Epithelial histogenesis during tooth development

Archives of Oral Biology

Volumn 54, Issue SUPPL. 1, 2009, Pages

  Lesot, H ^a,b,c   Brook, A H ^c  

^a INSERM   (France)

^b UNIVERSITÉ DE STRASBOURG   (France)

^c UNIVERSITY OF LIVERPOOL   (United Kingdom)

Author keywords

Epithelial histogenesis; Tooth development

Indexed keywords

ANIMAL; APOPTOSIS; ARTICLE; CELL DIFFERENTIATION; CYTOLOGY; EPITHELIUM CELL; EXTRACELLULAR MATRIX; MESODERM; METABOLISM; MOUSE; PHYSIOLOGY; PRENATAL DEVELOPMENT; SIGNAL TRANSDUCTION; TOOTH; TOOTH DEVELOPMENT; TOOTH FLORA;

ANIMALS; APOPTOSIS; CELL DIFFERENTIATION; ENAMEL ORGAN; EPITHELIAL CELLS; EXTRACELLULAR MATRIX; MESODERM; MICE; ODONTOGENESIS; SIGNAL TRANSDUCTION; TOOTH;

EID: 71549115159     PISSN: 00039969     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.archoralbio.2008.05.019     Document Type: Article

References (120)

1. Yoshiba K., Yoshiba N., Aberdam D., Meneguzzi G., Perrin-Schmitt F., Stoetzel C., et al. Expression and localization of laminin-5 subunits during mouse tooth development. Dev Dynam 211 2 (1998) 164-176
2. Nagai N., Nakano K., Sado Y., Naito I., Gunduz M., Tsujigiwa H., et al. Localization of type IV collagen a 1 to a 6 chains in basement membrane during mouse molar germ development. Int J Dev Biol 45 7 (2001) 827-831
3. Yoshiba N., Yoshiba K., Stoetzel C., Perrin-Schmitt F., Cam Y., Ruch J.V., et al. Temporospatial gene expression and protein localization of matrix metalloproteinases and their inhibitors during mouse molar tooth development. Dev Dynam 228 1 (2003) 105-112
4. Nadiri A., Kuchler-Bopp S., Haikel Y., and Lesot H. Immunolocalization of BMP-2/-4, FGF-4, and WNT10b in the developing mouse first lower molar. J Histochem Cytochem 52 1 (2004) 103-112
5. Salmivirta K., Gullberg D., Hirsch E., Altruda F., and Ekblom P. Integrin subunit expression associated with epithelial-mesenchymal interactions during murine tooth development. Dev Dynam 205 2 (1996) 104-113
6. Lesot H., Kieffer-Combeau S., Fausser J.L., Meyer J.M., Perrin-Schmitt F., Peterková R., et al. Cell-cell and cell-matrix interactions during initial enamel organ histomorphogenesis in the mouse. Connect Tissue Res 43 2-3 (2002) 191-200
7. Palacios J., Benito N., Berraquero R., Pizarro A., Cano A., and Gamallo C. Differential spatiotemporal expression of E- and P-cadherin during mouse tooth development. Int J Dev Biol 39 4 (1995) 663-666
8. Obara N., and Lesot H. Subcellular localization of beta-catenin and cadherin expression in the cap-stage enamel organ of the mouse molar. Histochem Cell Biol 121 4 (2004) 351-358
9. Ohazama A.C., Tucker ourtney J.M.A.S., Naito A., Tanaka S., Inoue J., and Sharpe P.T. Traf6 is essential for murine tooth cusp morphogenesis. Dev Dynam 229 1 (2004) 131-135
10. Nadiri A., Kuchler-Bopp S., Perrin-Schmitt F., and Lesot H. Expression patterns of BMPRs in the developing mouse molar. Cell Tissue Res 324 1 (2006) 33-40
11. Wolpert L. Cell boundaries: knowing who to mix with and what to shout or whisper. Development 130 19 (2003) 4497-4500
12. Ruch J.V., Lesot H., and Bègue-Kirn C. Odontoblast differentiation. Int J Dev Biol 39 1 (1995) 51-68
13. Ruch J.V., and Lesot H. Molecules implicated in odontoblast terminal differentiation and dentinogenesis. In: Teaford M., Smith M.M., and Ferguson M.W.J. (Eds). Development, function and evolution of teeth (2000), Cambridge University Press, Cambridge 22-36
