Literature DB >> 34353368

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

Takahito Moriwaki1, Akari Yoshimura2, Yuki Tamari3, Hiroyuki Sasanuma4, Shunichi Takeda4, Masayuki Seki2, Keizo Tano5.   

Abstract

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.
© 2021. The Author(s).

Entities:  

Year:  2021        PMID: 34353368     DOI: 10.1186/s41021-021-00211-4

Source DB:  PubMed          Journal:  Genes Environ        ISSN: 1880-7046


  22 in total

Review 1.  Peroxiredoxin, a novel family of peroxidases.

Authors:  S G Rhee; S W Kang; T S Chang; W Jeong; K Kim
Journal:  IUBMB Life       Date:  2001-07       Impact factor: 3.885

Review 2.  Evolution of the peroxiredoxins.

Authors:  Bernard Knoops; Eléonore Loumaye; Valérie Van Der Eecken
Journal:  Subcell Biochem       Date:  2007

3.  Crystal structure of a multifunctional 2-Cys peroxiredoxin heme-binding protein 23 kDa/proliferation-associated gene product.

Authors:  S Hirotsu; Y Abe; K Okada; N Nagahara; H Hori; T Nishino; T Hakoshima
Journal:  Proc Natl Acad Sci U S A       Date:  1999-10-26       Impact factor: 11.205

4.  Regulation of reactive oxygen species, DNA damage, and c-Myc function by peroxiredoxin 1.

Authors:  Rachel A Egler; Elaine Fernandes; Kristi Rothermund; Susan Sereika; Nadja de Souza-Pinto; Pawel Jaruga; Miral Dizdaroglu; Edward V Prochownik
Journal:  Oncogene       Date:  2005-12-01       Impact factor: 9.867

5.  Characterization of three isoforms of mammalian peroxiredoxin that reduce peroxides in the presence of thioredoxin.

Authors:  H Z Chae; H J Kim; S W Kang; S G Rhee
Journal:  Diabetes Res Clin Pract       Date:  1999-09       Impact factor: 5.602

Review 6.  Intracellular messenger function of hydrogen peroxide and its regulation by peroxiredoxins.

Authors:  Sue Goo Rhee; Sang Won Kang; Woojin Jeong; Tong-Shin Chang; Kap-Seok Yang; Hyun Ae Woo
Journal:  Curr Opin Cell Biol       Date:  2005-04       Impact factor: 8.382

Review 7.  Structure-based insights into the catalytic power and conformational dexterity of peroxiredoxins.

Authors:  Andrea Hall; Kimberly Nelson; Leslie B Poole; P Andrew Karplus
Journal:  Antioxid Redox Signal       Date:  2011-04-20       Impact factor: 8.401

8.  Essential role for the peroxiredoxin Prdx1 in erythrocyte antioxidant defence and tumour suppression.

Authors:  Carola A Neumann; Daniela S Krause; Christopher V Carman; Shampa Das; Devendra P Dubey; Jennifer L Abraham; Roderick T Bronson; Yuko Fujiwara; Stuart H Orkin; Richard A Van Etten
Journal:  Nature       Date:  2003-07-31       Impact factor: 49.962

Review 9.  Structure, mechanism and regulation of peroxiredoxins.

Authors:  Zachary A Wood; Ewald Schröder; J Robin Harris; Leslie B Poole
Journal:  Trends Biochem Sci       Date:  2003-01       Impact factor: 13.807

10.  The peroxidase PRDX1 inhibits the activated phenotype in mammary fibroblasts through regulating c-Jun N-terminal kinases.

Authors:  Agnieszka Jezierska-Drutel; Shireen Attaran; Barbara L Hopkins; John J Skoko; Steven A Rosenzweig; Carola A Neumann
Journal:  BMC Cancer       Date:  2019-08-16       Impact factor: 4.430

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.