Cargando…

A multifunctional neuromodulation platform utilizing Schwann cell-derived exosomes orchestrates bone microenvironment via immunomodulation, angiogenesis and osteogenesis

Recent evidence highlights multifaceted biological needs to recapitulate the bone microenvironment for bone regeneration. Neurotization has great potential for realizing multi-system modulations in bone tissue engineering (BTE). However, a neural strategy involving all the key bone repair steps temp...

Descripción completa

Detalles Bibliográficos
Autores principales: Hao, Zhichao, Ren, Lin, Zhang, Zhen, Yang, Zaiwu, Wu, Shujie, Liu, Gen, Cheng, Bin, Wu, Jun, Xia, Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9672134/
https://www.ncbi.nlm.nih.gov/pubmed/36439082
http://dx.doi.org/10.1016/j.bioactmat.2022.10.018
_version_ 1784832693968568320
author Hao, Zhichao
Ren, Lin
Zhang, Zhen
Yang, Zaiwu
Wu, Shujie
Liu, Gen
Cheng, Bin
Wu, Jun
Xia, Juan
author_facet Hao, Zhichao
Ren, Lin
Zhang, Zhen
Yang, Zaiwu
Wu, Shujie
Liu, Gen
Cheng, Bin
Wu, Jun
Xia, Juan
author_sort Hao, Zhichao
collection PubMed
description Recent evidence highlights multifaceted biological needs to recapitulate the bone microenvironment for bone regeneration. Neurotization has great potential for realizing multi-system modulations in bone tissue engineering (BTE). However, a neural strategy involving all the key bone repair steps temporally has not yet been reported. In this study, we reported the neural tissue engineering hydrogel-encapsulated Schwann cell-derived exosomes (SC Exo). This sustained-release SC Exo system prominently enhanced bone regeneration by promoting innervation, immunoregulation, vascularization, and osteogenesis in vivo. Moreover, the in vitro results further confirmed that this system significantly induced M2 polarization of macrophages, tube formation of HUVECs, and BMSCs osteogenic differentiation. Furthermore, BMSCs osteogenesis was promoted by upregulating the TGF-β1/SMAD2/3 signaling pathway. In summary, a novel cell-free and easily prepared SC Exo neural engineering was successfully developed to promote bone regeneration by orchestrating the entire bone healing microenvironment, which may provide a new strategy for tissue engineering and clinical treatment of bone defects.
format Online
Article
Text
id pubmed-9672134
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher KeAi Publishing
record_format MEDLINE/PubMed
spelling pubmed-96721342022-11-25 A multifunctional neuromodulation platform utilizing Schwann cell-derived exosomes orchestrates bone microenvironment via immunomodulation, angiogenesis and osteogenesis Hao, Zhichao Ren, Lin Zhang, Zhen Yang, Zaiwu Wu, Shujie Liu, Gen Cheng, Bin Wu, Jun Xia, Juan Bioact Mater Article Recent evidence highlights multifaceted biological needs to recapitulate the bone microenvironment for bone regeneration. Neurotization has great potential for realizing multi-system modulations in bone tissue engineering (BTE). However, a neural strategy involving all the key bone repair steps temporally has not yet been reported. In this study, we reported the neural tissue engineering hydrogel-encapsulated Schwann cell-derived exosomes (SC Exo). This sustained-release SC Exo system prominently enhanced bone regeneration by promoting innervation, immunoregulation, vascularization, and osteogenesis in vivo. Moreover, the in vitro results further confirmed that this system significantly induced M2 polarization of macrophages, tube formation of HUVECs, and BMSCs osteogenic differentiation. Furthermore, BMSCs osteogenesis was promoted by upregulating the TGF-β1/SMAD2/3 signaling pathway. In summary, a novel cell-free and easily prepared SC Exo neural engineering was successfully developed to promote bone regeneration by orchestrating the entire bone healing microenvironment, which may provide a new strategy for tissue engineering and clinical treatment of bone defects. KeAi Publishing 2022-11-14 /pmc/articles/PMC9672134/ /pubmed/36439082 http://dx.doi.org/10.1016/j.bioactmat.2022.10.018 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Hao, Zhichao
Ren, Lin
Zhang, Zhen
Yang, Zaiwu
Wu, Shujie
Liu, Gen
Cheng, Bin
Wu, Jun
Xia, Juan
A multifunctional neuromodulation platform utilizing Schwann cell-derived exosomes orchestrates bone microenvironment via immunomodulation, angiogenesis and osteogenesis
