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Calcium ions and osteoclastogenesis initiate the induction of bone formation by coral-derived macroporous constructs

Coral-derived calcium carbonate/hydroxyapatite macroporous constructs of the genus Goniopora with limited hydrothermal conversion to hydroxyapatite (7% HA/CC) initiate the induction of bone formation. Which are the molecular signals that initiate pattern formation and the induction of bone formation...

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Autores principales: Klar, Roland M, Duarte, Raquel, Dix-Peek, Therese, Dickens, Caroline, Ferretti, Carlo, Ripamonti, Ugo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4117557/
https://www.ncbi.nlm.nih.gov/pubmed/24106923
http://dx.doi.org/10.1111/jcmm.12125
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author Klar, Roland M
Duarte, Raquel
Dix-Peek, Therese
Dickens, Caroline
Ferretti, Carlo
Ripamonti, Ugo
author_facet Klar, Roland M
Duarte, Raquel
Dix-Peek, Therese
Dickens, Caroline
Ferretti, Carlo
Ripamonti, Ugo
author_sort Klar, Roland M
collection PubMed
description Coral-derived calcium carbonate/hydroxyapatite macroporous constructs of the genus Goniopora with limited hydrothermal conversion to hydroxyapatite (7% HA/CC) initiate the induction of bone formation. Which are the molecular signals that initiate pattern formation and the induction of bone formation? To evaluate the role of released calcium ions and osteoclastogenesis, 7% HA/CC was pre-loaded with either 500 μg of the calcium channel blocker, verapamil hydrochloride, or 240 μg of the osteoclast inhibitor, biphosphonate zoledronate, and implanted in the rectus abdominis muscle of six adult Chacma baboons Papio ursinus. Generated tissues on days 15, 60 and 90 were analysed by histomorphometry and qRT-PCR. On day 15, up-regulation of type IV collagen characterized all the implanted constructs correlating with vascular invasion. Zoledronate-treated specimens showed an important delay in tissue patterning and morphogenesis with limited bone formation. Osteoclastic inhibition yielded minimal, if any, bone formation by induction. 7% HA/CC pre-loaded with the Ca(++) channel blocker verapamil hydrochloride strongly inhibited the induction of bone formation. Down-regulation of bone morphogenetic protein-2 (BMP-2) together with up-regulation of Noggin genes correlated with limited bone formation in 7% HA/CC pre-loaded with either verapamil or zoledronate, indicating that the induction of bone formation by coral-derived macroporous constructs is via the BMPs pathway. The spontaneous induction of bone formation is initiated by a local peak of Ca(++) activating stem cell differentiation and the induction of bone formation.
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spelling pubmed-41175572014-12-03 Calcium ions and osteoclastogenesis initiate the induction of bone formation by coral-derived macroporous constructs Klar, Roland M Duarte, Raquel Dix-Peek, Therese Dickens, Caroline Ferretti, Carlo Ripamonti, Ugo J Cell Mol Med Original Articles Coral-derived calcium carbonate/hydroxyapatite macroporous constructs of the genus Goniopora with limited hydrothermal conversion to hydroxyapatite (7% HA/CC) initiate the induction of bone formation. Which are the molecular signals that initiate pattern formation and the induction of bone formation? To evaluate the role of released calcium ions and osteoclastogenesis, 7% HA/CC was pre-loaded with either 500 μg of the calcium channel blocker, verapamil hydrochloride, or 240 μg of the osteoclast inhibitor, biphosphonate zoledronate, and implanted in the rectus abdominis muscle of six adult Chacma baboons Papio ursinus. Generated tissues on days 15, 60 and 90 were analysed by histomorphometry and qRT-PCR. On day 15, up-regulation of type IV collagen characterized all the implanted constructs correlating with vascular invasion. Zoledronate-treated specimens showed an important delay in tissue patterning and morphogenesis with limited bone formation. Osteoclastic inhibition yielded minimal, if any, bone formation by induction. 7% HA/CC pre-loaded with the Ca(++) channel blocker verapamil hydrochloride strongly inhibited the induction of bone formation. Down-regulation of bone morphogenetic protein-2 (BMP-2) together with up-regulation of Noggin genes correlated with limited bone formation in 7% HA/CC pre-loaded with either verapamil or zoledronate, indicating that the induction of bone formation by coral-derived macroporous constructs is via the BMPs pathway. The spontaneous induction of bone formation is initiated by a local peak of Ca(++) activating stem cell differentiation and the induction of bone formation. John Wiley & Sons 2013-11 2013-09-23 /pmc/articles/PMC4117557/ /pubmed/24106923 http://dx.doi.org/10.1111/jcmm.12125 Text en Copyright © 2013 John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Klar, Roland M
Duarte, Raquel
Dix-Peek, Therese
Dickens, Caroline
Ferretti, Carlo
Ripamonti, Ugo
Calcium ions and osteoclastogenesis initiate the induction of bone formation by coral-derived macroporous constructs
title Calcium ions and osteoclastogenesis initiate the induction of bone formation by coral-derived macroporous constructs
title_full Calcium ions and osteoclastogenesis initiate the induction of bone formation by coral-derived macroporous constructs
title_fullStr Calcium ions and osteoclastogenesis initiate the induction of bone formation by coral-derived macroporous constructs
title_full_unstemmed Calcium ions and osteoclastogenesis initiate the induction of bone formation by coral-derived macroporous constructs
title_short Calcium ions and osteoclastogenesis initiate the induction of bone formation by coral-derived macroporous constructs
title_sort calcium ions and osteoclastogenesis initiate the induction of bone formation by coral-derived macroporous constructs
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4117557/
https://www.ncbi.nlm.nih.gov/pubmed/24106923
http://dx.doi.org/10.1111/jcmm.12125
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