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A Moderate Blast Exposure Results in Dysregulated Gene Network Activity Related to Cell Death, Survival, Structure, and Metabolism

Blast exposure is common in military personnel during training and combat operations, yet biological mechanisms related to cell survival and function that coordinate recovery remain poorly understood. This study explored how moderate blast exposure influences gene expression; specifically, gene-netw...

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Autores principales: Edwards, Katie A., Motamedi, Vida, Osier, Nicole D., Kim, Hyung-Suk, Yun, Sijung, Cho, Young-Eun, Lai, Chen, Dell, Kristine C., Carr, Walter, Walker, Peter, Ahlers, Stephen, LoPresti, Matthew, Yarnell, Angela, Tschiffley, Anna, Gill, Jessica M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054450/
https://www.ncbi.nlm.nih.gov/pubmed/32174881
http://dx.doi.org/10.3389/fneur.2020.00091
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author Edwards, Katie A.
Motamedi, Vida
Osier, Nicole D.
Kim, Hyung-Suk
Yun, Sijung
Cho, Young-Eun
Lai, Chen
Dell, Kristine C.
Carr, Walter
Walker, Peter
Ahlers, Stephen
LoPresti, Matthew
Yarnell, Angela
Tschiffley, Anna
Gill, Jessica M.
author_facet Edwards, Katie A.
Motamedi, Vida
Osier, Nicole D.
Kim, Hyung-Suk
Yun, Sijung
Cho, Young-Eun
Lai, Chen
Dell, Kristine C.
Carr, Walter
Walker, Peter
Ahlers, Stephen
LoPresti, Matthew
Yarnell, Angela
Tschiffley, Anna
Gill, Jessica M.
author_sort Edwards, Katie A.
collection PubMed
description Blast exposure is common in military personnel during training and combat operations, yet biological mechanisms related to cell survival and function that coordinate recovery remain poorly understood. This study explored how moderate blast exposure influences gene expression; specifically, gene-network changes following moderate blast exposure. On day 1 (baseline) of a 10-day military training program, blood samples were drawn, and health and demographic information collected. Helmets equipped with bilateral sensors worn throughout training measured overpressure in pounds per square inch (psi). On day 7, some participants experienced moderate blast exposure (peak pressure ≥5 psi). On day 10, 3 days post-exposure, blood was collected and compared to baseline with RNA-sequencing to establish gene expression changes. Based on dysregulation data from RNA-sequencing, followed by top gene networks identified with Ingenuity Pathway Analysis, a subset of genes was validated (NanoString). Five gene networks were dysregulated; specifically, two highly significant networks: (1) Cell Death and Survival (score: 42), including 70 genes, with 50 downregulated and (2) Cell Structure, Function, and Metabolism (score: 41), including 69 genes, with 41 downregulated. Genes related to ubiquitination, including neuronal development and repair: UPF1, RNA Helicase and ATPase (UPF1) was upregulated while UPF3 Regulator of Nonsense Transcripts Homolog B (UPF3B) was downregulated. Genes related to inflammation were upregulated, including AKT serine/threonine kinase 1 (AKT1), a gene coordinating cellular recovery following TBIs. Moderate blast exposure induced significant gene expression changes including gene networks involved in (1) cell death and survival and (2) cellular development and function. The present findings may have implications for understanding blast exposure pathology and subsequent recovery efforts.