title A multifunctional neuromodulation platform utilizing Schwann cell-derived exosomes orchestrates bone microenvironment via immunomodulation, angiogenesis and osteogenesis
title_full A multifunctional neuromodulation platform utilizing Schwann cell-derived exosomes orchestrates bone microenvironment via immunomodulation, angiogenesis and osteogenesis
title_fullStr A multifunctional neuromodulation platform utilizing Schwann cell-derived exosomes orchestrates bone microenvironment via immunomodulation, angiogenesis and osteogenesis
title_full_unstemmed A multifunctional neuromodulation platform utilizing Schwann cell-derived exosomes orchestrates bone microenvironment via immunomodulation, angiogenesis and osteogenesis
title_short A multifunctional neuromodulation platform utilizing Schwann cell-derived exosomes orchestrates bone microenvironment via immunomodulation, angiogenesis and osteogenesis
title_sort multifunctional neuromodulation platform utilizing schwann cell-derived exosomes orchestrates bone microenvironment via immunomodulation, angiogenesis and osteogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9672134/
https://www.ncbi.nlm.nih.gov/pubmed/36439082
http://dx.doi.org/10.1016/j.bioactmat.2022.10.018
work_keys_str_mv AT haozhichao amultifunctionalneuromodulationplatformutilizingschwanncellderivedexosomesorchestratesbonemicroenvironmentviaimmunomodulationangiogenesisandosteogenesis
AT renlin amultifunctionalneuromodulationplatformutilizingschwanncellderivedexosomesorchestratesbonemicroenvironmentviaimmunomodulationangiogenesisandosteogenesis
AT zhangzhen amultifunctionalneuromodulationplatformutilizingschwanncellderivedexosomesorchestratesbonemicroenvironmentviaimmunomodulationangiogenesisandosteogenesis
AT yangzaiwu amultifunctionalneuromodulationplatformutilizingschwanncellderivedexosomesorchestratesbonemicroenvironmentviaimmunomodulationangiogenesisandosteogenesis
AT wushujie amultifunctionalneuromodulationplatformutilizingschwanncellderivedexosomesorchestratesbonemicroenvironmentviaimmunomodulationangiogenesisandosteogenesis
AT liugen amultifunctionalneuromodulationplatformutilizingschwanncellderivedexosomesorchestratesbonemicroenvironmentviaimmunomodulationangiogenesisandosteogenesis
AT chengbin amultifunctionalneuromodulationplatformutilizingschwanncellderivedexosomesorchestratesbonemicroenvironmentviaimmunomodulationangiogenesisandosteogenesis
AT wujun amultifunctionalneuromodulationplatformutilizingschwanncellderivedexosomesorchestratesbonemicroenvironmentviaimmunomodulationangiogenesisandosteogenesis
AT xiajuan amultifunctionalneuromodulationplatformutilizingschwanncellderivedexosomesorchestratesbonemicroenvironmentviaimmunomodulationangiogenesisandosteogenesis
AT haozhichao multifunctionalneuromodulationplatformutilizingschwanncellderivedexosomesorchestratesbonemicroenvironmentviaimmunomodulationangiogenesisandosteogenesis
AT renlin multifunctionalneuromodulationplatformutilizingschwanncellderivedexosomesorchestratesbonemicroenvironmentviaimmunomodulationangiogenesisandosteogenesis
AT zhangzhen multifunctionalneuromodulationplatformutilizingschwanncellderivedexosomesorchestratesbonemicroenvironmentviaimmunomodulationangiogenesisandosteogenesis
AT yangzaiwu multifunctionalneuromodulationplatformutilizingschwanncellderivedexosomesorchestratesbonemicroenvironmentviaimmunomodulationangiogenesisandosteogenesis
AT wushujie multifunctionalneuromodulationplatformutilizingschwanncellderivedexosomesorchestratesbonemicroenvironmentviaimmunomodulationangiogenesisandosteogenesis
AT liugen multifunctionalneuromodulationplatformutilizingschwanncellderivedexosomesorchestratesbonemicroenvironmentviaimmunomodulationangiogenesisandosteogenesis
AT chengbin multifunctionalneuromodulationplatformutilizingschwanncellderivedexosomesorchestratesbonemicroenvironmentviaimmunomodulationangiogenesisandosteogenesis
AT wujun multifunctionalneuromodulationplatformutilizingschwanncellderivedexosomesorchestratesbonemicroenvironmentviaimmunomodulationangiogenesisandosteogenesis
AT xiajuan multifunctionalneuromodulationplatformutilizingschwanncellderivedexosomesorchestratesbonemicroenvironmentviaimmunomodulationangiogenesisandosteogenesis