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The maternal microbiome modulates fetal neurodevelopment in mice

机译:母体微生物组在小鼠中调节胎儿神经发育

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'Dysbiosis' of the maternal gut microbiome, in response to challenges such as infection(1), altered diet(2)and stress(3)during pregnancy, has been increasingly associated with abnormalities in brain function and behaviour of the offspring(4). However, it is unclear whether the maternal gut microbiome influences neurodevelopment during critical prenatal periods and in the absence of environmental challenges. Here we investigate how depletion and selective reconstitution of the maternal gut microbiome influences fetal neurodevelopment in mice. Embryos from antibiotic-treated and germ-free dams exhibited reduced brain expression of genes related to axonogenesis, deficient thalamocortical axons and impaired outgrowth of thalamic axons in response to cell-extrinsic factors. Gnotobiotic colonization of microbiome-depleted dams with a limited consortium of bacteria prevented abnormalities in fetal brain gene expression and thalamocortical axonogenesis. Metabolomic profiling revealed that the maternal microbiome regulates numerous small molecules in the maternal serum and the brains of fetal offspring. Select microbiota-dependent metabolites promoted axon outgrowth from fetal thalamic explants. Moreover, maternal supplementation with these metabolites abrogated deficiencies in fetal thalamocortical axons. Manipulation of the maternal microbiome and microbial metabolites during pregnancy yielded adult offspring with altered tactile sensitivity in two aversive somatosensory behavioural tasks, but no overt differences in many other sensorimotor behaviours. Together, our findings show that the maternal gut microbiome promotes fetal thalamocortical axonogenesis, probably through signalling by microbially modulated metabolites to neurons in the developing brain.Small molecules that arise from the maternal gut microbiome in pregnant dams promote fetal thalamocortical axonogenesis in their offspring.
机译:母体肠道微生物组的“缺陷”,响应于妊娠(1),改变的饮食(2)和妊娠期饮食(2)和应激(3)的挑战,越来越多地与后代脑功能和行为的异常相关(4) 。然而,目前尚不清楚母体肠道微生物组在关键产前期间是否影响神经发作,并且在没有环境挑战的情况下。在这里,我们研究母体肠道微生物组的耗尽和选择性重构如何影响小鼠的胎儿神经发育。来自抗生素治疗和无菌水坝的胚胎表现出与腋生发生相关的基因的脑表达,缺乏Thalamoctical轴突,响应于细胞外部因子,丘脑轴突的损伤患者。微生物组耗尽水坝的八噬菌体定植,细菌联盟有限,防止了胎儿脑基因表达和ThalamoColtical Assonogis的异常。代谢物分析表明,母体微生物组在母体血清中调节了许多小分子和胎儿后代的大脑。选择依赖胎儿丘脑外植体的Microbiota依赖性代谢物促进了Axon Fortrowth。此外,具有这些代谢物的母体补充,这些代谢物缺乏胎儿ThalamoCortical轴突。妊娠期间母体微生物组和微生物代谢物的操纵产生了成人后代,两种厌恶的躯体感应行为任务中的触觉敏感性改变,但许多其他感觉运动行为没有明显差异。我们的研究结果表明,母体肠道微生物组促进胎儿炎症性腋生,可能是通过通过通过微生物调制代谢物的信号传导至发育脑中的神经元。孕坝中母体肠道微生物组中出现的胎儿分子促进其后代胎儿神经元素。

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  • 来源
    《Nature》 |2020年第7828期|281-286|共6页
  • 作者单位

    Univ Calif Los Angeles Dept Integrat Biol & Physiol Los Angeles CA 90095 USA;

    Univ Calif Los Angeles Dept Integrat Biol & Physiol Los Angeles CA 90095 USA;

    NIDCR Oral Immun & Inflammat Sect NIH Bethesda MD USA;

    Univ Calif Los Angeles Dept Integrat Biol & Physiol Los Angeles CA 90095 USA;

    Univ Calif Los Angeles Dept Integrat Biol & Physiol Los Angeles CA 90095 USA;

    Univ Calif Los Angeles Dept Integrat Biol & Physiol Los Angeles CA 90095 USA;

    Univ Calif Los Angeles Dept Integrat Biol & Physiol Los Angeles CA 90095 USA;

    Univ Calif Los Angeles Dept Integrat Biol & Physiol Los Angeles CA 90095 USA;

    Univ Calif Los Angeles Dept Integrat Biol & Physiol Los Angeles CA 90095 USA;

    Univ Calif Los Angeles Dept Integrat Biol & Physiol Los Angeles CA 90095 USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 22:15:29

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