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Hippo pathway/Yap regulates primary enamel knot and dental cusp patterning in tooth morphogenesis

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Abstract

The shape of an individual tooth crown is primarily determined by the number and arrangement of its cusps, i.e., cusp patterning. Enamel knots that appear in the enamel organ during tooth morphogenesis have been suggested to play important roles in cusp patterning. Animal model studies have shown that the Hippo pathway effector Yap has a critical function in tooth morphogenesis. However, the role of the Hippo pathway/Yap in cusp patterning has not been well documented and its specific roles in tooth morphogenesis remain unclear. Here, we provide evidence that Yap is a key mediator in tooth cusp patterning. We demonstrate a correlation between Yap localization and cell proliferation in developing tooth germs. We also show that, between the cap stage and bell stage, Yap is crucial for the suppression of the primary enamel knot and for the patterning of secondary enamel knots, which are the future cusp regions. When Yap expression is stage-specifically knocked down during the cap stage, the activity of the primary enamel knot persists into the bell-stage tooth germ, leading to ectopic cusp formation. Our data reveal the importance of the Hippo pathway/Yap in enamel knots and in the proper patterning of tooth cusps.

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References

  • Camargo FD, Gokhale S, Johnnidis JB, Fu D, Bell GW, Jaenisch R, Brummelkamp TR (2007) YAP1 increases organ size and expands undifferentiated progenitor cells. Curr Biol 17:2054–2060

    Article  CAS  PubMed  Google Scholar 

  • Caton J, Tucker AS (2009) Current knowledge of tooth development: patterning and mineralization of the murine dentition. J Anat 214:502–515

    Article  PubMed Central  PubMed  Google Scholar 

  • Dong J, Feldmann G, Huang J, Wu S, Zhang N, Comerford SA, Gayyed MF, Anders RA, Maitra A, Pan D (2007) Elucidation of a universal size-control mechanism in Drosophila and mammals. Cell 130:1120–1133

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Jernvall J, Thesleff I (2000) Reiterative signaling and patterning during mammalian tooth morphogenesis. Mech Dev 92:19–29

    Article  CAS  PubMed  Google Scholar 

  • Jernvall J, Kettunen P, Karavanova I, Martin LB, Thesleff I (1994) 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 38:463–469

    CAS  PubMed  Google Scholar 

  • Lan Y, Jia S, Jiang R (2014) Molecular patterning of the mammalian dentition. Semin Cell Dev Biol 25–26:61–70

    Article  PubMed  Google Scholar 

  • Lee JM, Kwon HJ, Lai WF, Jung HS (2014) Requirement of Runx3 in pulmonary vasculogenesis. Cell Tissue Res 356:445–449

    Article  CAS  PubMed  Google Scholar 

  • Lee MJ, Kim EJ, Li L, Jung HS (2015) Roles of Wnt inhibitory factor 1 during tooth morphogenesis. Cell Tissue Res (in press)

  • Li L, Kwon HJ, Harada H, Ohshima H, Cho SW, Jung HS (2011) Expression patterns of ABCG2, Bmi-1, Oct-3/4, and Yap in the developing mouse incisor. Gene Expr Patterns 11:163–170

    Article  CAS  PubMed  Google Scholar 

  • Liu M, Zhao S, Wang XP (2014) YAP overexpression affects tooth morphogenesis and enamel knot patterning. J Dent Res 93:469–474

    Article  CAS  PubMed  Google Scholar 

  • Liu M, Zhao S, Lin Q, Wang XP (2015) YAP regulates the expression of Hoxa1 and Hoxc13 in mouse and human oral and skin epithelial tissues. Mol Cell Biol 35:1449–1461

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Tummers M, Thesleff I (2009) The importance of signal pathway modulation in all aspects of tooth development. J Exp Zool B Mol Dev Evol 312B:309–319

    Article  PubMed  Google Scholar 

  • Zhao B, Wei X, Li W, Udan RS, Yang Q, Kim J, Xie J, Ikenoue T, Yu J, Li L, Zheng P, Ye K, Chinnaiyan A, Halder G, Lai ZC, Guan KL (2007) Inactivation of YAP oncoprotein by the Hippo pathway is involved in cell contact inhibition and tissue growth control. Genes Dev 21:2747–2761

    Article  PubMed Central  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

This research was supported by a grant of the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI), funded by the Ministry of Health & Welfare, Republic of Korea (HI14C3266). This research was supported by a grant of the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI), funded by the Ministry of Health & Welfare, Republic of Korea (HI14C1817). This work was supported by the National Research Foundation of Korea(NRF) grant funded by the Korea government(MSIP) (No. 2014R1A2A1A11050764).This research was supported by the Bio & Medical Technology Development Program of the National Research Foundation (NRF) funded by the Korean government (MSIP) (No. 2012M3A9B4028738).

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Correspondence to Han-Sung Jung.

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Kwon, HJ.E., Li, L. & Jung, HS. Hippo pathway/Yap regulates primary enamel knot and dental cusp patterning in tooth morphogenesis. Cell Tissue Res 362, 447–451 (2015). https://doi.org/10.1007/s00441-015-2267-8

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  • DOI: https://doi.org/10.1007/s00441-015-2267-8

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