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Role of ALK5/Smad2/3 and MEK1/ERK Signaling in Transforming Growth Factor Beta 1-modulated Growth, Collagen Turnover, and Differentiation of Stem Cells from Apical Papilla of Human Tooth.
- Source :
-
Journal of endodontics [J Endod] 2015 Aug; Vol. 41 (8), pp. 1272-80. Date of Electronic Publication: 2015 May 19. - Publication Year :
- 2015
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Abstract
- Introduction: Transforming growth factor β1 (TGF-β1) plays an important role in cell proliferation, matrix formation, and odontogenesis. This study investigated the effects of TGF-β1 on stem cells from apical papilla (SCAPs) and its signaling by MEK/ERK and Smad2.<br />Methods: SCAPs were exposed to TGF-β1 with/without pretreatment and coincubation by SB431542 (an ALK5/Smad 2/3 inhibitor) or U0126 (a MEK/ERK inhibitor). Cell growth was examined by 3-(4,5-dimethylthiazol-2-yl)-2,5 diphenyl tetrazolium bromide assay or direct counting of viable cells. Collagen content was determined by using the Sircol collagen assay (Biocolor Ltd, Newtownabbey, Northern Ireland). Cell differentiation was evaluated by measuring alkaline phosphatase (ALP) activity. Smad2 and ERK1/2 phosphorylation was analyzed by Western blotting or PathScan phospho-enzyme-linked immunosorbent assay (Cell Signaling Technology Inc, Danvers, MA).<br />Results: TGF-β1 stimulated the growth and collagen content of cultured SCAPs. TGF-β1 stimulated ERK1/2 and Smad2 phosphorylation within 60 minutes of exposure. Pretreatment by U0126 and SB431542 effectively prevented the TGF-β1-induced cell growth and collagen content in SCAPs. TGF-β1 stimulated ALP activity at lower concentrations (0.1-1 ng/mL) but down-regulated ALP at higher concentrations (>5 ng/mL). U0126 prevented 0.5 ng/mL TGF-β1-induced ALP activity but showed little effect on 10 ng/mL TGF-β1-induced decline of ALP in SCAPs. Interestingly, SB431542 attenuated both the stimulatory and inhibitory effects on ALP by TGF-β1.<br />Conclusions: TGF-β1 may affect the proliferation, collagen turnover, and differentiation of SCAPs via differential activation of ALK5/Smad2 and MEK/ERK signaling. These results highlight the future use of TGF-β1 and SCAP for engineering of pulpal regeneration and apexogenesis.<br /> (Copyright © 2015 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Alkaline Phosphatase metabolism
Benzamides pharmacology
Butadienes pharmacology
Cell Differentiation drug effects
Cell Survival drug effects
Cell Survival physiology
Cells, Cultured
Child
Dental Papilla drug effects
Dioxoles pharmacology
Dose-Response Relationship, Drug
Enzyme Inhibitors pharmacology
Humans
MAP Kinase Kinase 1 antagonists & inhibitors
MAP Kinase Kinase 1 metabolism
MAP Kinase Signaling System drug effects
MAP Kinase Signaling System physiology
Nitriles pharmacology
Phosphorylation drug effects
Phosphorylation physiology
Protein Serine-Threonine Kinases antagonists & inhibitors
Protein Serine-Threonine Kinases metabolism
Receptor, Transforming Growth Factor-beta Type I
Receptors, Transforming Growth Factor beta antagonists & inhibitors
Receptors, Transforming Growth Factor beta metabolism
Smad2 Protein antagonists & inhibitors
Smad2 Protein metabolism
Smad3 Protein antagonists & inhibitors
Smad3 Protein metabolism
Stem Cells drug effects
Cell Differentiation physiology
Collagen metabolism
Dental Papilla physiology
Stem Cells physiology
Transforming Growth Factor beta1 metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1878-3554
- Volume :
- 41
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- Journal of endodontics
- Publication Type :
- Academic Journal
- Accession number :
- 26001858
- Full Text :
- https://doi.org/10.1016/j.joen.2015.03.022