Bone remodeling: A tissue-level process emerging from cell-level molecular algorithms

ABSTRACT: The human skeleton undergoes constant remodeling throughout the lifetime. Processes occurring on microscopic and molecular scales degrade bone and replace it with new, fully functional tissue. Multiple bone remodeling events occur simultaneously, continuously and independently throughout t...

Full description

Autores:
Fernández Arias, Clemente
Herrero García, Miguel Ángel
Echeverri Delgado, Luis Fernando
OleagaI, Gerardo
López García, José Manuel
Tipo de recurso:
Article of investigation
Fecha de publicación:
2018
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/23724
Acceso en línea:
http://hdl.handle.net/10495/23724
Palabra clave:
Remodelación Ósea
Bone Remodeling
Esqueleto humano
Human skeleton
Rights
openAccess
License
https://creativecommons.org/licenses/by/4.0/
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dc.title.spa.fl_str_mv Bone remodeling: A tissue-level process emerging from cell-level molecular algorithms
title Bone remodeling: A tissue-level process emerging from cell-level molecular algorithms
spellingShingle Bone remodeling: A tissue-level process emerging from cell-level molecular algorithms
Remodelación Ósea
Bone Remodeling
Esqueleto humano
Human skeleton
title_short Bone remodeling: A tissue-level process emerging from cell-level molecular algorithms
title_full Bone remodeling: A tissue-level process emerging from cell-level molecular algorithms
title_fullStr Bone remodeling: A tissue-level process emerging from cell-level molecular algorithms
title_full_unstemmed Bone remodeling: A tissue-level process emerging from cell-level molecular algorithms
title_sort Bone remodeling: A tissue-level process emerging from cell-level molecular algorithms
dc.creator.fl_str_mv Fernández Arias, Clemente
Herrero García, Miguel Ángel
Echeverri Delgado, Luis Fernando
OleagaI, Gerardo
López García, José Manuel
dc.contributor.author.none.fl_str_mv Fernández Arias, Clemente
Herrero García, Miguel Ángel
Echeverri Delgado, Luis Fernando
OleagaI, Gerardo
López García, José Manuel
dc.contributor.researchgroup.spa.fl_str_mv EMAC - Enseñanza de Matemáticas y Computación
dc.subject.decs.none.fl_str_mv Remodelación Ósea
Bone Remodeling
topic Remodelación Ósea
Bone Remodeling
Esqueleto humano
Human skeleton
dc.subject.lemb.none.fl_str_mv Esqueleto humano
Human skeleton
description ABSTRACT: The human skeleton undergoes constant remodeling throughout the lifetime. Processes occurring on microscopic and molecular scales degrade bone and replace it with new, fully functional tissue. Multiple bone remodeling events occur simultaneously, continuously and independently throughout the body, so that the entire skeleton is completely renewed about every ten years.Bone remodeling is performed by groups of cells called Bone Multicellular Units (BMU). BMUs consist of different cell types, some specialized in the resorption of old bone, others encharged with producing new bone to replace the former. These processes are tightly regulated so that the amount of new bone produced is in perfect equilibrium with that of old bone removed, thus maintaining bone microscopic structure.To date, many regulatory molecules involved in bone remodeling have been identified, but the precise mechanism of BMU operation remains to be fully elucidated. Given the complexity of the signaling pathways already known, one may question whether such complexity is an inherent requirement of the process or whether some subset of the multiple constituents could fulfill the essential role, leaving functional redundancy to serve an alternative safety role. We propose in this work a minimal model of BMU function that involves a limited number of signals able to account for fully functional BMU operation. Our main assumptions were i) at any given time, any cell within a BMU can select only one among a limited choice of decisions, i.e. divide, die, migrate or differentiate, ii) this decision is irreversibly determined by depletion of an appropriate internal inhibitor and iii) the dynamics of any such inhibitor are coupled to that of specific external mediators, such as hormones, cytokines, growth factors. It was thus shown that efficient BMU operation manifests as an emergent process, which results from the individual and collective decisions taken by cells within the BMU unit in the absence of any external planning.
publishDate 2018
dc.date.issued.none.fl_str_mv 2018
dc.date.accessioned.none.fl_str_mv 2021-11-03T15:52:07Z
dc.date.available.none.fl_str_mv 2021-11-03T15:52:07Z
dc.type.spa.fl_str_mv Artículo de investigación
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dc.identifier.citation.spa.fl_str_mv Arias, C., Herrero, M., Echeverri, L., Oleaga, G., López, J. (2018) Bone remodeling: A tissue-level process emerging from cell-level molecular algorithms. PLoS ONE 13(9): e0204171. https://doi.org/10.1371/journal.pone.0204171
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/10495/23724
dc.identifier.doi.none.fl_str_mv 10.1371/journal.pone.0204171
dc.identifier.eissn.none.fl_str_mv 1932-6203
identifier_str_mv Arias, C., Herrero, M., Echeverri, L., Oleaga, G., López, J. (2018) Bone remodeling: A tissue-level process emerging from cell-level molecular algorithms. PLoS ONE 13(9): e0204171. https://doi.org/10.1371/journal.pone.0204171
10.1371/journal.pone.0204171
1932-6203
url http://hdl.handle.net/10495/23724
dc.language.iso.spa.fl_str_mv eng
language eng
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dc.relation.citationvolume.spa.fl_str_mv 13
dc.relation.ispartofjournal.spa.fl_str_mv PLoS ONE
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dc.publisher.place.spa.fl_str_mv San Francisco, Estados Unidos
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spelling Fernández Arias, ClementeHerrero García, Miguel ÁngelEcheverri Delgado, Luis FernandoOleagaI, GerardoLópez García, José ManuelEMAC - Enseñanza de Matemáticas y Computación2021-11-03T15:52:07Z2021-11-03T15:52:07Z2018Arias, C., Herrero, M., Echeverri, L., Oleaga, G., López, J. (2018) Bone remodeling: A tissue-level process emerging from cell-level molecular algorithms. PLoS ONE 13(9): e0204171. https://doi.org/10.1371/journal.pone.0204171http://hdl.handle.net/10495/2372410.1371/journal.pone.02041711932-6203ABSTRACT: The human skeleton undergoes constant remodeling throughout the lifetime. Processes occurring on microscopic and molecular scales degrade bone and replace it with new, fully functional tissue. Multiple bone remodeling events occur simultaneously, continuously and independently throughout the body, so that the entire skeleton is completely renewed about every ten years.Bone remodeling is performed by groups of cells called Bone Multicellular Units (BMU). BMUs consist of different cell types, some specialized in the resorption of old bone, others encharged with producing new bone to replace the former. These processes are tightly regulated so that the amount of new bone produced is in perfect equilibrium with that of old bone removed, thus maintaining bone microscopic structure.To date, many regulatory molecules involved in bone remodeling have been identified, but the precise mechanism of BMU operation remains to be fully elucidated. Given the complexity of the signaling pathways already known, one may question whether such complexity is an inherent requirement of the process or whether some subset of the multiple constituents could fulfill the essential role, leaving functional redundancy to serve an alternative safety role. We propose in this work a minimal model of BMU function that involves a limited number of signals able to account for fully functional BMU operation. Our main assumptions were i) at any given time, any cell within a BMU can select only one among a limited choice of decisions, i.e. divide, die, migrate or differentiate, ii) this decision is irreversibly determined by depletion of an appropriate internal inhibitor and iii) the dynamics of any such inhibitor are coupled to that of specific external mediators, such as hormones, cytokines, growth factors. 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