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

Author

Listed:
  • Xiaobin Luo

    (Tsinghua University
    Tsinghua University)

  • Jia Yang

    (Tsinghua University)

  • Yonggang Zhao

    (Tubular Goods Research Institute of CNPC)

  • Toshitatsu Nagayasu

    (Tsinghua University)

  • Junlin Chen

    (Tsinghua University)

  • Peilun Hu

    (Tsinghua University
    Tsinghua University)

  • Zhi He

    (Tsinghua University)

  • Zifan Li

    (Tsinghua University)

  • Jun Wu

    (Chinese Academy of Sciences)

  • Zhe Zhao

    (Tsinghua University)

  • Guman Duan

    (Tsinghua University)

  • Xiaodan Sun

    (Tsinghua University)

  • Lingyun Zhao

    (Tsinghua University)

  • Yongwei Pan

    (Tsinghua University)

  • Xiumei Wang

    (Tsinghua University)

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.

Suggested Citation

  • Xiaobin Luo & Jia Yang & Yonggang Zhao & Toshitatsu Nagayasu & Junlin Chen & Peilun Hu & Zhi He & Zifan Li & Jun Wu & Zhe Zhao & Guman Duan & Xiaodan Sun & Lingyun Zhao & Yongwei Pan & Xiumei Wang, 2025. "Engineering spatially-confined conduits to tune nerve self-organization and allodynic responses via YAP-mediated mechanotransduction," Nature Communications, Nature, vol. 16(1), pages 1-20, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-024-55118-9
    DOI: 10.1038/s41467-024-55118-9
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    References listed on IDEAS

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    1. Lingchi Kong & Xin Gao & Xiangyun Yao & Haijiao Xie & Qinglin Kang & Wei Sun & Zhengwei You & Yun Qian & Cunyi Fan, 2024. "Multilevel neurium-mimetic individualized graft via additive manufacturing for efficient tissue repair," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
    2. Francesco De Logu & Romina Nassini & Alan Hegron & Lorenzo Landini & Dane D. Jensen & Rocco Latorre & Julia Ding & Matilde Marini & Daniel Souza Monteiro de Araujo & Paulina Ramírez-Garcia & Michael W, 2022. "Schwann cell endosome CGRP signals elicit periorbital mechanical allodynia in mice," Nature Communications, Nature, vol. 13(1), pages 1-19, December.
    3. Mariaceleste Aragona & Alejandro Sifrim & Milan Malfait & Yura Song & Jens Herck & Sophie Dekoninck & Souhir Gargouri & Gaëlle Lapouge & Benjamin Swedlund & Christine Dubois & Pieter Baatsen & Katlijn, 2020. "Mechanisms of stretch-mediated skin expansion at single-cell resolution," Nature, Nature, vol. 584(7820), pages 268-273, August.
    4. Stephanie J. Ellis & Nicholas C. Gomez & John Levorse & Aaron F. Mertz & Yejing Ge & Elaine Fuchs, 2019. "Distinct modes of cell competition shape mammalian tissue morphogenesis," Nature, Nature, vol. 569(7757), pages 497-502, May.
    5. Yuegui Guo & Zhehui Zhu & Zhenyu Huang & Long Cui & Wei Yu & Wanjin Hong & Zhaocai Zhou & Peng Du & Chen-Ying Liu, 2022. "CK2-induced cooperation of HHEX with the YAP-TEAD4 complex promotes colorectal tumorigenesis," Nature Communications, Nature, vol. 13(1), pages 1-17, December.
    6. Francesco De Logu & Romina Nassini & Serena Materazzi & Muryel Carvalho Gonçalves & Daniele Nosi & Duccio Rossi Degl’Innocenti & Ilaria M. Marone & Juliano Ferreira & Simone Li Puma & Silvia Benemei &, 2017. "Schwann cell TRPA1 mediates neuroinflammation that sustains macrophage-dependent neuropathic pain in mice," Nature Communications, Nature, vol. 8(1), pages 1-16, December.
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