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A novel animal model for neuroinflammation and white matter degeneration

Small interference RNA has been widely used to suppress gene expression. Three different short hairpin RNAs (shRNAs) against dopamine D1 receptor (Drd1), driven by mouse U6 promoter in self-complementary AAV8 vector (scAAV8), were used to silence mouse striatal Drd1 expression. Transduction of mouse...

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Detalles Bibliográficos
Autores principales: Ji, Baohu, Higa, Kerin, Soontornniyomkij, Virawudh, Miyanohara, Atsushi, Zhou, Xianjin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5669272/
https://www.ncbi.nlm.nih.gov/pubmed/29104820
http://dx.doi.org/10.7717/peerj.3905
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author Ji, Baohu
Higa, Kerin
Soontornniyomkij, Virawudh
Miyanohara, Atsushi
Zhou, Xianjin
author_facet Ji, Baohu
Higa, Kerin
Soontornniyomkij, Virawudh
Miyanohara, Atsushi
Zhou, Xianjin
author_sort Ji, Baohu
collection PubMed
description Small interference RNA has been widely used to suppress gene expression. Three different short hairpin RNAs (shRNAs) against dopamine D1 receptor (Drd1), driven by mouse U6 promoter in self-complementary AAV8 vector (scAAV8), were used to silence mouse striatal Drd1 expression. Transduction of mouse striatum with all three scAAV8-D1shRNA viruses, but not the control scAAV8 virus, causes extensive neuroinflammation, demyelination, and axon degeneration. RNA interference is known to be coupled to the innate immune system as a host cell defense against virus infection. Activation of the innate immune system may play a causal role in the development of neuroinflammation and white matter degeneration, providing a novel animal model for multiple sclerosis (MS) and other neuroinflammatory diseases.
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spelling pubmed-56692722017-11-03 A novel animal model for neuroinflammation and white matter degeneration Ji, Baohu Higa, Kerin Soontornniyomkij, Virawudh Miyanohara, Atsushi Zhou, Xianjin PeerJ Neuroscience Small interference RNA has been widely used to suppress gene expression. Three different short hairpin RNAs (shRNAs) against dopamine D1 receptor (Drd1), driven by mouse U6 promoter in self-complementary AAV8 vector (scAAV8), were used to silence mouse striatal Drd1 expression. Transduction of mouse striatum with all three scAAV8-D1shRNA viruses, but not the control scAAV8 virus, causes extensive neuroinflammation, demyelination, and axon degeneration. RNA interference is known to be coupled to the innate immune system as a host cell defense against virus infection. Activation of the innate immune system may play a causal role in the development of neuroinflammation and white matter degeneration, providing a novel animal model for multiple sclerosis (MS) and other neuroinflammatory diseases. PeerJ Inc. 2017-10-31 /pmc/articles/PMC5669272/ /pubmed/29104820 http://dx.doi.org/10.7717/peerj.3905 Text en ©2017 Ji et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Neuroscience
Ji, Baohu
Higa, Kerin
Soontornniyomkij, Virawudh
Miyanohara, Atsushi
Zhou, Xianjin
A novel animal model for neuroinflammation and white matter degeneration
title A novel animal model for neuroinflammation and white matter degeneration
title_full A novel animal model for neuroinflammation and white matter degeneration
title_fullStr A novel animal model for neuroinflammation and white matter degeneration
title_full_unstemmed A novel animal model for neuroinflammation and white matter degeneration
title_short A novel animal model for neuroinflammation and white matter degeneration
title_sort novel animal model for neuroinflammation and white matter degeneration
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5669272/
https://www.ncbi.nlm.nih.gov/pubmed/29104820
http://dx.doi.org/10.7717/peerj.3905
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