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A Novel in vivo Gene Transfer Technique and in vitro Cell Based Assays for the Study of Bone Loss in Musculoskeletal Disorders
Published on: June 8, 2014
Chemically modified tetracyclines act through multiple mechanisms directly on osteoclast precursors
S G Holmes1, K Still, D J Buttle
1Academic Unit of Child Health, Division of Clinical Sciences (South), University of Sheffield, Stephenson Wing, Sheffield Children's Hospital NHS Trust, Western Bank, Sheffield S10 2TH, UK.
Abstract:
Chemically modified tetracyclines (CMTs) are thought to inhibit bone resorption primarily through their ability to inhibit matrix metalloproteinases (MMPs). We have previously demonstrated that some tetracycline compounds (TCs) induce apoptosis in mature rabbit osteoclasts and inhibit osteoclastic resorption in mouse osteoblast/marrow co-cultures in vitro. In this report, we now show that non-antibiotic analogues of doxycycline (CMT-3) and minocycline (CMT-8) are potent inhibitors of osteoclastogenesis in vitro from human peripheral blood mononuclear cells (PBMC) stimulated with macrophage colony stimulating factor (MCSF) and receptor activator of NF-kappaB ligand (RANKL), through an action that is independent of osteoblast-osteoclast interactions. Osteoclast formation over 20 days was completely abrogated when CMT-3 or CMT-8 were included in PBMC cultures at a concentration of 250 ng/ml, although doxycycline at this concentration reduced osteoclast formation to ca. 50% of control. CMT-3 and CMT-8 also significantly induced apoptosis over 24 h in mature osteoclasts generated over 20 days when added to cultures at 5 microg/ml or more. In a time-course experiment, apoptosis was evident after a delay of 1-2 h following treatment of mature osteoclasts with CMT-3 at 20 microg/ml. The broad-spectrum MMP inhibitor BB94 (Batimastat) did not recapitulate the apoptosis induced by CMT-3, even at a concentration where MMP-13 activity was completely inhibited. There was no evidence for an anabolic effect of any of the TCs on osteoblast lineage cells in a calcifying fibroblastic colony (CFU-f) formation assay, where CMT-3 partially inhibited CFU-f formation at 5 microg/ml. Our data indicate that inhibition of osteoclast formation and induction of osteoclast apoptosis are pharmacologically significant actions of CMTs in inhibiting bone resorption, and that osteoclast apoptosis cannot be attributed to the ability of CMTs to inhibit MMPs or to actions mediated by osteoblastic lineage cells.
Insights
Chemically modified tetracyclines (CMTs) potently inhibit osteoclast formation and induce osteoclast apoptosis, independent of matrix metalloproteinase (MMP) inhibition. These findings highlight CMTs as promising agents for treating bone resorption disorders.
Area of Science:
- Biochemistry
- Cell Biology
- Pharmacology
Background:
- Chemically modified tetracyclines (CMTs) are investigated for inhibiting bone resorption, primarily attributed to matrix metalloproteinase (MMP) inhibition.
- Previous studies showed tetracycline compounds (TCs) induce osteoclast apoptosis and inhibit resorption in co-cultures.
- The precise mechanisms underlying CMTs' effects on bone resorption require further elucidation.
Purpose of the Study:
- To investigate the effects of non-antibiotic CMTs (CMT-3 and CMT-8) on osteoclastogenesis and osteoclast apoptosis in vitro.
- To determine if the observed effects are mediated by MMP inhibition or osteoblast-osteoclast interactions.
- To evaluate the potential anabolic effects of CMTs on osteoblast lineage cells.
Main Methods:
- Osteoclastogenesis assays using human peripheral blood mononuclear cells (PBMCs) stimulated with MCSF and RANKL.
- Apoptosis assays on mature osteoclasts treated with CMT-3, CMT-8, doxycycline, and BB94.
- Calcinogenic fibroblastic colony (CFU-f) formation assays to assess effects on osteoblast lineage cells.
Main Results:
- CMT-3 and CMT-8 completely abrogated osteoclast formation at 250 ng/ml, while doxycycline reduced it by 50%.
- CMT-3 and CMT-8 significantly induced osteoclast apoptosis at concentrations of 5 microg/ml or higher.
- The MMP inhibitor BB94 did not replicate the apoptosis induced by CMT-3, and CMT-3 partially inhibited CFU-f formation.
- Osteoclast apoptosis was independent of MMP inhibition and osteoblast lineage cell interactions.
Conclusions:
- CMT-3 and CMT-8 are potent inhibitors of osteoclast formation and inducers of osteoclast apoptosis.
- These effects are independent of MMP inhibition and osteoblast-mediated actions.
- CMTs demonstrate significant pharmacological actions in inhibiting bone resorption through direct effects on osteoclasts.
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