Whole Genome Transcriptome Analysis in a Genetic Model of Gulf War Illness
Public Domain
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2020/03/01
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Details
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Personal Author:Ashbrook D ; Jones BC ; Lu L ; Miller DB ; Mulligan MK ; O'Callaghan JP ; Williams RW ; Xu F ; Ashbrook D ; Jones BC ; Lu L ; Miller DB ; Mulligan MK ; O'Callaghan JP ; Williams RW ; Xu F
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Description:Gulf War illness (GWI) affected up to 30% of the nearly one million personnel sent to the Persian Gulf in 1991. The probable cause was exposure to organophosphorus compounds coupled with high circulating glucocorticoids as would be expected in a combat theater. Previously, we developed a mouse model consisting of 7 days of exposure to corticosterone in the drinking water followed by injection with diisopropylflurophosphate (DFP, surrogate for sarin) and assessment of pro-inflammatory cytokines in frontal cortex and hippocampus 6h after DFP treatment. In order to assess genetic-based individual differences in susceptibility to developing GWI, we applied the model to male and female C57BL/6J and DBA/2J mice. Consequently we observed wide-genetic differences in pro-inflammatory gene expression by qPCR in the prefrontal cortex. We then subjected the prefrontal cortex to genome-wide transcriptome response by RNA-seq, comparing the combined corticosterone- DFP treatment. Gene ontology analysis showed altered immune function and apoptosis as the top systems affected. We also verified a previous nomination of Spondin 1 and ILb1 as candidate genes underlying individual differences in susceptibility. [Description provided by NIOSH]
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ISSN:1096-6080
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Volume:174
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Issue:1
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NIOSHTIC Number:nn:20058989
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Citation:Toxicologist 2020 Mar; 174(1):488
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Federal Fiscal Year:2020
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Peer Reviewed:False
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Source Full Name:The Toxicologist. Society of Toxicology 59th Annual Meeting and ToxExpo, March 15-19, 2020, Anaheim, California
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Main Document Checksum:urn:sha-512:1097600a6eb134b0303dd01d087f1b429de9e627c9900cc83bc062f04d9cc639ff70dc4f6e9e871ef4771ddba973464b425f8ea91e45c4b6f87098cdf63eadb5
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