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Effects of Ethanol on Expression of Coding and Noncoding RNAs in Murine Neuroblastoma Neuro2a Cells.
Choi, Mi Ran; Cho, Sinyoung; Kim, Dai-Jin; Choi, Jung-Seok; Jin, Yeung-Bae; Kim, Miran; Chang, Hye Jin; Jeon, Seong Ho; Yang, Young Duk; Lee, Sang-Rae.
Afiliación
  • Choi MR; Laboratory Animal Research Center, Ajou University School of Medicine, Suwon 16499, Korea.
  • Cho S; Department of Pharmacy, College of Pharmacy and Institute of Pharmaceutical Sciences, CHA University, Pocheon 11160, Korea.
  • Kim DJ; Department of Psychiatry, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul 06591, Korea.
  • Choi JS; Department of Psychiatry, Samsung Medical Center, Seoul 06351, Korea.
  • Jin YB; Department of Laboratory Animal Medicine, College of Veterinary Medicine, Gyeongsang National University, Jinju 52828, Korea.
  • Kim M; Department of Obstetrics and Gynecology, Ajou University School of Medicine, Suwon 16499, Korea.
  • Chang HJ; Department of Obstetrics and Gynecology, Ajou University School of Medicine, Suwon 16499, Korea.
  • Jeon SH; Department of Pharmacy, College of Pharmacy and Institute of Pharmaceutical Sciences, CHA University, Pocheon 11160, Korea.
  • Yang YD; Department of Pharmacy, College of Pharmacy and Institute of Pharmaceutical Sciences, CHA University, Pocheon 11160, Korea.
  • Lee SR; Laboratory Animal Research Center, Ajou University School of Medicine, Suwon 16499, Korea.
Int J Mol Sci ; 23(13)2022 Jun 30.
Article en En | MEDLINE | ID: mdl-35806296
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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Texto completo: 1 Base de datos: MEDLINE Asunto principal: ARN Largo no Codificante / Neuroblastoma Límite: Animals Idioma: En Revista: Int J Mol Sci Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: ARN Largo no Codificante / Neuroblastoma Límite: Animals Idioma: En Revista: Int J Mol Sci Año: 2022 Tipo del documento: Article