Physiology and Behavior Laboratory, Swiss Federal Institute of Technology (ETH) Zurich, Schwerzenbach, Switzerland.
Department of Psychiatry, Columbia University, New York City, USA.
Sci Rep. 2018 May 29;8(1):8344. doi: 10.1038/s41598-018-26631-x.
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.
内侧前额叶皮层(mPFC)是高级认知功能的主要调节者,是唯一在青春期晚期成熟的大脑区域。在此期间,mPFC 对压力事件或营养不足敏感。例如,青春期高脂肪饮食(HFD)喂养会明显损害前额叶依赖的认知。它还在 mPFC 内的细胞和突触尺度上引发多种变化,表明 HFD 在这个成熟期间引发了主要的转录事件。这种转录重编程的性质尚不清楚,但可能包括表观遗传过程,特别是 microRNAs,已知其可直接调节突触功能。我们在青春期小鼠 mPFC 中使用高通量筛选,鉴定出 38 种 microRNAs 受 HFD 差异调节,特别是 mir-30e-5p。我们使用荧光素酶测定来证实 mir-30e-5p 对选定靶标:Ephrin-A3 的功能影响。通过对预测的 microRNA 靶标的全局途径分析,我们确定了可能受 HFD 影响的生物学途径。轴突导向是 top-1 途径,通过鉴定 HFD 后轴突导向分子的基因表达变化来验证。我们的发现描绘了青春期 HFD 诱导的 mPFC 内主要的 microRNA 转录重编程。这些结果将有助于理解 microRNAs 在早期生活环境事件后认知缺陷出现中的贡献。