Connective tissue fibroblasts and Tcf4 regulate myogenesis

Development

Volumn 138, Issue 2, 2011, Pages 371-384

  Mathew, Sam J ^a   Hansen, Jody M ^a   Merrell, Allyson J ^a   Murphy, Malea M ^a   Lawson, Jennifer A ^a   Hutcheson, David A ^a   Hansen, Mark S ^a   Angus Hill, Melinda ^a   Kardon, Gabrielle ^a  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

Author keywords

Connective tissue; Mouse; Myogenesis; Myosin; Tcf4; Tcf7l2

Indexed keywords

MYOSIN HEAVY CHAIN; TRANSCRIPTION FACTOR 7 LIKE 2; TRANSCRIPTION FACTOR TCF4; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ARTICLE; CELL MATURATION; CONNECTIVE TISSUE; CONTROLLED STUDY; DIAPHRAGM MUSCLE; EMBRYO; FIBROBLAST; FLUORESCENCE ACTIVATED CELL SORTING; GENE EXPRESSION; GENETIC MANIPULATION; GERM LINE; IMMUNOFLUORESCENCE MICROSCOPY; LIMB; MOUSE; MUSCLE DEVELOPMENT; MYOBLAST; NONHUMAN; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SKELETAL MUSCLE; WESTERN BLOTTING;

ANIMALS; BASIC HELIX-LOOP-HELIX LEUCINE ZIPPER TRANSCRIPTION FACTORS; BETA CATENIN; CONNECTIVE TISSUE; FEMALE; FIBROBLASTS; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GREEN FLUORESCENT PROTEINS; MALE; MICE; MICE, KNOCKOUT; MICE, TRANSGENIC; MUSCLE DEVELOPMENT; MUSCLE FIBERS, FAST-TWITCH; MUSCLE FIBERS, SLOW-TWITCH; MUSCLE, SKELETAL; PREGNANCY; SIGNAL TRANSDUCTION;

MUS;

EID: 78751475042     PISSN: 09501991     EISSN: 14779129     Source Type: Journal    
DOI: 10.1242/dev.057463     Document Type: Article

References (65)

