Cargando…

The Effect of RADA16-I and CDNF on Neurogenesis and Neuroprotection in Brain Ischemia-Reperfusion Injury

Scaffold materials, neurotrophic factors, and seed cells are three elements of neural tissue engineering. As well-known self-assembling peptide-based hydrogels, RADA16-I and modified peptides are attractive matrices for neural tissue engineering. In addition to its neuroprotective effects, cerebral...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Xingyu, Ren, Haiyuan, Peng, Ai, Cheng, Haoyang, Chen, Jiahao, Xia, Xue, Liu, Ting, Wang, Xiaojing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836142/
https://www.ncbi.nlm.nih.gov/pubmed/35163360
http://dx.doi.org/10.3390/ijms23031436
_version_ 1784649604096065536
author Liu, Xingyu
Ren, Haiyuan
Peng, Ai
Cheng, Haoyang
Chen, Jiahao
Xia, Xue
Liu, Ting
Wang, Xiaojing
author_facet Liu, Xingyu
Ren, Haiyuan
Peng, Ai
Cheng, Haoyang
Chen, Jiahao
Xia, Xue
Liu, Ting
Wang, Xiaojing
author_sort Liu, Xingyu
collection PubMed
description Scaffold materials, neurotrophic factors, and seed cells are three elements of neural tissue engineering. As well-known self-assembling peptide-based hydrogels, RADA16-I and modified peptides are attractive matrices for neural tissue engineering. In addition to its neuroprotective effects, cerebral dopamine neurotrophic factor (CDNF) has been reported to promote the proliferation, migration, and differentiation of neural stem cells (NSCs). However, the role of RADA16-I combined with CDNF on NSCs remains unknown. First, the effect of RADA16-I hydrogel and CDNF on the proliferation and differentiation of cultured NSCs was investigated. Next, RADA16-I hydrogel and CDNF were microinjected into the lateral ventricle (LV) of middle cerebral artery occlusion (MCAO) rats to activate endogenous NSCs. CDNF promoted the proliferation of NSCs, while RADA16-I induced the neural differentiation of NSCs in vitro. Importantly, both RADA16-I and CDNF promoted the proliferation, migration, and differentiation of endogenous NSCs by activating the ERK1/2 and STAT3 pathways, and CDNF exerted an obvious neuroprotective effect on brain ischemia-reperfusion injury. These findings provide new information regarding the application of the scaffold material RADA16-I hydrogel and the neurotrophic factor CDNF in neural tissue engineering and suggest that RADA16-I hydrogel and CDNF microinjection may represent a novel therapeutic strategy for the treatment of stroke.
format Online
Article
Text
id pubmed-8836142
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-88361422022-02-12 The Effect of RADA16-I and CDNF on Neurogenesis and Neuroprotection in Brain Ischemia-Reperfusion Injury Liu, Xingyu Ren, Haiyuan Peng, Ai Cheng, Haoyang Chen, Jiahao Xia, Xue Liu, Ting Wang, Xiaojing Int J Mol Sci Article Scaffold materials, neurotrophic factors, and seed cells are three elements of neural tissue engineering. As well-known self-assembling peptide-based hydrogels, RADA16-I and modified peptides are attractive matrices for neural tissue engineering. In addition to its neuroprotective effects, cerebral dopamine neurotrophic factor (CDNF) has been reported to promote the proliferation, migration, and differentiation of neural stem cells (NSCs). However, the role of RADA16-I combined with CDNF on NSCs remains unknown. First, the effect of RADA16-I hydrogel and CDNF on the proliferation and differentiation of cultured NSCs was investigated. Next, RADA16-I hydrogel and CDNF were microinjected into the lateral ventricle (LV) of middle cerebral