Back to Search
Start Over
Harmine promotes molar root development via SMAD1/5/8 phosphorylation.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2018 Mar 11; Vol. 497 (3), pp. 924-929. Date of Electronic Publication: 2017 Dec 15. - Publication Year :
- 2018
-
Abstract
- Tooth and bone are major tissues involved in physiological calcification in the body, and they use similar molecular pathways for development, homeostasis, and regeneration. Harmine (HMN) is a natural small compound that stimulates osteoblast differentiation in vitro and in vivo. Here we examined the biological effect of HMN on the postnatal development of molar tooth roots and periodontal tissues. HMN supported the formation of tooth roots and periodontal tissues in developing tooth germs. In tooth germ organ culture, HMN promoted the elongation of Hertwig's epithelial root sheath (HERS) and stimulated cell proliferation in HERS and dental follicle-derived tissues, including dental papillae and dental follicles. HMN stimulated cell proliferation and cell movement of HERS-derived cells without mesenchymal cells in vitro and directly induced the phosphorylation of SMAD1/5/8 protein in HERS-derived cells. Our results indicated that HMN was the first natural small compound to stimulate postnatal development of tooth germs.<br /> (Copyright © 2017 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Cell Movement drug effects
Cell Proliferation drug effects
Mice, Inbred C57BL
Molar growth & development
Molar metabolism
Smad1 Protein analysis
Smad5 Protein analysis
Smad8 Protein analysis
Tooth Root growth & development
Tooth Root metabolism
Harmine pharmacology
Molar drug effects
Phosphorylation drug effects
Smad1 Protein metabolism
Smad5 Protein metabolism
Smad8 Protein metabolism
Tooth Root drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2104
- Volume :
- 497
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 29253570
- Full Text :
- https://doi.org/10.1016/j.bbrc.2017.12.062