1. Agbulut, O., Noirez, P., Beaumont, F. and Butler-Browne, G. (2003). Myosin heavy chain isoforms in postnatal muscle development of mice. Biol. Cell 95, 399-406.
2. Anakwe, K., Robson, L., Hadley, J., Buxton, P., Church, V., Allen, S., Hartmann, C., Harfe, B., Nohno, T., Brown, A. M. et al. (2003). Wnt signalling regulates myogenic differentiation in the developing avian wing. Development 130, 3503-3514.
3. Armand, O., Boutineau, A. M., Mauger, A., Pautou, M. P. and Kieny, M. (1983). Origin of satellite cells in avian skeletal muscles. Arch. Anat. Microsc. Morphol. Exp. 72, 163-181.
4. Biressi, S., Molinaro, M. and Cossu, G. (2007). Cellular heterogeneity during vertebrate skeletal muscle development. Dev. Biol. 308, 281-293.
5. Borg, T. K. and Caulfield, J. B. (1980). Morphology of connective tissue in skeletal muscle. Tissue Cell 12, 197-207.
6. Brack, A. S., Conboy, M. J., Roy, S., Lee, M., Kuo, C. J., Keller, C. and Rando, T. A. (2007). Increased Wnt signaling during aging alters muscle stem cell fate and increases fibrosis. Science 317, 807-810.
7. Bradford, M. M. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72, 248-254.
8. Butler, J., Cosmos, E. and Cauwenbergs, P. (1988). Positional signals: evidence for a possible role in muscle fibre-type patterning of the embryonic avian limb. Development 102, 762-772.
9. Chevallier, A., Kieny, M. and Mauger, A. (1977). Limb-somite relationship: origin of the limb musculature. J. Embryol. Exp. Morphol. 41, 245-258.
10. Christ, B., Jacob, H. J. and Jacob, M. (1977). Experimental analysis of the origin of the wing musculature in avian embryos. Anat. Embryol. 150, 171-186.
11. Cooper, S. T., Maxwell, A. L., Kizana, E., Ghoddusi, M., Hardeman, E. C., Alexander, I. E., Allen, D. G. and North, K. N. (2004). C2C12 co-culture on a fibroblast substratum enables sustained survival of contractile, highly differentiated myotubes with peripheral nuclei and adult fast myosin expression. Cell Motil. Cytoskeleton 58, 200-211.
12. Dahlman, J. M., Bakkar, N., He, W. and Guttridge, D. C. (2010). NF-kappaB functions in stromal fibroblasts to regulate early postnatal muscle development. J. Biol. Chem. 285, 5479-5487.
13. Duchenne, G. B. (1968). Studies on pseudohypertrophic muscular paralysis or myosclerotic paralysis. Arch. Neurol. 19, 629-636.
14. Duprez, D., Lapointe, F., Edom-Vovard, F., Kostakopoulou, K. and Robson, L. (1999). Sonic hedgehog (SHH) specifies muscle pattern at tissue and cellular chick level, in the chick limb bud. Mech. Dev. 82, 151-163.
15. Emerson, C. P., Jr and Hauschka, S. D. (2004). Embryonic origins of skeletal muscles. In Myology, Vol. 1 (ed. A. G. Engel and C. Franzini-Armstrong), pp. 3- 44. New York: McGraw-Hill.
16. Engleka, K. A., Gitler, A. D., Zhang, M., Zhou, D. D., High, F. A. and Epstein, J. A. (2005). Insertion of Cre into the Pax3 locus creates a new allele of Splotch and identifies unexpected Pax3 derivatives. Dev. Biol. 280, 396-406.
17. Grim, M. and Wachtler, F. (1991). Muscle morphogenesis in the absence of myogenic cells. Anat. Embryol. 183, 67-70.
18. Gunning, P. and Hardeman, E. (1991). Multiple mechanisms regulate muscle fiber diversity. FASEB J. 5, 3064-3070.
19. Hagiwara, N., Yeh, M. and Liu, A. (2007). Sox6 is required for normal fiber type differentiation of fetal skeletal muscle in mice. Dev. Dyn. 236, 2062-2076.
20. Hasson, P., DeLaurier, A., Bennett, M., Grigorieva, E., Naiche, L. A., Papaioannou, V. E., Mohun, T. J. and Logan, M. P. (2010). Tbx4 and tbx5 acting in connective tissue are required for limb muscle and tendon patterning. Dev. Cell 18, 148-156.
21. Hutcheson, D. A. and Kardon, G. (2009). Genetic manipulations reveal dynamic cell and gene functions: cre-ating a new view of myogenesis. Cell Cycle 8, 3675-3678.
22. Hutcheson, D. A., Zhao, J., Merrell, A., Haldar, M. and Kardon, G. (2009). Embryonic and fetal limb myogenic cells are derived from developmentally distinct progenitors and have different requirements for beta-catenin. Genes Dev. 23, 997-1013.
23. Issa, L. L., Palmer, S. J., Guven, K. L., Santucci, N., Hodgson, V. R., Popovic, K., Joya, J. E. and Hardeman, E. C. (2006). MusTRD can regulate postnatal fiber-specific expression. Dev. Biol. 293, 104-115.
