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The brain targeted delivery of programmed cell death 4 specific siRNA protects mice from CRS-induced depressive behavior
Depression is one of the most common psychiatric disorders. Recently, studies demonstrate that antidepressants generating BDNF not only maintain synaptic signal transmission but also repress neuroinflammatory cytokines such as IL-6 and IL-1β. Therefore, promoting BDNF expression provides a strategy...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8590023/ https://www.ncbi.nlm.nih.gov/pubmed/34772918 http://dx.doi.org/10.1038/s41419-021-04361-9 |
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author | Jia, Yufeng Zhuang, Xiao Zhang, Yi Zhao, Ming Chen, Nuo Li, Wen Zhu, Faliang Guo, Chun Li, Yan Wang, Qun Li, Yuan Zhang, Lining |
author_facet | Jia, Yufeng Zhuang, Xiao Zhang, Yi Zhao, Ming Chen, Nuo Li, Wen Zhu, Faliang Guo, Chun Li, Yan Wang, Qun Li, Yuan Zhang, Lining |
author_sort | Jia, Yufeng |
collection | PubMed |
description | Depression is one of the most common psychiatric disorders. Recently, studies demonstrate that antidepressants generating BDNF not only maintain synaptic signal transmission but also repress neuroinflammatory cytokines such as IL-6 and IL-1β. Therefore, promoting BDNF expression provides a strategy for the treatment of depression. Our recent research has indicated that programmed cell death 4 (Pdcd4) is a new target for antidepressant treatment by facilitating BDNF. Herein, we modified Pdcd4 specific small interfering RNA (siPdcd4) with the rabies virus glycoprotein peptide (RVG/siPdcd4) which enables it cross the blood-brain barrier (BBB). We found that RVG/siPdcd4 complex was selectively delivered to neurons and microglia and silenced the expression of Pdcd4, thereby up-regulating the level of BDNF and down-regulating IL-6 and IL-1β expression. More importantly, RVG/siPdcd4 injection attenuated synaptic plasticity impairment and protected mice from CRS-induced depressive behavior. These findings suggest that RVG/siPdcd4 complex is a potential therapeutic medicine for depression. |
format | Online Article Text |
id | pubmed-8590023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85900232021-11-15 The brain targeted delivery of programmed cell death 4 specific siRNA protects mice from CRS-induced depressive behavior Jia, Yufeng Zhuang, Xiao Zhang, Yi Zhao, Ming Chen, Nuo Li, Wen Zhu, Faliang Guo, Chun Li, Yan Wang, Qun Li, Yuan Zhang, Lining Cell Death Dis Article Depression is one of the most common psychiatric disorders. Recently, studies demonstrate that antidepressants generating BDNF not only maintain synaptic signal transmission but also repress neuroinflammatory cytokines such as IL-6 and IL-1β. Therefore, promoting BDNF expression provides a strategy for the treatment of depression. Our recent research has indicated that programmed cell death 4 (Pdcd4) is a new target for antidepressant treatment by facilitating BDNF. Herein, we modified Pdcd4 specific small interfering RNA (siPdcd4) with the rabies virus glycoprotein peptide (RVG/siPdcd4) which enables it cross the blood-brain barrier (BBB). We found that RVG/siPdcd4 complex was selectively delivered to neurons and microglia and silenced the expression of Pdcd4, thereby up-regulating the level of BDNF and down-regulating IL-6 and IL-1β expression. More importantly, RVG/siPdcd4 injection attenuated synaptic plasticity impairment and protected mice from CRS-induced depressive behavior. These findings suggest that RVG/siPdcd4 complex is a potential therapeutic medicine for depression. Nature Publishing Group UK 2021-11-12 /pmc/articles/PMC8590023/ /pubmed/34772918 http://dx.doi.org/10.1038/s41419-021-04361-9 Text en © The Author(s) 2021 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Jia, Yufeng Zhuang, Xiao Zhang, Yi Zhao, Ming Chen, Nuo Li, Wen Zhu, Faliang Guo, Chun Li, Yan Wang, Qun Li, Yuan Zhang, Lining The brain targeted delivery of programmed cell death 4 specific siRNA protects mice from CRS-induced depressive behavior |
title | The brain targeted delivery of programmed cell death 4 specific siRNA protects mice from CRS-induced depressive behavior |
title_full | The brain targeted delivery of programmed cell death 4 specific siRNA protects mice from CRS-induced depressive behavior |
title_fullStr | The brain targeted delivery of programmed cell death 4 specific siRNA protects mice from CRS-induced depressive behavior |
title_full_unstemmed | The brain targeted delivery of programmed cell death 4 specific siRNA protects mice from CRS-induced depressive behavior |
title_short | The brain targeted delivery of programmed cell death 4 specific siRNA protects mice from CRS-induced depressive behavior |
title_sort | brain targeted delivery of programmed cell death 4 specific sirna protects mice from crs-induced depressive behavior |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8590023/ https://www.ncbi.nlm.nih.gov/pubmed/34772918 http://dx.doi.org/10.1038/s41419-021-04361-9 |
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