Foxc2 induces Wnt4 and Bmp4 expression during muscle regeneration and osteogenesis

Cell Death and Differentiation

Volumn 20, Issue 8, 2013, Pages 1031-1042

  Gozo, M C ^a   Aspuria, P J ^a   Cheon, D J ^a   Walts, A E ^a   Berel, D ^a   Miura, N ^b   Karlan, B Y ^a   Orsulic, S ^a  

^a CEDARS SINAI MEDICAL CENTER   (United States)

^b HAMAMATSU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

Bmp4; Foxc2; Myogenesis; Osteogenesis; Wnt4

Indexed keywords

BONE MORPHOGENETIC PROTEIN 4; RHOA GUANINE NUCLEOTIDE BINDING PROTEIN; TRANSCRIPTION FACTOR FOXC2; WNT4 PROTEIN;

ANIMAL CELL; ARTICLE; BONE DEVELOPMENT; CELL DIFFERENTIATION; CELL FUSION; CELL PROLIFERATION; CONTROLLED STUDY; DOWN REGULATION; MOUSE; MUSCLE DEVELOPMENT; MUSCLE REGENERATION; MYOBLAST; MYOTUBE; NONHUMAN; OSSIFYING MYOSITIS; OSTEOBLAST; PREMATURITY; PRIORITY JOURNAL; PROTEIN EXPRESSION; SKELETAL MUSCLE SATELLITE CELL; WNT SIGNALING PATHWAY;

ANIMALS; BONE MORPHOGENETIC PROTEIN 4; CELL DIFFERENTIATION; CELL LINE; CELL PROLIFERATION; FIBROBLASTS; FORKHEAD TRANSCRIPTION FACTORS; MICE; MICE, INBRED C57BL; MODELS, ANIMAL; MUSCLE, SKELETAL; MYOBLASTS, SKELETAL; MYOD PROTEIN; NIH 3T3 CELLS; OSTEOGENESIS; PAX7 TRANSCRIPTION FACTOR; REGENERATION; SIGNAL TRANSDUCTION; WNT4 PROTEIN;

MOUSE MAMMARY TUMOR VIRUS;

EID: 84880290546     PISSN: 13509047     EISSN: 14765403     Source Type: Journal    
DOI: 10.1038/cdd.2013.34     Document Type: Article

References (44)

