Cargando…

Engineered Sensory Nerve Guides Self‐Adaptive Bone Healing via NGF‐TrkA Signaling Pathway

The upstream role of sensory innervation during bone homeostasis is widely underestimated in bone repairing strategies. Herein, a neuromodulation approach is proposed to orchestrate bone defect healing by constructing engineered sensory nerves (eSN) in situ to leverage the adaptation feature of SN d...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Zengjie, Wang, Fangqian, Huang, Xin, Sun, Hangxiang, Xu, Jianxiang, Qu, Hao, Yan, Xiaobo, Shi, Wei, Teng, Wangsiyuan, Jin, Xiaoqiang, Shao, Zhenxuan, Zhang, Yongxing, Zhao, Shenzhi, Wu, Yan, Ye, Zhaoming, Yu, Xiaohua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10074090/
https://www.ncbi.nlm.nih.gov/pubmed/36725311
http://dx.doi.org/10.1002/advs.202206155
_version_ 1785019703201103872
author Zhang, Zengjie
Wang, Fangqian
Huang, Xin
Sun, Hangxiang
Xu, Jianxiang
Qu, Hao
Yan, Xiaobo
Shi, Wei
Teng, Wangsiyuan
Jin, Xiaoqiang
Shao, Zhenxuan
Zhang, Yongxing
Zhao, Shenzhi
Wu, Yan
Ye, Zhaoming
Yu, Xiaohua
author_facet Zhang, Zengjie
Wang, Fangqian
Huang, Xin
Sun, Hangxiang
Xu, Jianxiang
Qu, Hao
Yan, Xiaobo
Shi, Wei
Teng, Wangsiyuan
Jin, Xiaoqiang
Shao, Zhenxuan
Zhang, Yongxing
Zhao, Shenzhi
Wu, Yan
Ye, Zhaoming
Yu, Xiaohua
author_sort Zhang, Zengjie
collection PubMed
description The upstream role of sensory innervation during bone homeostasis is widely underestimated in bone repairing strategies. Herein, a neuromodulation approach is proposed to orchestrate bone defect healing by constructing engineered sensory nerves (eSN) in situ to leverage the adaptation feature of SN during tissue formation. NGF liberated from ECM‐constructed eSN effectively promotes sensory neuron differentiation and enhances CGRP secretion, which lead to improved RAOECs mobility and osteogenic differentiation of BMSC. In turn, such eSN effectively drives ossification in vivo via NGF‐TrkA signaling pathway, which substantially accelerates critical size bone defect healing. More importantly, eSN also adaptively suppresses excessive bone formation and promotes bone remodeling by activating osteoclasts via CGRP‐dependent mechanism when combined with BMP‐2 delivery, which ingeniously alleviates side effects of BMP‐2. In sum, this eSN approach offers a valuable avenue to harness the adaptive role of neural system to optimize bone homeostasis under various clinical scenario.
