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Rab5促进斑马鱼Mauthner轴突再生和功能恢复的机制。

Mechanism by which Rab5 promotes regeneration and functional recovery of zebrafish Mauthner axons.

作者信息

Cui Jiantao, Shen Yueru, Song Zheng, Fan Dinggang, Hu Bing

机构信息

Center for Advanced Interdisciplinary Science and Biomedicine of IHM, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui Province, China.

出版信息

Neural Regen Res. 2025 Jun 1;20(6):1816-1824. doi: 10.4103/NRR.NRR-D-23-00529. Epub 2024 Apr 3.

DOI:10.4103/NRR.NRR-D-23-00529
PMID:39104118
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11688562/
Abstract

JOURNAL/nrgr/04.03/01300535-202506000-00031/figure1/v/2024-08-05T133530Z/r/image-tiff Rab5 is a GTPase protein that is involved in intracellular membrane trafficking. It functions by binding to various effector proteins and regulating cellular responses, including the formation of transport vesicles and their fusion with the cellular membrane. Rab5 has been reported to play an important role in the development of the zebrafish embryo; however, its role in axonal regeneration in the central nervous system remains unclear. In this study, we established a zebrafish Mauthner cell model of axonal injury using single-cell electroporation and two-photon axotomy techniques. We found that overexpression of Rab5 in single Mauthner cells promoted marked axonal regeneration and increased the number of intra-axonal transport vesicles. In contrast, treatment of zebrafish larvae with the Rab kinase inhibitor CID-1067700 markedly inhibited axonal regeneration in Mauthner cells. We also found that Rab5 activated phosphatidylinositol 3-kinase (PI3K) during axonal repair of Mauthner cells and promoted the recovery of zebrafish locomotor function. Additionally, rapamycin, an inhibitor of the mechanistic target of rapamycin downstream of PI3K, markedly hindered axonal regeneration. These findings suggest that Rab5 promotes the axonal regeneration of injured zebrafish Mauthner cells by activating the PI3K signaling pathway.

摘要

《期刊》/nrgr/04.03/01300535 - 202506000 - 00031/图1/v/2024 - 08 - 05T133530Z/图像 - tiff Rab5是一种参与细胞内膜运输的GTP酶蛋白。它通过与各种效应蛋白结合并调节细胞反应来发挥作用,包括运输小泡的形成及其与细胞膜的融合。据报道,Rab5在斑马鱼胚胎发育中起重要作用;然而,其在中枢神经系统轴突再生中的作用仍不清楚。在本研究中,我们使用单细胞电穿孔和双光子轴突切断技术建立了斑马鱼Mauthner细胞轴突损伤模型。我们发现,在单个Mauthner细胞中过表达Rab5可显著促进轴突再生,并增加轴突内运输小泡的数量。相反,用Rab激酶抑制剂CID - 1067700处理斑马鱼幼虫可显著抑制Mauthner细胞的轴突再生。我们还发现,Rab5在Mauthner细胞轴突修复过程中激活磷脂酰肌醇3激酶(PI3K),并促进斑马鱼运动功能的恢复。此外,雷帕霉素是PI3K下游雷帕霉素作用靶点的抑制剂,它显著阻碍轴突再生。这些发现表明,Rab5通过激活PI3K信号通路促进受伤斑马鱼Mauthner细胞的轴突再生。

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Neural Regen Res. 2024 Jul 1;19(7):1618-1624. doi: 10.4103/1673-5374.387973. Epub 2023 Nov 8.
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Wolfram syndrome 1b mutation suppresses Mauthner-cell axon regeneration via ER stress signal pathway.
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Acta Neuropathol Commun. 2022 Dec 17;10(1):184. doi: 10.1186/s40478-022-01484-8.
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Driving axon regeneration by orchestrating neuronal and non-neuronal innate immune responses via the IFNγ-cGAS-STING axis.通过 IFNγ-cGAS-STING 轴协调神经元和非神经元固有免疫反应来驱动轴突再生。
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