Chronic exposure of humans to high level natural background radiation leads to robust expression of protective stress response proteins

Author:

Nishad S.,Chauhan Pankaj Kumar,Sowdhamini R.,Ghosh Anu

Abstract

AbstractUnderstanding exposures to low doses of ionizing radiation are relevant since most environmental, diagnostic radiology and occupational exposures lie in this region. However, the molecular mechanisms that drive cellular responses at these doses, and the subsequent health outcomes, remain unclear. A local monazite-rich high level natural radiation area (HLNRA) in the state of Kerala on the south-west coast of Indian subcontinent show radiation doses extending from ≤ 1 to ≥ 45 mGy/y and thus, serve as a model resource to understand low dose mechanisms directly on healthy humans. We performed quantitative discovery proteomics based on multiplexed isobaric tags (iTRAQ) coupled with LC–MS/MS on human peripheral blood mononuclear cells from HLNRA individuals. Several proteins involved in diverse biological processes such as DNA repair, RNA processing, chromatin modifications and cytoskeletal organization showed distinct expression in HLNRA individuals, suggestive of both recovery and adaptation to low dose radiation. In protein–protein interaction (PPI) networks, YWHAZ (14-3-3ζ) emerged as the top-most hub protein that may direct phosphorylation driven pro-survival cellular processes against radiation stress. PPI networks also identified an integral role for the cytoskeletal protein ACTB, signaling protein PRKACA; and the molecular chaperone HSPA8. The data will allow better integration of radiation biology and epidemiology for risk assessment [Data are available via ProteomeXchange with identifier PXD022380].

Funder

Bhabha Atomic Research Centre, India

National Centre for Biological Sciences, India

J.C. Bose Fellowship, Science and Engineering Research Board, Department of Science and Technology, Government of India

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Reference79 articles.

1. United Nations Scientific Committee on the Effects of Atomic Radiation (UNSCEAR). Biological Mechanisms of Radiation Actions at Low Doses. A White Paper to Guide the Scientific Committee‘s Future Programme of Work (United Nations, New York, 2012).

2. Valentin, J. Low-dose extrapolation of radiation-related cancer risk. Ann. ICRP 35, 1–140. https://doi.org/10.1016/j.icrp.2005.11.002 (2005).

3. United Nations Scientific Committee on the Effects of Atomic Radiations (UNSCEAR). Sources and Effects of Ionising Radiation Annex B Exposures from Natural Radiation Sources (United Nations, New York, 2000).

4. Sohrabi, M. World high background natural radiation areas: Need to protect public from radiation exposure. Radiat. Meas. 50, 166–171. https://doi.org/10.1016/j.radmeas.2012.03.011 (2013).

5. World Health Organization (WHO). Effects of Radiation on Human Heredity: Investigations of Areas of High Natural Radiation. WHO Technical Report Series No. 166 (WHO, Geneva, 1959).

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