artery occlusion (MCAO) rats to activate endogenous NSCs. CDNF promoted the proliferation of NSCs, while RADA16-I induced the neural differentiation of NSCs in vitro. Importantly, both RADA16-I and CDNF promoted the proliferation, migration, and differentiation of endogenous NSCs by activating the ERK1/2 and STAT3 pathways, and CDNF exerted an obvious neuroprotective effect on brain ischemia-reperfusion injury. These findings provide new information regarding the application of the scaffold material RADA16-I hydrogel and the neurotrophic factor CDNF in neural tissue engineering and suggest that RADA16-I hydrogel and CDNF microinjection may represent a novel therapeutic strategy for the treatment of stroke. MDPI 2022-01-27 /pmc/articles/PMC8836142/ /pubmed/35163360 http://dx.doi.org/10.3390/ijms23031436 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Liu, Xingyu
Ren, Haiyuan
Peng, Ai
Cheng, Haoyang
Chen, Jiahao
Xia, Xue
Liu, Ting
Wang, Xiaojing
The Effect of RADA16-I and CDNF on Neurogenesis and Neuroprotection in Brain Ischemia-Reperfusion Injury
title The Effect of RADA16-I and CDNF on Neurogenesis and Neuroprotection in Brain Ischemia-Reperfusion Injury
title_full The Effect of RADA16-I and CDNF on Neurogenesis and Neuroprotection in Brain Ischemia-Reperfusion Injury
title_fullStr The Effect of RADA16-I and CDNF on Neurogenesis and Neuroprotection in Brain Ischemia-Reperfusion Injury
title_full_unstemmed The Effect of RADA16-I and CDNF on Neurogenesis and Neuroprotection in Brain Ischemia-Reperfusion Injury
title_short The Effect of RADA16-I and CDNF on Neurogenesis and Neuroprotection in Brain Ischemia-Reperfusion Injury
title_sort effect of rada16-i and cdnf on neurogenesis and neuroprotection in brain ischemia-reperfusion injury
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836142/
https://www.ncbi.nlm.nih.gov/pubmed/35163360
http://dx.doi.org/10.3390/ijms23031436
work_keys_str_mv AT liuxingyu theeffectofrada16iandcdnfonneurogenesisandneuroprotectioninbrainischemiareperfusioninjury
AT renhaiyuan theeffectofrada16iandcdnfonneurogenesisandneuroprotectioninbrainischemiareperfusioninjury
AT pengai theeffectofrada16iandcdnfonneurogenesisandneuroprotectioninbrainischemiareperfusioninjury
AT chenghaoyang theeffectofrada16iandcdnfonneurogenesisandneuroprotectioninbrainischemiareperfusioninjury
AT chenjiahao theeffectofrada16iandcdnfonneurogenesisandneuroprotectioninbrainischemiareperfusioninjury
AT xiaxue theeffectofrada16iandcdnfonneurogenesisandneuroprotectioninbrainischemiareperfusioninjury
AT liuting theeffectofrada16iandcdnfonneurogenesisandneuroprotectioninbrainischemiareperfusioninjury
AT wangxiaojing theeffectofrada16iandcdnfonneurogenesisandneuroprotectioninbrainischemiareperfusioninjury
AT liuxingyu effectofrada16iandcdnfonneurogenesisandneuroprotectioninbrainischemiareperfusioninjury
AT renhaiyuan effectofrada16iandcdnfonneurogenesisandneuroprotectioninbrainischemiareperfusioninjury
AT pengai effectofrada16iandcdnfonneurogenesisandneuroprotectioninbrainischemiareperfusioninjury
AT chenghaoyang effectofrada16iandcdnfonneurogenesisandneuroprotectioninbrainischemiareperfusioninjury
AT chenjiahao effectofrada16iandcdnfonneurogenesisandneuroprotectioninbrainischemiareperfusioninjury
AT xiaxue effectofrada16iandcdnfonneurogenesisandneuroprotectioninbrainischemiareperfusioninjury
AT liuting effectofrada16iandcdnfonneurogenesisandneuroprotectioninbrainischemiareperfusioninjury
AT wangxiaojing effectofrada16iandcdnfonneurogenesisandneuroprotectioninbrainischemiareperfusioninjury