1. Allbrook DB, Han MF, Hellmuth AE. Population of muscle satellite cells in relation to age and mitotic activity. Pathology 1971; 3: 223-243.
2. Zammit PS, Heslop L, Hudon V, Rosenblatt JD, Tajbakhsh S, Buckingham ME et al. Kinetics of myoblast proliferation show that resident satellite cells are competent to fully regenerate skeletal muscle fibers. Exp Cell Res 2002; 281: 39-49.
3. Tedesco FS, Dellavalle A, Diaz-Manera J, Messina G, Cossu G. Repairing skeletal muscle: regenerative potential of skeletal muscle stem cells. J Clin Invest 2010; 120: 11-19.
4. Jackson WM, Aragon AB, Bulken-Hoover JD, Nesti LJ, Tuan RS. Putative heterotopic ossification progenitor cells derived from traumatized muscle. J Orthop Res 2009; 27: 1645-1651.
5. Zundel WS, Tyler FH. The muscular dystrophies. N Engl J Med 1965; 273: 596-601; CONCL.
6. Frank NY, Kho AT, Schatton T, Murphy GF, Molloy MJ, Zhan Q et al. Regulation of myogenic progenitor proliferation in human fetal skeletal muscle by BMP4 and its antagonist Gremlin. J Cell Biol 2006; 175: 99-110.
7. Ono Y, Calhabeu F, Morgan JE, Katagiri T, Amthor H, Zammit PS. BMP signalling permits population expansion by preventing premature myogenic differentiation in muscle satellite cells. Cell Death Differ 2011; 18: 222-234.
8. Clever JL, Sakai Y, Wang RA, Schneider DB. Inefficient skeletal muscle repair in inhibitor of differentiation knockout mice suggests a crucial role for BMP signaling during adult muscle regeneration. Am J Physiol Cell Physiol 2010; 298: C1087-C1099.
9. Bandyopadhyay A, Tsuji K, Cox K, Harfe BD, Rosen V, Tabin CJ. Genetic analysis of the roles of BMP2, BMP4, and BMP7 in limb patterning and skeletogenesis. PLoS Genet 2006; 2: e216.
10. Dahlqvist C, Blokzijl A, Chapman G, Falk A, Dannaeus K, Ibanez CF et al. Functional Notch signaling is required for BMP4-induced inhibition of myogenic differentiation. Development 2003; 130: 6089-6099.
11. Polesskaya A, Seale P, Rudnicki MA. Wnt signaling induces the myogenic specification of resident CD45+ adult stem cells during muscle regeneration. Cell 2003; 113: 841-852.
12. Bernardi H, Gay S, Fedon Y, Vernus B, Bonnieu A, Bacou F. Wnt4 activates the canonical beta-catenin pathway and regulates negatively myostatin: functional implication in myogenesis. Am J Physiol Cell Physiol 2011; 300: C1122-C1138.
13. Sethi JK, Vidal-Puig A. Wnt signalling and the control of cellular metabolism. Biochem J 2010; 427: 1-17.
14. Guo X, Wang XF. Signaling cross-talk between TGF-beta/BMP and other pathways. Cell Res 2009; 19: 71-88.
15. Hu MC, Rosenblum ND. Smad1, beta-catenin and Tcf4 associate in a molecular complex with the Myc promoter in dysplastic renal tissue and cooperate to control Myc transcription. Development 2005; 132: 215-225.
16. Labbe E, Letamendia A, Attisano L. Association of Smads with lymphoid enhancer binding factor 1/T cell-specific factor mediates cooperative signaling by the transforming growth factor-beta and wnt pathways. Proc Natl Acad Sci USA 2000; 97: 8358-8363.
17. Hannenhalli S, Kaestner KH. The evolution of Fox genes and their role in development and disease. Nat Rev Genet 2009; 10: 233-240.
18. Nifuji A, Miura N, Kato N, Kellermann O, Noda M. Bone morphogenetic protein regulation of forkhead/winged helix transcription factor Foxc2 (Mfh1) in a murine mesodermal cell line C1 and in skeletal precursor cells. J Bone Miner Res 2001; 16: 1765-1771.
19. Davis KE, Moldes M, Farmer SR. The forkhead transcription factor FoxC2 inhibits white adipocyte differentiation. J Biol Chem 2004; 279: 42453-42461.
20. Perez VA, Ali Z, Alastalo TP, Ikeno F, Sawada H, Lai YJ et al. BMP promotes motility and represses growth of smooth muscle cells by activation of tandem Wnt pathways. J Cell Biol 2011; 192: 171-188.
21. Habas R, Kato Y, He X. Wnt/Frizzled activation of Rho regulates vertebrate gastrulation and requires a novel Formin homology protein Daam1. Cell 2001; 107: 843-854.
22. Nishiyama T, Kii I, Kudo A. Inactivation of Rho/ROCK signaling is crucial for the nuclear accumulation of FKHR and myoblast fusion. J Biol Chem 2004; 279: 47311-47319.
