Cargando…

Gene-metabolite networks associated with impediment of bone fracture repair in spaceflight

Adverse effects of spaceflight on musculoskeletal health increase the risk of bone injury and impairment of fracture healing. Its yet elusive molecular comprehension warrants immediate attention, since space travel is becoming more frequent. Here we examined the effects of spaceflight on bone fractu...

Descripción completa

Detalles Bibliográficos
Autores principales: Chakraborty, Nabarun, Zamarioli, Ariane, Gautam, Aarti, Campbell, Ross, Mendenhall, Stephen K, Childress, Paul J., Dimitrov, George, Sowe, Bintu, Tucker, Aamir, Zhao, Liming, Hammamieh, Rasha, Kacena, Melissa A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8220416/
https://www.ncbi.nlm.nih.gov/pubmed/34194674
http://dx.doi.org/10.1016/j.csbj.2021.05.050
_version_ 1783711144055144448
author Chakraborty, Nabarun
Zamarioli, Ariane
Gautam, Aarti
Campbell, Ross
Mendenhall, Stephen K
Childress, Paul J.
Dimitrov, George
Sowe, Bintu
Tucker, Aamir
Zhao, Liming
Hammamieh, Rasha
Kacena, Melissa A.
author_facet Chakraborty, Nabarun
Zamarioli, Ariane
Gautam, Aarti
Campbell, Ross
Mendenhall, Stephen K
Childress, Paul J.
Dimitrov, George
Sowe, Bintu
Tucker, Aamir
Zhao, Liming
Hammamieh, Rasha
Kacena, Melissa A.
author_sort Chakraborty, Nabarun
collection PubMed
description Adverse effects of spaceflight on musculoskeletal health increase the risk of bone injury and impairment of fracture healing. Its yet elusive molecular comprehension warrants immediate attention, since space travel is becoming more frequent. Here we examined the effects of spaceflight on bone fracture healing using a 2 mm femoral segmental bone defect (SBD) model. Forty, 9-week-old, male C57BL/6J mice were randomized into 4 groups: 1) Sham surgery on Ground (G-Sham); 2) Sham surgery housed in Spaceflight (FLT-Sham); 3) SBD surgery on Ground (G-Surgery); and 4) SBD surgery housed in Spaceflight (FLT-Surgery). Surgery procedures occurred 4 days prior to launch; post-launch, the spaceflight mice were house in the rodent habitats on the International Space Station (ISS) for approximately 4 weeks before euthanasia. Mice remaining on the Earth were subjected to identical housing and experimental conditions. The right femur from half of the spaceflight and ground groups was investigated by micro-computed tomography (µCT). In the remaining mice, the callus regions from surgery groups and corresponding femoral segments in sham mice were probed by global transcriptomic and metabolomic assays. µCT confirmed escalated bone loss in FLT-Sham compared to G-Sham mice. Comparing to their respective on-ground counterparts, the morbidity gene-network signal was inhibited in sham spaceflight mice but activated in the spaceflight callus. µCT analyses of spaceflight callus revealed increased trabecular spacing and decreased trabecular connectivity. Activated apoptotic signals in spaceflight callus were synchronized with inhibited cell migration signals that potentially hindered the wound site to recruit growth factors. A major pro-apoptotic and anti-migration gene network, namely the RANK-NFκB axis, emerged as the central node in spaceflight callus. Concluding, spaceflight suppressed a unique biomolecular mechanism in callus tissue to facilitate a failed regeneration, which merits a customized intervention strategy.
format Online
Article
Text
id pubmed-8220416
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Research Network of Computational and Structural Biotechnology
record_format MEDLINE/PubMed
spelling pubmed-82204162021-06-29 Gene-metabolite networks associated with impediment of bone fracture repair in spaceflight Chakraborty, Nabarun Zamarioli, Ariane Gautam, Aarti Campbell, Ross Mendenhall, Stephen K Childress, Paul J. Dimitrov, George Sowe, Bintu Tucker, Aamir Zhao, Liming Hammamieh, Rasha Kacena, Melissa A. Comput Struct Biotechnol J Research Article Adverse effects of spaceflight on musculoskeletal health increase the risk of bone injury and impairment of fracture healing. Its yet elusive molecular comprehension warrants immediate attention, since space travel is becoming more frequent. Here we examined the effects of