14. Schmitt R., and Ruch J.V. In vitro synchronization of embryonic mouse incisor preodontoblasts and preameloblasts: repercussions on terminal differentiation. Eur J Oral Sci 108 4 (2000) 311-319
15. Gumbiner B.M. Regulation of cadherin-mediated adhesion in morphogenesis. Nat Rev Mol Cell Biol 6 8 (2005) 622-634
16. Hu B., Nadiri A., Bopp-Küchler S., Perrin-Schmitt F., and Lesot H. Dental epithelial histomorphogenesis in vitro. J Dent Res 84 6 (2005) 521-525
17. Gamer L.W., Nove J., and Rosen V. Return of the chalones. Dev Cell 4 2 (2003) 143-144
18. Hata R.I. Where am i? How a cell recognizes its positional information during morphogenesis. Cell Biol Int 20 1 (1996) 59-65
19. Morgan M.R., Humphries M.J., and Bass M.D. Synergistic control of cell adhesion by integrins and syndecans. Nat Rev Mol Cell Biol 8 12 (2007) 957-969
20. Bitgood M.J., and McMahon A.P. Hedgehog and Bmp genes are coexpressed at many diverse sites of cell-cell interaction in the mouse embryo. Dev Biol 172 1 (1995) 126-138
21. Hardcastle Z., Mo R., Hui C.C., and Sharpe P.T. The Shh signalling pathway in tooth development: defects in Gli2 and Gli3 mutants. Development 125 15 (1998) 2803-2811
22. Sarkar L., Cobourne M., Naylor S., Smalley M., Dale T., and Sharpe P.T. Wnt/Shh interactions regulate ectodermal boundary formation during mammalian tooth development. Proc Natl Acad Sci USA 97 9 (2000) 4520-4524
23. Peterková R., Kristenová P., Lesot H., Lisi S., Vonesch J.L., Gendrault J.L., et al. Different morphotypes of the tabby (EDA) dentition in the mouse mandible result from a defect in the mesio-distal segmentation of dental epithelium. Orthod Craniofac Res 5 4 (2002) 215-226
24. Klein O.D., Minowada G., Peterkova R., Kangas A., Yu B.D., Lesot H., et al. Sprouty genes control diastema tooth development via bidirectional antagonism of epithelial-mesenchymal FGF signaling. Dev Cell 11 2 (2006) 181-190
25. Thomas B.L., Tucker A.S., Qui M., Ferguson C.A., Hardcastle Z., Rubenstein J.L., et al. Role of Dlx-1 and Dlx-2 genes in patterning of the murine dentition. Development 124 23 (1997) 4811-4818
26. Ferguson C.A., Tucker A.S., Christensen L., Lau A.L., Matzuk M.M., and Sharpe P.T. Activin is an essential early mesenchymal signal in tooth development that is required for patterning of the murine dentition. Genes Dev 12 16 (1998) 2636-2649
27. Pourtois M. Contribution to the study of tooth buds in the mouse. I. Periods of induction and morphodifferentiation. Arch Biol (Liege) 72 (1961) 17-95
28. Peterková R., Lesot H., Vonesch J.L., Peterka M., and Ruch J.V. Mouse molar morphogenesis revisited by three-dimensional reconstruction. I. Analysis of initial stages of the first upper molar development revealed two transient buds. Int J Dev Biol 40 5 (1996) 1009-1016
29. Fausser J.L., Schlepp O., Aberdam D., Meneguzzi G., Ruch J.V., and Lesot H. Localization of antigens associated with adherens junctions, desmosomes, and hemidesmosomes during murine molar morphogenesis. Differentiation 63 1 (1998) 1-11
30. Obara N., Suzuki Y., Nagai Y., and Takeda M. Expression of E- and P-cadherin during tooth morphogenesis and cytodifferentiation of ameloblasts. Anat Embryol (Berlin) 197 6 (1998) 469-475
