A Hedgehog–Foxf axis coordinates dental follicle-derived alveolar bone formation

Mizuki Nagata, Gaurav T. Gadhvi, Taishi Komori, Yuki Arai, Chiaki Tsutsumi-Arai, Angel Ka Yan Chu, Seth N. Nye, Yuntao Yang, Shion Orikasa, Akira Takahashi, Peter Carlsson, W. Jim Zheng, Joshua D. Welch, Noriaki Ono and Wanida Ono ()
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Mizuki Nagata: University of Texas Health Science Center at Houston School of Dentistry
Gaurav T. Gadhvi: University of Michigan
Taishi Komori: University of Texas Health Science Center at Houston School of Dentistry
Yuki Arai: University of Texas Health Science Center at Houston School of Dentistry
Chiaki Tsutsumi-Arai: University of Texas Health Science Center at Houston School of Dentistry
Angel Ka Yan Chu: University of Michigan
Seth N. Nye: University of Michigan School of Dentistry
Yuntao Yang: University of Texas Health Science Center at Houston
Shion Orikasa: University of Texas Health Science Center at Houston School of Dentistry
Akira Takahashi: Kyushu University
Peter Carlsson: University of Gothenburg
W. Jim Zheng: University of Texas Health Science Center at Houston
Joshua D. Welch: University of Michigan
Noriaki Ono: University of Texas Health Science Center at Houston School of Dentistry
Wanida Ono: University of Texas Health Science Center at Houston School of Dentistry

Nature Communications, 2025, vol. 16, issue 1, 1-21

Abstract: Abstract The alveolar bone is a specialized mineralized structure supporting the lifelong functionality of the tooth in mastication. The alveolar bone develops from the dental follicle (DF) during tooth root formation due to deliberate epithelial–mesenchymal interactions. However, how DF progenitor cell fates are regulated toward alveolar bone osteoblasts remains unknown. We find that Hedgehog signaling activities are transiently activated during the onset of tooth root formation and alveolar bone formation. Parathyroid hormone-related protein (PTHrP)-expressing DF cells are highly responsive to Hedgehog signaling, yet constitutive Hedgehog activation using Pthrp-creER and Ptch1-floxed alleles potently suppresses alveolar osteoblast and ligament differentiation of PTHrP+ DF cells, resulting in striking susceptibility to alveolar bone loss. Concomitant inactivation of Hedgehog-target Foxf1 factor in Hedgehog-activated PTHrP+ DF cells partially rescued alveolar bone defects. Therefore, the Hedgehog–Foxf pathway needs to be suppressed to drive alveolar bone osteoblast fates of PTHrP+ DF cells, unraveling a unique tooth-specific mechanism of bone formation requiring deliberate on-off regulations of Hedgehog signaling.

Date: 2025
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DOI: 10.1038/s41467-025-61050-3

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