Molecular genetics of ameloblast cell lineage

Journal of Experimental Zoology Part B: Molecular and Developmental Evolution

Volumn 312, Issue 5, 2009, Pages 437-444

  Bei, Marianna ^a  

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMALIA;

ANIMAL; CELL ADHESION; CELL DIFFERENTIATION; CYTOLOGY; ENAMEL; GENETICS; GROWTH, DEVELOPMENT AND AGING; HUMAN; LIFE CYCLE; METHODOLOGY; MOLECULAR BIOLOGY; MORPHOGENESIS; MOUSE; ODONTOBLAST; PHYSIOLOGY; REVIEW; TOOTH; TOOTH CROWN; TRANSGENIC MOUSE;

ANIMALS; CELL ADHESION; CELL DIFFERENTIATION; DENTAL ENAMEL; HUMANS; LIFE CYCLE STAGES; MICE; MICE, TRANSGENIC; MOLECULAR BIOLOGY; MORPHOGENESIS; ODONTOBLASTS; TOOTH; TOOTH CROWN;

EID: 67651204860     PISSN: 15525007     EISSN: 15525015     Source Type: Journal    
DOI: 10.1002/jez.b.21261     Document Type: Article

References (62)

1. Aberdam D, Aguzzi A, Baudoin C, Galliano MF, Ortonne JP, Meneguzzi G. 1994. Developmental expression of nicein adhesion protein (laminin-5) subunits suggests multiple morphogenic roles. Cell Adhes Commun 2:115-129.
2. Åberg T, Wozney J, Thesleff I. 1997. Expression patterns of bone morphogenetic proteins (Bmps) in the developing mouse tooth suggest roles in morphogenesis and cell differentiation. Dev Dyn 210: 383-396.
3. Aldred MJ, Savarirayan R, Crawford PJ. 2003. Amelogenesis imperfecta: a classification and catalogue for the 21st century. Oral Dis 9: 19-23.
4. Baker SE, Hopkinson SB, Fitchmun M, Andreason GL, Frasier F, Plopper G, Quaranta V, Jones JC. 1996. Laminin-5 and hemidesmosomes: role of the alpha 3 chain subunit in hemidesmosome stability and assembly. J Cell Sci 109: 2509-2520.
5. Bartlett JD, Beniash E, Lee DH, Smith CE. 2004. Decreased mineral content in MMP-20 null mouse enamel is prominent during the maturation stage. J Dent Res 83: 909-913.
6. Begue-Kirn C, Krebsbach PH, Bartlett JD, Butler WT. 1998. Dentin sialoprotein, dentin phosphoprotein, enamelysin and ameloblastin: tooth-specific molecules that are distinctively expressed during murine dental differentiation. Eur J Oral Sci 106: 963-970.
7. Bei M, Stowell S, Maas R. 2004. Msx2 controls ameloblast terminal differentiation. Dev Dyn 231: 758-765.
8. Bouwman P, Gollner H, Elasser HP, Eckhoff G, Karis A, Grosveld F, Philipsen S, Suske G. 2000. Transcription factor Sp3 is essential for post-natal survival and late tooth development. EMBO J 19: 655-661.
9. Brain EB, Wigglesworth JS. 1968. Developing teeth in epidermolysis bullosa hereditaria letalis. A histological study. Br Dent J 124: 255-260.
10. Caterina JJ, Skobe Z, Shi J, Ding Y, Simmer JP, Birkedal-Hansen H, Bartlett JD. 2002. Enamelysin (matrix metalloproteinase 20)-deficient mice display an amelogenesis imperfecta phenotype. J Biol Chem 277: 49598-49604.
11. Christiano AM, Pulkkinen L, McGrath JA, Uitto J. 1997. Mutation-based prenatal diagnosis of Herlitz junctional epidermolysis bullosa. Prenat Diagn 17: 343-354.
12. Coin R, Haikel Y, Ruch JV. 1999. Effects of apatite, transforming growth factor beta-1, bone morphogenetic protein-2 and interleukin-7 on ameloblast differentiation in vitro. Eur J Oral Sci 107: 487-495.
13. Collier PM, Sauk JJ, Rosenbloom SJ, Yuan ZA, Gibson CW. 1997. An amelogenin gene defect associated with human X-linked amelogenesis imperfecta. Arch Oral Biol 42: 235-242.
