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SiRNA in MSC-derived exosomes silences CTGF gene for locomotor recovery in spinal cord injury rats

BACKGROUND: How to obtain a small interfering RNA (siRNA) vector has become a moot point in recent years. Exosomes (Exo) show advantages of long survival time in vivo, high transmission efficiency, and easy penetration across the blood-spinal cord barrier, renowned as excellent carriers of bioactive...

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Autores principales: Huang, Wei, Qu, Mingjia, Li, Lu, Liu, Tao, Lin, Miaoman, Yu, Xiaobing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8193895/
https://www.ncbi.nlm.nih.gov/pubmed/34112262
http://dx.doi.org/10.1186/s13287-021-02401-x
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author Huang, Wei
Qu, Mingjia
Li, Lu
Liu, Tao
Lin, Miaoman
Yu, Xiaobing
author_facet Huang, Wei
Qu, Mingjia
Li, Lu
Liu, Tao
Lin, Miaoman
Yu, Xiaobing
author_sort Huang, Wei
collection PubMed
description BACKGROUND: How to obtain a small interfering RNA (siRNA) vector has become a moot point in recent years. Exosomes (Exo) show advantages of long survival time in vivo, high transmission efficiency, and easy penetration across the blood-spinal cord barrier, renowned as excellent carriers of bioactive substances. METHODS: We applied mesenchymal stem cell (MSC)-derived exosomes as the delivery of synthesized siRNA, which were extracted from rat bone marrow. We constructed exosomes-siRNA (Exo-siRNA) that could specifically silence CTGF gene in the injury sites by electroporation. During the administration, we injected Exo-siRNA into the tail vein of SCI rats, RESULTS: In vivo and in vitro experiments showed that Exo-siRNA not only effectively inhibited the expressions of CTGF gene, but quenched inflammation, and thwarted neuronal apoptosis and reactive astrocytes and glial scar formation. Besides, it significantly upregulated several neurotrophic factors and anti-inflammatory factors, acting as a facilitator of locomotor recovery of rats with spinal cord injury (SCI). CONCLUSIONS: In conclusion, this study has combined the thoroughness of gene therapy and the excellent drug-loading characteristics of Exo for the precise treatment of SCI, which will shed new light on the drug-loading field of Exo.
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spelling pubmed-81938952021-06-15 SiRNA in MSC-derived exosomes silences CTGF gene for locomotor recovery in spinal cord injury rats Huang, Wei Qu, Mingjia Li, Lu Liu, Tao Lin, Miaoman Yu, Xiaobing Stem Cell Res Ther Research BACKGROUND: How to obtain a small interfering RNA (siRNA) vector has become a moot point in recent years. Exosomes (Exo) show advantages of long survival time in vivo, high transmission efficiency, and easy penetration across the blood-spinal cord barrier, renowned as excellent carriers of bioactive substances. METHODS: We applied mesenchymal stem cell (MSC)-derived exosomes as the delivery of synthesized siRNA, which were extracted from rat bone marrow. We constructed exosomes-siRNA (Exo-siRNA) that could specifically silence CTGF gene in the injury sites by electroporation. During the administration, we injected Exo-siRNA into the tail vein of SCI rats, RESULTS: In vivo and in vitro experiments showed that Exo-siRNA not only effectively inhibited the expressions of CTGF gene, but quenched inflammation, and thwarted neuronal apoptosis and reactive astrocytes and glial scar formation. Besides, it significantly upregulated several neurotrophic factors and anti-inflammatory factors, acting as a facilitator of locomotor recovery of rats with spinal cord injury (SCI). CONCLUSIONS: In conclusion, this study has combined the thoroughness of gene therapy and the excellent drug-loading characteristics of Exo for the precise treatment of SCI, which will shed new light on the drug-loading field of Exo. BioMed Central 2021-06-10 /pmc/articles/PMC8193895/ /pubmed/34112262 http://dx.doi.org/10.1186/s13287-021-02401-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (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
Huang, Wei
Qu, Mingjia
Li, Lu
Liu, Tao
Lin, Miaoman
Yu, Xiaobing
SiRNA in MSC-derived exosomes silences CTGF gene for locomotor recovery in spinal cord injury rats
title SiRNA in MSC-derived exosomes silences CTGF gene for locomotor recovery in spinal cord injury rats
title_full SiRNA in MSC-derived exosomes silences CTGF gene for locomotor recovery in spinal cord injury rats
title_fullStr SiRNA in MSC-derived exosomes silences CTGF gene for locomotor recovery in spinal cord injury rats
title_full_unstemmed SiRNA in MSC-derived exosomes silences CTGF gene for locomotor recovery in spinal cord injury rats
title_short SiRNA in MSC-derived exosomes silences CTGF gene for locomotor recovery in spinal cord injury rats
title_sort sirna in msc-derived exosomes silences ctgf gene for locomotor recovery in spinal cord injury rats
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8193895/
https://www.ncbi.nlm.nih.gov/pubmed/34112262
http://dx.doi.org/10.1186/s13287-021-02401-x
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