Development of an in vitro culture system for the study of osteoclast activity and function

Resorption is a difficult process to study in vivo because of the complex organization of mineralized tissue. The objective of this study was to develop an in vitro culture system for studying osteoclast attachment and activity. Transparent, microporous substrata were prepared using radio frequency-sputtering techniques to apply a thin layer of hydroxyapatite on polycarbonate filters previously coated with Type I collagen. Dentinoclasts isolated from the root surface of rat molar teeth undergoing inflammatory resorption and osteoclasts isolated from the endosteal surfaces of rat long bones were incubated on the experimental substrata. The culture system proved successful, supporting osteoclast viability and activity as demonstrated by cellular attachment and spreading seen by scanning electron microscopy. Activity was further demonstrated by monitoring acid production using a fluorescent probe, acridine orange. Isolated osteoclasts or dentinoclasts, when combined with synthetically prepared substrata, were observed to respond by mechanisms comparable to those that occur in vivo. Therefore, the system developed permits basic observations of osteoclasts in an in vitro system.