14. Dassule H, Lewis P, Bei M, Maas R, McMahon AP. 2000. Sonic hedgehog regulates growth and morphogenesis of the tooth. Development 127: 4775-4785.
15. Dobrowolski R, Sasse P, Schrickel JW, Watkins M, Kim JS, Rackauskas M, Troatz C, Ghanem A, Tiemann K, Degen J, Bukauskas FF, Civitelli R, Lewalter T, Fleischmann BK, Willecke K. 2008. The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodi-gital dysplasia in humans. Hum Mol Genet 17: 539-554.
16. Fausser J, Schlepp O, Aberdam D, Meneguzzi G, Ruch JV, Lesot H. 1998. Localization of antigens associated with adherens junctions, desmosomes and hemidesmosomes during murine molar morphogenesis. Differentiation 63: 1-11.
17. Fukumoto S, Kiba T, Hall B, Iehara N, Nakamura T, Longnecker G, Krebsbach PH, Nanci A, Kulkarni AB, Yamada Y. 2004. Ameloblastin is a cell adhesion molecule required for maintaining the differentiation state of amelo-blasts. J Biol Chem 167: 973-983.
18. Fukumoto S, Yamada A, Nonaka K, Yamada Y. 2005. Essential roles of ameloblastin in maintaining ameloblast differentiation and enamel formation. Cells Tissues Organs 181: 189-195.
19. Garrod D, Chidgey M, North A. 1996. Desmosomes: differentiation, development, dynamics and disease. Curr Opin Cell Biol 8: 670-678.
20. Gibson CW, Yuan ZA, Hall B, Longenecker G, Chen E, Thyagarajan T, Sreenath T, Wright JT, Decker S, Piddington R, Harrison G, Kulkarni AB. 2001. Amelogenin-deficient mice display an amelogenesis imperfecta phenotype. J Biol Chem 276: 31871-31875.
21. Green KJ, Jones JCR. 1996. Desmosomes and hemidesmosomes: structure and function of molecular components. FASEB J 10: 871-881.
22. Gritli-Linde A., Bei M, Maas R, Zhang XM, Linde A, McMahon AP. 2002. Shh signaling within the dental epithelium is necessary for cell proliferation, growth and polarization. Development 129: 5323-5337.
23. Hart PS, Aldred MJ, Crawford PJ, Wright NJ, Hart TC, Wright JT. 2002. Amelogenesis imperfecta phenotype-genotype correlations with two amelogenin gene mutations. Arch Oral Biol 47: 261-265.
24. Hart PS, Hart TC, Michalec MD, Ryu OH, Simmons D, Hong S, Wright JT. 2004. Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta. J Med Genet 41: 545-549.
25. Hu JC, Sun X, Zhang C, Liu S, Bartlett JD, Simmer JP. 2002. Enamelysin and kallikrein-4 mRNA expression in developing mouse molars. Eur J Oral Sci 1: 307-315.
26. Hu JC, Hu Y, Smith CE, McKee MD, Wright JT, Yamakoshi Y, Papagerakis P, Hunter GK, Feng JQ, Yamakoshi F, Simmer JP. 2008. Enamel defects and ameloblast-specific expression in Enam knock-out/lacz knock-in mice. J Biol Chem 283: 10858-10871.
27. Karcher-Djuricic V, Staubli A, Meyer JM, Ruch JV. 1985. Acellular dental matrices promote functional differentiation of ameloblasts. Differentiation 29: 169-175.
28. Kim JW, Simmer JP, Hu YY, Lin BP, Boyd C, Wright JT, Yamada CJ, Rayes SK, Feigal RJ, Hu JC. 2004. Amelogenin p.M1T and p.W4S mutations underlying hypoplastic X-linked amelogenesis imperfecta. J Dent Res 83: 378-383.
29. Kim JW, Simmer JP, Hart TC, Hart PS, Ramaswami MD, Bartlett JD, Hu JC. 2005. MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imper-fecta. J Med Genet 42: 271-275.
