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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Research Network of Computational and Structural Biotechnology
2021
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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 |
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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 |
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