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Cited 6 time in webofscience Cited 5 time in scopus
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Effects of Ethanol on Expression of Coding and Noncoding RNAs in Murine Neuroblastoma Neuro2a Cellsopen access

Authors
Choi, Mi RanCho, SinyoungKim, Dai-JinChoi, Jung-SeokJin, Yeung-BaeKim, MiranChang, Hye JinJeon, Seong HoYang, Young DukLee, Sang-Rae
Issue Date
Jul-2022
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Keywords
ethanol; transcriptome profiling; lncRNA; Cebpd; Rnu3a
Citation
International Journal of Molecular Sciences, v.23, no.13
Indexed
SCIE
SCOPUS
Journal Title
International Journal of Molecular Sciences
Volume
23
Number
13
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/1084
DOI
10.3390/ijms23137294
ISSN
1661-6596
1422-0067
Abstract
Excessive use of alcohol can induce neurobiological and neuropathological alterations in the brain, including the hippocampus and forebrain, through changes in neurotransmitter systems, hormonal systems, and neuroimmune processes. We aimed to investigate the effects of ethanol on the expression of coding and noncoding RNAs in a brain-derived cell line exposed to ethanol. After exposing Neuro2a cells, a neuroblastoma cell line, to ethanol for 24 and 72 h, we observed cell proliferation and analyzed up- and downregulated mRNAs and long noncoding RNAs (lncRNAs) using total RNA-Seq technology. We validated the differential expression of some mRNAs and lncRNAs by RT-qPCR and analyzed the expression of Cebpd and Rnu3a through knock-down of Cebpd. Cell proliferation was significantly reduced in cells exposed to 100 mM ethanol for 72 h, with 1773 transcripts up- or downregulated by greater than three-fold in ethanol-treated cells compared to controls. Of these, 514 were identified as lncRNAs. Differentially expressed mRNAs and lncRNAs were mainly observed in cells exposed to ethanol for 72 h, in which Atm and Cnr1 decreased, but Trib3, Cebpd, and Spdef increased. On the other hand, lncRNAs Kcnq1ot1, Tug1, and Xist were changed by ethanol, and Rnu3a in particular was greatly increased by chronic ethanol treatment through inhibition of Cebpd. Our results increase the understanding of cellular and molecular mechanisms related to coding and noncoding RNAs in an in vitro model of acute and chronic exposure to ethanol.
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