Robust differential gene expression patterns in the pre-frontal cortex of male mice exposed to an occupationally relevant dose of laboratory generated wildfire smoke.

IF 3.4 3区 医学 Q2 TOXICOLOGY Toxicological Sciences Pub Date : 2024-08-06 DOI:10.1093/toxsci/kfae097
Adam Schuller, Jessica Oakes, Tom Larocca, Jacqueline Matz, Matthew Eden, Chiara Bellini, Luke Montrose
{"title":"Robust differential gene expression patterns in the pre-frontal cortex of male mice exposed to an occupationally relevant dose of laboratory generated wildfire smoke.","authors":"Adam Schuller, Jessica Oakes, Tom Larocca, Jacqueline Matz, Matthew Eden, Chiara Bellini, Luke Montrose","doi":"10.1093/toxsci/kfae097","DOIUrl":null,"url":null,"abstract":"<p><p>Wildfires have become common global phenomena concurrent with warmer and drier climates and are now major contributors to ambient air pollution world-wide. Exposure to wildfire smoke has been classically associated with adverse cardiopulmonary health outcomes, especially in vulnerable populations. Recent work has expanded our understanding of wildfire smoke toxicology to include effects on the central nervous system and reproductive function; however, the neurotoxic profile of this toxicant remains ill-explored in an occupational context. Here, we sought to address this by using RNA sequencing to examine transcriptomic signatures in the pre-frontal cortex of male mice modeling career wildland firefighter smoke exposure. We report robust changes in gene expression profiles between smoke exposed samples and filtered air controls, evidenced by 2,862 differentially expressed genes (51.2% increased). We further characterized the functional relevance of these genes highlighting enriched pathways related to synaptic transmission, neuroplasticity, blood-brain barrier integrity, and neurotransmitter metabolism. Additionally, we identified possible contributors to these alterations through protein-protein interaction network mapping, which revealed a central node at ß-catenin and secondary hubs centered around mitochondrial oxidases, the Wnt signaling pathway, and gene expression machinery. The data reported here will serve as the foundation for future experiments aiming to characterize the phenotypic effects and mechanistic underpinnings of occupational wildfire smoke neurotoxicology.</p>","PeriodicalId":23178,"journal":{"name":"Toxicological Sciences","volume":null,"pages":null},"PeriodicalIF":3.4000,"publicationDate":"2024-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Toxicological Sciences","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/toxsci/kfae097","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"TOXICOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Wildfires have become common global phenomena concurrent with warmer and drier climates and are now major contributors to ambient air pollution world-wide. Exposure to wildfire smoke has been classically associated with adverse cardiopulmonary health outcomes, especially in vulnerable populations. Recent work has expanded our understanding of wildfire smoke toxicology to include effects on the central nervous system and reproductive function; however, the neurotoxic profile of this toxicant remains ill-explored in an occupational context. Here, we sought to address this by using RNA sequencing to examine transcriptomic signatures in the pre-frontal cortex of male mice modeling career wildland firefighter smoke exposure. We report robust changes in gene expression profiles between smoke exposed samples and filtered air controls, evidenced by 2,862 differentially expressed genes (51.2% increased). We further characterized the functional relevance of these genes highlighting enriched pathways related to synaptic transmission, neuroplasticity, blood-brain barrier integrity, and neurotransmitter metabolism. Additionally, we identified possible contributors to these alterations through protein-protein interaction network mapping, which revealed a central node at ß-catenin and secondary hubs centered around mitochondrial oxidases, the Wnt signaling pathway, and gene expression machinery. The data reported here will serve as the foundation for future experiments aiming to characterize the phenotypic effects and mechanistic underpinnings of occupational wildfire smoke neurotoxicology.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
雄性小鼠暴露于与职业相关剂量的实验室产生的野火烟雾后,其前额叶皮层出现了强大的差异基因表达模式。
野火已成为一种常见的全球现象,与此同时,气候也变得更加温暖和干燥,目前已成为造成全球环境空气污染的主要因素。暴露于野火烟雾中通常会对心肺健康造成不良影响,尤其是对弱势群体而言。最近的研究拓展了我们对野火烟雾毒理学的认识,包括对中枢神经系统和生殖功能的影响;然而,这种毒物的神经毒性特征在职业环境中仍未得到充分探索。为了解决这个问题,我们使用 RNA 测序技术研究了模拟野外消防员烟雾暴露的雄性小鼠前额叶皮层的转录组特征。我们报告了烟雾暴露样本与过滤空气对照组之间基因表达谱的显著变化,2862 个差异表达基因(增加 51.2%)证明了这一点。我们进一步描述了这些基因的功能相关性,突出了与突触传递、神经可塑性、血脑屏障完整性和神经递质代谢相关的丰富通路。此外,我们还通过蛋白质-蛋白质相互作用网络图谱确定了这些改变的可能促成因素,该图谱显示ß-catenin为中心节点,线粒体氧化酶、Wnt信号通路和基因表达机制为次级中心。本文报告的数据将为今后旨在描述职业性野火烟雾神经毒理学表型效应和机理基础的实验奠定基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Toxicological Sciences
Toxicological Sciences 医学-毒理学
CiteScore
7.70
自引率
7.90%
发文量
118
审稿时长
1.5 months
期刊介绍: The mission of Toxicological Sciences, the official journal of the Society of Toxicology, is to publish a broad spectrum of impactful research in the field of toxicology. The primary focus of Toxicological Sciences is on original research articles. The journal also provides expert insight via contemporary and systematic reviews, as well as forum articles and editorial content that addresses important topics in the field. The scope of Toxicological Sciences is focused on a broad spectrum of impactful toxicological research that will advance the multidisciplinary field of toxicology ranging from basic research to model development and application, and decision making. Submissions will include diverse technologies and approaches including, but not limited to: bioinformatics and computational biology, biochemistry, exposure science, histopathology, mass spectrometry, molecular biology, population-based sciences, tissue and cell-based systems, and whole-animal studies. Integrative approaches that combine realistic exposure scenarios with impactful analyses that move the field forward are encouraged.
期刊最新文献
Immune checkpoint blockade lowers the threshold of naïve T-cell priming to drug-associated antigens in a dose-dependent fashion Urinary bladder carcinogenic potential of 4,4’-methylenebis(2-chloroaniline) in humanized-liver mice Pharmacokinetic Analysis of Nicotine and Its Metabolites (Cotinine and trans-3′-Hydroxycotinine) in Male Sprague-Dawley Rats Following Nose-Only Inhalation, Oral Gavage, and Intravenous Infusion of Nicotine Unraveling the Hemolytic Toxicity Tapestry of Peptides using Chemical Space Complex Networks Exploring the Interplay Between Cannabinoids and Thymic Functions
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1