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RNA Sequencing of Human Peripheral Blood Cells Indicates Upregulation of Immune-Related Genes in Huntington's Disease

Huntington's disease (HD) is an autosomal dominantly inherited neurodegenerative disorder caused by a trinucleotide repeat expansion in the Huntingtin gene. As disease-modifying therapies for HD are being developed, peripheral blood cells may be used to indicate disease progression and to monit...

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Autores principales: Andrade-Navarro, Miguel A., Mühlenberg, Katja, Spruth, Eike J., Mah, Nancy, González-López, Adrián, Andreani, Tommaso, Russ, Jenny, Huska, Matthew R., Muro, Enrique M., Fontaine, Jean-Fred, Amstislavskiy, Vyacheslav, Soldatov, Alexei, Nietfeld, Wilfried, Wanker, Erich E., Priller, Josef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7731869/
https://www.ncbi.nlm.nih.gov/pubmed/33329316
http://dx.doi.org/10.3389/fneur.2020.573560
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author Andrade-Navarro, Miguel A.
Mühlenberg, Katja
Spruth, Eike J.
Mah, Nancy
González-López, Adrián
Andreani, Tommaso
Russ, Jenny
Huska, Matthew R.
Muro, Enrique M.
Fontaine, Jean-Fred
Amstislavskiy, Vyacheslav
Soldatov, Alexei
Nietfeld, Wilfried
Wanker, Erich E.
Priller, Josef
author_facet Andrade-Navarro, Miguel A.
Mühlenberg, Katja
Spruth, Eike J.
Mah, Nancy
González-López, Adrián
Andreani, Tommaso
Russ, Jenny
Huska, Matthew R.
Muro, Enrique M.
Fontaine, Jean-Fred
Amstislavskiy, Vyacheslav
Soldatov, Alexei
Nietfeld, Wilfried
Wanker, Erich E.
Priller, Josef
author_sort Andrade-Navarro, Miguel A.
collection PubMed
description Huntington's disease (HD) is an autosomal dominantly inherited neurodegenerative disorder caused by a trinucleotide repeat expansion in the Huntingtin gene. As disease-modifying therapies for HD are being developed, peripheral blood cells may be used to indicate disease progression and to monitor treatment response. In order to investigate whether gene expression changes can be found in the blood of individuals with HD that distinguish them from healthy controls, we performed transcriptome analysis by next-generation sequencing (RNA-seq). We detected a gene expression signature consistent with dysregulation of immune-related functions and inflammatory response in peripheral blood from HD cases vs. controls, including induction of the interferon response genes, IFITM3, IFI6 and IRF7. Our results suggest that it is possible to detect gene expression changes in blood samples from individuals with HD, which may reflect the immune pathology associated with the disease.
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spelling pubmed-77318692020-12-15 RNA Sequencing of Human Peripheral Blood Cells Indicates Upregulation of Immune-Related Genes in Huntington's Disease Andrade-Navarro, Miguel A. Mühlenberg, Katja Spruth, Eike J. Mah, Nancy González-López, Adrián Andreani, Tommaso Russ, Jenny Huska, Matthew R. Muro, Enrique M. Fontaine, Jean-Fred Amstislavskiy, Vyacheslav Soldatov, Alexei Nietfeld, Wilfried Wanker, Erich E. Priller, Josef Front Neurol Neurology Huntington's disease (HD) is an autosomal dominantly inherited neurodegenerative disorder caused by a trinucleotide repeat expansion in the Huntingtin gene. As disease-modifying therapies for HD are being developed, peripheral blood cells may be used to indicate disease progression and to monitor treatment response. In order to investigate whether gene expression changes can be found in the blood of individuals with HD that distinguish them from healthy controls, we performed transcriptome analysis by next-generation sequencing (RNA-seq). We detected a gene expression signature consistent with dysregulation of immune-related functions and inflammatory response in peripheral blood from HD cases vs. controls, including induction of the interferon response genes, IFITM3, IFI6 and IRF7. Our results suggest that it is possible to detect gene expression changes in blood samples from individuals with HD, which may reflect the immune pathology associated with the disease. Frontiers Media S.A. 2020-11-27 /pmc/articles/PMC7731869/ /pubmed/33329316 http://dx.doi.org/10.3389/fneur.2020.573560 Text en Copyright © 2020 Andrade-Navarro, Mühlenberg, Spruth, Mah, González-López, Andreani, Russ, Huska, Muro, Fontaine, Amstislavskiy, Soldatov, Nietfeld, Wanker and Priller. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Andrade-Navarro, Miguel A.
Mühlenberg, Katja
Spruth, Eike J.
Mah, Nancy
González-López, Adrián
Andreani, Tommaso
Russ, Jenny
Huska, Matthew R.
Muro, Enrique M.
Fontaine, Jean-Fred
Amstislavskiy, Vyacheslav
Soldatov, Alexei
Nietfeld, Wilfried
Wanker, Erich E.
Priller, Josef
RNA Sequencing of Human Peripheral Blood Cells Indicates Upregulation of Immune-Related Genes in Huntington's Disease
title RNA Sequencing of Human Peripheral Blood Cells Indicates Upregulation of Immune-Related Genes in Huntington's Disease
title_full RNA Sequencing of Human Peripheral Blood Cells Indicates Upregulation of Immune-Related Genes in Huntington's Disease
title_fullStr RNA Sequencing of Human Peripheral Blood Cells Indicates Upregulation of Immune-Related Genes in Huntington's Disease
title_full_unstemmed RNA Sequencing of Human Peripheral Blood Cells Indicates Upregulation of Immune-Related Genes in Huntington's Disease
title_short RNA Sequencing of Human Peripheral Blood Cells Indicates Upregulation of Immune-Related Genes in Huntington's Disease
title_sort rna sequencing of human peripheral blood cells indicates upregulation of immune-related genes in huntington's disease
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7731869/
https://www.ncbi.nlm.nih.gov/pubmed/33329316
http://dx.doi.org/10.3389/fneur.2020.573560
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