测量发育中的小鼠胚胎的脑室内压力:揭示大脑发育的重复机械线索。

IF 1.7 4区 生物学 Q4 CELL BIOLOGY
Mami Akaike, Jun Hatakeyama, Yuta Nakashima, Kenji Shimamura
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引用次数: 0

摘要

在包括人类在内的生物体中,从单个受精卵构建其形态的发育过程不仅受到遗传调控的影响,还受到各种外部因素的影响。其中一个因素是机械刺激。虽然机械力被认为在发育过程中有助于大脑的形成,但神经发生过程中脑室内压力的定量信息仍然有限。我们开发了一种高时间分辨率的系统,有效地使用压阻式传感器来测量E12.5至E16.5(胚胎期)的小鼠胚胎的脑室内压力。体外测量显示,脑室内压力从E12.5时的53.76±4.16 Pa增加到E16.5时的158.10±19.94 Pa。在子宫内的分析发现了与子宫收缩同步的惊人周期性,在E12.5时达到1430±195.2 Pa,表明动态机械刺激超出了子宫外观察。此外,E9.0-E15.5的穿孔实验显示,压力释放后神经上皮迅速增厚,根尖表面收缩,表明脑室内正压的拉伸作用。这种效应在E15.5后减弱,这意味着张力减弱或神经上皮变得更加强健。这些结果强调了胚胎脑室内压力的动态性,由内部流体产生和子宫力控制,并强调了机械线索在神经上皮结构中的重要性。我们的发现为阐明机械力如何与遗传和分子过程相结合来塑造正常的大脑发育提供了一个垫脚石,并可能为大脑进化提供新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Measuring intraventricular pressure in developing mouse embryos: Uncovering a repetitive mechanical cue for brain development.

In living organisms, including humans, the developmental processes that construct their morphology from a single fertilized egg are influenced not only by genetic regulation but also by various external factors. One such factor is mechanical stimulation. Although mechanical forces are suggested to contribute to brain formation during development, quantitative information on intraventricular pressure during neurogenesis remains limited. We developed a high time-resolution system efficiently using a piezoresistive sensor to measure brain intraventricular pressure in mouse embryos from E12.5 to E16.5 (embryonic stages in days). Ex utero measurements revealed intraventricular pressure increasing from 53.76 ± 4.16 Pa at E12.5 to 158.10 ± 19.94 Pa by E16.5. In utero analyses uncovered striking periodicity in sync with uterine contractions, reaching up to 1430 ± 195.2 Pa at E12.5, indicating dynamic mechanical stimuli beyond ex utero observations. Additionally, perforation experiments at E9.0-E15.5 showed rapid neuroepithelial thickening and apical surface contraction upon pressure release, indicative of a tensile effect by the positive intraventricular pressure. This effect diminished after E15.5, implying that tension wanes or the neuroepithelium becomes more robust. These results highlight the dynamic nature of embryonic intraventricular pressure, governed by internal fluid production and uterine forces, and emphasize the importance of mechanical cues in neuroepithelial architecture. Our findings provide a steppingstone to clarify how mechanical forces integrate with genetic and molecular processes to shape normal brain development and may render new perspectives on brain evolution.

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来源期刊
Development Growth & Differentiation
Development Growth & Differentiation 生物-发育生物学
CiteScore
4.60
自引率
4.00%
发文量
62
审稿时长
6 months
期刊介绍: Development Growth & Differentiation (DGD) publishes three types of articles: original, resource, and review papers. Original papers are on any subjects having a context in development, growth, and differentiation processes in animals, plants, and microorganisms, dealing with molecular, genetic, cellular and organismal phenomena including metamorphosis and regeneration, while using experimental, theoretical, and bioinformatic approaches. Papers on other related fields are also welcome, such as stem cell biology, genomics, neuroscience, Evodevo, Ecodevo, and medical science as well as related methodology (new or revised techniques) and bioresources. Resource papers describe a dataset, such as whole genome sequences and expressed sequence tags (ESTs), with some biological insights, which should be valuable for studying the subjects as mentioned above. Submission of review papers is also encouraged, especially those providing a new scope based on the authors’ own study, or a summarization of their study series.
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