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spelling pubmed-70544502020-03-13 A Moderate Blast Exposure Results in Dysregulated Gene Network Activity Related to Cell Death, Survival, Structure, and Metabolism Edwards, Katie A. Motamedi, Vida Osier, Nicole D. Kim, Hyung-Suk Yun, Sijung Cho, Young-Eun Lai, Chen Dell, Kristine C. Carr, Walter Walker, Peter Ahlers, Stephen LoPresti, Matthew Yarnell, Angela Tschiffley, Anna Gill, Jessica M. Front Neurol Neurology Blast exposure is common in military personnel during training and combat operations, yet biological mechanisms related to cell survival and function that coordinate recovery remain poorly understood. This study explored how moderate blast exposure influences gene expression; specifically, gene-network changes following moderate blast exposure. On day 1 (baseline) of a 10-day military training program, blood samples were drawn, and health and demographic information collected. Helmets equipped with bilateral sensors worn throughout training measured overpressure in pounds per square inch (psi). On day 7, some participants experienced moderate blast exposure (peak pressure ≥5 psi). On day 10, 3 days post-exposure, blood was collected and compared to baseline with RNA-sequencing to establish gene expression changes. Based on dysregulation data from RNA-sequencing, followed by top gene networks identified with Ingenuity Pathway Analysis, a subset of genes was validated (NanoString). Five gene networks were dysregulated; specifically, two highly significant networks: (1) Cell Death and Survival (score: 42), including 70 genes, with 50 downregulated and (2) Cell Structure, Function, and Metabolism (score: 41), including 69 genes, with 41 downregulated. Genes related to ubiquitination, including neuronal development and repair: UPF1, RNA Helicase and ATPase (UPF1) was upregulated while UPF3 Regulator of Nonsense Transcripts Homolog B (UPF3B) was downregulated. Genes related to inflammation were upregulated, including AKT serine/threonine kinase 1 (AKT1), a gene coordinating cellular recovery following TBIs. Moderate blast exposure induced significant gene expression changes including gene networks involved in (1) cell death and survival and (2) cellular development and function. The present findings may have implications for understanding blast exposure pathology and subsequent recovery efforts. Frontiers Media S.A. 2020-02-26 /pmc/articles/PMC7054450/ /pubmed/32174881 http://dx.doi.org/10.3389/fneur.2020.00091 Text en At least a portion of this work is authored by Katie A. Edwards, Vida Motamedi, Nicole D. Osier, Hyung-Suk Kim, Young-Eun Cho, Chen Lai, Kristine C. Dell, Walter Carr, Peter Walker, Stephen Ahlers, Matthew LoPresti, Angela Yarnell, Anna Tschiffley and Jessica M. Gill on behalf of the U.S. Government and, as regards Katie A. Edwards, Vida Motamedi, Nicole D. Osier, Hyung-Suk Kim, Young-Eun Cho, Chen Lai, Kristine C. Dell, Walter Carr, Peter Walker, Stephen Ahlers, Matthew LoPresti, Angela Yarnell, Anna Tschiffley and Jessica M. Gill and the U.S. Government, is not subject to copyright protection in the United States. Foreign and other copyrights may apply. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Edwards, Katie A.
Motamedi, Vida
Osier, Nicole D.
Kim, Hyung-Suk
Yun, Sijung
Cho, Young-Eun
Lai, Chen
Dell, Kristine C.
Carr, Walter
Walker, Peter
Ahlers, Stephen
LoPresti, Matthew
Yarnell, Angela
Tschiffley, Anna
Gill, Jessica M.
A Moderate Blast Exposure Results in Dysregulated Gene Network Activity Related to Cell Death, Survival, Structure, and Metabolism
title A Moderate Blast Exposure Results in Dysregulated Gene Network Activity Related to Cell Death, Survival, Structure, and Metabolism
title_full A Moderate Blast Exposure Results in Dysregulated Gene Network Activity Related to Cell Death, Survival, Structure, and Metabolism
title_fullStr A Moderate Blast Exposure Results in Dysregulated Gene Network Activity Related to Cell Death, Survival, Structure, and Metabolism
title_full_unstemmed A Moderate Blast Exposure Results in Dysregulated Gene Network Activity Related to Cell Death, Survival, Structure, and Metabolism
title_short A Moderate Blast Exposure Results in Dysregulated Gene Network Activity Related to Cell Death, Survival, Structure, and Metabolism
title_sort moderate blast exposure results in dysregulated gene network activity related to cell death, survival, structure, and metabolism
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054450/
https://www.ncbi.nlm.nih.gov/pubmed/32174881
http://dx.doi.org/10.3389/fneur.2020.00091
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