Cargando…
Autologous olfactory mucosa mesenchymal stem cells treatment improves the neural network in chronic refractory epilepsy
BACKGROUND AND AIMS: Refractory epilepsy is also known as drug-resistant epilepsy with limited clinical treatment. Benefitting from its safety and easy availability, olfactory mucosa mesenchymal stem cells (OM-MSCs) are considered a preferable MSC source for clinical application. This study aims to...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10483711/ https://www.ncbi.nlm.nih.gov/pubmed/37674249 http://dx.doi.org/10.1186/s13287-023-03458-6 |
_version_ | 1785102440151908352 |
---|---|
author | Liu, Zheng-Zhao Huang, Yan Hong, Chun-Gu Wang, Xin Duan, Ran Liu, Jian-Yang He, Jia-Lin Duan, Da Xie, Hui Lu, Ming |
author_facet | Liu, Zheng-Zhao Huang, Yan Hong, Chun-Gu Wang, Xin Duan, Ran Liu, Jian-Yang He, Jia-Lin Duan, Da Xie, Hui Lu, Ming |
author_sort | Liu, Zheng-Zhao |
collection | PubMed |
description | BACKGROUND AND AIMS: Refractory epilepsy is also known as drug-resistant epilepsy with limited clinical treatment. Benefitting from its safety and easy availability, olfactory mucosa mesenchymal stem cells (OM-MSCs) are considered a preferable MSC source for clinical application. This study aims to investigate whether OM-MSCs are a promising alternative source for treating refractory epilepsy clinically and uncover the mechanism by OM-MSCs administration on an epileptic mouse model. METHODS: OM-MSCs were isolated from turbinal and characterized by flow cytometry. Autologous human OM-MSCs treatment on a patient was carried out using intrathecal administration. Epileptic mouse model was established by 1 mg/kg scopolamine and 300 mg/kg pilocarpine treatment (intraperitoneal). Stereotaxic microinjection was employed to deliver the mouse OM-MSCs. Mouse electroencephalograph recording was used to investigate the seizures. Brain structure was evaluated by magnetic resonance imaging (MRI). Immunohistochemical and immunofluorescent staining of GFAP, IBA1, MAP2, TUBB3, OLIG2, CD4, CD25, and FOXP3 was carried out to investigate the neural cells and Treg cells. QRT-PCR and ELISA were performed to determine the cytokines (Il1b, Il6, Tnf, Il10) on mRNA and protein level. Y-maze, the object location test, and novel object recognition test were performed to measure the cognitive function. Footprint test, rotarod test, balance beam test, and grip strength test were conducted to evaluate the locomotive function. Von Frey testing was carried out to assess the mechanical allodynia. RESULTS: Many beneficial effects of the OM-MSC treatment on disease status, including seizure type, frequency, severity, duration, and cognitive function, and no apparent adverse effects were observed at the 8-year follow-up case. Brain MRI indicated that autologous OM-MSC treatment alleviated brain atrophy in epilepsy patients. A study in an epileptic mouse model revealed that OM-MSC treatment recruited Treg cells to the brain, inhibited inflammation, rebuilt the neural network, and improved the cognitive, locomotive, and perceptive functions of epileptic mice. CONCLUSIONS: Autologous OM-MSC treatment is efficacious for improving chronic refractory epilepsy, suggesting a future therapeutic candidate for epilepsy. Trial registration: The study was registered with Chinese Clinical Trial Registry (ChiCTR2200055357). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-023-03458-6. |
format | Online Article Text |
id | pubmed-10483711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-104837112023-09-08 Autologous olfactory mucosa mesenchymal stem cells treatment improves the neural network in chronic refractory epilepsy Liu, Zheng-Zhao Huang, Yan Hong, Chun-Gu Wang, Xin Duan, Ran Liu, Jian-Yang He, Jia-Lin Duan, Da Xie, Hui Lu, Ming Stem Cell Res Ther Research BACKGROUND AND AIMS: Refractory epilepsy is also known as drug-resistant epilepsy with limited clinical treatment. Benefitting from its safety and easy availability, olfactory mucosa mesenchymal stem cells (OM-MSCs) are considered a preferable MSC source for clinical application. This study aims to investigate whether OM-MSCs are a promising alternative source for treating refractory epilepsy clinically and uncover the mechanism by OM-MSCs administration on an epileptic mouse model. METHODS: OM-MSCs were isolated from turbinal and characterized by flow cytometry. Autologous human OM-MSCs treatment on a patient