Radiation-induced signaling results in mitochondrial impairment in mouse heart at 4 weeks after exposure to X-rays.

<h4>Background</h4>Radiation therapy treatment of breast cancer, Hodgkin's disease or childhood cancers expose the heart to high local radiation doses, causing an increased risk of cardiovascular disease in the survivors decades after the treatment. The mechanisms that underlie the...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Zarko Barjaktarovic, Dominik Schmaltz, Alena Shyla, Omid Azimzadeh, Sabine Schulz, Julia Haagen, Wolfgang Dörr, Hakan Sarioglu, Alexander Schäfer, Michael J Atkinson, Hans Zischka, Soile Tapio
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2011
Materias:
R
Q
Acceso en línea:https://doaj.org/article/8c87f624a23c4ce1bbf2eb43fadcbd47
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:8c87f624a23c4ce1bbf2eb43fadcbd47
record_format dspace
spelling oai:doaj.org-article:8c87f624a23c4ce1bbf2eb43fadcbd472021-11-18T07:32:46ZRadiation-induced signaling results in mitochondrial impairment in mouse heart at 4 weeks after exposure to X-rays.1932-620310.1371/journal.pone.0027811https://doaj.org/article/8c87f624a23c4ce1bbf2eb43fadcbd472011-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22174747/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>Radiation therapy treatment of breast cancer, Hodgkin's disease or childhood cancers expose the heart to high local radiation doses, causing an increased risk of cardiovascular disease in the survivors decades after the treatment. The mechanisms that underlie the radiation damage remain poorly understood so far. Previous data show that impairment of mitochondrial oxidative metabolism is directly linked to the development of cardiovascular disease.<h4>Methodology/principal findings</h4>In this study, the radiation-induced in vivo effects on cardiac mitochondrial proteome and function were investigated. C57BL/6N mice were exposed to local irradiation of the heart with doses of 0.2 Gy or 2 Gy (X-ray, 200 kV) at the age of eight weeks, the control mice were sham-irradiated. After four weeks the cardiac mitochondria were isolated and tested for proteomic and functional alterations. Two complementary proteomics approaches using both peptide and protein quantification strategies showed radiation-induced deregulation of 25 proteins in total. Three main biological categories were affected: the oxidative phophorylation, the pyruvate metabolism, and the cytoskeletal structure. The mitochondria exposed to high-dose irradiation showed functional impairment reflected as partial deactivation of Complex I (32%) and Complex III (11%), decreased succinate-driven respiratory capacity (13%), increased level of reactive oxygen species and enhanced oxidation of mitochondrial proteins. The changes in the pyruvate metabolism and structural proteins were seen with both low and high radiation doses.<h4>Conclusion/significance</h4>This is the first study showing the biological alterations in the murine heart mitochondria several weeks after the exposure to low- and high-dose of ionizing radiation. Our results show that doses, equivalent to a single dose in radiotherapy, cause long-lasting changes in mitochondrial oxidative metabolism and mitochondria-associated cytoskeleton. This prompts us to propose that these first pathological changes lead to an increased risk of cardiovascular disease after radiation exposure.Zarko BarjaktarovicDominik SchmaltzAlena ShylaOmid AzimzadehSabine SchulzJulia HaagenWolfgang DörrHakan SariogluAlexander SchäferMichael J AtkinsonHans ZischkaSoile TapioPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 6, Iss 12, p e27811 (2011)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Zarko Barjaktarovic
Dominik Schmaltz
Alena Shyla
Omid Azimzadeh
Sabine Schulz
Julia Haagen
Wolfgang Dörr
Hakan Sarioglu
Alexander Schäfer
Michael J Atkinson
Hans Zischka
Soile Tapio
Radiation-induced signaling results in mitochondrial impairment in mouse heart at 4 weeks after exposure to X-rays.