31. Braga V. Epithelial cell shape: cadherins and small GTPases. Exp Cell Res 261 1 (2000) 83-90
32. Vasioukhin V., and Fuchs E. Actin dynamics and cell-cell adhesion in epithelia. Curr Opin Cell Biol 13 1 (2001) 76-84
33. Carthew R.W. Adhesion proteins and the control of cell shape. Curr Opin Genet Dev 15 4 (2005) 358-363
34. Chausovsky A., Waterman H., Elbaum M., Yarden Y., Geiger B., and Bershadsky A.D. Molecular requirements for the effect of neuregulin on cell spreading, motility and colony organization. Oncogene 19 7 (2000) 878-888
35. Mège R.M., Gavard J., and Lambert M. Regulation of cell-cell junctions by the cytoskeleton. Curr Opin Cell Biol 18 5 (2006) 541-548
36. Vleminckx K., and Kemler R. Cadherins and tissue formation: integrating adhesion and signaling. Bioessays 21 3 (1999) 211-220
37. Nelson W.J., and Nusse R. Convergence of Wnt, beta-catenin, and cadherin pathways. Science 303 5663 (2004) 1483-1487
38. Meyer C.J., Alenghat F.J., Rim P., Fong J.H., Fabry B., and Ingber D.E. Mechanical control of cyclic AMP signalling and gene transcription through integrins. Nat Cell Biol 2 9 (2000) 666-668
39. Ko K.S., Arora P.D., and McCulloch C.A. Cadherins mediate intercellular mechanical signaling in fibroblasts by activation of stretch-sensitive calcium-permeable channels. J Biol Chem 276 38 (2001) 35967-35977
40. Ingber D.E. Mechanical control of tissue morphogenesis during embryological development. Int J Dev Biol 50 2-3 (2006) 255-266
41. Ingber D.E., Madri J.A., and Jamieson J.D. Role of basal lamina in neoplastic disorganization of tissue architecture. Proc Natl Acad Sci USA 78 6 (1981) 3901-3905
42. Ingber D.E., and Tensegrity I. Cell structure and hierarchical systems biology. J Cell Sci 116 Pt 7 (2003) 1157-1173
43. Ingber D.E., and Tensegrity I.I. How structural networks influence cellular information processing networks. J Cell Sci 116 Part 8 (2003) 1397-1408
44. Edwards G., and Streuli C. Signalling in extracellular-matrix-mediated control of epithelial cell phenotype. Biochem Soc Trans 23 3 (1995) 464-468
45. Larsen M., Artym V.V., Green J.A., and Yamada K.M. The matrix reorganized: extracellular matrix remodeling and integrin signaling. Curr Opin Cell Biol 18 5 (2006) 463-471
46. Zaidel-Bar R., Itzkovitz S., Ma'ayan A., Iyengar R., and Geiger B. Functional atlas of the integrin adhesome. Nat Cell Biol 9 8 (2007) 858-867
47. Coin R., Lesot H., Vonesch J.L., Haikel Y., and Ruch J.V. Aspects of cell proliferation kinetics of the inner dental epithelium during mouse molar and incisor morphogenesis: a reappraisal of the role of the enamel knot area. Int J Dev Biol 43 3 (1999) 261-267
48. Shigemura N., Kiyoshima T., Kobayashi I., Matsuo K., Yamaza H., Akamine A., et al. The distribution of BrdU- and TUNEL-positive cells during odontogenesis in mouse lower first molars. Histochem J 31 6 (1999) 367-377
49. Lisi S., Peterková R., Peterka M., Vonesch J.L., Ruch J.V., and Lesot H. Tooth morphogenesis and pattern of odontoblast differentiation. Connect Tissue Res 44 Suppl 1 (2003) 167-170
50. Obara N., and Lesot H. Asymmetrical growth, differential cell proliferation, and dynamic cell rearrangement underlie epithelial morphogenesis in mouse molar development. Cell Tissue Res 330 3 (2007) 461-473
