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通过YAP介导的机械转导构建空间受限的管道以调节神经自组织和异常性疼痛反应。

Engineering spatially-confined conduits to tune nerve self-organization and allodynic responses via YAP-mediated mechanotransduction.

作者信息

Luo Xiaobin, Yang Jia, Zhao Yonggang, Nagayasu Toshitatsu, Chen Junlin, Hu Peilun, He Zhi, Li Zifan, Wu Jun, Zhao Zhe, Duan Guman, Sun Xiaodan, Zhao Lingyun, Pan Yongwei, Wang Xiumei

机构信息

State Key Laboratory of New Ceramics and Fine Processing, School of Materials Science and Engineering, Tsinghua University, Beijing, 100084, China.

Department of Orthopedics, Beijing Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua University, Beijing, 102218, China.

出版信息

Nat Commun. 2025 Jan 2;16(1):66. doi: 10.1038/s41467-024-55118-9.

DOI:10.1038/s41467-024-55118-9
PMID:39746959
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11695937/
Abstract

Chronic allodynia stemming from peripheral stump neuromas can persist for extended periods, significantly compromising patients' quality of life. Conventional managements for nerve stumps have demonstrated limited effectiveness in ensuring their orderly termination. In this study, we present a spatially confined conduit strategy, designed to enhance the self-organization of regenerating nerves after truncation. This innovative approach elegantly enables the autonomous slowing of axonal outgrowth in response to the gradually constricting space, concurrently suppressing neuroinflammation through YAP-mediated mechanotransduction activation. Meanwhile, the decelerating axons exhibit excellent alignment and remyelination, thereby helping to prevent failure modes in nerve self-organization, such as axonal twisting in congested regions and overgrowth beyond the conduit's capacity. Additionally, proteins associated with mechanical allodynia, including TRPA1 and CGRP, exhibit a gradual reduction in expression as spatial constraints tighten, a trend inversely validated by the administration of the YAP-targeted inhibitor Verteporfin. This spatially confined conduit strategy significantly alleviates allodynia, thus preventing autotomy behavior and reducing pain-induced gait alterations.

摘要

源于外周残端神经瘤的慢性痛觉过敏可能会持续很长时间,严重影响患者的生活质量。传统的神经残端处理方法在确保其有序终止方面效果有限。在本研究中,我们提出了一种空间受限导管策略,旨在增强截断后再生神经的自组织能力。这种创新方法巧妙地使轴突生长在空间逐渐变窄时自主减缓,同时通过YAP介导的机械转导激活抑制神经炎症。与此同时,减速的轴突表现出良好的排列和髓鞘再生,从而有助于防止神经自组织中的失败模式,如在拥挤区域的轴突扭曲和超出导管容量的过度生长。此外,随着空间限制加剧,与机械性痛觉过敏相关的蛋白质,包括TRPA1和CGRP,其表达逐渐降低,通过给予YAP靶向抑制剂维替泊芬得到了相反趋势的验证。这种空间受限导管策略显著减轻了痛觉过敏,从而防止自残行为并减少疼痛引起的步态改变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cbe/11695937/2fad24f14390/41467_2024_55118_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cbe/11695937/8293fd818e67/41467_2024_55118_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cbe/11695937/f6935a757031/41467_2024_55118_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cbe/11695937/98670c9539b3/41467_2024_55118_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cbe/11695937/882e4bcfd903/41467_2024_55118_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cbe/11695937/24315397e5f3/41467_2024_55118_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cbe/11695937/2fad24f14390/41467_2024_55118_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cbe/11695937/8293fd818e67/41467_2024_55118_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cbe/11695937/f15fd8929fe9/41467_2024_55118_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cbe/11695937/920ac33c8350/41467_2024_55118_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cbe/11695937/f6935a757031/41467_2024_55118_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cbe/11695937/98670c9539b3/41467_2024_55118_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cbe/11695937/882e4bcfd903/41467_2024_55118_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cbe/11695937/24315397e5f3/41467_2024_55118_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cbe/11695937/2fad24f14390/41467_2024_55118_Fig8_HTML.jpg

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