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PRDX1 is essential for the viability and maintenance of reactive oxygen species in chicken DT40

BACKGROUND: Peroxiredoxin 1 (PRDX1) is a member of a ubiquitous family of thiol peroxidases that catalyze the reduction of peroxides, including hydrogen peroxide. It functions as an antioxidant enzyme, similar to catalase and glutathione peroxidase. PRDX1 was recently shown act as a sensor of reacti...

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Autores principales: Moriwaki, Takahito, Yoshimura, Akari, Tamari, Yuki, Sasanuma, Hiroyuki, Takeda, Shunichi, Seki, Masayuki, Tano, Keizo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8340460/
https://www.ncbi.nlm.nih.gov/pubmed/34353368
http://dx.doi.org/10.1186/s41021-021-00211-4
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author Moriwaki, Takahito
Yoshimura, Akari
Tamari, Yuki
Sasanuma, Hiroyuki
Takeda, Shunichi
Seki, Masayuki
Tano, Keizo
author_facet Moriwaki, Takahito
Yoshimura, Akari
Tamari, Yuki
Sasanuma, Hiroyuki
Takeda, Shunichi
Seki, Masayuki
Tano, Keizo
author_sort Moriwaki, Takahito
collection PubMed
description BACKGROUND: Peroxiredoxin 1 (PRDX1) is a member of a ubiquitous family of thiol peroxidases that catalyze the reduction of peroxides, including hydrogen peroxide. It functions as an antioxidant enzyme, similar to catalase and glutathione peroxidase. PRDX1 was recently shown act as a sensor of reactive oxygen species (ROS) and play a role in ROS-dependent intracellular signaling pathways. To investigate its physiological functions, PRDX1 was conditionally disrupted in chicken DT40 cells in the present study. RESULTS: The depletion of PRDX1 resulted in cell death with increased levels of intracellular ROS. PRDX1-depleted cells did not show the accumulation of chromosomal breaks or sister chromatid exchange (SCE). These results suggest that cell death in PRDX1-depleted cells was not due to DNA damage. 2-Mercaptoethanol protected against cell death in PRDX1-depleted cells and also suppressed elevations in ROS. CONCLUSIONS: PRDX1 is essential in chicken DT40 cells and plays an important role in maintaining intracellular ROS homeostasis (or in the fine-tuning of cellular ROS levels). Cells deficient in PRDX1 may be used as an endogenously deregulated ROS model to elucidate the physiological roles of ROS in maintaining proper cell growth.
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spelling pubmed-83404602021-08-06 PRDX1 is essential for the viability and maintenance of reactive oxygen species in chicken DT40 Moriwaki, Takahito Yoshimura, Akari Tamari, Yuki Sasanuma, Hiroyuki Takeda, Shunichi Seki, Masayuki Tano, Keizo Genes Environ Research BACKGROUND: Peroxiredoxin 1 (PRDX1) is a member of a ubiquitous family of thiol peroxidases that catalyze the reduction of peroxides, including hydrogen peroxide. It functions as an antioxidant enzyme, similar to catalase and glutathione peroxidase. PRDX1 was recently shown act as a sensor of reactive oxygen species (ROS) and play a role in ROS-dependent intracellular signaling pathways. To investigate its physiological functions, PRDX1 was conditionally disrupted in chicken DT40 cells in the present study. RESULTS: The depletion of PRDX1 resulted in cell death with increased levels of intracellular ROS. PRDX1-depleted cells did not show the accumulation of chromosomal breaks or sister chromatid exchange (SCE). These results suggest that cell death in PRDX1-depleted cells was not due to DNA damage. 2-Mercaptoethanol protected against cell death in PRDX1-depleted cells and also suppressed elevations in ROS. CONCLUSIONS: PRDX1 is essential in chicken DT40 cells and plays an important role in maintaining intracellular ROS homeostasis (or in the fine-tuning of cellular ROS levels). Cells deficient in PRDX1 may be used as an endogenously deregulated ROS model to elucidate the physiological roles of ROS in maintaining proper cell growth. BioMed Central 2021-08-05 /pmc/articles/PMC8340460/ /pubmed/34353368 http://dx.doi.org/10.1186/s41021-021-00211-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Moriwaki, Takahito
Yoshimura, Akari
Tamari, Yuki
Sasanuma, Hiroyuki
Takeda, Shunichi
Seki, Masayuki
Tano, Keizo
PRDX1 is essential for the viability and maintenance of reactive oxygen species in chicken DT40
title PRDX1 is essential for the viability and maintenance of reactive oxygen species in chicken DT40
title_full PRDX1 is essential for the viability and maintenance of reactive oxygen species in chicken DT40
title_fullStr PRDX1 is essential for the viability and maintenance of reactive oxygen species in chicken DT40
title_full_unstemmed PRDX1 is essential for the viability and maintenance of reactive oxygen species in chicken DT40
title_short PRDX1 is essential for the viability and maintenance of reactive oxygen species in chicken DT40
title_sort prdx1 is essential for the viability and maintenance of reactive oxygen species in chicken dt40
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8340460/
https://www.ncbi.nlm.nih.gov/pubmed/34353368
http://dx.doi.org/10.1186/s41021-021-00211-4
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