24. Jacob, H. J. and Christ, B. (1980). On the formation of muscle pattern in the chick limb. In Teratology of the Limbs (ed. H.-J. Merker, H. Nau and D. Neubert), pp. 89-97. Berlin: Walter de Gruyter and Company.
25. Joe, A. W., Yi, L., Natarajan, A., Le Grand, F., So, L., Wang, J., Rudnicki, M. A. and Rossi, F. M. (2010). Muscle injury activates resident fibro/adipogenic progenitors that facilitate myogenesis. Nat. Cell Biol. 12, 153-163.
26. Kardon, G., Campbell, J. K. and Tabin, C. J. (2002). Local extrinsic signals determine muscle and endothelial cell fate and patterning in the vertebrate limb. Dev. Cell 3, 533-545.
27. Kardon, G., Harfe, B. D. and Tabin, C. J. (2003). A Tcf4-positive mesodermal population provides a prepattern for vertebrate limb muscle patterning. Dev. Cell 5, 937-944.
28. Kassar-Duchossoy, L., Gayraud-Morel, B., Gomes, D., Rocancourt, D., Buckingham, M., Shinin, V. and Tajbakhsh, S. (2004). Mrf4 determines skeletal muscle identity in Myf5:Myod double-mutant mice. Nature 431, 466-471.
29. Kassar-Duchossoy, L., Giacone, E., Gayraud-Morel, B., Jory, A., Gomes, D. and Tajbakhsh, S. (2005). Pax3/Pax7 mark a novel population of primitive myogenic cells during development. Genes Dev. 19, 1426-1431.
30. Keller, C., Arenkiel, B. R., Coffin, C. M., El-Bardeesy, N., DePinho, R. A. and Capecchi, M. R. (2004). Alveolar rhabdomyosarcomas in conditional Pax3:Fkhr mice: cooperativity of Ink4a/ARF and Trp53 loss of function. Genes Dev. 18, 2614-2626.
31. Komiya, Y. and Habas, R. (2008). Wnt signal transduction pathways. Organogenesis 4, 68-75.
32. Korinek, V., Barker, N., Moerer, P., van Donselaar, E., Huls, G., Peters, P. J. and Clevers, H. (1998). Depletion of epithelial stem-cell compartments in the small intestine of mice lacking Tcf-4. Nat. Genet. 19, 379-383.
33. Kusner, L. L., Young, A., Tjoe, S., Leahy, P. and Kaminski, H. J. (2010). Perimysial fibroblasts of extraocular muscle, as unique as the muscle fibers. Invest. Ophthalmol. Vis. Sci. 51, 192-200.
34. Lanser, M. E. and Fallon, J. F. (1987). Development of wing-bud-derived muscles in normal and wingless chick embryos: a computer-assisted three-dimensional reconstruction study of muscle pattern formation in the absence of skeletal elements. Anat. Rec. 217, 61-78.
35. Le, Y., Miller, J. L. and Sauer, B. (1999). GFPcre fusion vectors with enhanced expression. Anal. Biochem. 270, 334-336.
36. Lu, B. D., Allen, D. L., Leinwand, L. A. and Lyons, G. E. (1999). Spatial and temporal changes in myosin heavy chain gene expression in skeletal muscle development. Dev. Biol. 216, 312-326.
37. Melone, M. A., Peluso, G., Galderisi, U., Petillo, O. and Cotrufo, R. (2000). Increased expression of IGF-binding protein-5 in Duchenne muscular dystrophy (DMD) fibroblasts correlates with the fibroblast-induced downregulation of DMD myoblast growth: an in vitro analysis. J. Cell Physiol. 185, 143-153.
38. Messina, G., Biressi, S., Monteverde, S., Magli, A., Cassano, M., Perani, L., Roncaglia, E., Tagliafico, E., Starnes, L., Campbell, C. E. et al. (2010). Nfix regulates fetal-specific transcription in developing skeletal muscle. Cell 140, 554-566.
39. Muzumdar, M. D., Tasic, B., Miyamichi, K., Li, L. and Luo, L. (2007). A global double-fluorescent Cre reporter mouse. Genesis 45, 593-605.
40. Nagy, A., Gertsenstein, M., Vintersten, K., and Behringer, R. (2002). Manipulating the Mouse Embryo: A Laboratory Manual, 3rd edition. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press.
41. Nikovits, W., Jr, Cann, G. M., Huang, R., Christ, B. and Stockdale, F. E. (2001). Patterning of fast and slow fibers within embryonic muscles is established independently of signals from the surrounding mesenchyme. Development 128, 2537-2544.
42. Niro, C., Demignon, J., Vincent, S., Liu, Y., Giordani, J., Sgarioto, N., Favier, M., Guillet-Deniau, I., Blais, A. and Maire, P. (2010). Six1 and Six4 gene expression is necessary to activate the fast-type muscle gene program in the mouse primary myotome. Dev. Biol. 338, 168-182.
