Cargando…
Induced neural stem cell grafts exert neuroprotection through an interaction between Crry and Akt in a mouse model of closed head injury
BACKGROUND: Recently, growing evidence has indicated an important role of the complement system, a crucial component of immunity, in mediating neuroinflammation and promoting neuronal apoptosis following closed head injury (CHI). We previously reported that transplanted induced neural stem cells (iN...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7881465/ https://www.ncbi.nlm.nih.gov/pubmed/33579360 http://dx.doi.org/10.1186/s13287-021-02186-z |
_version_ | 1783650883296296960 |
---|---|
author | Gao, Mou Dong, Qin Wang, Wenjia Yang, Zhijun Guo, Lili Lu, Yingzhou Ding, Boyun Chen, Lihua Zhang, Jianning Xu, Ruxiang |
author_facet | Gao, Mou Dong, Qin Wang, Wenjia Yang, Zhijun Guo, Lili Lu, Yingzhou Ding, Boyun Chen, Lihua Zhang, Jianning Xu, Ruxiang |
author_sort | Gao, Mou |
collection | PubMed |
description | BACKGROUND: Recently, growing evidence has indicated an important role of the complement system, a crucial component of immunity, in mediating neuroinflammation and promoting neuronal apoptosis following closed head injury (CHI). We previously reported that transplanted induced neural stem cells (iNSCs) pre-treated with CHI mouse serum could enhance complement receptor type 1-related protein y (Crry) expression and ameliorate complement-mediated damage in mouse CHI models. However, the mechanism underlying the elevated levels of Crry expression remains elusive. METHODS: CHI models were established using a standardized weight-drop device. We collected CHI mouse serum at 12 h post-trauma. RT-QPCR assay, western blot analysis, complement deposition assay, Akt inhibition assay, flow cytometry, cell transplantation, and functional assay were utilized to clarify the mechanism of Crry expression in iNSCs receiving CHI mouse serum treatment. RESULTS: We observed dramatic increases in the levels of Crry expression and Akt activation in iNSCs receiving CHI mouse serum treatment. Remarkably, Akt inhibition led to the reduction of Crry expression in iNSCs. Intriguingly, the treatment of iNSC-derived neurons with recombinant complement receptor 2-conjugated Crry (CR2-Crry), which inhibits all complement pathways, substantially enhanced Crry expression and Akt activation in neurons after CHI mouse serum treatment. In subsequent in vitro experiments of pre-treatment of iNSCs with CR2-Crry, we observed significant increases in the levels of Crry expression and Akt activation in iNSCs and iNSC-derived astrocytes and neurons post-treatment with CHI mouse serum. Additionally, an in vivo study showed that intracerebral-transplanted iNSCs pre-treated with CR2-Crry markedly enhanced Crry expression in neurons and protected neurons from complement-dependent damage in the brains of CHI mice. CONCLUSION: INSCs receiving CR2-Crry pre-treatment increased the levels of Crry expression in iNSCs and iNSC-derived astrocytes and neurons and attenuated complement-mediated injury following CHI. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-021-02186-z. |
format | Online Article Text |
id | pubmed-7881465 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78814652021-02-17 Induced neural stem cell grafts exert neuroprotection through an interaction between Crry and Akt in a mouse model of closed head injury Gao, Mou Dong, Qin Wang, Wenjia Yang, Zhijun Guo, Lili Lu, Yingzhou Ding, Boyun Chen, Lihua Zhang, Jianning Xu, Ruxiang Stem Cell Res Ther Research BACKGROUND: Recently, growing evidence has indicated an important role of the complement system, a crucial component of immunity, in mediating neuroinflammation and promoting neuronal apoptosis following closed head injury (CHI). We previously reported that transplanted induced neural stem cells (iNSCs) pre-treated with CHI mouse serum could enhance complement receptor type 1-related protein y (Crry) expression and ameliorate complement-mediated damage in mouse CHI models. However, the mechanism underlying the elevated levels of Crry expression remains elusive. METHODS: CHI models were established using a standardized weight-drop device. We collected CHI mouse serum at 12 h post-trauma. RT-QPCR assay, western