Cargando…

Phosphoproteomics Profiling of Human Skin Fibroblast Cells Reveals Pathways and Proteins Affected by Low Doses of Ionizing Radiation

BACKGROUND: High doses of ionizing radiation result in biological damage; however, the precise relationships between long-term health effects, including cancer, and low-dose exposures remain poorly understood and are currently extrapolated using high-dose exposure data. Identifying the signaling pat...

Descripción completa

Detalles Bibliográficos
Autores principales: Yang, Feng, Waters, Katrina M., Miller, John H., Gritsenko, Marina A., Zhao, Rui, Du, Xiuxia, Livesay, Eric A., Purvine, Samuel O., Monroe, Matthew E., Wang, Yingchun, Camp, David G., Smith, Richard D., Stenoien, David L.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2994767/
https://www.ncbi.nlm.nih.gov/pubmed/21152398
http://dx.doi.org/10.1371/journal.pone.0014152
_version_ 1782192993037451264
author Yang, Feng
Waters, Katrina M.
Miller, John H.
Gritsenko, Marina A.
Zhao, Rui
Du, Xiuxia
Livesay, Eric A.
Purvine, Samuel O.
Monroe, Matthew E.
Wang, Yingchun
Camp, David G.
Smith, Richard D.
Stenoien, David L.
author_facet Yang, Feng
Waters, Katrina M.
Miller, John H.
Gritsenko, Marina A.
Zhao, Rui
Du, Xiuxia
Livesay, Eric A.
Purvine, Samuel O.
Monroe, Matthew E.
Wang, Yingchun
Camp, David G.
Smith, Richard D.
Stenoien, David L.
author_sort Yang, Feng
collection PubMed
description BACKGROUND: High doses of ionizing radiation result in biological damage; however, the precise relationships between long-term health effects, including cancer, and low-dose exposures remain poorly understood and are currently extrapolated using high-dose exposure data. Identifying the signaling pathways and individual proteins affected at the post-translational level by radiation should shed valuable insight into the molecular mechanisms that regulate dose-dependent responses to radiation. PRINCIPAL FINDINGS: We have identified 7117 unique phosphopeptides (2566 phosphoproteins) from control and irradiated (2 and 50 cGy) primary human skin fibroblasts 1 h post-exposure. Semi-quantitative label-free analyses were performed to identify phosphopeptides that are apparently altered by radiation exposure. This screen identified phosphorylation sites on proteins with known roles in radiation responses including TP53BP1 as well as previously unidentified radiation-responsive proteins such as the candidate tumor suppressor SASH1. Bioinformatic analyses suggest that low and high doses of radiation affect both overlapping and unique biological processes and suggest a role for MAP kinase and protein kinase A (PKA) signaling in the radiation response as well as differential regulation of p53 networks at low and high doses of radiation. CONCLUSIONS: Our results represent the most comprehensive analysis of the phosphoproteomes of human primary fibroblasts exposed to multiple doses of ionizing radiation published to date and provide a basis for the systems-level identification of biological processes, molecular pathways and individual proteins regulated in a dose dependent manner by ionizing radiation. Further study of these modified proteins and affected networks should help to define the molecular mechanisms that regulate biological responses to radiation at different radiation doses and elucidate the impact of low-dose radiation exposure on human health.
format Text
id pubmed-2994767
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-29947672010-12-08 Phosphoproteomics Profiling of Human Skin Fibroblast Cells Reveals Pathways and Proteins Affected by Low Doses of Ionizing Radiation Yang, Feng Waters, Katrina M. Miller, John H. Gritsenko, Marina A. Zhao, Rui Du, Xiuxia Livesay, Eric A. Purvine, Samuel O. Monroe, Matthew E. Wang, Yingchun Camp, David G. Smith, Richard D. Stenoien, David L. PLoS One Research Article BACKGROUND: High doses of ionizing radiation result in biological damage; however, the precise relationships between long-term health effects, including cancer, and low-dose exposures remain poorly understood and are currently extrapolated using high-dose exposure data. Identifying the signaling pathways and individual proteins affected at the post-translational level by radiation should shed valuable insight into the molecular mechanisms that regulate dose-dependent responses to radiation. PRINCIPAL FINDINGS: We have identified 7117 unique phosphopeptides (2566 phosphoproteins) from control and irradiated (2 and 50 cGy) primary human skin fibroblasts 1 h post-exposure. Semi-quantitative label-free