Materials and Reagents

Equipment

Procedure

Osteoclasts were plated (250,000 cells/well) in the presence and absence of calvarial osteoblasts in 96-well plates, previously equipped with bone slices.
Cells were cultured in appropriate media for at least 14 days at 37 °C.
After this time cells were washed twice with PBS and removed from bone slices via ultrasonication in 250 µl of 70% isopropanol for at least 15 min at high power.
Note: A volume of 250 µl of 70% isopropanol before ultrasonication makes it easier to get rid of the cells.
Resorption pit formation was visualized by 100 µl toluidine blue (1%; dissolved in water) staining for 2 min at RT.
The slices were then rinsed with 250 µl MilliQ water at least 5 times to wash out residues.
Resorption pits are now stained in dark blue (Figure 1) and resorption area can be quantified via Osteomeasure System or resorption pits/well can be counted via light microscopy.

Figure 1. Resorption pit formation

Acknowledgments

This protocol was adapted from the previously published paper Scholtysek et al. (2013).

References

Scholtysek, C., Katzenbeisser, J., Fu, H., Uderhardt, S., Ipseiz, N., Stoll, C., Zaiss, M. M., Stock, M., Donhauser, L., Bohm, C., Kleyer, A., Hess, A., Engelke, K., David, J. P., Djouad, F., Tuckermann, J. P., Desvergne, B., Schett, G. and Krönke, G. (2013). PPARbeta/delta governs Wnt signaling and bone turnover. Nat Med 19(5): 608-613.