A Wnt10a-Notch signaling axis controls Hertwig’s epithelial root sheath cell behaviors during root furcation patterning

Kai Sun1, Miao Yu1, Jiayu Wang1, Hu Zhao2, Haochen Liu1, Hailan Feng1, Yang Liu1, Dong Han1

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International Journal of Oral Science ›› 2024, Vol. 16 ›› Issue (0) : 25. DOI: 10.1038/s41368-024-00288-x
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A Wnt10a-Notch signaling axis controls Hertwig’s epithelial root sheath cell behaviors during root furcation patterning

  • Kai Sun1, Miao Yu1, Jiayu Wang1, Hu Zhao2, Haochen Liu1, Hailan Feng1, Yang Liu1, Dong Han1
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Abstract

Human with bi-allelic WNT10A mutations and epithelial Wnt10a knockout mice present enlarged pulp chamber and apical displacement of the root furcation of multi-rooted teeth, known as taurodontism; thus, indicating the critical role of Wnt10a in tooth root morphogenesis. However, the endogenous mechanism by which epithelial Wnt10a regulates Hertwig’s epithelial root sheath (HERS) cellular behaviors and contributes to root furcation patterning remains unclear. In this study, we found that HERS in the presumptive root furcating region failed to elongate at an appropriate horizontal level in K14-Cre;Wnt10afl/fl mice from post-natal day 0.5 (PN0.5) to PN4.5. EdU assays and immunofluorescent staining of cyclin D1 revealed significantly decreased proliferation activity of inner enamel epithelial (IEE) cells of HERS in K14-Cre;Wnt10afl/fl mice at PN2.5 and PN3.5. Immunofluorescent staining of E-Cadherin and acetyl-α-Tubulin demonstrated that the IEE cells of HERS tended to divide perpendicularly to the horizontal plane, which impaired the horizontal extension of HERS in the presumptive root furcating region of K14-Cre;Wnt10afl/fl mice. RNA-seq and immunofluorescence showed that the expressions of Jag1 and Notch2 were downregulated in IEE cells of HERS in K14-Cre;Wnt10afl/fl mice. Furthermore, after activation of Notch signaling in K14-Cre;Wnt10afl/fl molars by Notch2 adenovirus and kidney capsule grafts, the root furcation defect was partially rescued. Taken together, our study demonstrates that an epithelial Wnt10a-Notch signaling axis is crucial for modulating HERS cell proper proliferation and horizontal-oriented division during tooth root furcation morphogenesis.

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Kai Sun, Miao Yu, Jiayu Wang, Hu Zhao, Haochen Liu, Hailan Feng, Yang Liu, …Dong Han. A Wnt10a-Notch signaling axis controls Hertwig’s epithelial root sheath cell behaviors during root furcation patterning. International Journal of Oral Science, 2024, 16(0): 25 https://doi.org/10.1038/s41368-024-00288-x

