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定量蛋白质组学揭示的导向景观控制成年视觉系统中的神经再支配。

Guidance landscapes unveiled by quantitative proteomics to control reinnervation in adult visual system.

机构信息

University Grenoble Alpes, Inserm, U1216, Grenoble Institut Neurosciences, 38000, Grenoble, France.

University Grenoble Alpes, INSERM, CEA, UMR BioSanté U1292, CNRS, CEA, FR2048, 38000, Grenoble, France.

出版信息

Nat Commun. 2022 Oct 13;13(1):6040. doi: 10.1038/s41467-022-33799-4.

DOI:10.1038/s41467-022-33799-4
PMID:36229455
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9561644/
Abstract

In the injured adult central nervous system (CNS), activation of pro-growth molecular pathways in neurons leads to long-distance regeneration. However, most regenerative fibers display guidance defects, which prevent reinnervation and functional recovery. Therefore, the molecular characterization of the proper target regions of regenerative axons is essential to uncover the modalities of adult reinnervation. In this study, we use mass spectrometry (MS)-based quantitative proteomics to address the proteomes of major nuclei of the adult visual system. These analyses reveal that guidance-associated molecules are expressed in adult visual targets. Moreover, we show that bilateral optic nerve injury modulates the expression of specific proteins. In contrast, the expression of guidance molecules remains steady. Finally, we show that regenerative axons are able to respond to guidance cues ex vivo, suggesting that these molecules possibly interfere with brain target reinnervation in adult. Using a long-distance regeneration model, we further demonstrate that the silencing of specific guidance signaling leads to rerouting of regenerative axons in vivo. Altogether, our results suggest ways to modulate axon guidance of regenerative neurons to achieve circuit repair in adult.

摘要

在受伤的成人中枢神经系统 (CNS) 中,神经元中促生长分子途径的激活导致长距离再生。然而,大多数再生纤维表现出导向缺陷,这阻止了再神经支配和功能恢复。因此,对再生轴突的适当靶区的分子特征进行表征对于揭示成人再神经支配的方式至关重要。在这项研究中,我们使用基于质谱 (MS) 的定量蛋白质组学来解决成年视觉系统主要核的蛋白质组。这些分析表明,导向相关分子在成年视觉靶标中表达。此外,我们表明双侧视神经损伤会调节特定蛋白质的表达。相比之下,导向分子的表达保持稳定。最后,我们表明再生轴突能够在体外对导向线索做出反应,这表明这些分子可能会干扰成年大脑靶标再神经支配。使用长距离再生模型,我们进一步证明,特定导向信号的沉默会导致体内再生轴突的改道。总之,我们的研究结果为调节再生神经元的轴突导向以实现成年的回路修复提供了思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7808/9561644/76791bffd128/41467_2022_33799_Fig8_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7808/9561644/7dc934d11b51/41467_2022_33799_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7808/9561644/76791bffd128/41467_2022_33799_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7808/9561644/e75dc9e8459c/41467_2022_33799_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7808/9561644/ec0b162136da/41467_2022_33799_Fig2_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7808/9561644/d584d08c39fa/41467_2022_33799_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7808/9561644/b6dc1535ab0f/41467_2022_33799_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7808/9561644/053f28fafdea/41467_2022_33799_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7808/9561644/7dc934d11b51/41467_2022_33799_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7808/9561644/76791bffd128/41467_2022_33799_Fig8_HTML.jpg

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