The knowledge of how cells respond to different treatments in terms of their migration potential could improve bone regeneration and osseointegration of dental implants. The objective of this study was to elucidate the effects of various chemoattractants, bone morphogenetic protein-2 (BMP-2), low-level laser therapy (LLLT), and cone beam computed tomography (CBCT) on the migration of dental follicle stem cells (DFSCs). The chemoattractants used in our study were the serum-free (SF) conditioned media that were harvested from osteoblast cell cultures seeded on the surface of titanium implantsTi6Al7Nb (TiCtrl), implants infiltrated with hydroxyapatite (TiHA), with silicatitanate (TiSiO2), and from culture of DFSCs cultivated on TiCtrl implants. We used the scratch migration assay to evaluate the influence of BMP-2, LLLT therapy, and CBCT on the migration potential of DFSCs. The migration scratch assay indicates that the BMP-2 growth factor is able to increase the DFSC migration compared to control culturing medium and regardless of laser or CBCT exposure. The results demonstrate the importance of improving the implant surface with HA, SiO2, and DFSCs. Stimulated DFSCs will secrete growth factors which will act as chemoattractants for the stem cells of the implant host. Adding growth factors such as BMP-2 can improve the migration process of DFSCs.