References

1. He, Y. D.et al.Site-specific function and regulation of Osterix in tooth root formation.Int Endod. J. 49, 1124-1131 (2016).
2. Regalo, S. C.et al.Evaluation of molar and incisor bite force in indigenous compared with white population in Brazil.Arch. Oral. Biol. 53, 282-286 (2008).
3. Li, J., Parada, C.& Chai, Y. Cellular and molecular mechanisms of tooth root development.Development 144, 374-384 (2017).
4. Huang X., Xu X., Bringas, P. Jr, Hung, Y. P.& Chai, Y. Smad4-Shh-Nfic signaling cascade-mediated epithelial-mesenchymal interaction is crucial in regulating tooth root development.J. Bone Min. Res 25, 1167-1178 (2010).
5. Madan A. K.& Kramer, B. Immunolocalization of fibroblast growth factor-2 (FGF-2) in the developing root and supporting structures of the murine tooth.J. Mol. Histol. 36, 171-178 (2005).
6. Rakian, A.et al.Bone morphogenetic protein-2 gene controls tooth root development in coordination with formation of the periodontium.Int J. Oral. Sci. 5, 75-84 (2013).
7. Wang Y., Cox M. K., Coricor G., MacDougall, M. & Serra, R. Inactivation of Tgfbr2 in Osterix-Cre expressing dental mesenchyme disrupts molar root formation.Dev. Biol. 382, 27-37 (2013).
8. Chu, E. Y.et al.Full Spectrum of Postnatal Tooth Phenotypes in a Novel Irf6 Cleft Lip Model.J. Dent. Res 95, 1265-1273 (2016).
9. Fons Romero, J. M. et al. The Impact of the Eda Pathway on Tooth Root Development.J. Dent. Res 96, 1290-1297 (2017).
10. Li, X.et al.Development of immortalized Hertwig’s epithelial root sheath cell lines for cementum and dentin regeneration.Stem Cell Res Ther. 10, 3(2019).
11. Yu T.& Klein, O. D. Molecular and cellular mechanisms of tooth development, homeostasis and repair.Development 147, dev184754 (2020).
12. Sakano, M.et al.Cell dynamics in cervical loop epithelium during transition from crown to root: implications for Hertwig’s epithelial root sheath formation.J. Periodontal Res 48, 262-267 (2013).
13. Zeichner-David, M. et al. Role of Hertwig’s epithelial root sheath cells in tooth root development.Dev. Dyn. 228, 651-663 (2003).
14. Dineshshankar, J.et al.Taurodontism.J. Pharm. Bioallied Sci. 6, S13-S15 (2014).
15. Jayashankara C., Shivanna A. K., Sridhara K.& Kumar, P. S. Taurodontism: A dental rarity.J. Oral. Maxillofac. Pathol. 17, 478(2013).
16. Kim T. H., Bae C. H., Yang S., Park J. C.& Cho, E. S. Nfic regulates tooth root patterning and growth.Anat. Cell Biol. 48, 188-194 (2015).
17. Simon, Y.et al.Cephalometric assessment of craniofacial dysmorphologies in relation with Msx2 mutations in mouse.Orthod. Craniofac Res 17, 92-105 (2014).
18. Yu, M.et al.Epithelial Wnt10a Is Essential for Tooth Root Furcation Morphogenesis.J. Dent. Res 99, 311-319 (2020).
19. Dassule H. R.& McMahon, A. P. Analysis of epithelial-mesenchymal interactions in the initial morphogenesis of the mammalian tooth.Dev. Biol. 202, 215-227 (1998).
20. Yamashiro, T.et al.Wnt10a regulates dentin sialophosphoprotein mRNA expression and possibly links odontoblast differentiation and tooth morphogenesis.Differentiation 75, 452-462 (2007).
21. Hamada, Y.et al.Mutation in ankyrin repeats of the mouse Notch2 gene induces early embryonic lethality.Development 126, 3415-3424 (1999).
22. McDaniell, R.et al. NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway.Am. J. Hum. Genet 79, 169-173 (2006).
23. Mitsiadis T. A., Graf D., Luder H., Gridley T.& Bluteau, G. BMPs and FGFs target Notch signalling via jagged 2 to regulate tooth morphogenesis and cytodifferentiation.Development 137, 3025-3035 (2010).
24. Mitsiadis, T. A.et al.Notch Signaling Pathway in Tooth Shape Variations throughout Evolution.Cells 12, 761(2023).
25. Cai X., Gong P., Huang Y.& Lin, Y. Notch signalling pathway in tooth development and adult dental cells.Cell Prolif. 44, 495-507 (2011).
26. Gillies T. E.& Cabernard, C. Cell division orientation in animals.Curr. Biol. 21, R599-R609 (2011).
27. Michel M.& Dahmann, C. Memorizing Shape to Orient Cell Division.Dev. Cell 36, 589-590 (2016).
28. Huang, S.et al.Jagged1/Notch2 controls kidney fibrosis via Tfam-mediated metabolic reprogramming.PLoS Biol. 16, e2005233(2018).
29. Ungerbäck J., Elander N., Grünberg J., Sigvardsson M.& Söderkvist, P. The Notch-2 gene is regulated by Wnt signaling in cultured colorectal cancer cells.PLoS One 6, e17957(2011).
30. Hirata, A.et al.Dose-dependent roles for canonical Wnt signalling in de novo crypt formation and cell cycle properties of the colonic epithelium.Development 140, 66-75 (2013).
31. Tamura M.& Nemoto, E. Role of the Wnt signaling molecules in the tooth.Jpn Dent. Sci. Rev. 52, 75-83 (2016).
32. Tokavanich N., Wein M. N., English J. D., Ono N.& Ono, W. The Role of Wnt Signaling in Postnatal Tooth Root Development.Front Dent. Med 2, 769134(2021).
33. He, J.et al.Lhx6 regulates canonical Wnt signaling to control the fate of mesenchymal progenitor cells during mouse molar root patterning.PLoS Genet 17, e1009320(2021).
34. Balic A.& Thesleff, I. Tissue Interactions Regulating Tooth Development and Renewal.Curr. Top. Dev. Biol. 115, 157-186 (2015).
35. Bosshardt D. D.& Nanci, A. Immunolocalization of epithelial and mesenchymal matrix constituents in association with inner enamel epithelial cells.J. Histochem Cytochem 46, 135-142 (1998).
36. Surendran K., Selassie M., Liapis H., Krigman H.& Kopan, R. Reduced Notch signaling leads to renal cysts and papillary microadenomas.J. Am. Soc. Nephrol. 21, 819-832 (2010).
37. Zhou, Y.et al.Notch2 regulates BMP signaling and epithelial morphogenesis in the ciliary body of the mouse eye.Proc. Natl Acad. Sci. USA 110, 8966-8971 (2013).
38. Ronchini C.& Capobianco, A. J. Induction of cyclin D1 transcription and CDK2 activity by Notch(ic): implication for cell cycle disruption in transformation by Notch(ic).Mol. Cell Biol. 21, 5925-5934 (2001).
39. Li, A.et al.Shaping organs by a wingless-int/Notch/nonmuscle myosin module which orients feather bud elongation.Proc. Natl Acad. Sci. USA 110, E1452-E1461 (2013).
40. Hayward, P., Kalmar, T.& Arias, A. M. Wnt/Notch signalling and information processing during development.Development 135, 411-424 (2008).
41. Cardiff, R. D., Miller, C. H.& Munn, R. J. Manual hematoxylin and eosin staining of mouse tissue sections.Cold Spring Harb. Protoc. 2014, 655-658 (2014).
42. Li, J.et al.SMAD4-mediated WNT signaling controls the fate of cranial neural crest cells during tooth morphogenesis.Development 138, 1977-1989 (2011).
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