51. Ozawa M., Baribault H., and Kemler R. The cytoplasmic domain of the cell adhesion molecule uvomorulin associates with three independent proteins structurally related in different species. EMBO J 8 6 (1989) 1711-1717
52. Logan C.Y., and Nusse R. The Wnt signaling pathway in development and disease. Annu Rev Cell Dev Biol 20 (2004) 781-810
53. Keränen S.V., Aberg T., Kettunen P., Thesleff I., and Jernvall J. Association of developmental regulatory genes with the development of different molar tooth shapes in two species of rodents. Dev Genes Evol 208 9 (1998) 477-486
54. Jernvall J., and Thesleff I. Reiterative signaling and patterning during mammalian tooth morphogenesis. Mech Dev 92 1 (2000) 19-29
55. Peterková R., Peterka M., Viriot L., and Lesot H. Development of the vestigial tooth primordia as part of mouse odontogenesis. Connect Tissue Res 43 2-3 (2002) 120-128
56. Lesot H., Peterková R., Schmitt R., Meyer J.M., Viriot L., Vonesch J.L., et al. Initial features of the inner dental epithelium histo-morphogenesis in the first lower molar in mouse. Int J Dev Biol 43 3 (1999) 245-254
57. Jernvall J., Kettunen P., Karavanova I., Martin L.B., and Thesleff I. Evidence for the role of the enamel knot as a control center in mammalian tooth cusp formation: non-dividing cells express growth stimulating Fgf-4 gene. Int J Dev Biol 38 3 (1994) 463-469
58. Byrne C. Regulation of gene expression in developing epidermal epithelia. Bioessays 19 8 (1997) 691-698
59. Kelley M.W. Regulation of cell fate in the sensory epithelia of the inner ear. Nat Rev Neurosci 7 11 (2006) 837-849
60. Metallo C.M., Ji L., de Pablo J.J., and Palecek S.P. Retinoic acid and bone morphogenetic protein signaling synergize to efficiently direct epithelial differentiation of human embryonic stem cells. Stem Cells; 26 2 (2008) 372-380
61. Kindaichi K. An electron microscopic study of cell death in molar tooth germ epithelia of mouse embryos. Arch Histol Jpn 43 4 (1980) 289-304
62. Lesot H., Vonesch J.L., Peterka M., Turecková J., Peterková R., and Ruch J.V. Mouse molar morphogenesis revisited by three-dimensional reconstruction. II. Spatial distribution of mitoses and apoptosis in cap to bell staged first and second upper molar teeth. Int J Dev Biol 40 5 (1996) 1017-1031
63. Jernvall J., Aberg T., Kettunen P., Keränen S., and Thesleff I. The life history of an embryonic signaling center: BMP-4 induces p21 and is associated with apoptosis in the mouse tooth enamel knot. Development 125 2 (1998) 161-169
64. Peterková R., Peterka M., and Lesot H. The developing mouse dentition: a new tool for apoptosis study. Ann NY Acad Sci 1010 (2003) 453-466
65. Matalova E., Tucker A.S., and Sharpe P.T. Death in the life of a tooth. J Dent Res 83 1 (2004) 11-16
66. Yoshiba K., Yoshiba N., Aberdam D., Meneguzzi G., Perrin-Schmitt F., Stoetzel C., et al. Differential expression of laminin-5 subunits during incisor and molar development in the mouse. Int J Dev Biol 44 3 (2000) 337-340
67. Sarkar L., and Sharpe P.T. Expression of Wnt signalling pathway genes during tooth development. Mech Dev 85 1-2 (1999) 197-200
68. Løes S., Luukko K., Kvinnsland I.H., and Kettunen P. Slit1 is specifically expressed in the primary and secondary enamel knots during molar tooth cusp formation. Mech Dev 107 1-2 (2001) 155-157