spaceflight on bone fracture healing using a 2 mm femoral segmental bone defect (SBD) model. Forty, 9-week-old, male C57BL/6J mice were randomized into 4 groups: 1) Sham surgery on Ground (G-Sham); 2) Sham surgery housed in Spaceflight (FLT-Sham); 3) SBD surgery on Ground (G-Surgery); and 4) SBD surgery housed in Spaceflight (FLT-Surgery). Surgery procedures occurred 4 days prior to launch; post-launch, the spaceflight mice were house in the rodent habitats on the International Space Station (ISS) for approximately 4 weeks before euthanasia. Mice remaining on the Earth were subjected to identical housing and experimental conditions. The right femur from half of the spaceflight and ground groups was investigated by micro-computed tomography (µCT). In the remaining mice, the callus regions from surgery groups and corresponding femoral segments in sham mice were probed by global transcriptomic and metabolomic assays. µCT confirmed escalated bone loss in FLT-Sham compared to G-Sham mice. Comparing to their respective on-ground counterparts, the morbidity gene-network signal was inhibited in sham spaceflight mice but activated in the spaceflight callus. µCT analyses of spaceflight callus revealed increased trabecular spacing and decreased trabecular connectivity. Activated apoptotic signals in spaceflight callus were synchronized with inhibited cell migration signals that potentially hindered the wound site to recruit growth factors. A major pro-apoptotic and anti-migration gene network, namely the RANK-NFκB axis, emerged as the central node in spaceflight callus. Concluding, spaceflight suppressed a unique biomolecular mechanism in callus tissue to facilitate a failed regeneration, which merits a customized intervention strategy. Research Network of Computational and Structural Biotechnology 2021-06-08 /pmc/articles/PMC8220416/ /pubmed/34194674 http://dx.doi.org/10.1016/j.csbj.2021.05.050 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Chakraborty, Nabarun
Zamarioli, Ariane
Gautam, Aarti
Campbell, Ross
Mendenhall, Stephen K
Childress, Paul J.
Dimitrov, George
Sowe, Bintu
Tucker, Aamir
Zhao, Liming
Hammamieh, Rasha
Kacena, Melissa A.
Gene-metabolite networks associated with impediment of bone fracture repair in spaceflight
title Gene-metabolite networks associated with impediment of bone fracture repair in spaceflight
title_full Gene-metabolite networks associated with impediment of bone fracture repair in spaceflight
title_fullStr Gene-metabolite networks associated with impediment of bone fracture repair in spaceflight
title_full_unstemmed Gene-metabolite networks associated with impediment of bone fracture repair in spaceflight
title_short Gene-metabolite networks associated with impediment of bone fracture repair in spaceflight
title_sort gene-metabolite networks associated with impediment of bone fracture repair in spaceflight
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8220416/
https://www.ncbi.nlm.nih.gov/pubmed/34194674
http://dx.doi.org/10.1016/j.csbj.2021.05.050
work_keys_str_mv AT chakrabortynabarun genemetabolitenetworksassociatedwithimpedimentofbonefracturerepairinspaceflight
AT zamarioliariane genemetabolitenetworksassociatedwithimpedimentofbonefracturerepairinspaceflight
AT gautamaarti genemetabolitenetworksassociatedwithimpedimentofbonefracturerepairinspaceflight
AT campbellross genemetabolitenetworksassociatedwithimpedimentofbonefracturerepairinspaceflight
AT mendenhallstephenk genemetabolitenetworksassociatedwithimpedimentofbonefracturerepairinspaceflight
AT childresspaulj genemetabolitenetworksassociatedwithimpedimentofbonefracturerepairinspaceflight
AT dimitrovgeorge genemetabolitenetworksassociatedwithimpedimentofbonefracturerepairinspaceflight
AT sowebintu genemetabolitenetworksassociatedwithimpedimentofbonefracturerepairinspaceflight
AT tuckeraamir genemetabolitenetworksassociatedwithimpedimentofbonefracturerepairinspaceflight
AT zhaoliming genemetabolitenetworksassociatedwithimpedimentofbonefracturerepairinspaceflight
AT hammamiehrasha genemetabolitenetworksassociatedwithimpedimentofbonefracturerepairinspaceflight
AT kacenamelissaa genemetabolitenetworksassociatedwithimpedimentofbonefracturerepairinspaceflight