30. Kim JW, Lee SK, Lee ZH, Park JC, Lee KE, Lee MH, Park JT, Seo BM, Hu JC, Simmer JP. 2008. FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfecta. Am J Hum Genet 82: 489-494.
31. Kivirikko S, McGrath JA, Baudoin C, Aberdam D, Ciatti S, Dunnill MG, McMillan JR, Eady RA, Ortonne JP, Meneguzzi G. 1995. A homozygous nonsense mutation in the a 3 chain gene of laminin 5 (LAMA3) in lethal (Herlitz) junctional epidermolysis bullosa. Hum Mol Genet 4: 959-964.
32. Kollar EJ, Baird GR. 1970. Tissue interactions in embryonic mouse tooth germs II. The inductive role of the dental papilla. J Embryol Exp Morphol 24: 173-186.
33. Kollar EJ, Lumsden AGS. 1979. Tooth morphogenesis: the role of the innervation during induction and pattern formation. J Biol Buccale 7: 49-60.
34. Krebsbach PH, Lee SK, Matsuki Y, Kozak CA, Yamada KM, Yamada Y. 1996. Full-length sequence, localization, and chromosomal mapping of ameloblastin. A novel tooth-specific gene. J Biol Chem 271: 4431-4435.
35. Lee SK, Hu JC, Bartlett JD, Lee KE, Lin BP, Simmer JP, Kim JW. 2008. Mutational spectrum of FAM83H: the C-terminal portion is required for tooth enamel calcification. Hum Mutat 29: 95-99.
36. Lench NJ, Winter GB. 1995. Characterisation of molecular defects in X-linked amelogenesis imperfecta (AIH1). Hum Mutat 5: 251-259.
37. Lezot F, Thomas B, Greene SR, Hotton D, Yuan Z, Castaneda B, Bolanos A, Depew M, Sharpe P, Gibson CW, Berdal A. 2008. Physiological implications of DLX homeo-proteins in enamel formation. J Cell Physiol 216: 688-697.
38. McGrath JA, Kivirikko S, Ciatti S, Moss C, Dunnill GS, Eady RA, Rodeck CH, Christiano AM, Uitto J. 1995. A homozygous nonsense mutation in the a 3 chain gene of laminin 5 (LAMA3) in Herlitz junctional epidermolysis bullosa: prenatal exclusion in a fetus at risk. Genomics 29: 282-284.
39. Meyer JM, Ruch JV, Kubler MD, Kupferle C, Lesot H. 1995. Cultured incisors display major modifications in basal lamina deposition without further effect on odontoblast differentiation. Cell Tissue Res 279: 135-147.
40. Millar SE, Koyama E, Reddy ST, Andl T, Gaddapara T, Piddington R, Gibson CW. 2003. Over-and ectopic expression of Wnt3 causes progressive loss of ameloblasts in postnatal mouse incisor teeth. Connect Tissue Res 44: 124-129.
41. Moffatt P, Smith CE, Sooknanan R, St-Arnaud R, Nanci A. 2006a. Identification of secreted and membrane proteins in the rat incisor enamel organ using a signal-trap screening approach. Eur J Oral Sci 114: 139-146.
42. Moffatt P, Smith CE, St-Arnaud R, Simmons D, Wright JT, Nanci A. 2006b. Cloning of rat amelotin and localization of the protein to the basal lamina of maturation stage ameloblasts and junctional epithelium. Biochem J 399: 37-46.
43. Mustonen T, Ilmonen M, Pummila M, Kangas AT, Laurikkala J, Jaatinen R, Pispa J, Gaide O, Schneider P, Thesleff I, Mikkola ML. 2004. Ectodysplasin A1 promotes placodal cell fate during early morphogenesis of ectodermal appendages. Development 131: 4907-4919.
44. Nakamura T, deVega S, Fukumoto S, Jimenez L, Unda F, Yamada Y. 2008. Transcription factor epiprofin is essential for tooth morphogenesis by regulating epithelial cell fate and tooth number. J Biol Chem 283: 4825-4833.
