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Mechanisms for Interferon-α-Induced Depression and Neural Stem Cell Dysfunction
New neurons generated by the neural stem cells (NSCs) in the adult hippocampus play an important role in emotional regulation and respond to the action of antidepressants. Depression is a common and serious side effect of interferon-α (IFN-α), which limits its use as an antiviral and antitumor drug....
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4110771/ https://www.ncbi.nlm.nih.gov/pubmed/25068123 http://dx.doi.org/10.1016/j.stemcr.2014.05.015 |
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author | Zheng, Lian-Shun Hitoshi, Seiji Kaneko, Naoko Takao, Keizo Miyakawa, Tsuyoshi Tanaka, Yasuhito Xia, Hongjing Kalinke, Ulrich Kudo, Koutaro Kanba, Shigenobu Ikenaka, Kazuhiro Sawamoto, Kazunobu |
author_facet | Zheng, Lian-Shun Hitoshi, Seiji Kaneko, Naoko Takao, Keizo Miyakawa, Tsuyoshi Tanaka, Yasuhito Xia, Hongjing Kalinke, Ulrich Kudo, Koutaro Kanba, Shigenobu Ikenaka, Kazuhiro Sawamoto, Kazunobu |
author_sort | Zheng, Lian-Shun |
collection | PubMed |
description | New neurons generated by the neural stem cells (NSCs) in the adult hippocampus play an important role in emotional regulation and respond to the action of antidepressants. Depression is a common and serious side effect of interferon-α (IFN-α), which limits its use as an antiviral and antitumor drug. However, the mechanism(s) underlying IFN-induced depression are largely unknown. Using a comprehensive battery of behavioral tests, we found that mice subjected to IFN-α treatment exhibited a depression-like phenotype. IFN-α directly suppressed NSC proliferation, resulting in the reduced generation of new neurons. Brain-specific mouse knockout of the IFN-α receptor prevented IFN-α-induced depressive behavioral phenotypes and the inhibition of neurogenesis, suggesting that IFN-α suppresses hippocampal neurogenesis and induces depression via its receptor in the brain. These findings provide insight for understanding the neuropathology underlying IFN-α-induced depression and for developing new strategies for the prevention and treatment of IFN-α-induced depressive effects. |
format | Online Article Text |
id | pubmed-4110771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-41107712014-07-25 Mechanisms for Interferon-α-Induced Depression and Neural Stem Cell Dysfunction Zheng, Lian-Shun Hitoshi, Seiji Kaneko, Naoko Takao, Keizo Miyakawa, Tsuyoshi Tanaka, Yasuhito Xia, Hongjing Kalinke, Ulrich Kudo, Koutaro Kanba, Shigenobu Ikenaka, Kazuhiro Sawamoto, Kazunobu Stem Cell Reports Article New neurons generated by the neural stem cells (NSCs) in the adult hippocampus play an important role in emotional regulation and respond to the action of antidepressants. Depression is a common and serious side effect of interferon-α (IFN-α), which limits its use as an antiviral and antitumor drug. However, the mechanism(s) underlying IFN-induced depression are largely unknown. Using a comprehensive battery of behavioral tests, we found that mice subjected to IFN-α treatment exhibited a depression-like phenotype. IFN-α directly suppressed NSC proliferation, resulting in the reduced generation of new neurons. Brain-specific mouse knockout of the IFN-α receptor prevented IFN-α-induced depressive behavioral phenotypes and the inhibition of neurogenesis, suggesting that IFN-α suppresses hippocampal neurogenesis and induces depression via its receptor in the brain. These findings provide insight for understanding the neuropathology underlying IFN-α-induced depression and for developing new strategies for the prevention and treatment of IFN-α-induced depressive effects. Elsevier 2014-06-26 /pmc/articles/PMC4110771/ /pubmed/25068123 http://dx.doi.org/10.1016/j.stemcr.2014.05.015 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/). |
spellingShingle | Article Zheng, Lian-Shun Hitoshi, Seiji Kaneko, Naoko Takao, Keizo Miyakawa, Tsuyoshi Tanaka, Yasuhito Xia, Hongjing Kalinke, Ulrich Kudo, Koutaro Kanba, Shigenobu Ikenaka, Kazuhiro Sawamoto, Kazunobu Mechanisms for Interferon-α-Induced Depression and Neural Stem Cell Dysfunction |
title | Mechanisms for Interferon-α-Induced Depression and Neural Stem Cell Dysfunction |
title_full | Mechanisms for Interferon-α-Induced Depression and Neural Stem Cell Dysfunction |
title_fullStr | Mechanisms for Interferon-α-Induced Depression and Neural Stem Cell Dysfunction |
title_full_unstemmed | Mechanisms for Interferon-α-Induced Depression and Neural Stem Cell Dysfunction |
title_short | Mechanisms for Interferon-α-Induced Depression and Neural Stem Cell Dysfunction |
title_sort | mechanisms for interferon-α-induced depression and neural stem cell dysfunction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4110771/ https://www.ncbi.nlm.nih.gov/pubmed/25068123 http://dx.doi.org/10.1016/j.stemcr.2014.05.015 |
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