Extracellular Vesicles Released by Lactobacillus paracasei Mitigate Stress-induced Transcriptional Changes and Depression-like Behavior in Mice.

IF 1.8 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Hyejin Kwon, Eun-Hwa Lee, Juli Choi, Jin-Young Park, Yoon-Keun Kim, Pyung-Lim Han
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Abstract

Various probiotic strains have been reported to affect emotional behavior. However, the underlying mechanisms by which specific probiotic strains change brain function are not clearly understood. Here, we report that extracellular vesicles derived from Lactobacillus paracasei (Lpc-EV) have an ability to produce genome-wide changes against glucocorticoid (GC)-induced transcriptional responses in HT22 hippocampal neuronal cells. Genome-wide analysis using microarray assay followed by Rank-Rank Hypergeometric Overlap (RRHO) method leads to identify the top 20%-ranked 1,754 genes up- or down-regulated following GC treatment and their altered expressions are reversed by Lpc-EV in HT22 cells. Serial k-means clustering combined with Gene Ontology enrichment analyses indicate that the identified genes can be grouped into multiple functional clusters that contain functional modules of "responses to stress or steroid hormones", "histone modification", and "regulating MAPK signaling pathways". While all the selected genes respond to GC and Lpc-EV at certain levels, the present study focuses on the clusters that contain Mkp-1, Fkbp5, and Mecp2, the genes characterized to respond to GC and Lpc-EV in opposite directions in HT22 cells. A translational study indicates that the expression levels of Mkp-1, Fkbp5, and Mecp2 are changed in the hippocampus of mice exposed to chronic stress in the same directions as those following GC treatment in HT22 cells, whereas Lpc-EV treatment restored stress-induced changes of those factors, and alleviated stress-induced depressive-like behavior. These results suggest that Lpc-EV cargo contains bioactive components that directly induce genome-wide transcriptional responses against GC-induced transcriptional and behavioral changes.

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副干酪乳杆菌释放的细胞外小泡缓解小鼠应激诱导的转录变化和抑郁样行为。
据报道,各种益生菌菌株会影响情绪行为。然而,特定益生菌菌株改变大脑功能的潜在机制尚不清楚。在这里,我们报道了来源于副干酪乳杆菌(Lpc-EV)的细胞外小泡具有在HT22海马神经元细胞中产生对抗糖皮质激素(GC)诱导的转录反应的全基因组变化的能力。使用微阵列分析和秩-秩超几何重叠(RRHO)方法进行全基因组分析,可以识别出GC处理后排名前20%的1754个上调或下调的基因,并且它们改变的表达被HT22细胞中的Lpc EV逆转。系列k均值聚类与基因本体富集分析相结合表明,已鉴定的基因可以分为多个功能簇,这些功能簇包含“对应激或类固醇激素的反应”、“组蛋白修饰”和“调节MAPK信号通路”的功能模块。虽然所有选定的基因都在一定水平上对GC和Lpc EV做出反应,但本研究的重点是含有Mkp-1、Fkbp5和Mecp2的簇,这些基因在HT22细胞中以相反的方向对GC和Lpc EV做出反应。一项转化研究表明,在暴露于慢性应激的小鼠海马中,Mkp-1、Fkbp5和Mecp2的表达水平在HT22细胞中以与GC处理后相同的方向发生变化,而Lpc-EV处理恢复了应激诱导的这些因素的变化,并减轻了应力诱导的抑郁样行为。这些结果表明,Lpc EV货物含有直接诱导全基因组转录反应以对抗GC诱导的转录和行为变化的生物活性成分。
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来源期刊
Experimental Neurobiology
Experimental Neurobiology Neuroscience-Cellular and Molecular Neuroscience
CiteScore
4.30
自引率
4.20%
发文量
29
期刊介绍: Experimental Neurobiology is an international forum for interdisciplinary investigations of the nervous system. The journal aims to publish papers that present novel observations in all fields of neuroscience, encompassing cellular & molecular neuroscience, development/differentiation/plasticity, neurobiology of disease, systems/cognitive/behavioral neuroscience, drug development & industrial application, brain-machine interface, methodologies/tools, and clinical neuroscience. It should be of interest to a broad scientific audience working on the biochemical, molecular biological, cell biological, pharmacological, physiological, psychophysical, clinical, anatomical, cognitive, and biotechnological aspects of neuroscience. The journal publishes both original research articles and review articles. Experimental Neurobiology is an open access, peer-reviewed online journal. The journal is published jointly by The Korean Society for Brain and Neural Sciences & The Korean Society for Neurodegenerative Disease.
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