Cargando…

Osteoclastic differentiation and resorption is modulated by bioactive metal ions Co(2+), Cu(2+) and Cr(3+) incorporated into calcium phosphate bone cements

Biologically active metal ions in low doses have the potential to accelerate bone defect healing. For successful remodelling the interaction of bone graft materials with both bone-forming osteoblasts and bone resorbing osteoclasts is crucial. In the present study brushite forming calcium phosphate c...

Descripción completa

Detalles Bibliográficos
Autores principales: Bernhardt, Anne, Schamel, Martha, Gbureck, Uwe, Gelinsky, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5538673/
https://www.ncbi.nlm.nih.gov/pubmed/28763481
http://dx.doi.org/10.1371/journal.pone.0182109
_version_ 1783254384292921344
author Bernhardt, Anne
Schamel, Martha
Gbureck, Uwe
Gelinsky, Michael
author_facet Bernhardt, Anne
Schamel, Martha
Gbureck, Uwe
Gelinsky, Michael
author_sort Bernhardt, Anne
collection PubMed
description Biologically active metal ions in low doses have the potential to accelerate bone defect healing. For successful remodelling the interaction of bone graft materials with both bone-forming osteoblasts and bone resorbing osteoclasts is crucial. In the present study brushite forming calcium phosphate cements (CPC) were doped with Co(2+), Cu(2+) and Cr(3+) and the influence of these materials on osteoclast differentiation and activity was examined. Human osteoclasts were differentiated from human peripheral blood mononuclear cells (PBMC) both on the surface and in indirect contact to the materials on dentin discs. Release of calcium, phosphate and bioactive metal ions was determined using ICP-MS both in the presence and absence of the cells. While Co(2+) and Cu(2+) showed a burst release, Cr(3+) was released steadily at very low concentrations (below 1 μM) and both calcium and phosphate release of the cements was considerably changed in the Cr(3+) modified samples. Direct cultivation of PBMC/osteoclasts on Co(2+) cements showed lower attached cell number compared to the reference but high activity of osteoclast specific enzymes tartrate resistant acid phosphatase (TRAP), carbonic anhydrase II (CAII) and cathepsin K (CTSK) and significantly increased gene expression of vitronectin receptor. Indirect cultivation with diluted Co(2+) cement extracts revealed highest resorbed area compared to all other modifications and the reference. Cu(2+) cements had cytotoxic effect on PBMC/osteoclasts during direct cultivation, while indirect cultivation with diluted extracts from Cu(2+) cements did not provoke cytotoxic effects but a strictly inhibited resorption. Cr(3+) doped cements did not show cytotoxic effects at all. Gene expression and enzyme activity of CTSK was significantly increased in direct culture. Indirect cultivation with Cr(3+) doped cements revealed significantly higher resorbed area compared to the reference. In conclusion Cr(3+) doped calcium phosphate cements are an innovative cement modification because of their high cytocompatibility and support of active resorption by osteoclasts.
format Online
Article
Text
id pubmed-5538673
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-55386732017-08-07 Osteoclastic differentiation and resorption is modulated by bioactive metal ions Co(2+), Cu(2+) and Cr(3+) incorporated into calcium phosphate bone cements Bernhardt, Anne Schamel, Martha Gbureck, Uwe Gelinsky, Michael PLoS One Research Article Biologically active metal ions in low doses have the potential to accelerate bone defect healing. For successful remodelling the interaction of bone graft materials with both bone-forming osteoblasts and bone resorbing osteoclasts is crucial. In the present study brushite forming calcium phosphate cements (CPC) were doped with Co(2+), Cu(2+) and Cr(3+) and the influence of these materials on osteoclast differentiation and activity was examined. Human osteoclasts were differentiated from human peripheral blood mononuclear cells (PBMC) both on the surface and in indirect contact to the materials on dentin discs. Release of calcium, phosphate and bioactive metal ions was determined using ICP-MS both in the presence and absence of the cells. While Co(2+) and Cu(2+) showed a burst release, Cr(3+) was released steadily at very low concentrations (below 1 μM) and both calcium and phosphate release of the cements was considerably changed in the Cr(3+) modified samples. Direct cultivation of PBMC/osteoclasts on Co(2+) cements showed lower attached cell number compared to the reference but high activity of osteoclast specific enzymes tartrate resistant acid phosphatase (TRAP), carbonic anhydrase II (CAII) and cathepsin K (CTSK) and significantly increased gene expression of vitronectin receptor. Indirect cultivation with diluted Co(2+) cement extracts revealed highest resorbed area compared to all other modifications and the reference. Cu(2+) cements had cytotoxic effect on PBMC/osteoclasts during direct cultivation, while indirect cultivation with diluted extracts from Cu(2+) cements did not provoke cytotoxic effects but a strictly inhibited resorption. Cr(3+) doped cements did not show cytotoxic effects at all. Gene expression and enzyme activity of CTSK was significantly increased in direct culture. Indirect cultivation with Cr(3+) doped cements revealed significantly higher resorbed area compared to the reference. In conclusion Cr(3+) doped calcium phosphate cements are an innovative cement modification because of their high cytocompatibility and support of active resorption by osteoclasts. Public Library of Science 2017-08-01 /pmc/articles/PMC5538673/ /pubmed/28763481 http://dx.doi.org/10.1371/journal.pone.0182109 Text en © 2017 Bernhardt et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Bernhardt, Anne
Schamel, Martha
Gbureck, Uwe
Gelinsky, Michael
Osteoclastic differentiation and resorption is modulated by bioactive metal ions Co(2+), Cu(2+) and Cr(3+) incorporated into calcium phosphate bone cements
title Osteoclastic differentiation and resorption is modulated by bioactive metal ions Co(2+), Cu(2+) and Cr(3+) incorporated into calcium phosphate bone cements
title_full Osteoclastic differentiation and resorption is modulated by bioactive metal ions Co(2+), Cu(2+) and Cr(3+) incorporated into calcium phosphate bone cements
title_fullStr Osteoclastic differentiation and resorption is modulated by bioactive metal ions Co(2+), Cu(2+) and Cr(3+) incorporated into calcium phosphate bone cements
title_full_unstemmed Osteoclastic differentiation and resorption is modulated by bioactive metal ions Co(2+), Cu(2+) and Cr(3+) incorporated into calcium phosphate bone cements
title_short Osteoclastic differentiation and resorption is modulated by bioactive metal ions Co(2+), Cu(2+) and Cr(3+) incorporated into calcium phosphate bone cements
title_sort osteoclastic differentiation and resorption is modulated by bioactive metal ions co(2+), cu(2+) and cr(3+) incorporated into calcium phosphate bone cements
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5538673/
https://www.ncbi.nlm.nih.gov/pubmed/28763481
http://dx.doi.org/10.1371/journal.pone.0182109
work_keys_str_mv AT bernhardtanne osteoclasticdifferentiationandresorptionismodulatedbybioactivemetalionsco2cu2andcr3incorporatedintocalciumphosphatebonecements
AT schamelmartha osteoclasticdifferentiationandresorptionismodulatedbybioactivemetalionsco2cu2andcr3incorporatedintocalciumphosphatebonecements
AT gbureckuwe osteoclasticdifferentiationandresorptionismodulatedbybioactivemetalionsco2cu2andcr3incorporatedintocalciumphosphatebonecements
AT gelinskymichael osteoclasticdifferentiationandresorptionismodulatedbybioactivemetalionsco2cu2andcr3incorporatedintocalciumphosphatebonecements