format Online
Article
Text
id pubmed-10074090
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-100740902023-04-06 Engineered Sensory Nerve Guides Self‐Adaptive Bone Healing via NGF‐TrkA Signaling Pathway Zhang, Zengjie Wang, Fangqian Huang, Xin Sun, Hangxiang Xu, Jianxiang Qu, Hao Yan, Xiaobo Shi, Wei Teng, Wangsiyuan Jin, Xiaoqiang Shao, Zhenxuan Zhang, Yongxing Zhao, Shenzhi Wu, Yan Ye, Zhaoming Yu, Xiaohua Adv Sci (Weinh) Research Articles The upstream role of sensory innervation during bone homeostasis is widely underestimated in bone repairing strategies. Herein, a neuromodulation approach is proposed to orchestrate bone defect healing by constructing engineered sensory nerves (eSN) in situ to leverage the adaptation feature of SN during tissue formation. NGF liberated from ECM‐constructed eSN effectively promotes sensory neuron differentiation and enhances CGRP secretion, which lead to improved RAOECs mobility and osteogenic differentiation of BMSC. In turn, such eSN effectively drives ossification in vivo via NGF‐TrkA signaling pathway, which substantially accelerates critical size bone defect healing. More importantly, eSN also adaptively suppresses excessive bone formation and promotes bone remodeling by activating osteoclasts via CGRP‐dependent mechanism when combined with BMP‐2 delivery, which ingeniously alleviates side effects of BMP‐2. In sum, this eSN approach offers a valuable avenue to harness the adaptive role of neural system to optimize bone homeostasis under various clinical scenario. John Wiley and Sons Inc. 2023-02-01 /pmc/articles/PMC10074090/ /pubmed/36725311 http://dx.doi.org/10.1002/advs.202206155 Text en © 2023 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Zhang, Zengjie
Wang, Fangqian
Huang, Xin
Sun, Hangxiang
Xu, Jianxiang
Qu, Hao
Yan, Xiaobo
Shi, Wei
Teng, Wangsiyuan
Jin, Xiaoqiang
Shao, Zhenxuan
Zhang, Yongxing
Zhao, Shenzhi
Wu, Yan
Ye, Zhaoming
Yu, Xiaohua
Engineered Sensory Nerve Guides Self‐Adaptive Bone Healing via NGF‐TrkA Signaling Pathway
title Engineered Sensory Nerve Guides Self‐Adaptive Bone Healing via NGF‐TrkA Signaling Pathway
title_full Engineered Sensory Nerve Guides Self‐Adaptive Bone Healing via NGF‐TrkA Signaling Pathway
title_fullStr Engineered Sensory Nerve Guides Self‐Adaptive Bone Healing via NGF‐TrkA Signaling Pathway
title_full_unstemmed Engineered Sensory Nerve Guides Self‐Adaptive Bone Healing via NGF‐TrkA Signaling Pathway
title_short Engineered Sensory Nerve Guides Self‐Adaptive Bone Healing via NGF‐TrkA Signaling Pathway
title_sort engineered sensory nerve guides self‐adaptive bone healing via ngf‐trka signaling pathway
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10074090/
https://www.ncbi.nlm.nih.gov/pubmed/36725311
http://dx.doi.org/10.1002/advs.202206155
work_keys_str_mv AT zhangzengjie engineeredsensorynerveguidesselfadaptivebonehealingviangftrkasignalingpathway
AT wangfangqian engineeredsensorynerveguidesselfadaptivebonehealingviangftrkasignalingpathway
AT huangxin engineeredsensorynerveguidesselfadaptivebonehealingviangftrkasignalingpathway
AT sunhangxiang engineeredsensorynerveguidesselfadaptivebonehealingviangftrkasignalingpathway
AT xujianxiang engineeredsensorynerveguidesselfadaptivebonehealingviangftrkasignalingpathway
AT quhao engineeredsensorynerveguidesselfadaptivebonehealingviangftrkasignalingpathway
AT yanxiaobo engineeredsensorynerveguidesselfadaptivebonehealingviangftrkasignalingpathway
AT shiwei engineeredsensorynerveguidesselfadaptivebonehealingviangftrkasignalingpathway
AT tengwangsiyuan engineeredsensorynerveguidesselfadaptivebonehealingviangftrkasignalingpathway
AT jinxiaoqiang engineeredsensorynerveguidesselfadaptivebonehealingviangftrkasignalingpathway
AT shaozhenxuan engineeredsensorynerveguidesselfadaptivebonehealingviangftrkasignalingpathway
AT zhangyongxing engineeredsensorynerveguidesselfadaptivebonehealingviangftrkasignalingpathway
AT zhaoshenzhi engineeredsensorynerveguidesselfadaptivebonehealingviangftrkasignalingpathway
AT wuyan engineeredsensorynerveguidesselfadaptivebonehealingviangftrkasignalingpathway
AT yezhaoming engineeredsensorynerveguidesselfadaptivebonehealingviangftrkasignalingpathway
AT yuxiaohua engineeredsensorynerveguidesselfadaptivebonehealingviangftrkasignalingpathway