69. Iseki S., Araga A., Ohuchi H., Nohno T., Yoshioka H., Hayashi F., et al. Sonic hedgehog is expressed in epithelial cells during development of whisker, hair, and tooth. Biochem Biophys Res Commun 218 3 (1996) 688-693
70. Dassule H.R., Lewis P., Bei M., Maas R., and McMahon A.P. Sonic hedgehog regulates growth and morphogenesis of the tooth. Development 127 22 (2000) 4775-4785
71. Tucker A.S., Headon D.J., Schneider P., Ferguson B.M., Overbeek P., Tschopp J., et al. Edar/Eda interactions regulate enamel knot formation in tooth morphogenesis. Development 127 21 (2000) 4691-4700
72. Miletich I., and Sharpe P.T. Normal and abnormal dental development. Hum Mol Genet 12 Spec No 1 (2003) R69-73
73. Bei M., Stowell S., and Maas R. Msx2 controls ameloblast terminal differentiation. Dev Dynam 231 4 (2004) 758-765
74. Neumann M., and Affolter M. Remodelling epithelial tubes through cell rearrangements: from cells to molecules. EMBO Rep 7 1 (2006) 36-40
75. Pispa J., Jung H.S., Jernvall J., Kettunen P., Mustonen T., Tabata M.J., et al. Cusp patterning defect in Tabby mouse teeth and its partial rescue by FGF. Dev Biol 216 2 (1999) 521-534
76. Miard S., Peterková R., Vonesch J.L., Peterka M., Ruch J.V., and Lesot H. Alterations in the incisor development in the Tabby mouse. Int J Dev Biol 43 6 (1999) 517-529
77. Kettunen P., Spencer-Dene B., Furmanek T., Kvinnsland I.H., Dickson C., Thesleff I., et al. Fgfr2b mediated epithelial-mesenchymal interactions coordinate tooth morphogenesis and dental trigeminal axon patterning. Mech Dev 124 11-12 (2007) 868-883
78. Tepass U., Godt D., and Winklbauer R. Cell sorting in animal development: signalling and adhesive mechanisms in the formation of tissue boundaries. Curr Opin Genet Dev 12 5 (2002) 572-582
79. Meyer J.M., Steuer P., Obara N., Vonesch J.L., and et Lesot H. Histogenesis of the inner dental epithelium during molar development in the mouse. In: Zadzinska E. (Ed). Current trends in dental morphology research (2005), University of Lodz Press, Lodz 411-419
80. Nishikawa S., and Sasaki F. DNA localization in nuclear fragments of apoptotic ameloblasts using anti-DNA immunoelectron microscopy: programmed cell death of ameloblasts. Histochem Cell Biol 104 2 (1995) 151-159
81. Bronckers A.L., Lyaruu D.M., Goei W., Litz M., Luo G., Karsenty G., et al. Nuclear DNA fragmentation during postnatal tooth development of mouse and hamster and during dentin repair in the rat. Eur J Oral Sci 104 2 (Part 1) (1996) 102-111
82. Olive M., and Ruch J.V. Does the basement membrane control the mitotic activity of the inner dental epithelium of the embryonic mouse first lower molar. Dev Biol 93 2 (1982) 301-307
83. Viriot L., Peterková R., Vonesch J.L., Peterka M., Ruch J.V., and Lesot H. Mouse molar morphogenesis revisited by three-dimensional reconstruction. III. Spatial distribution of mitoses and apoptoses up to bell-staged first lower molar teeth. Int J Dev Biol 41 5 (1997) 679-690
84. Bernfield M.R., and Banerjee S.D. The basal lamina in epithelial-mesenchymal interactions. In: Kefalides N. (Ed). Biology and chemistry of basement membranes (1978), Academic Press, New York 137-148
85. Ekblom P., Alitalo K., Vaheri A., Timpl R., and Saxén L. Induction of a basement membrane glycoprotein in embryonic kidney: possible role of laminin in morphogenesis. Proc Natl Acad Sci USA 77 1 (1980) 485-489
