|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
Development, Vol 127, Issue 22 4775-4785, Copyright © 2000 by Company of Biologists
JOURNAL ARTICLES |
HR Dassule, P Lewis, M Bei, R Maas and AP McMahon
Department of Molecular and Cellular Biology, The Biolabs, Divinity Avenue, Cambridge, MA 02138, USA.
During mammalian tooth development, the oral ectoderm and mesenchyme coordinate their growth and differentiation to give rise to organs with precise shapes, sizes and functions. The initial ingrowth of the dental epithelium and its associated dental mesenchyme gives rise to the tooth bud. Next, the epithelial component folds to give the tooth its shape. Coincident with this process, adjacent epithelial and mesenchymal cells differentiate into enamel-secreting ameloblasts and dentin-secreting odontoblasts, respectively. Growth, morphogenesis and differentiation of the epithelium and mesenchyme are coordinated by secreted signaling proteins. Sonic hedgehog (Shh) encodes a signaling peptide which is present in the oral epithelium prior to invagination and in the tooth epithelium throughout its development. We have addressed the role of Shh in the developing tooth in mouse by using a conditional allele to remove Shh activity shortly after ingrowth of the dental epithelium. Reduction and then loss of Shh function results in a cap stage tooth rudiment in which the morphology is severely disrupted. The overall size of the tooth is reduced and both the lingual epithelial invagination and the dental cord are absent. However, the enamel knot, a putative organizer of crown formation, is present and expresses Fgf4, Wnt10b, Bmp2 and Lef1, as in the wild type. At birth, the size and the shape of the teeth are severely affected and the polarity and organization of the ameloblast and odontoblast layers is disrupted. However, both dentin- and enamel-specific markers are expressed and a large amount of tooth-specific extracellular matrix is produced. This observation was confirmed by grafting studies in which tooth rudiments were cultured for several days under kidney capsules. Under these conditions, both enamel and dentin were deposited even though the enamel and dentin layers remained disorganized. These studies demonstrate that Shh regulates growth and determines the shape of the tooth. However, Shh signaling is not essential for differentiation of ameloblasts or odontoblasts.
This article has been cited by other articles:
![]() |
K.-A. Nakrieko, I. Welch, H. Dupuis, D. Bryce, A. Pajak, R. St. Arnaud, S. Dedhar, S. J. A. D'Souza, and L. Dagnino Impaired Hair Follicle Morphogenesis and Polarized Keratinocyte Movement upon Conditional Inactivation of Integrin-linked Kinase in the Epidermis Mol. Biol. Cell, April 1, 2008; 19(4): 1462 - 1473. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Takamori, R. Hosokawa, X. Xu, X. Deng, P. Bringas Jr., and Y. Chai Epithelial Fibroblast Growth Factor Receptor 1 Regulates Enamel Formation J. Dent. Res., March 1, 2008; 87(3): 238 - 243. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Nakamura, S. de Vega, S. Fukumoto, L. Jimenez, F. Unda, and Y. Yamada Transcription Factor Epiprofin Is Essential for Tooth Morphogenesis by Regulating Epithelial Cell Fate and Tooth Number J. Biol. Chem., February 22, 2008; 283(8): 4825 - 4833. [Abstract] [Full Text] [PDF] |
||||
![]() |
O. D. Klein, D. B. Lyons, G. Balooch, G. W. Marshall, M. A. Basson, M. Peterka, T. Boran, R. Peterkova, and G. R. Martin An FGF signaling loop sustains the generation of differentiated progeny from stem cells in mouse incisors Development, January 15, 2008; 135(2): 377 - 385. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. M. Azarova, Y. L. Lyu, C.-P. Lin, Y.-C. Tsai, J. Y.-N. Lau, J. C. Wang, and L. F. Liu From the Cover: Roles of DNA topoisomerase II isozymes in chemotherapy and secondary malignancies PNAS, June 26, 2007; 104(26): 11014 - 11019. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Pummila, I. Fliniaux, R. Jaatinen, M. J. James, J. Laurikkala, P. Schneider, I. Thesleff, and M. L. Mikkola Ectodysplasin has a dual role in ectodermal organogenesis: inhibition of Bmp activity and induction of Shh expression Development, January 1, 2007; 134(1): 117 - 125. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. J. Hatsell and P. Cowin Gli3-mediated repression of Hedgehog targets is required for normal mammary development Development, September 15, 2006; 133(18): 3661 - 3670. [Abstract] [Full Text] [PDF] |
||||
![]() |
