Regulation of the regenerative activity of dental pulp stem cells from exfoliated deciduous teeth (SHED) of children by TGF-β1 is associated with ALK5/Smad2, TAK1, p38 and MEK/ERK signaling

Transforming growth factor-beta 1 (TGF-beta 1) regulates wound healing/regeneration and aging processes. Dental pulp stem cells from human exfoliated deciduous teeth (SHED) are cell sources for treatment of age-related disorders. We studied the effect of TGF-beta 1 on SHED and related signaling. SHED were treated with TGF-beta 1 with/without pretreatment/co-incubation by SB431542, U0126, 5Z-7-oxozeaenol or SB203580. Sircol collagen assay, 3-(4,5-Dimethylthiazol-2-yl)-2,5diphenyl tetrazolium bromide (MTT) assay, alkaline phosphatase (ALP) assay, RT-PCR, western blotting and PathScan phospho-ELISA were used to measure the effects. We found that SHED expressed ALK1, ALK3, ALK5, TGF-RII, betaglycan and endoglin mRNA. TGF-I31 stimulated p-Smad2, p-TAK1, p-ERK, p-p38 and cyclooxygenase-2 (COX-2) protein expression. It enhanced proliferation and collagen content of SHED that were attenuated by SB431542, 5Z-7-oxozeaenol and SB203580, but not U0126. TGF-beta 1 (0.5-1 ng/ml) stimulated ALP of SHED, whereas 5-10 ng/ml TGF-beta 1 suppressed ALP. SB431542 reversed the effects of TGF-beta 1. However, 5Z-7-oxozeaenol, SB203580 and U0126 only reversed the stimulatory effect of TGF beta 1 on ALP. Four inhibitors attenuated TGF-beta 1-induced COX-2 expression. TGF-beta 1-stimulated TIMP-1 and Ncadherin was inhibited by SB431542 and 5Z-7-oxozeaenol. These results indicate that TGF-beta 1 affects SHED by differential regulation of ALK5/Smad2/3, TAK1, p38 and MEK/ERK. TGF-beta 1 and SHED could potentially be used for tissue engineering/regeneration and treatment of age-related diseases.