86. Salazar-Ciudad I., and Jernvall J. A gene network model accounting for development and evolution of mammalian teeth. Proc Natl Acad Sci USA 99 12 (2002) 8116-8120
87. Schmitt R., Lesot H., Vonesch J.L., and Ruch J.V. Mouse odontogenesis in vitro: the cap-stage mesenchyme controls individual molar crown morphogenesis. Int J Dev Biol 43 3 (1999) 255-260
88. Matalova E., Antonarakis G.S., Sharpe P.T., and Tucker A.S. Cell lineage of primary and secondary enamel knots. Dev Dynam 233 3 (2005) 754-759
89. Coin R., Kieffer S., Lesot H., Vonesch J.L., and Ruch J.V. Inhibition of apoptosis in the primary enamel knot does not affect specific tooth crown morphogenesis in the mouse. Int J Dev Biol 44 4 (2000) 389-396
90. Satokata I., Ma L., Ohshima H., Bei M., Woo I., Nishizawa K., et al. Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation. Nat Genet 24 4 (2000) 391-395
91. Mittenthal J.E., and Jacobson A.G. The mechanics of morphogenesis in multicellular embryos. In: Akkas N. (Ed). Biomechanics of active movement and deformation of cells (1990), Springer-Verlag, Berlin 295-401
92. Hardin J., and Walston T. Models of morphogenesis: the mechanisms and mechanics of cell rearrangement. Curr Opin Genet Dev 14 4 (2004) 399-406
93. Ruch J.V. Determinisms of odontogenesis. Revis Biol Cell 14 (1987) 1-99
94. Zeichner-David M., Diekwisch T., Fincham A., Lau E., MacDougall M., Moradian-Oldak J., et al. Control of ameloblast differentiation. Int J Dev Biol 39 1 (1995) 69-92
95. Gaunt W.A. The development of enamel and dentine on the molars of the mouse, with an account of the enamel-free areas. Acta Anat (Basel) 28 1-2 (1956) 111-134
96. Starr D.A. Communication between the cytoskeleton and the nuclear envelope to position the nucleus. Mol Biosyst 3 9 (2007) 583-589
97. Karim A., and Warshawsky H. The effect of colcemid on the structure and secretory activity of ameloblasts in the rat incisor as shown by radioautography after injection of 3H-proline. Anat Rec 195 4 (1979) 587-609
98. Nishikawa S., and Kitamura H. Morphology and distribution of microtubules in the presecretory and secretory ameloblasts of the rat incisor. Anat Rec 202 3 (1982) 305-316
99. Hawkinson R.W., and Eisenmann D.R. Electron microscopy of dentinal tubule sclerosis in the enamel-free region of the rat molar. Arch Oral Biol 28 5 (1983) 409-414
100. Barrows M.J., Ashrafi S.H., and Weber D.F. Microradiographic and electron microscopic observations of the enamel-covered dentine in rat molars. Arch Oral Biol 29 6 (1984) 461-466
101. Sakakura Y., Fujiwara N., and Nawa T. Epithelial cytodifferentiation and extracellular matrix formation in enamel-free areas of the occlusal cusp during development of mouse molars: light and electron microscopic studies. Am J Anat 184 4 (1989) 287-297
102. Diab M.M., and Zaki A.E. Morphology and cytidine-5′-monophosphatase cytochemistry of odontogenic epithelium at the enamel-free areas of mouse molars. Arch Oral Biol 36 5 (1991) 361-370
103. Inai T., Nagata K., Kukita T., and Kurisu K. Demonstration of amelogenin in the enamel-free cusps of rat molar tooth germs: immunofluorescent and immunoelectron microscopic studies. Anat Rec 233 4 (1992) 588-596
104. Sutcliffe J.E., and Owens P.D. Microscopy of resorption of enamel and dentine from the cusp tips of the molar teeth of rats. Arch Oral Biol 26 1 (1981) 29-39
