Effects of apatite, transforming growth factor beta-1, bone morphogenetic protein-2 and interleukin-7 on ameloblast differentiation in vitro.

Preameloblasts overtly differentiate in vitro when recombined with cell-free predentin-dentin. The predentin-dentin components able to trigger ameloblast terminal differentiation have not been identified, but some growth factors (members of the TGF beta superfamily) have been demonstrated to be associated with this matrix, and in situ hybridization has demonstrated the presence of transcripts for TGF beta s and BMP-2 in odontoblasts facing differentiating ameloblasts. Moreover, intense expression of receptors for the cytokine interleukin-7 (IL-7) in polarizing ameloblasts has been reported. In this study, isolated E-18 and E-19 mouse molar enamel organs were cultured in vitro in presence of BMP-2, TGF beta-1, IL-7 or synthetic apatite. TGF beta-1 and BMP-2 combined with heparin induced cytodifferentiation of ameloblasts. IL-7 maintained the polarized state of ameloblasts. BMP-2-soaked apatite induced functional differentiation of ameloblasts (secretion of amelogenin). Integrating these data with previous work, a working hypothesis concerning the control of ameloblast terminal differentiation is presented: members of the TGF beta superfamily secreted by odontoblasts might be trapped by predentin components first and then by dentin apatites, and these growth factors might trigger the cytological-functional sequence of ameloblast terminal differentiation.