Your browser doesn't support javascript.
loading
MicroRNA Expression Profiling in the Prefrontal Cortex: Putative Mechanisms for the Cognitive Effects of Adolescent High Fat Feeding.
Labouesse, Marie A; Polesel, Marcello; Clementi, Elena; Müller, Flavia; Markkanen, Enni; Mouttet, Forouhar; Cattaneo, Annamaria; Richetto, Juliet.
Afiliação
  • Labouesse MA; Physiology and Behavior Laboratory, Swiss Federal Institute of Technology (ETH) Zurich, Schwerzenbach, Switzerland.
  • Polesel M; Department of Psychiatry, Columbia University, New York City, USA.
  • Clementi E; Institute of Anatomy, University of Zurich, Zurich, Switzerland.
  • Müller F; Institute of Veterinary Pharmacology and Toxicology, University of Zurich - Vetsuisse, Zurich, Switzerland.
  • Markkanen E; Institute of Veterinary Pharmacology and Toxicology, University of Zurich - Vetsuisse, Zurich, Switzerland.
  • Mouttet F; Institute of Veterinary Pharmacology and Toxicology, University of Zurich - Vetsuisse, Zurich, Switzerland.
  • Cattaneo A; Physiology and Behavior Laboratory, Swiss Federal Institute of Technology (ETH) Zurich, Schwerzenbach, Switzerland.
  • Richetto J; Biological Psychiatry Laboratory, IRCCS Fatebenefratelli San Giovanni di Dio, Brescia, Italy.
Sci Rep ; 8(1): 8344, 2018 05 29.
Article em En | MEDLINE | ID: mdl-29844565
The medial prefrontal cortex (mPFC), master regulator of higher-order cognitive functions, is the only brain region that matures until late adolescence. During this period, the mPFC is sensitive to stressful events or suboptimal nutrition. For instance, high-fat diet (HFD) feeding during adolescence markedly impairs prefrontal-dependent cognition. It also provokes multiple changes at the cellular and synaptic scales within the mPFC, suggesting that major transcriptional events are elicited by HFD during this maturational period. The nature of this transcriptional reprogramming remains unknown, but may include epigenetic processes, in particular microRNAs, known to directly regulate synaptic functions. We used high-throughput screening in the adolescent mouse mPFC and identified 38 microRNAs differentially regulated by HFD, in particular mir-30e-5p. We used a luciferase assay to confirm the functional effect of mir-30e-5p on a chosen target: Ephrin-A3. Using global pathway analyses of predicted microRNA targets, we identified biological pathways putatively affected by HFD. Axon guidance was the top-1 pathway, validated by identifying gene expression changes of axon guidance molecules following HFD. Our findings delineate major microRNA transcriptional reprogramming within the mPFC induced by adolescent HFD. These results will help understanding the contribution of microRNAs in the emergence of cognitive deficits following early-life environmental events.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Perfilação da Expressão Gênica / MicroRNAs Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Perfilação da Expressão Gênica / MicroRNAs Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2018 Tipo de documento: Article