ISOLATION OF OSTEOGENIC PROGENITORS FROM HUMAN AMNIOTIC FLUID USING A SINGLE STEP CULTURE PROTOCOL

Background: Stem cells isolated from amniotic fluid are known to be able to differentiate into different cells types, being thus considered as a potential tool for cellular therapy of different human diseases. In the present study, we report a nove! single step protocol for the osteoblastic differentiation of human arrmiotic fluid cells. Results: The described protocol is able to previde osteoblastic cells producing nodules of calcium mineralization within 18 days from withdrawal of amniotic fluid sarnples. These cells display a full expression of markers of osteogenic differentiation (COLl, OC, OPN, OCN, OPG, BSP, Runx2) within 30 days from withdrawal. In arder to test the ability of these cells to proliferate on surfaces commonly used in oral osteointegrated implantology, we carried out cultures onto different test disks, narnely smooth copper, machined titanium and Sandblasted and Acid Etching titanium (SLA titanium). Electron microscopy analysis evidenced the best celi gro'Nth on this latter surface. Conclusions: The described protocol provides an efficient and time-saving tool for the production of osteogenic cells from amniotic fluid that in the future could be used in ora! osteointegrated implantology.