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High Concentrations of Polyelectrolyte Complex Nanoparticles Decrease Activity of Osteoclasts
Fracture treatment in osteoporotic patients is still challenging. Osteoporosis emerges when there is an imbalance between bone formation and resorption in favor of resorption by osteoclasts. Thus, new implant materials for osteoporotic fracture treatment should promote bone formation and reduce bone...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6630339/ https://www.ncbi.nlm.nih.gov/pubmed/31242715 http://dx.doi.org/10.3390/molecules24122346 |
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author | Kauschke, Vivien Hessland, Felix Maximilian Vehlow, David Müller, Martin Heiss, Christian Lips, Katrin Susanne |
author_facet | Kauschke, Vivien Hessland, Felix Maximilian Vehlow, David Müller, Martin Heiss, Christian Lips, Katrin Susanne |
author_sort | Kauschke, Vivien |
collection | PubMed |
description | Fracture treatment in osteoporotic patients is still challenging. Osteoporosis emerges when there is an imbalance between bone formation and resorption in favor of resorption by osteoclasts. Thus, new implant materials for osteoporotic fracture treatment should promote bone formation and reduce bone resorption. Nanoparticles can serve as drug delivery systems for growth factors like Brain-Derived Neurotrophic Factor (BDNF), which stimulated osteoblast differentiation. Therefore, polyelectrolyte complex nanoparticles (PEC-NPs) consisting of poly(l-lysine) (PLL) and cellulose sulfate (CS), with or without addition of BDNF, were used to analyze their effect on osteoclasts in vitro. Live cell images showed that osteoclast numbers decreased after application of high PLL/CS PEC-NPs concentrations independent of whether BDNF was added or not. Real-time RT-PCR revealed that relative mRNA expression of cathepsin K and calcitonin receptor significantly declined after incubation of osteoclasts with high concentrations of PLL/CS PEC-NPs. Furthermore, Enzyme-Linked Immunosorbent Assay indicated that tartrate-resistant acidic phosphatase 5b activity was significantly reduced in the presence of high PLL/CS PEC-NPs concentrations. Consistent with these results, the pit formation analysis showed that less hydroxyapatite was resorbed by osteoclasts after incubation with high concentrations of PLL/CS PEC-NPs. BDNF had no influence on osteoclasts. We conclude that highly concentrated PLL/CS PEC-NPs dosages decreased osteoclastogenesis and osteoclasts activity. Moreover, BDNF might be a promising growth factor for osteoporotic fracture treatment since it did not increase osteoclast activity. |
format | Online Article Text |
id | pubmed-6630339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66303392019-08-19 High Concentrations of Polyelectrolyte Complex Nanoparticles Decrease Activity of Osteoclasts Kauschke, Vivien Hessland, Felix Maximilian Vehlow, David Müller, Martin Heiss, Christian Lips, Katrin Susanne Molecules Article Fracture treatment in osteoporotic patients is still challenging. Osteoporosis emerges when there is an imbalance between bone formation and resorption in favor of resorption by osteoclasts. Thus, new implant materials for osteoporotic fracture treatment should promote bone formation and reduce bone resorption. Nanoparticles can serve as drug delivery systems for growth factors like Brain-Derived Neurotrophic Factor (BDNF), which stimulated osteoblast differentiation. Therefore, polyelectrolyte complex nanoparticles (PEC-NPs) consisting of poly(l-lysine) (PLL) and cellulose sulfate (CS), with or without addition of BDNF, were used to analyze their effect on osteoclasts in vitro. Live cell images showed that osteoclast numbers decreased after application of high PLL/CS PEC-NPs concentrations independent of whether BDNF was added or not. Real-time RT-PCR revealed that relative mRNA expression of cathepsin K and calcitonin receptor significantly declined after incubation of osteoclasts with high concentrations of PLL/CS PEC-NPs. Furthermore, Enzyme-Linked Immunosorbent Assay indicated that tartrate-resistant acidic phosphatase 5b activity was significantly reduced in the presence of high PLL/CS PEC-NPs concentrations. Consistent with these results, the pit formation analysis showed that less hydroxyapatite was resorbed by osteoclasts after incubation with high concentrations of PLL/CS PEC-NPs. BDNF had no influence on osteoclasts. We conclude that highly concentrated PLL/CS PEC-NPs dosages decreased osteoclastogenesis and osteoclasts activity. Moreover, BDNF might be a promising growth factor for osteoporotic fracture treatment since it did not increase osteoclast activity. MDPI 2019-06-25 /pmc/articles/PMC6630339/ /pubmed/31242715 http://dx.doi.org/10.3390/molecules24122346 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kauschke, Vivien Hessland, Felix Maximilian Vehlow, David Müller, Martin Heiss, Christian Lips, Katrin Susanne High Concentrations of Polyelectrolyte Complex Nanoparticles Decrease Activity of Osteoclasts |
title | High Concentrations of Polyelectrolyte Complex Nanoparticles Decrease Activity of Osteoclasts |
title_full | High Concentrations of Polyelectrolyte Complex Nanoparticles Decrease Activity of Osteoclasts |
title_fullStr | High Concentrations of Polyelectrolyte Complex Nanoparticles Decrease Activity of Osteoclasts |
title_full_unstemmed | High Concentrations of Polyelectrolyte Complex Nanoparticles Decrease Activity of Osteoclasts |
title_short | High Concentrations of Polyelectrolyte Complex Nanoparticles Decrease Activity of Osteoclasts |
title_sort | high concentrations of polyelectrolyte complex nanoparticles decrease activity of osteoclasts |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6630339/ https://www.ncbi.nlm.nih.gov/pubmed/31242715 http://dx.doi.org/10.3390/molecules24122346 |
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