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Published on: June 9, 2014
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.
Abstract:
Equine osteoclast-like cells (OCLs) were generated from the bone marrow (BM) of two ponies and one horse in the presence of RANKL, the receptor activator of NF kappa B ligand and macrophage colony-stimulating factor (M-CSF). The phenotype of these cells was confirmed by demonstration of characteristics typical of osteoclasts (OCs) including: the expression of tartrate-resistant acid phosphatase (TRAP), the vitronectin receptor (VNR) and the calcitonin receptor (CTR), the demonstration of responsiveness to calcitonin (CT) and the ability to form resorption lacunae on ivory slices and calcium phosphate films. The bisphosphonate pamidronate (APD) dose-dependently inhibited resorption of calcium phosphate films by equine OCLs with an IC(50) of 5.8 x 10(-7) M in one horse. APD also dose-dependently inhibited the number of OCLs present in BM cultures after 7 days. However, this effect is most likely attributable to increased OCL death rather than decreased OCL formation. Paradoxically, ADP appeared to cause an early, transient, increase in OCL formation in BM cultures, however, this effect was reversed after 7 days. These preliminary in vitro data support the potential use of APD in clinical conditions characterised by increased bone turnover such as osteomyelitis, osteitis, septic osteoarthritis, navicular disease, cystic bone lesions and immobilisation-induced osteoporosis and provide useful information for future pharmacokinetic studies and clinical trials in vivo.
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