45. Nanci A. 2007. Ten Cate's oral histology: development, structure, and function, 7th edition. St. Louis, MO: Mosby Inc.
46. Pasqualini R, Bodorova J, Song Y, Hemler ME. 1993. A study of the structure, function and distribution of b5 integrin using novel anti-b5 monoclonal antibodies. J Cell Sci 105: 101-111.
47. Ruspita I, Miyoshi K, Muto T, Abe K, Horiguchi T, Noma T. 2008. Sp6 downregulation of follistatin gene expression in ameloblasts. J Med Invest 55: 87-98.
48. Ryan MC, Lee K, Miyashita Y, Carter WG. 1999. Targeted disruption of the LAMA 3 gene in mice reveals abnormalities in survival and late stage differentiation of epithelial cells. J Cell Biol 145: 1309-1323.
49. Salmivirta K, Gullberg D, Hirsch E, Altruda F, Ekblom P. 1996. Integrin subunit expression associated with epithelial-mesenchymal interactions during murine tooth development. Dev Dyn 205: 104-113.
50. Satokata I, Ma L, Ohshima H, Bei M, Woo I, Nishizawa K, Maeda T, Takano Y, Uchiyama I, Heaney S, Peters H, Tang Z, Maxson R, Maas R. 2000. Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation. Nat Genet 24: 391-395.
51. Suda N, Kitahara Y, Ohyama K. 2006. A case of amelogenesis imperfecta, cleft lip and palate and polycystic kidney disease. Orthod Craniofac Res 1: 52-56.
52. Thesleff I, Hurmerinta K. 1981. Tissue interactions in tooth development. Differentiation 18: 75-88.
53. Thesleff I, Nieminen P. 2005. Tooth induction. Encyclopedia of life sciences. Chichester, UK: Wiley.
54. Vidal F, Baudoin C, Miquel C, Galliano MF, Christiano AM, Uitto J, Ortonne JP, Meneguzzi G. 1995. Cloning of the laminin 5a3 chain gene (LAMA3) and identification of a homozygous deletion in a patient with Herlitz junctional epidermolysis bullosa. Genomics 30: 273-280.
55. Wang XP, Suomalainen M, Jorgez CJ, Matzuk MM, Werner S, Thesleff I. 2004. Follistatin regulates enamel patterning in mouse incisors by asymmetrically inhibiting BMP signaling and ameloblast differentiation. Dev Cell 7: 719-730.
56. Wang XP, Suomalainen M, Felszeghy S, Zelarayan LC, Alonso MT, Plikus MV, Maas RL, Chuong CM, Schimmang T, Thesleff I. 2007. An integrated gene regulatory network controls stem cell proliferation in teeth. PLoS Biol 5:e159.
57. Witkop Jr CJ. 1988. Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classification. J Oral Pathol 17: 547-553.
58. Wright JT. 2006. The molecular etiologies and associated phenotypes of amelogenesis imperfecta. Am J Med Genet 140: 2547-2555.
59. Wright JT, Hart PS, Aldred MJ, Seow K, Crawford PJ, Hong SP, Gibson CW, Hart TC. 2003. Relationship of phenotype and genotype in X-linked amelogenesis imperfecta. Connect Tissue Res 44: 72-78.
60. Yoshiba K, Yoshiba N, Aberdam D, Meneguzzi G, Perrin-Schmitt F, Stoetzel C, Ruch JV, Lesot H. 1998. Expression and localization of laminin-5 subunits during mouse tooth development. Dev Dyn 211: 164-176.
61. Zeichner-David M, Diekwisch T, Fincham A, Lau E, MacDougall M, Moradian-Oldak J, Simmer J, Snead M, Slavkin HC. 1995. Control of ameloblast differentiation. Int J Dev Biol 39: 69-92.
62. Zhou H, Nichols A, Wohlwend A, Bolon I, Vassali JD. 1999. Extracellular proteolysis alters tooth development in transgenic mice expressing urokinase-type plasminogen activator in the enamel organ. Development 126:903-912.