was carried out using intrathecal administration. Epileptic mouse model was established by 1 mg/kg scopolamine and 300 mg/kg pilocarpine treatment (intraperitoneal). Stereotaxic microinjection was employed to deliver the mouse OM-MSCs. Mouse electroencephalograph recording was used to investigate the seizures. Brain structure was evaluated by magnetic resonance imaging (MRI). Immunohistochemical and immunofluorescent staining of GFAP, IBA1, MAP2, TUBB3, OLIG2, CD4, CD25, and FOXP3 was carried out to investigate the neural cells and Treg cells. QRT-PCR and ELISA were performed to determine the cytokines (Il1b, Il6, Tnf, Il10) on mRNA and protein level. Y-maze, the object location test, and novel object recognition test were performed to measure the cognitive function. Footprint test, rotarod test, balance beam test, and grip strength test were conducted to evaluate the locomotive function. Von Frey testing was carried out to assess the mechanical allodynia. RESULTS: Many beneficial effects of the OM-MSC treatment on disease status, including seizure type, frequency, severity, duration, and cognitive function, and no apparent adverse effects were observed at the 8-year follow-up case. Brain MRI indicated that autologous OM-MSC treatment alleviated brain atrophy in epilepsy patients. A study in an epileptic mouse model revealed that OM-MSC treatment recruited Treg cells to the brain, inhibited inflammation, rebuilt the neural network, and improved the cognitive, locomotive, and perceptive functions of epileptic mice. CONCLUSIONS: Autologous OM-MSC treatment is efficacious for improving chronic refractory epilepsy, suggesting a future therapeutic candidate for epilepsy. Trial registration: The study was registered with Chinese Clinical Trial Registry (ChiCTR2200055357). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13287-023-03458-6. BioMed Central 2023-09-07 /pmc/articles/PMC10483711/ /pubmed/37674249 http://dx.doi.org/10.1186/s13287-023-03458-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Liu, Zheng-Zhao Huang, Yan Hong, Chun-Gu Wang, Xin Duan, Ran Liu, Jian-Yang He, Jia-Lin Duan, Da Xie, Hui Lu, Ming Autologous olfactory mucosa mesenchymal stem cells treatment improves the neural network in chronic refractory epilepsy |
title | Autologous olfactory mucosa mesenchymal stem cells treatment improves the neural network in chronic refractory epilepsy |
title_full | Autologous olfactory mucosa mesenchymal stem cells treatment improves the neural network in chronic refractory epilepsy |
title_fullStr | Autologous olfactory mucosa mesenchymal stem cells treatment improves the neural network in chronic refractory epilepsy |
title_full_unstemmed | Autologous olfactory mucosa mesenchymal stem cells treatment improves the neural network in chronic refractory epilepsy |
title_short | Autologous olfactory mucosa mesenchymal stem cells treatment improves the neural network in chronic refractory epilepsy |
title_sort | autologous olfactory mucosa mesenchymal stem cells treatment improves the neural network in chronic refractory epilepsy |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10483711/ https://www.ncbi.nlm.nih.gov/pubmed/37674249 http://dx.doi.org/10.1186/s13287-023-03458-6 |
work_keys_str_mv | AT liuzhengzhao autologousolfactorymucosamesenchymalstemcellstreatmentimprovestheneuralnetworkinchronicrefractoryepilepsy AT huangyan autologousolfactorymucosamesenchymalstemcellstreatmentimprovestheneuralnetworkinchronicrefractoryepilepsy AT hongchungu autologousolfactorymucosamesenchymalstemcellstreatmentimprovestheneuralnetworkinchronicrefractoryepilepsy AT wangxin autologousolfactorymucosamesenchymalstemcellstreatmentimprovestheneuralnetworkinchronicrefractoryepilepsy AT duanran autologousolfactorymucosamesenchymalstemcellstreatmentimprovestheneuralnetworkinchronicrefractoryepilepsy AT liujianyang autologousolfactorymucosamesenchymalstemcellstreatmentimprovestheneuralnetworkinchronicrefractoryepilepsy AT hejialin autologousolfactorymucosamesenchymalstemcellstreatmentimprovestheneuralnetworkinchronicrefractoryepilepsy AT duanda autologousolfactorymucosamesenchymalstemcellstreatmentimprovestheneuralnetworkinchronicrefractoryepilepsy AT xiehui autologousolfactorymucosamesenchymalstemcellstreatmentimprovestheneuralnetworkinchronicrefractoryepilepsy AT luming autologousolfactorymucosamesenchymalstemcellstreatmentimprovestheneuralnetworkinchronicrefractoryepilepsy |