Overexpression of catalase in mitochondria mitigates changes in hippocampal cytokine expression following simulated microgravity and isolation

Abstract Isolation on Earth can alter physiology and signaling of organs systems, including the central nervous system. Although not in complete solitude, astronauts operate in an isolated environment during spaceflight. In this study, we determined the effects of isolation and simulated microgravit...

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Autores principales: Linda Rubinstein, Ann-Sofie Schreurs, Samantha M. Torres, Sonette Steczina, Moniece G. Lowe, Frederico Kiffer, Antiño R. Allen, April E. Ronca, Marianne B. Sowa, Ruth K. Globus, Candice G. T. Tahimic
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/3e9da7ae8c2a4834b6f11f00fed4c348
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spelling oai:doaj.org-article:3e9da7ae8c2a4834b6f11f00fed4c3482021-12-02T15:39:42ZOverexpression of catalase in mitochondria mitigates changes in hippocampal cytokine expression following simulated microgravity and isolation10.1038/s41526-021-00152-w2373-8065https://doaj.org/article/3e9da7ae8c2a4834b6f11f00fed4c3482021-07-01T00:00:00Zhttps://doi.org/10.1038/s41526-021-00152-whttps://doaj.org/toc/2373-8065Abstract Isolation on Earth can alter physiology and signaling of organs systems, including the central nervous system. Although not in complete solitude, astronauts operate in an isolated environment during spaceflight. In this study, we determined the effects of isolation and simulated microgravity solely or combined, on the inflammatory cytokine milieu of the hippocampus. Adult female wild-type mice underwent simulated microgravity by hindlimb unloading for 30 days in single or social (paired) housing. In hippocampus, simulated microgravity and isolation each regulate a discrete repertoire of cytokines associated with inflammation. Their combined effects are not additive. A model for mitochondrial reactive oxygen species (ROS) quenching via targeted overexpression of the human catalase gene to the mitochondria (MCAT mice), are protected from isolation- and/or simulated microgravity-induced changes in cytokine expression. These findings suggest a key role for mitochondrial ROS signaling in neuroinflammatory responses to spaceflight and prolonged bedrest, isolation, and confinement on Earth.Linda RubinsteinAnn-Sofie SchreursSamantha M. TorresSonette SteczinaMoniece G. LoweFrederico KifferAntiño R. AllenApril E. RoncaMarianne B. SowaRuth K. GlobusCandice G. T. TahimicNature PortfolioarticleBiotechnologyTP248.13-248.65PhysiologyQP1-981ENnpj Microgravity, Vol 7, Iss 1, Pp 1-9 (2021)
institution DOAJ
collection DOAJ
language EN
topic Biotechnology
TP248.13-248.65
Physiology
QP1-981
spellingShingle Biotechnology
TP248.13-248.65
Physiology
QP1-981
Linda Rubinstein
Ann-Sofie Schreurs
Samantha M. Torres
Sonette Steczina
Moniece G. Lowe
Frederico Kiffer
Antiño R. Allen
April E. Ronca
Marianne B. Sowa
Ruth K. Globus
Candice G. T. Tahimic
Overexpression of catalase in mitochondria mitigates changes in hippocampal cytokine expression following simulated microgravity and isolation
description Abstract Isolation on Earth can alter physiology and signaling of organs systems, including the central nervous system. Although not in complete solitude, astronauts operate in an isolated environment during spaceflight. In this study, we determined the effects of isolation and simulated microgravity solely or combined, on the inflammatory cytokine milieu of the hippocampus. Adult female wild-type mice underwent simulated microgravity by hindlimb unloading for 30 days in single or social (paired) housing. In hippocampus, simulated microgravity and isolation each regulate a discrete repertoire of cytokines associated with inflammation. Their combined effects are not additive. A model for mitochondrial reactive oxygen species (ROS) quenching via targeted overexpression of the human catalase gene to the mitochondria (MCAT mice), are protected from isolation- and/or simulated microgravity-induced changes in cytokine expression. These findings suggest a key role for mitochondrial ROS signaling in neuroinflammatory responses to spaceflight and prolonged bedrest, isolation, and confinement on Earth.
format article
author Linda Rubinstein
Ann-Sofie Schreurs
Samantha M. Torres
Sonette Steczina
Moniece G. Lowe
Frederico Kiffer
Antiño R. Allen
April E. Ronca
Marianne B. Sowa
Ruth K. Globus
Candice G. T. Tahimic
author_facet Linda Rubinstein
Ann-Sofie Schreurs
Samantha M. Torres
Sonette Steczina
Moniece G. Lowe
Frederico Kiffer
Antiño R. Allen
April E. Ronca
Marianne B. Sowa
Ruth K. Globus
Candice G. T. Tahimic
author_sort Linda Rubinstein
title Overexpression of catalase in mitochondria mitigates changes in hippocampal cytokine expression following simulated microgravity and isolation
title_short Overexpression of catalase in mitochondria mitigates changes in hippocampal cytokine expression following simulated microgravity and isolation
title_full Overexpression of catalase in mitochondria mitigates changes in hippocampal cytokine expression following simulated microgravity and isolation
title_fullStr Overexpression of catalase in mitochondria mitigates changes in hippocampal cytokine expression following simulated microgravity and isolation
title_full_unstemmed Overexpression of catalase in mitochondria mitigates changes in hippocampal cytokine expression following simulated microgravity and isolation
title_sort overexpression of catalase in mitochondria mitigates changes in hippocampal cytokine expression following simulated microgravity and isolation
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/3e9da7ae8c2a4834b6f11f00fed4c348
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