Serum lipidomic analysis from mixed neutron/X-ray radiation fields reveals a hyperlipidemic and pro-inflammatory phenotype.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
14 03 2019
Historique:
received: 22 10 2018
accepted: 27 02 2019
entrez: 16 3 2019
pubmed: 16 3 2019
medline: 29 9 2020
Statut: epublish

Résumé

Heightened threats for nuclear terrorism using improvised nuclear devices (IND) necessitate the development of biodosimetry assays that could rapidly assess thousands of individuals. However, the radiation exposures from an IND may be complex due to mixed fields of neutrons and photons (γ-rays), shielding from buildings, and proximity to the epicenter among others. In this study we utilized lipidomics to analyze serum samples from mice exposed to various percentages of neutrons and X-rays to a total dose of 3 Gy. Triacylglycerides, phosphatidylserines, lysophosphatidylethanolamines, lysophosphatidylcholines (LPCs), sphingolipids, and cholesteryl esters all showed delayed increases at day 7 compared to day 1 after irradiation, while diacylglycerides decreased in mixed field exposures and phosphatidylcholines (PCs) remained largely unchanged. Individual lipid molecules with a high degree of unsaturation exhibited the highest fold changes in mixed fields compared to photons alone. More importantly, the increased ratio of LPCs to PCs of each irradiation group compared to control could be used as a radiation biomarker and highlights the existence of a pro-inflammatory phenotype. The results showed that even a small percentage of neutrons in a mixed field can lead to high biological responses with implications for accurate biodosimetry, triage and medical managements of exposed populations.

Identifiants

pubmed: 30872747
doi: 10.1038/s41598-019-41083-7
pii: 10.1038/s41598-019-41083-7
pmc: PMC6418166
doi:

Substances chimiques

Lipids 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

4539

Subventions

Organisme : NCI NIH HHS
ID : P30 CA051008
Pays : United States
Organisme : NIAID NIH HHS
ID : U19 AI067773
Pays : United States

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Auteurs

Evagelia C Laiakis (EC)

Department of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA. ecl28@georgetown.edu.
Department of Biochemistry and Molecular & Cellular Biology, Georgetown University, Washington, DC, USA. ecl28@georgetown.edu.

Monica Pujol Canadell (MP)

Center for Radiological Research, Columbia University, New York, NY, USA.

Veljko Grilj (V)

Radiological Research Accelerator Facility, Columbia University, Irvington, NY, USA.

Andrew D Harken (AD)

Radiological Research Accelerator Facility, Columbia University, Irvington, NY, USA.

Guy Y Garty (GY)

Radiological Research Accelerator Facility, Columbia University, Irvington, NY, USA.

Giuseppe Astarita (G)

Department of Biochemistry and Molecular & Cellular Biology, Georgetown University, Washington, DC, USA.

David J Brenner (DJ)

Center for Radiological Research, Columbia University, New York, NY, USA.

Lubomir Smilenov (L)

Center for Radiological Research, Columbia University, New York, NY, USA.

Albert J Fornace (AJ)

Department of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.
Department of Biochemistry and Molecular & Cellular Biology, Georgetown University, Washington, DC, USA.

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Classifications MeSH