X.-M. Gu, H.-S. Zhao, L.-S. Sun, and T.-J. Li PTCH Mutations in Sporadic and Gorlin-syndrome-related Odontogenic Keratocysts J. Dent. Res., September 1, 2006; 85(9): 859 - 863. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Grachtchouk, J. Liu, A. Wang, L. Wei, C. K. Bichakjian, J. Garlick, A. F. Paulino, T. Giordano, and A. A. Dlugosz Odontogenic Keratocysts Arise from Quiescent Epithelial Rests and Are Associated with Deregulated Hedgehog Signaling in Mice and Humans Am. J. Pathol., September 1, 2006; 169(3): 806 - 814. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Nakatomi, I. Morita, K. Eto, and M.S. Ota Sonic Hedgehog Signaling is Important in Tooth Root Development. J. Dent. Res., May 1, 2006; 85(5): 427 - 431. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Fukumoto, J. H. Miner, H. Ida, E. Fukumoto, K. Yuasa, H. Miyazaki, M. P. Hoffman, and Y. Yamada Laminin {alpha}5 Is Required for Dental Epithelium Growth and Polarity and the Development of Tooth Bud and Shape J. Biol. Chem., February 24, 2006; 281(8): 5008 - 5016. [Abstract] [Full Text] [PDF] |
||||
![]() |
Q. Xu, C. P. Wonders, and S. A. Anderson Sonic hedgehog maintains the identity of cortical interneuron progenitors in the ventral telencephalon Development, November 15, 2005; 132(22): 4987 - 4998. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Fukumoto, T. Kiba, B. Hall, N. Iehara, T. Nakamura, G. Longenecker, P. H. Krebsbach, A. Nanci, A. B. Kulkarni, and Y. Yamada Ameloblastin is a cell adhesion molecule required for maintaining the differentiation state of ameloblasts J. Cell Biol., December 6, 2004; 167(5): 973 - 983. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Fan, C. V. Pepicelli, C. C. Dibble, W. Catbagan, J. L. Zarycki, R. Laciak, J. Gipp, A. Shaw, M. L. G. Lamm, A. Munoz, et al. Hedgehog Signaling Promotes Prostate Xenograft Tumor Growth Endocrinology, August 1, 2004; 145(8): 3961 - 3970. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. T. Cobourne, I. Miletich, and P. T. Sharpe Restriction of sonic hedgehog signalling during early tooth development Development, June 15, 2004; 131(12): 2875 - 2885. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Andl, K. Ahn, A. Kairo, E. Y. Chu, L. Wine-Lee, S. T. Reddy, N. J. Croft, J. A. Cebra-Thomas, D. Metzger, P. Chambon, et al. Epithelial Bmpr1a regulates differentiation and proliferation in postnatal hair follicles and is essential for tooth development Development, May 15, 2004; 131(10): 2257 - 2268. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Jeong, J. Mao, T. Tenzen, A. H. Kottmann, and A. P. McMahon Hedgehog signaling in the neural crest cells regulates the patterning and growth of facial primordia Genes & Dev., April 15, 2004; 18(8): 937 - 951. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. O. Walterhouse, M. L.G. Lamm, E. Villavicencio, and P. M. Iannaccone Emerging Roles for Hedgehog-Patched-Gli Signal Transduction in Reproduction Biol Reprod, July 1, 2003; 69(1): 8 - 14. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Miletich and P. T. Sharpe Normal and abnormal dental development Hum. Mol. Genet., April 2, 2003; 12(90001): R69 - 73. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Yu, T. J. Carroll, and A. P. McMahon Sonic hedgehog regulates proliferation and differentiation of mesenchymal cells in the mouse metanephric kidney Development, March 13, 2003; 129(22): 5301 - 5312. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Steele-Perkins, K. G. Butz, G. E. Lyons, M. Zeichner-David, H.-J. Kim, M.-I. Cho, and R. M. Gronostajski Essential Role for NFI-C/CTF Transcription-Replication Factor in Tooth Root Development Mol. Cell. Biol., February 1, 2003; 23(3): 1075 - 1084. [Abstract] [Full Text] |
||||
![]() |
K. Kratochwil, J. Galceran, S. Tontsch, W. Roth, and R. Grosschedl FGF4, a direct target of LEF1 and Wnt signaling, can rescue the arrest of tooth organogenesis in Lef1-/- mice Genes & Dev., December 15, 2002; 16(24): 3173 - 3185. [Abstract] [Full Text] [PDF] |
||||
![]() |
D.C. Barreto, A.E. Bale, L. De Marco, and R.S. Gomez Immunolocalization of PTCH Protein in Odontogenic Cysts and Tumors J. Dent. Res., November 1, 2002; 81(11): 757 - 760. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Quint, A. Smith, F. Avaron, L. Laforest, J. Miles, W. Gaffield, and M.-A. Akimenko From the Cover: Bone patterning is altered in the regenerating zebrafish caudal fin after ectopic expression of sonic hedgehog and bmp2b or exposure to cyclopamine PNAS, June 25, 2002; 99(13): 8713 - 8718. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Salazar-Ciudad and J. Jernvall A gene network model accounting for development and evolution of mammalian teeth PNAS, June 11, 2002; 99(12): 8116 - 8120. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Gritli-Linde, M. Bei, R. Maas, X. M. Zhang, A. Linde, and A. P. McMahon Shh signaling within the dental epithelium is necessary for cell proliferation, growth and polarization Development, January 12, 2002; 129(23): 5323 - 5337. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Haraguchi, R. Mo, C.-c. Hui, J. Motoyama, S. Makino, T. Shiroishi, W. Gaffield, and G. Yamada Unique functions of Sonic hedgehog signaling during external genitalia development Development, November 1, 2001; 128(21): 4241 - 4250. [Abstract] [Full Text] [PDF] |
||||