23. Fortier M, Comunale F, Kucharczak J, Blangy A, Charrasse S, Gauthier-Rouviere C. RhoE controls myoblast alignment prior fusion through RhoA and ROCK. Cell Death Differ 2008; 15: 1221-1231.
24. Retting KN, Song B, Yoon BS, Lyons KM. BMP canonical Smad signaling through Smad1 and Smad5 is required for endochondral bone formation. Development 2009; 136: 1093-1104.
25. Bryson-Richardson R, JCurrie PD. The genetics of vertebrate myogenesis. Nat Rev Genet 2008; 9: 632-646.
26. Daczewska M, Picchio L, Jagla T, Figeac N, Jagla K. Muscle development and regeneration in normal and pathological conditions: learning from Drosophila. Curr Pharm Des 2010; 16: 929-941.
27. Amthor H, Christ B, Weil M, Patel K. The importance of timing differentiation during limb muscle development. Curr Biol 1998; 8: 642-652.
28. Zhao P, Hoffman EP. Embryonic myogenesis pathways in muscle regeneration. Dev Dyn 2004; 229: 380-392.
29. Brack AS, Conboy IM, Conboy MJ, Shen J, Rando TA. A temporal switch from notch to Wnt signaling in muscle stem cells is necessary for normal adult myogenesis. Cell Stem Cell 2008; 2: 50-59.
30. Chang J, SonoyamaW,Wang Z, Jin Q, Zhang C, Krebsbach PH et al. Noncanonical Wnt-4 signaling enhances bone regeneration of mesenchymal stem cells in craniofacial defects through activation of p38 MAPK. J Biol Chem 2007; 282: 30938-30948.
31. Trompouki E, Bowman TV, Lawton LN, Fan ZP, Wu DC, DiBiase A et al. Lineage regulators direct BMP and Wnt pathways to cell-specific programs during differentiation and regeneration. Cell 2011; 147: 577-589.
32. Fukuda T, Kokabu S, Ohte S, Sasanuma H, Kanomata K, Yoneyama K et al. Canonical Wnts and BMPs cooperatively induce osteoblastic differentiation through a GSK3beta-dependent and beta-catenin-independent mechanism. Differentiation 2010; 80: 46-52.
33. McBeath R, Pirone DM, Nelson CM, Bhadriraju K, Chen CS. Cell shape, cytoskeletal tension, and RhoA regulate stem cell lineage commitment. Dev Cell 2004; 6: 483-495.
34. Li G, Peng H, Corsi K, Usas A, Olshanski A, Huard J. Differential effect of BMP4 on NIH/ 3T3 and C2C12 cells: implications for endochondral bone formation. J Bone Miner Res 2005; 20: 1611-1623.
35. Friedrichs M, Wirsdoerfer F, Flohe SB, Schneider S, Wuelling M, Vortkamp A. BMP signaling balances proliferation and differentiation of muscle satellite cell descendants. BMC Cell Biol 2011; 12: 26.
36. Hannallah D, Peng H, Young B, Usas A, Gearhart B, Huard J. Retroviral delivery of Noggin inhibits the formation of heterotopic ossification induced by BMP-4, demineralized bone matrix, and trauma in an animal model. J Bone Joint Surg Am 2004; 86-A: 80-91.
37. Liu K, Tripp S, Layfield LJ. Heterotopic ossification: review of histologic findings and tissue distribution in a 10-year experience. Pathol Res Pract 2007; 203: 633-640.
38. Weber FE, Schmokel H, Oelgeschlager M, Nickel J, Maly FE, Hortschansky P et al. Deletion mutants of BMP folding variants act as BMP antagonists and are efficient inhibitors for heterotopic ossification. J Bone Miner Res 2003; 18: 2142-2151.
39. Gannon FH, Kaplan FS, Olmsted E, Finkel GC, Zasloff MA, Shore E. Bone morphogenetic protein 2/4 in early fibromatous lesions of fibrodysplasia ossificans progressiva. Hum Pathol 1997; 28: 339-343.
40. Kan L, Kessler JA. Animal models of typical heterotopic ossification. J Biomed Biotechnol 2011; 2011: 309287.
41. Hong JH, Hwang ES, McManus MT, Amsterdam A, Tian Y, Kalmukova R et al. TAZ, a transcriptional modulator of mesenchymal stem cell differentiation. Science 2005; 309: 1074-1078.
42. Veeman MT, Slusarski DC, Kaykas A, Louie SH, Moon RT. Zebrafish prickle, a modulator of noncanonical Wnt/Fz signaling, regulates gastrulation movements. Curr Biol 2003; 13: 680-685.
43. Miao J, Mu D, Ergel B, Singavarapu R, Duan Z, Powers S et al. Hepsin colocalizes with desmosomes and induces progression of ovarian cancer in a mouse model. Int J Cancer 2008; 123: 2041-2047.
44. Huang da W, Sherman BT, Lempicki RA. Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nat Protoc 2009; 4: 44-57.