Generation and activity of equine osteoclasts in vitro: effects of the bisphosphonate pamidronate (APD)

A W Gray1, M E Davies, L B Jeffcott

  • 1Equine Orthopaedic Research Group, University of Cambridge, Department of Clinical Veterinary Medicine, Madingley Road, Cambridge, UK.

Insights

Pamidronate (APD) effectively inhibits equine osteoclast-like cells (OCLs) in vitro, showing potential for treating equine bone diseases with high turnover. Further research is needed for clinical application.

Area of Science:

  • Veterinary Medicine
  • Cell Biology
  • Pharmacology

Background:

  • Osteoclasts (OCs) are crucial for bone remodeling.
  • Equine bone diseases often involve increased bone turnover.
  • In vitro models are needed to study equine osteoclast function and drug efficacy.

Purpose of the Study:

  • To generate and characterize equine osteoclast-like cells (OCLs) in vitro.
  • To evaluate the in vitro effects of pamidronate (APD) on equine OCLs.
  • To assess the potential of APD for treating equine conditions with increased bone turnover.

Main Methods:

  • Equine bone marrow (BM) cells were cultured with RANKL and M-CSF to generate OCLs.
  • OCL phenotype was confirmed by TRAP, VNR, and CTR expression, calcitonin responsiveness, and resorption assays.
  • The effect of APD on OCL resorption and cell number was assessed in a dose-dependent manner.

Main Results:

  • Equine OCLs were successfully generated and characterized by standard osteoclast markers and functions.
  • Pamidronate (APD) dose-dependently inhibited OCL-mediated resorption of calcium phosphate films (IC50 = 5.8 x 10(-7) M).
  • APD also inhibited OCL numbers in BM cultures, likely due to increased cell death rather than reduced formation.

Conclusions:

  • Preliminary in vitro data suggest APD is a potent inhibitor of equine osteoclast-like cells.
  • APD shows promise for treating equine conditions characterized by excessive bone resorption.
  • Further in vivo studies are warranted to explore APD's pharmacokinetic profile and clinical efficacy in horses.