blot analysis, complement deposition assay, Akt inhibition assay, flow cytometry, cell transplantation, and functional assay were utilized to clarify the mechanism of Crry expression in iNSCs receiving CHI mouse serum treatment. RESULTS: We observed dramatic increases in the levels of Crry expression and Akt activation in iNSCs receiving CHI mouse serum treatment. Remarkably, Akt inhibition led to the reduction of Crry expression in iNSCs. Intriguingly, the treatment of iNSC-derived neurons with recombinant complement receptor 2-conjugated Crry (CR2-Crry), which inhibits all complement pathways, substantially enhanced Crry expression and Akt activation in neurons after CHI mouse serum treatment. In subsequent in vitro experiments of pre-treatment of iNSCs with CR2-Crry, we observed significant increases in the levels of Crry expression and Akt activation in iNSCs and iNSC-derived astrocytes and neurons post-treatment with CHI mouse serum. Additionally, an in vivo study showed that intracerebral-transplanted iNSCs pre-treated with CR2-Crry markedly enhanced Crry expression in neurons and protected neurons from complement-dependent damage in the brains of CHI mice. CONCLUSION: INSCs receiving CR2-Crry pre-treatment increased the levels of Crry expression in iNSCs and iNSC-derived astrocytes and neurons and attenuated complement-mediated injury following CHI. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-021-02186-z. BioMed Central 2021-02-12 /pmc/articles/PMC7881465/ /pubmed/33579360 http://dx.doi.org/10.1186/s13287-021-02186-z Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Gao, Mou Dong, Qin Wang, Wenjia Yang, Zhijun Guo, Lili Lu, Yingzhou Ding, Boyun Chen, Lihua Zhang, Jianning Xu, Ruxiang Induced neural stem cell grafts exert neuroprotection through an interaction between Crry and Akt in a mouse model of closed head injury |
title | Induced neural stem cell grafts exert neuroprotection through an interaction between Crry and Akt in a mouse model of closed head injury |
title_full | Induced neural stem cell grafts exert neuroprotection through an interaction between Crry and Akt in a mouse model of closed head injury |
title_fullStr | Induced neural stem cell grafts exert neuroprotection through an interaction between Crry and Akt in a mouse model of closed head injury |
title_full_unstemmed | Induced neural stem cell grafts exert neuroprotection through an interaction between Crry and Akt in a mouse model of closed head injury |
title_short | Induced neural stem cell grafts exert neuroprotection through an interaction between Crry and Akt in a mouse model of closed head injury |
title_sort | induced neural stem cell grafts exert neuroprotection through an interaction between crry and akt in a mouse model of closed head injury |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7881465/ https://www.ncbi.nlm.nih.gov/pubmed/33579360 http://dx.doi.org/10.1186/s13287-021-02186-z |
work_keys_str_mv | AT gaomou inducedneuralstemcellgraftsexertneuroprotectionthroughaninteractionbetweencrryandaktinamousemodelofclosedheadinjury AT dongqin inducedneuralstemcellgraftsexertneuroprotectionthroughaninteractionbetweencrryandaktinamousemodelofclosedheadinjury AT wangwenjia inducedneuralstemcellgraftsexertneuroprotectionthroughaninteractionbetweencrryandaktinamousemodelofclosedheadinjury AT yangzhijun inducedneuralstemcellgraftsexertneuroprotectionthroughaninteractionbetweencrryandaktinamousemodelofclosedheadinjury AT guolili inducedneuralstemcellgraftsexertneuroprotectionthroughaninteractionbetweencrryandaktinamousemodelofclosedheadinjury AT luyingzhou inducedneuralstemcellgraftsexertneuroprotectionthroughaninteractionbetweencrryandaktinamousemodelofclosedheadinjury AT dingboyun inducedneuralstemcellgraftsexertneuroprotectionthroughaninteractionbetweencrryandaktinamousemodelofclosedheadinjury AT chenlihua inducedneuralstemcellgraftsexertneuroprotectionthroughaninteractionbetweencrryandaktinamousemodelofclosedheadinjury AT zhangjianning inducedneuralstemcellgraftsexertneuroprotectionthroughaninteractionbetweencrryandaktinamousemodelofclosedheadinjury AT xuruxiang inducedneuralstemcellgraftsexertneuroprotectionthroughaninteractionbetweencrryandaktinamousemodelofclosedheadinjury |