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Bakshi, M.V. ; Azimzadeh, O. ; Barjaktarovic, Z. ; Kempf, S.J. ; Merl-Pham, J. ; Hauck, S.M. ; Buratovic, S.* ; Eriksson, P.* ; Atkinson, M.J. ; Tapio, S.

Total body exposure to low-dose ionizing radiation induces long-term alterations to the liver proteome of neonatally exposed mice.

J. Proteome Res. 14, 366-373 (2015)
Postprint DOI PMC
Open Access Green
Tens of thousands of people are being exposed daily to environmental low-dose gamma radiation. Epidemiological data indicate that such low radiation doses may negatively affect liver function and result in the development of liver disease. However, the biological mechanisms behind these adverse effects are unknown. The aim of this study was to investigate radiation-induced damage in the liver after low radiation doses. Neonatal male NMRI mice were exposed to total body irradiation on postnatal day 10 using acute single doses ranging from 0.02 to 1.0 Gy. Early (1 day) and late (7 months) changes in the liver proteome were tracked using isotope-coded protein label technology and quantitative mass spectrometry. Our data indicate that low and moderate radiation doses induce an immediate inhibition of the glycolysis pathway and pyruvate dehydrogenase availability in the liver. Furthermore, they lead to significant long-term alterations in lipid metabolism and increased liver inflammation accompanying inactivation of the transcription factor peroxisome proliferator-activated receptor alpha. This study contributes to the understanding of the potential risk of liver damage in populations environmentally exposed to ionizing radiation.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Icpl ; Liver ; Low-dose Ionizing Radiation ; Metabolic Crosstalk ; Ppar Alpha ; Proteomics; Peroxisome Proliferator; Ppar-alpha; Hepatocellular Carcinomas; Mitochondrial Dysfunction; Solid Tumors; Mouse-liver; Gamma-rays; Label-free; Heart; Rat
ISSN (print) / ISBN 1535-3893
e-ISSN 1535-3907
Zeitschrift Journal of Proteome Research
Quellenangaben Band: 14, Heft: 1, Seiten: 366-373 Artikelnummer: , Supplement: ,
Verlag American Chemical Society (ACS)
Verlagsort Washington
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Radiation Biology (ISB)
CF Metabolomics & Proteomics (CF-MPC)