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Activation of NF-κB/p65 Facilitates Early Chondrogenic Differentiation during Endochondral Ossification

BACKGROUND: NF-κB/p65 has been reported to be involved in regulation of chondrogenic differentiation. However, its function in relation to key chondrogenic factor Sox9 and onset of chondrogenesis during endochondral ossification is poorly understood. We hypothesized that the early onset of chondroge...

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Autores principales: Caron, Marjolein M. J., Emans, Pieter J., Surtel, Don A. M., Cremers, Andy, Voncken, Jan Willem, Welting, Tim J. M., van Rhijn, Lodewijk W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3299787/
https://www.ncbi.nlm.nih.gov/pubmed/22428055
http://dx.doi.org/10.1371/journal.pone.0033467
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author Caron, Marjolein M. J.
Emans, Pieter J.
Surtel, Don A. M.
Cremers, Andy
Voncken, Jan Willem
Welting, Tim J. M.
van Rhijn, Lodewijk W.
author_facet Caron, Marjolein M. J.
Emans, Pieter J.
Surtel, Don A. M.
Cremers, Andy
Voncken, Jan Willem
Welting, Tim J. M.
van Rhijn, Lodewijk W.
author_sort Caron, Marjolein M. J.
collection PubMed
description BACKGROUND: NF-κB/p65 has been reported to be involved in regulation of chondrogenic differentiation. However, its function in relation to key chondrogenic factor Sox9 and onset of chondrogenesis during endochondral ossification is poorly understood. We hypothesized that the early onset of chondrogenic differentiation is initiated by transient NF-κB/p65 signaling. METHODOLOGY/PRINCIPAL FINDINGS: The role of NF-κB/p65 in early chondrogenesis was investigated in different in vitro, ex vivo and in vivo endochondral models: ATDC5 cells, hBMSCs, chicken periosteal explants and growth plates of 6 weeks old mice. NF-κB/p65 activation was manipulated using pharmacological inhibitors, RNAi and activating agents. Gene expression and protein expression analysis, and (immuno)histochemical stainings were employed to determine the role of NF-κB/p65 in the chondrogenic phase of endochondral development. Our data show that chondrogenic differentiation is facilitated by early transient activation of NF-κB/p65. NF-κB/p65-mediated signaling determines early expression of Sox9 and facilitates the subsequent chondrogenic differentiation programming by signaling through key chondrogenic pathways. CONCLUSIONS/SIGNIFICANCE: The presented data demonstrate that NF-κB/p65 signaling, as well as its intensity and timing, represents one of the transcriptional regulatory mechanisms of the chondrogenic developmental program of chondroprogenitor cells during endochondral ossification. Importantly, these results provide novel possibilities to improve the success of cartilage and bone regenerative techniques.
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spelling pubmed-32997872012-03-16 Activation of NF-κB/p65 Facilitates Early Chondrogenic Differentiation during Endochondral Ossification Caron, Marjolein M. J. Emans, Pieter J. Surtel, Don A. M. Cremers, Andy Voncken, Jan Willem Welting, Tim J. M. van Rhijn, Lodewijk W. PLoS One Research Article BACKGROUND: NF-κB/p65 has been reported to be involved in regulation of chondrogenic differentiation. However, its function in relation to key chondrogenic factor Sox9 and onset of chondrogenesis during endochondral ossification is poorly understood. We hypothesized that the early onset of chondrogenic differentiation is initiated by transient NF-κB/p65 signaling. METHODOLOGY/PRINCIPAL FINDINGS: The role of NF-κB/p65 in early chondrogenesis was investigated in different in vitro, ex vivo and in vivo endochondral models: ATDC5 cells, hBMSCs, chicken periosteal explants and growth plates of 6 weeks old mice. NF-κB/p65 activation was manipulated using pharmacological inhibitors, RNAi and activating agents. Gene expression and protein expression analysis, and (immuno)histochemical stainings were employed to determine the role of NF-κB/p65 in the chondrogenic phase of endochondral development. Our data show that chondrogenic differentiation is facilitated by early transient activation of NF-κB/p65. NF-κB/p65-mediated signaling determines early expression of Sox9 and facilitates the subsequent chondrogenic differentiation programming by signaling through key chondrogenic pathways. CONCLUSIONS/SIGNIFICANCE: The presented data demonstrate that NF-κB/p65 signaling, as well as its intensity and timing, represents one of the transcriptional regulatory mechanisms of the chondrogenic developmental program of chondroprogenitor cells during endochondral ossification. Importantly, these results provide novel possibilities to improve the success of cartilage and bone regenerative techniques. Public Library of Science 2012-03-12 /pmc/articles/PMC3299787/ /pubmed/22428055 http://dx.doi.org/10.1371/journal.pone.0033467 Text en Caron 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
Caron, Marjolein M. J.
Emans, Pieter J.
Surtel, Don A. M.
Cremers, Andy
Voncken, Jan Willem
Welting, Tim J. M.
van Rhijn, Lodewijk W.
Activation of NF-κB/p65 Facilitates Early Chondrogenic Differentiation during Endochondral Ossification
title Activation of NF-κB/p65 Facilitates Early Chondrogenic Differentiation during Endochondral Ossification
title_full Activation of NF-κB/p65 Facilitates Early Chondrogenic Differentiation during Endochondral Ossification
title_fullStr Activation of NF-κB/p65 Facilitates Early Chondrogenic Differentiation during Endochondral Ossification
title_full_unstemmed Activation of NF-κB/p65 Facilitates Early Chondrogenic Differentiation during Endochondral Ossification
title_short Activation of NF-κB/p65 Facilitates Early Chondrogenic Differentiation during Endochondral Ossification
title_sort activation of nf-κb/p65 facilitates early chondrogenic differentiation during endochondral ossification
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3299787/
https://www.ncbi.nlm.nih.gov/pubmed/22428055
http://dx.doi.org/10.1371/journal.pone.0033467
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