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BMP‐Smad Signaling Regulates Postnatal Crown Dentinogenesis in Mouse Molar

Dentinogenesis, a formation of dentin by odontoblasts, is an essential process during tooth development. Bone morphogenetic proteins (BMPs) are one of the most crucial growth factors that contribute to dentin formation. However, it is still unclear how BMP signaling pathways regulate postnatal crown...

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Autores principales: Omi, Maiko, Kulkarni, Anshul K, Raichur, Anagha, Fox, Mason, Uptergrove, Amber, Zhang, Honghao, Mishina, Yuji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7017888/
https://www.ncbi.nlm.nih.gov/pubmed/32149267
http://dx.doi.org/10.1002/jbm4.10249
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author Omi, Maiko
Kulkarni, Anshul K
Raichur, Anagha
Fox, Mason
Uptergrove, Amber
Zhang, Honghao
Mishina, Yuji
author_facet Omi, Maiko
Kulkarni, Anshul K
Raichur, Anagha
Fox, Mason
Uptergrove, Amber
Zhang, Honghao
Mishina, Yuji
author_sort Omi, Maiko
collection PubMed
description Dentinogenesis, a formation of dentin by odontoblasts, is an essential process during tooth development. Bone morphogenetic proteins (BMPs) are one of the most crucial growth factors that contribute to dentin formation. However, it is still unclear how BMP signaling pathways regulate postnatal crown and root dentinogenesis. BMPs transduce signals through canonical Smad and non‐Smad signaling pathways including p38 and ERK signaling pathways. To investigate the roles of Smad and non‐Smad signaling pathways in dentinogenesis, we conditionally deleted Bmpr1a, which encodes the type 1A receptor for BMPs, to remove both Smad and non‐Smad pathways in Osterix‐expressing cells. We also expressed a constitutively activated form of Bmpr1a (caBmpr1a) to increase Smad1/5/9 signaling activity without altered non‐Smad activity in odontoblasts. To understand the function of BMP signaling during postnatal dentin formation, Cre activity was induced at the day of birth. Our results showed that loss of BmpR1A in odontoblasts resulted in impaired dentin formation and short molar roots at postnatal day 21. Bmpr1a cKO mice displayed a reduction of dentin matrix production compared to controls associated with increased cell proliferation and reduced Osx and Dspp expression. In contrast, caBmpr1a mutant mice that show increased Smad1/5/9 signaling activity resulted in no overt tooth phenotype. To further dissect the functions of each signaling activity, we generated Bmpr1a cKO mice also expressing caBmpr1a to restore only Smad1/5/9 signaling activity. Restoring Smad activity in the compound mutant mice rescued impaired crown dentin formation in the Bmpr1a cKO mice; however, impaired root dentin formation and short roots were not changed. These results suggest that BMP‐Smad signaling in odontoblasts is responsible for crown dentin formation, while non‐Smad signaling may play a major role in root dentin formation and elongation. © 2019 The Authors. JBMR Plus published by Wiley Periodicals, Inc. on behalf of American Society for Bone and Mineral Research. © 2019 The Authors. JBMR Plus published by Wiley Periodicals, Inc. on behalf of American Society for Bone and Mineral Research.
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spelling pubmed-70178882020-03-06 BMP‐Smad Signaling Regulates Postnatal Crown Dentinogenesis in Mouse Molar Omi, Maiko Kulkarni, Anshul K Raichur, Anagha Fox, Mason Uptergrove, Amber Zhang, Honghao Mishina, Yuji JBMR Plus Original Articles Dentinogenesis, a formation of dentin by odontoblasts, is an essential process during tooth development. Bone morphogenetic proteins (BMPs) are one of the most crucial growth factors that contribute to dentin formation. However, it is still unclear how BMP signaling pathways regulate postnatal crown and root dentinogenesis. BMPs transduce signals through canonical Smad and non‐Smad signaling pathways including p38 and ERK signaling pathways. To investigate the roles of Smad and non‐Smad signaling pathways in dentinogenesis, we conditionally deleted Bmpr1a, which encodes the type 1A receptor for BMPs, to remove both Smad and non‐Smad pathways in Osterix‐expressing cells. We also expressed a constitutively activated form of Bmpr1a (caBmpr1a) to increase Smad1/5/9 signaling activity without altered non‐Smad activity in odontoblasts. To understand the function of BMP signaling during postnatal dentin formation, Cre activity was induced at the day of birth. Our results showed that loss of BmpR1A in odontoblasts resulted in impaired dentin formation and short molar roots at postnatal day 21. Bmpr1a cKO mice displayed a reduction of dentin matrix production compared to controls associated with increased cell proliferation and reduced Osx and Dspp expression. In contrast, caBmpr1a mutant mice that show increased Smad1/5/9 signaling activity resulted in no overt tooth phenotype. To further dissect the functions of each signaling activity, we generated Bmpr1a cKO mice also expressing caBmpr1a to restore only Smad1/5/9 signaling activity. Restoring Smad activity in the compound mutant mice rescued impaired crown dentin formation in the Bmpr1a cKO mice; however, impaired root dentin formation and short roots were not changed. These results suggest that BMP‐Smad signaling in odontoblasts is responsible for crown dentin formation, while non‐Smad signaling may play a major role in root dentin formation and elongation. © 2019 The Authors. JBMR Plus published by Wiley Periodicals, Inc. on behalf of American Society for Bone and Mineral Research. © 2019 The Authors. JBMR Plus published by Wiley Periodicals, Inc. on behalf of American Society for Bone and Mineral Research. John Wiley & Sons, Inc. 2019-11-14 /pmc/articles/PMC7017888/ /pubmed/32149267 http://dx.doi.org/10.1002/jbm4.10249 Text en © 2019 The Authors. JBMR Plus published by Wiley Periodicals, Inc. on behalf of American Society for Bone and Mineral Research. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Omi, Maiko
Kulkarni, Anshul K
Raichur, Anagha
Fox, Mason
Uptergrove, Amber
Zhang, Honghao
Mishina, Yuji
BMP‐Smad Signaling Regulates Postnatal Crown Dentinogenesis in Mouse Molar
title BMP‐Smad Signaling Regulates Postnatal Crown Dentinogenesis in Mouse Molar
title_full BMP‐Smad Signaling Regulates Postnatal Crown Dentinogenesis in Mouse Molar
title_fullStr BMP‐Smad Signaling Regulates Postnatal Crown Dentinogenesis in Mouse Molar
title_full_unstemmed BMP‐Smad Signaling Regulates Postnatal Crown Dentinogenesis in Mouse Molar
title_short BMP‐Smad Signaling Regulates Postnatal Crown Dentinogenesis in Mouse Molar
title_sort bmp‐smad signaling regulates postnatal crown dentinogenesis in mouse molar
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7017888/
https://www.ncbi.nlm.nih.gov/pubmed/32149267
http://dx.doi.org/10.1002/jbm4.10249
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