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膈肌及其运动神经支配的左右不对称的遗传特征。

Genetic specification of left-right asymmetry in the diaphragm muscles and their motor innervation.

机构信息

University of Lyon, Claude Bernard University Lyon 1, INMG UMR CNRS 5310, INSERM U1217, Lyon, France.

Department of Pediatrics, University of Michigan Medical Center, Ann Arbor, United States.

出版信息

Elife. 2017 Jun 22;6:e18481. doi: 10.7554/eLife.18481.

Abstract

The diaphragm muscle is essential for breathing in mammals. Its asymmetric elevation during contraction correlates with morphological features suggestive of inherent left-right (L/R) asymmetry. Whether this asymmetry is due to L versus R differences in the muscle or in the phrenic nerve activity is unknown. Here, we have combined the analysis of genetically modified mouse models with transcriptomic analysis to show that both the diaphragm muscle and phrenic nerves have asymmetries, which can be established independently of each other during early embryogenesis in pathway instructed by Nodal, a morphogen that also conveys asymmetry in other organs. We further found that phrenic motoneurons receive an early L/R genetic imprint, with L versus R differences both in Slit/Robo signaling and MMP2 activity and in the contribution of both pathways to establish phrenic nerve asymmetry. Our study therefore demonstrates L-R imprinting of spinal motoneurons and describes how L/R modulation of axon guidance signaling helps to match neural circuit formation to organ asymmetry.

摘要

膈肌是哺乳动物呼吸的重要组成部分。它在收缩时的不对称抬高与形态特征相关,提示其存在固有左右(L/R)不对称性。这种不对称性是由于肌肉或膈神经活动中的 L 与 R 差异引起的尚不清楚。在这里,我们结合了基因修饰小鼠模型与转录组分析,结果表明膈肌和膈神经都存在不对称性,这种不对称性可以在由形态发生因子 Nodal 指导的早期胚胎发育过程中独立建立,Nodal 也能在其他器官中传递不对称性。我们进一步发现,膈运动神经元接受早期的 L/R 遗传印记,Slit/Robo 信号和 MMP2 活性中的 L 与 R 差异,以及这两条途径对建立膈神经不对称性的贡献。因此,我们的研究证明了脊髓运动神经元的 L-R 印迹,并描述了如何调节轴突导向信号来帮助将神经回路形成与器官不对称性相匹配。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01f1/5481184/94c5625dad02/elife-18481-fig1.jpg

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