Real-time analysis of osteoclast resorption and fusion dynamics in response to bone resorption inhibitors

Preety Panwar, Jacob Bastholm Olesen, Galia Blum, Jean-Marie Delaissé, Kent Søe*, Dieter Brömme*

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

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Abstract

Cathepsin K (CatK), an essential collagenase in osteoclasts (OCs), is a potential therapeutic target for the treatment of osteoporosis. Using live-cell imaging, we monitored the bone resorptive behaviour of OCs during dose-dependent inhibition of CatK by an ectosteric (Tanshinone IIA sulfonate) and an active site inhibitor (odanacatib). CatK inhibition caused drastic reductions in the overall resorption speed of OCs. At IC 50 CatK-inhibitor concentration, OCs reduced about 40% of their trench-forming capacity and at fourfold IC 50 concentrations, a > 95% reduction was observed. The majority of CatK-inhibited OCs (~ 75%) were involved in resorption-migration-resorption episodes forming adjacent pits, while ~ 25% were stagnating OCs which remained associated with the same excavation. We also observed fusions of OCs during the resorption process both in control and inhibitor-treated conditions, which increased their resorption speeds by 30-50%. Inhibitor IC 50-concentrations increased OC-fusion by twofold. Nevertheless, more fusion could not counterweigh the overall loss of resorption activity by inhibitors. Using an activity-based probe, we demonstrated the presence of active CatK at the resorbing front in pits and trenches. In conclusion, our data document how OCs respond to CatK-inhibition with respect to movement, bone resorption activity, and their attempt to compensate for inhibition by activating fusion.

Original languageEnglish
Article number7358
JournalScientific Reports
Volume14
Number of pages15
ISSN2045-2322
DOIs
Publication statusPublished - 28. Mar 2024

Keywords

  • Active-site probe
  • Bone resorption
  • Cathepsin K
  • Cell fusion
  • Human osteoclast
  • Live-imaging

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