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Synergistic activity of polarised osteoblasts inside condensations cause their differentiation
Condensation of pre-osteogenic, or pre-chondrogenic, cells is the first of a series of processes that initiate skeletal development. We present a validated, novel, three-dimensional agent-based model of in vitro intramembranous osteogenic condensation. The model, informed by system heterogeneity and...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4491713/ https://www.ncbi.nlm.nih.gov/pubmed/26146365 http://dx.doi.org/10.1038/srep11838 |
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author | Kaul, Himanshu Hall, Brian K. Newby, Chris Ventikos, Yiannis |
author_facet | Kaul, Himanshu Hall, Brian K. Newby, Chris Ventikos, Yiannis |
author_sort | Kaul, Himanshu |
collection | PubMed |
description | Condensation of pre-osteogenic, or pre-chondrogenic, cells is the first of a series of processes that initiate skeletal development. We present a validated, novel, three-dimensional agent-based model of in vitro intramembranous osteogenic condensation. The model, informed by system heterogeneity and relying on an interaction-reliant strategy, is shown to be sensitive to ‘rules’ capturing condensation growth and can be employed to track activity of individual cells to observe their macroscopic impact. It, therefore, makes available previously inaccessible data, offering new insights and providing a new context for exploring the emergence, as well as normal and abnormal development, of osteogenic structures. Of the several stages of condensation we investigate osteoblast ‘burial’ within the osteoid they deposit. The mechanisms underlying entrapment – required for osteoblasts to differentiate into osteocytes – remain a matter of conjecture with several hypotheses claiming to capture this important transition. Computational examination of this transition indicates that osteoblasts neither turn off nor slow down their matrix secreting genes – a widely held view; nor do they secrete matrix randomly. The model further reveals that osteoblasts display polarised behaviour to deposit osteoid. This is both an important addition to our understanding of condensation and an important validation of the model’s utility. |
format | Online Article Text |
id | pubmed-4491713 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-44917132015-07-08 Synergistic activity of polarised osteoblasts inside condensations cause their differentiation Kaul, Himanshu Hall, Brian K. Newby, Chris Ventikos, Yiannis Sci Rep Article Condensation of pre-osteogenic, or pre-chondrogenic, cells is the first of a series of processes that initiate skeletal development. We present a validated, novel, three-dimensional agent-based model of in vitro intramembranous osteogenic condensation. The model, informed by system heterogeneity and relying on an interaction-reliant strategy, is shown to be sensitive to ‘rules’ capturing condensation growth and can be employed to track activity of individual cells to observe their macroscopic impact. It, therefore, makes available previously inaccessible data, offering new insights and providing a new context for exploring the emergence, as well as normal and abnormal development, of osteogenic structures. Of the several stages of condensation we investigate osteoblast ‘burial’ within the osteoid they deposit. The mechanisms underlying entrapment – required for osteoblasts to differentiate into osteocytes – remain a matter of conjecture with several hypotheses claiming to capture this important transition. Computational examination of this transition indicates that osteoblasts neither turn off nor slow down their matrix secreting genes – a widely held view; nor do they secrete matrix randomly. The model further reveals that osteoblasts display polarised behaviour to deposit osteoid. This is both an important addition to our understanding of condensation and an important validation of the model’s utility. Nature Publishing Group 2015-07-06 /pmc/articles/PMC4491713/ /pubmed/26146365 http://dx.doi.org/10.1038/srep11838 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Kaul, Himanshu Hall, Brian K. Newby, Chris Ventikos, Yiannis Synergistic activity of polarised osteoblasts inside condensations cause their differentiation |
title | Synergistic activity of polarised osteoblasts inside condensations cause their differentiation |
title_full | Synergistic activity of polarised osteoblasts inside condensations cause their differentiation |
title_fullStr | Synergistic activity of polarised osteoblasts inside condensations cause their differentiation |
title_full_unstemmed | Synergistic activity of polarised osteoblasts inside condensations cause their differentiation |
title_short | Synergistic activity of polarised osteoblasts inside condensations cause their differentiation |
title_sort | synergistic activity of polarised osteoblasts inside condensations cause their differentiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4491713/ https://www.ncbi.nlm.nih.gov/pubmed/26146365 http://dx.doi.org/10.1038/srep11838 |
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