43. Oh, M., Rybkin, I. I., Copeland, V., Czubryt, M. P., Shelton, J. M., van Rooij, E., Richardson, J. A., Hill, J. A., De Windt, L. J., Bassel-Duby, R. et al. (2005). Calcineurin is necessary for the maintenance but not embryonic development of slow muscle fibers. Mol. Cell. Biol. 25, 6629-6638.
44. Quinn, L. S., Ong, L. D. and Roeder, R. A. (1990). Paracrine control of myoblast proliferation and differentiation by fibroblasts. Dev. Biol. 140, 8-19.
45. Relaix, F., Rocancourt, D., Mansouri, A. and Buckingham, M. (2005). A Pax3/Pax7-dependent population of skeletal muscle progenitor cells. Nature 435, 945-953.
46. Richler, C. and Yaffe, D. (1970). The in vitro cultivation and differentiation capacities of myogenic cell lines. Dev. Biol. 23, 1-22.
47. Robson, L. G., Kara, T., Crawley, A. and Tickle, C. (1994). Tissue and cellular patterning of the musculature in chick wings. Development 120, 1265-1276.
48. Rodriguez, C. I., Buchholz, F., Galloway, J., Sequerra, R., Kasper, J., Ayala, R., Stewart, A. F. and Dymecki, S. M. (2000). High-efficiency deleter mice show that FLPe is an alternative to Cre-loxP. Nat. Genet. 25, 139-140.
49. Rubinstein, N. A. and Kelly, A. M. (2004). The diversity of muscle fiber types and its origin during development. In Myology (ed. A. G. Engel and C. Franzini- Armstrong), pp. 87-103. New York: McGraw-Hill.
50. Sanes, J. (2004). The extracellular matrix. In Myology, Vol. 1 (ed. A. Engel and C. Franzini-Armstrong), pp. 471-487. New York: McGraw-Hill.
51. Schiaffino, S. and Reggiani, C. (1996). Molecular diversity of myofibrillar proteins: gene regulation and functional significance. Physiol. Rev. 76, 371-423.
52. Shanely, R. A., Zwetsloot, K. A., Childs, T. E., Lees, S. J., Tsika, R. W. and Booth, F. W. (2009). IGF-I activates the mouse type IIb myosin heavy chain gene. Am. J. Physiol. Cell Physiol. 297, C1019-C1027.
53. Soriano, P. (1999). Generalized lacZ expression with the ROSA26 Cre reporter strain. Nat. Genet. 21, 70-71.
54. Srinivas, S., Watanabe, T., Lin, C. S., William, C. M., Tanabe, Y., Jessell, T. M. and Costantini, F. (2001). Cre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus. BMC Dev. Biol. 1, 4.
55. Stallcup, W. B. (2002). The NG2 proteoglycan: past insights and future prospects. J. Neurocytol. 31, 423-435.
56. Stockdale, F. E. (1992). Myogenic cell lineages. Dev. Biol. 154, 284-298.
57. Tang, S. H., Silva, F. J., Tsark, W. M. and Mann, J. R. (2002). A Cre/loxP-deleter transgenic line in mouse strain 129S1/SvImJ. Genesis 32, 199-202.
58. Tomasek, J. J., Gabbiani, G., Hinz, B., Chaponnier, C. and Brown, R. A. (2002). Myofibroblasts and mechano-regulation of connective tissue remodelling. Nat. Rev. Mol. Cell Biol. 3, 349-363.
59. Van Swearingen, J. and Lance-Jones, C. (1995). Slow and fast muscle fibers are preferentially derived from myoblasts migrating into the chick limb bud at different developmental times. Dev. Biol. 170, 321-337.
60. Van Vliet, E., Melis, M. and Van Ewijk, W. (1984). Monoclonal antibodies to stromal cell types of the mouse thymus. Eur. J. Immunol. 14, 524-529.
61. Wang, H., Noulet, F., Edom-Vovard, F., Le Grand, F. and Duprez, D. (2010). Bmp signaling at the tips of skeletal muscles regulates the number of fetal muscle progenitors and satellite cells during development. Dev. Cell 18, 643-654.
62. White, R. B., Bierinx, A. S., Gnocchi, V. F. and Zammit, P. S. (2010). Dynamics of muscle fibre growth during postnatal mouse development. BMC Dev. Biol. 10, 21.
63. Wigmore, P. M. and Evans, D. J. (2002). Molecular and cellular mechanisms involved in the generation of fiber diversity during myogenesis. Int. Rev. Cytol. 216, 175-232.
64. Wu, S., Wu, Y. and Capecchi, M. R. (2006). Motoneurons and oligodendrocytes are sequentially generated from neural stem cells but do not appear to share common lineage-restricted progenitors in vivo. Development 133, 581-590.
65. Zou, Y., Zhang, R. Z., Sabatelli, P., Chu, M. L. and Bonnemann, C. G. (2008). Muscle interstitial fibroblasts are the main source of collagen VI synthesis in skeletal muscle: implications for congenital muscular dystrophy types Ullrich and Bethlem. J. Neuropathol. Exp. Neurol. 67, 144-154.