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Podoplanin Immunopositive Lymphatic Vessels at the Implant Interface in a Rat Model of Osteoporotic Fractures
Insertion of bone substitution materials accelerates healing of osteoporotic fractures. Biodegradable materials are preferred for application in osteoporotic patients to avoid a second surgery for implant replacement. Degraded implant fragments are often absorbed by macrophages that are removed from...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793947/ https://www.ncbi.nlm.nih.gov/pubmed/24130867 http://dx.doi.org/10.1371/journal.pone.0077259 |
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author | Lips, Katrin Susanne Kauschke, Vivien Hartmann, Sonja Thormann, Ulrich Ray, Seemun Kampschulte, Marian Langheinrich, Alexander Schumacher, Matthias Gelinsky, Michael Heinemann, Sascha Hanke, Thomas Kautz, Armin R. Schnabelrauch, Matthias Schnettler, Reinhard Heiss, Christian Alt, Volker Kilian, Olaf |
author_facet | Lips, Katrin Susanne Kauschke, Vivien Hartmann, Sonja Thormann, Ulrich Ray, Seemun Kampschulte, Marian Langheinrich, Alexander Schumacher, Matthias Gelinsky, Michael Heinemann, Sascha Hanke, Thomas Kautz, Armin R. Schnabelrauch, Matthias Schnettler, Reinhard Heiss, Christian Alt, Volker Kilian, Olaf |
author_sort | Lips, Katrin Susanne |
collection | PubMed |
description | Insertion of bone substitution materials accelerates healing of osteoporotic fractures. Biodegradable materials are preferred for application in osteoporotic patients to avoid a second surgery for implant replacement. Degraded implant fragments are often absorbed by macrophages that are removed from the fracture side via passage through veins or lymphatic vessels. We investigated if lymphatic vessels occur in osteoporotic bone defects and whether they are regulated by the use of different materials. To address this issue osteoporosis was induced in rats using the classical method of bilateral ovariectomy and additional calcium and vitamin deficient diet. In addition, wedge-shaped defects of 3, 4, or 5 mm were generated in the distal metaphyseal area of femur via osteotomy. The 4 mm defects were subsequently used for implantation studies where bone substitution materials of calcium phosphate cement, composites of collagen and silica, and iron foams with interconnecting pores were inserted. Different materials were partly additionally functionalized by strontium or bisphosphonate whose positive effects in osteoporosis treatment are well known. The lymphatic vessels were identified by immunohistochemistry using an antibody against podoplanin. Podoplanin immunopositive lymphatic vessels were detected in the granulation tissue filling the fracture gap, surrounding the implant and growing into the iron foam through its interconnected pores. Significant more lymphatic capillaries were counted at the implant interface of composite, strontium and bisphosphonate functionalized iron foam. A significant increase was also observed in the number of lymphatics situated in the pores of strontium coated iron foam. In conclusion, our results indicate the occurrence of lymphatic vessels in osteoporotic bone. Our results show that lymphatic vessels are localized at the implant interface and in the fracture gap where they might be involved in the removal of lymphocytes, macrophages, debris and the implants degradation products. Therefore the lymphatic vessels are involved in implant integration and fracture healing. |
format | Online Article Text |
id | pubmed-3793947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37939472013-10-15 Podoplanin Immunopositive Lymphatic Vessels at the Implant Interface in a Rat Model of Osteoporotic Fractures Lips, Katrin Susanne Kauschke, Vivien Hartmann, Sonja Thormann, Ulrich Ray, Seemun Kampschulte, Marian Langheinrich, Alexander Schumacher, Matthias Gelinsky, Michael Heinemann, Sascha Hanke, Thomas Kautz, Armin R. Schnabelrauch, Matthias Schnettler, Reinhard Heiss, Christian Alt, Volker Kilian, Olaf PLoS One Research Article Insertion of bone substitution materials accelerates healing of osteoporotic fractures. Biodegradable materials are preferred for application in osteoporotic patients to avoid a second surgery for implant replacement. Degraded implant fragments are often absorbed by macrophages that are removed from the fracture side via passage through veins or lymphatic vessels. We investigated if lymphatic vessels occur in osteoporotic bone defects and whether they are regulated by the use of different materials. To address this issue osteoporosis was induced in rats using the classical method of bilateral ovariectomy and additional calcium and vitamin deficient diet. In addition, wedge-shaped defects of 3, 4, or 5 mm were generated in the distal metaphyseal area of femur via osteotomy. The 4 mm defects were subsequently used for implantation studies where bone substitution materials of calcium phosphate cement, composites of collagen and silica, and iron foams with interconnecting pores were inserted. Different materials were partly additionally functionalized by strontium or bisphosphonate whose positive effects in osteoporosis treatment are well known. The lymphatic vessels were identified by immunohistochemistry using an antibody against podoplanin. Podoplanin immunopositive lymphatic vessels were detected in the granulation tissue filling the fracture gap, surrounding the implant and growing into the iron foam through its interconnected pores. Significant more lymphatic capillaries were counted at the implant interface of composite, strontium and bisphosphonate functionalized iron foam. A significant increase was also observed in the number of lymphatics situated in the pores of strontium coated iron foam. In conclusion, our results indicate the occurrence of lymphatic vessels in osteoporotic bone. Our results show that lymphatic vessels are localized at the implant interface and in the fracture gap where they might be involved in the removal of lymphocytes, macrophages, debris and the implants degradation products. Therefore the lymphatic vessels are involved in implant integration and fracture healing. Public Library of Science 2013-10-09 /pmc/articles/PMC3793947/ /pubmed/24130867 http://dx.doi.org/10.1371/journal.pone.0077259 Text en © 2013 Lips 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Lips, Katrin Susanne Kauschke, Vivien Hartmann, Sonja Thormann, Ulrich Ray, Seemun Kampschulte, Marian Langheinrich, Alexander Schumacher, Matthias Gelinsky, Michael Heinemann, Sascha Hanke, Thomas Kautz, Armin R. Schnabelrauch, Matthias Schnettler, Reinhard Heiss, Christian Alt, Volker Kilian, Olaf Podoplanin Immunopositive Lymphatic Vessels at the Implant Interface in a Rat Model of Osteoporotic Fractures |
title | Podoplanin Immunopositive Lymphatic Vessels at the Implant Interface in a Rat Model of Osteoporotic Fractures |
title_full | Podoplanin Immunopositive Lymphatic Vessels at the Implant Interface in a Rat Model of Osteoporotic Fractures |
title_fullStr | Podoplanin Immunopositive Lymphatic Vessels at the Implant Interface in a Rat Model of Osteoporotic Fractures |
title_full_unstemmed | Podoplanin Immunopositive Lymphatic Vessels at the Implant Interface in a Rat Model of Osteoporotic Fractures |
title_short | Podoplanin Immunopositive Lymphatic Vessels at the Implant Interface in a Rat Model of Osteoporotic Fractures |
title_sort | podoplanin immunopositive lymphatic vessels at the implant interface in a rat model of osteoporotic fractures |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793947/ https://www.ncbi.nlm.nih.gov/pubmed/24130867 http://dx.doi.org/10.1371/journal.pone.0077259 |
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