description <h4>Background</h4>Radiation therapy treatment of breast cancer, Hodgkin's disease or childhood cancers expose the heart to high local radiation doses, causing an increased risk of cardiovascular disease in the survivors decades after the treatment. The mechanisms that underlie the radiation damage remain poorly understood so far. Previous data show that impairment of mitochondrial oxidative metabolism is directly linked to the development of cardiovascular disease.<h4>Methodology/principal findings</h4>In this study, the radiation-induced in vivo effects on cardiac mitochondrial proteome and function were investigated. C57BL/6N mice were exposed to local irradiation of the heart with doses of 0.2 Gy or 2 Gy (X-ray, 200 kV) at the age of eight weeks, the control mice were sham-irradiated. After four weeks the cardiac mitochondria were isolated and tested for proteomic and functional alterations. Two complementary proteomics approaches using both peptide and protein quantification strategies showed radiation-induced deregulation of 25 proteins in total. Three main biological categories were affected: the oxidative phophorylation, the pyruvate metabolism, and the cytoskeletal structure. The mitochondria exposed to high-dose irradiation showed functional impairment reflected as partial deactivation of Complex I (32%) and Complex III (11%), decreased succinate-driven respiratory capacity (13%), increased level of reactive oxygen species and enhanced oxidation of mitochondrial proteins. The changes in the pyruvate metabolism and structural proteins were seen with both low and high radiation doses.<h4>Conclusion/significance</h4>This is the first study showing the biological alterations in the murine heart mitochondria several weeks after the exposure to low- and high-dose of ionizing radiation. Our results show that doses, equivalent to a single dose in radiotherapy, cause long-lasting changes in mitochondrial oxidative metabolism and mitochondria-associated cytoskeleton. This prompts us to propose that these first pathological changes lead to an increased risk of cardiovascular disease after radiation exposure.
format article
author Zarko Barjaktarovic
Dominik Schmaltz
Alena Shyla
Omid Azimzadeh
Sabine Schulz
Julia Haagen
Wolfgang Dörr
Hakan Sarioglu
Alexander Schäfer
Michael J Atkinson
Hans Zischka
Soile Tapio
author_facet Zarko Barjaktarovic
Dominik Schmaltz
Alena Shyla
Omid Azimzadeh
Sabine Schulz
Julia Haagen
Wolfgang Dörr
Hakan Sarioglu
Alexander Schäfer
Michael J Atkinson
Hans Zischka
Soile Tapio
author_sort Zarko Barjaktarovic
title Radiation-induced signaling results in mitochondrial impairment in mouse heart at 4 weeks after exposure to X-rays.
title_short Radiation-induced signaling results in mitochondrial impairment in mouse heart at 4 weeks after exposure to X-rays.
title_full Radiation-induced signaling results in mitochondrial impairment in mouse heart at 4 weeks after exposure to X-rays.
title_fullStr Radiation-induced signaling results in mitochondrial impairment in mouse heart at 4 weeks after exposure to X-rays.
title_full_unstemmed Radiation-induced signaling results in mitochondrial impairment in mouse heart at 4 weeks after exposure to X-rays.
title_sort radiation-induced signaling results in mitochondrial impairment in mouse heart at 4 weeks after exposure to x-rays.
publisher Public Library of Science (PLoS)
publishDate 2011
url https://doaj.org/article/8c87f624a23c4ce1bbf2eb43fadcbd47
work_keys_str_mv AT zarkobarjaktarovic radiationinducedsignalingresultsinmitochondrialimpairmentinmouseheartat4weeksafterexposuretoxrays
AT dominikschmaltz radiationinducedsignalingresultsinmitochondrialimpairmentinmouseheartat4weeksafterexposuretoxrays
AT alenashyla radiationinducedsignalingresultsinmitochondrialimpairmentinmouseheartat4weeksafterexposuretoxrays
AT omidazimzadeh radiationinducedsignalingresultsinmitochondrialimpairmentinmouseheartat4weeksafterexposuretoxrays
AT sabineschulz radiationinducedsignalingresultsinmitochondrialimpairmentinmouseheartat4weeksafterexposuretoxrays
AT juliahaagen radiationinducedsignalingresultsinmitochondrialimpairmentinmouseheartat4weeksafterexposuretoxrays
AT wolfgangdorr radiationinducedsignalingresultsinmitochondrialimpairmentinmouseheartat4weeksafterexposuretoxrays
AT hakansarioglu radiationinducedsignalingresultsinmitochondrialimpairmentinmouseheartat4weeksafterexposuretoxrays
AT alexanderschafer radiationinducedsignalingresultsinmitochondrialimpairmentinmouseheartat4weeksafterexposuretoxrays
AT michaeljatkinson radiationinducedsignalingresultsinmitochondrialimpairmentinmouseheartat4weeksafterexposuretoxrays
AT hanszischka radiationinducedsignalingresultsinmitochondrialimpairmentinmouseheartat4weeksafterexposuretoxrays
AT soiletapio radiationinducedsignalingresultsinmitochondrialimpairmentinmouseheartat4weeksafterexposuretoxrays
_version_ 1718423299248095232