analyses were performed to identify phosphopeptides that are apparently altered by radiation exposure. This screen identified phosphorylation sites on proteins with known roles in radiation responses including TP53BP1 as well as previously unidentified radiation-responsive proteins such as the candidate tumor suppressor SASH1. Bioinformatic analyses suggest that low and high doses of radiation affect both overlapping and unique biological processes and suggest a role for MAP kinase and protein kinase A (PKA) signaling in the radiation response as well as differential regulation of p53 networks at low and high doses of radiation. CONCLUSIONS: Our results represent the most comprehensive analysis of the phosphoproteomes of human primary fibroblasts exposed to multiple doses of ionizing radiation published to date and provide a basis for the systems-level identification of biological processes, molecular pathways and individual proteins regulated in a dose dependent manner by ionizing radiation. Further study of these modified proteins and affected networks should help to define the molecular mechanisms that regulate biological responses to radiation at different radiation doses and elucidate the impact of low-dose radiation exposure on human health. Public Library of Science 2010-11-30 /pmc/articles/PMC2994767/ /pubmed/21152398 http://dx.doi.org/10.1371/journal.pone.0014152 Text en Yang et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Yang, Feng
Waters, Katrina M.
Miller, John H.
Gritsenko, Marina A.
Zhao, Rui
Du, Xiuxia
Livesay, Eric A.
Purvine, Samuel O.
Monroe, Matthew E.
Wang, Yingchun
Camp, David G.
Smith, Richard D.
Stenoien, David L.
Phosphoproteomics Profiling of Human Skin Fibroblast Cells Reveals Pathways and Proteins Affected by Low Doses of Ionizing Radiation
title Phosphoproteomics Profiling of Human Skin Fibroblast Cells Reveals Pathways and Proteins Affected by Low Doses of Ionizing Radiation
title_full Phosphoproteomics Profiling of Human Skin Fibroblast Cells Reveals Pathways and Proteins Affected by Low Doses of Ionizing Radiation
title_fullStr Phosphoproteomics Profiling of Human Skin Fibroblast Cells Reveals Pathways and Proteins Affected by Low Doses of Ionizing Radiation
title_full_unstemmed Phosphoproteomics Profiling of Human Skin Fibroblast Cells Reveals Pathways and Proteins Affected by Low Doses of Ionizing Radiation
title_short Phosphoproteomics Profiling of Human Skin Fibroblast Cells Reveals Pathways and Proteins Affected by Low Doses of Ionizing Radiation
title_sort phosphoproteomics profiling of human skin fibroblast cells reveals pathways and proteins affected by low doses of ionizing radiation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2994767/
https://www.ncbi.nlm.nih.gov/pubmed/21152398
http://dx.doi.org/10.1371/journal.pone.0014152
work_keys_str_mv AT yangfeng phosphoproteomicsprofilingofhumanskinfibroblastcellsrevealspathwaysandproteinsaffectedbylowdosesofionizingradiation
AT waterskatrinam phosphoproteomicsprofilingofhumanskinfibroblastcellsrevealspathwaysandproteinsaffectedbylowdosesofionizingradiation
AT millerjohnh phosphoproteomicsprofilingofhumanskinfibroblastcellsrevealspathwaysandproteinsaffectedbylowdosesofionizingradiation
AT gritsenkomarinaa phosphoproteomicsprofilingofhumanskinfibroblastcellsrevealspathwaysandproteinsaffectedbylowdosesofionizingradiation
AT zhaorui phosphoproteomicsprofilingofhumanskinfibroblastcellsrevealspathwaysandproteinsaffectedbylowdosesofionizingradiation
AT duxiuxia phosphoproteomicsprofilingofhumanskinfibroblastcellsrevealspathwaysandproteinsaffectedbylowdosesofionizingradiation
AT livesayerica phosphoproteomicsprofilingofhumanskinfibroblastcellsrevealspathwaysandproteinsaffectedbylowdosesofionizingradiation
AT purvinesamuelo phosphoproteomicsprofilingofhumanskinfibroblastcellsrevealspathwaysandproteinsaffectedbylowdosesofionizingradiation
AT monroematthewe phosphoproteomicsprofilingofhumanskinfibroblastcellsrevealspathwaysandproteinsaffectedbylowdosesofionizingradiation
AT wangyingchun phosphoproteomicsprofilingofhumanskinfibroblastcellsrevealspathwaysandproteinsaffectedbylowdosesofionizingradiation
AT campdavidg phosphoproteomicsprofilingofhumanskinfibroblastcellsrevealspathwaysandproteinsaffectedbylowdosesofionizingradiation
AT smithrichardd phosphoproteomicsprofilingofhumanskinfibroblastcellsrevealspathwaysandproteinsaffectedbylowdosesofionizingradiation
AT stenoiendavidl phosphoproteomicsprofilingofhumanskinfibroblastcellsrevealspathwaysandproteinsaffectedbylowdosesofionizingradiation