bud differentiation. J. Cell Biol. 107:1988;2191-2197.
53. Wernig A., Irintchev A., Hartling A., Stephan G., Zimmermann K., Starzinski-Powitz A. Formation of a new muscle fibres and tumours after injection of cultured myogenic cells. J. Neurocytol. 20:1991;982-997.
54. Wieczorek D., Periasamy M., Butler-Browne G., Whalen R., Nadal-Ginard B. Co-expression of multiple myosin heavy chain genes, in addition to a specific one, in extraocular musculature. J. Cell Biol. 101:1985;618-629.
55. Whalen R., Harris J., Butler-Browne G., Sesodia S. Expression of myosin isoforms during notexin-induced regeneration of rat soleus muscles. Dev. Biol. 141:1990;24-40.
56. Yaffe D. Retention of differentiation potentialities during prolonged cultivation of myogenic cells. Proc. Natl. Acad. Sci. USA. 61:1968;477-483.
57. Zhang W., Behringer R., Olson E. Inactivation of the myogenic bHLH gene MRF4 results in up-regulation of myogenin and rib abnormalities. Gene Dev. 9:1995;1388-1399.