105. Luukko K., Løes S., Furmanek T., Fjeld K., Kvinnsland I.H., and Kettunen P. Identification of a novel putative signaling center, the tertiary enamel knot in the postnatal mouse molar tooth. Mech Dev 120 3 (2003) 270-276
106. Smith C.E., and Warshawsky H. Cellular renewal in the enamel organ and the odontoblast layer of the rat incisor as followed by radioautography using 3H-thymidine. Anat Rec 183 4 (1975) 523-561
107. Smith C.E., and Warshawsky H. Histological and three-dimensional organization of the odontogenic organ in the lower incisor of 100 g rats. Am J Anat 142 4 (1975) 403-429
108. Harada H., Mitsuyasu T., Toyono T., and Toyoshima K. Epithelial stem cells in teeth. Odontology 90 1 (2002) 1-6
109. Tummers M., and Thesleff I. Root or crown: a developmental choice orchestrated by the differential regulation of the epithelial stem cell niche in the tooth of two rodent species. Development 130 6 (2003) 1049-1057
110. Smith C.E., and Warshawsky H. Movement of entire cell populations during renewal of the rat incisor as shown by radio-autography after labeling with 3H-thymidine, the concept of a continuously differentiating cross-sectional segment. (With an appendix on the development of the periodontal ligament). Am J Anat 145 2 (1976) 225-259
111. Harada H., Kettunen P., Jung H.S., Mustonen T., Wang Y.A., and Thesleff I. Localization of putative stem cells in dental epithelium and their association with notch and FGF signaling. J Cell Biol 147 1 (1999) 105-120
112. Harada H., Toyono T., Toyoshima K., Yamasaki M., Itoh N., Kato S., et al. FGF10 maintains stem cell compartment in developing mouse incisors. Development 129 6 (2002) 1533-1541
113. Yokohama-Tamaki T., Ohshima H., Fujiwara N., Takada Y., Ichimori Y., Wakisaka S., et al. Cessation of Fgf10 signaling, resulting in a defective dental epithelial stem cell compartment, leads to the transition from crown to root formation. Development 133 7 (2006) 1359-1366
114. Tummers M., Yamashiro T., and Thesleff I. Modulation of epithelial cell fate of the root in vitro. J Dent Res 86 11 (2007) 1063-1067
115. Ausprunk D.H., and Folkman J. Migration and proliferation of endothelial cells in preformed and newly formed blood vessels during tumor angiogenesis. Microvasc Res 14 1 (1977) 53-65
116. Meyer J.M., Ruch J.V., Kubler M.D., Kupferle C., and Lesot H. Cultured incisors display major modifications in basal lamina deposition without further effect on odontoblast differentiation. Cell Tissue Res 279 1 (1995) 135-147
117. Amar S., Karcher-Djuricic V., Meyer J.M., and Ruch J.V. The lingual (root analogue) and the labial (crown analogue) mouse incisor dentin promotes ameloblast differentiation. Arch Anat Microsc Morphol Exp 75 4 (1986/1987) 229-239
118. Amar S., Luo W., Snead M.L., and Ruch J.V. Amelogenin gene expression in mouse incisor heterotopic recombinations. Differentiation 41 1 (1989) 56-61
119. Ruch J.V. Patterned distribution of differentiating dental cells: facts and hypotheses. J Biol Buccale 18 2 (1990) 91-98
120. Nso M., Senger B., and Ruch J.V. Scoring mitotic activity in longitudinal sections of mouse embryonic incisors: significant differences exist for labial and lingual inner dental epithelia. J Craniofac Genet Dev Biol 12 3 (1992) 159-166