Integrative genomic and proteomic analyses identifies glycerol-3-phosphate acyltransferase as a target of low-dose ionizing radiation in EBV infected-B cells. (2nd January 2016)

• Record Type: Journal Article
• Authors: Tabe, Yoko; Hatanaka, Yasuhito; Nakashiro, Mayumi; Sekihara, Kazumasa; Yamamoto, Shinichi; Matsushita, Hiromichi; Kazuno, Saiko; Fujimura, Tsutomu; Ikegami, Takako; Nakanaga, Keita; Matsumoto, Hirotaka; Ueno, Takashi; Aoki, Junken; Yokomizo, Takehiko; Konopleva, Marina; Andreeff, Michael; Miida, Takashi; Iwabuchi, Kazuhisa; Sasai, Keisuke
• Is Part Of: International journal of radiation biology. Volume 92:Number 1(2016:Jan.)
• Page Start: 24
• Page End: 34
• Publication Date: 2016-01-02
• Subjects: Low-dose ionizing radiation (LDIR) -- glycerol-3-phosphate acyltransferase (GPAM) -- Epstein-Barr virus-infected B-cells (EBV-B) -- microRNA (miRNA) -- isobaric tags for relative and absolute quantification (iTRAQ); Radiation -- Physiological effect -- Periodicals; Radiobiology -- Periodicals; 571.45
• DOI: 10.3109/09553002.2015.1106021
• Languages: English
• ISSNs: 0955-3002

Abstract

Abstract: Purpose : We sought to gain a better understanding of the low-dose ionizing radiation (LDIR)-induced molecular changes in transformed pre-malignant cells in their microenvironment. Materials and methods : The cellular response to LDIR was compared and contrasted using immortalized human Epstein-Barr virus-infected B-cells (EBV-B) in mono-culture, co-culture with human bone marrow derived stromal cells (MSC), or under the LDIR-induced bystander effect. The resulting alterations in protein and gene expression (including microRNA, miRNA) were evaluated by isobaric tags for relative and absolute quantification (iTRAQ) proteomics assay, western blot, cDNA array and quantitative reverse transcription polymerase chain reaction (RT-PCR), respectively. Results : The miRNAs let7a, miR-15b, miR-16, and miR-21, and a lipid metabolic miRNA hub miR- 23b, were upregulated after LDIR exposure in the mono-cultured EBV-B cells, but were downregulated in EBV-B cells co-irradiated with MSC. A lipid biosynthesis enzyme glycerol-3-phosphate acyltransferase, the common target of these miRNA, was downregulated at the level of protein and mRNA expression in the LDIR-exposed, mono-cultured EBV-B cells and upregulated MSC co-cultured EBV-B cells. Conclusions : These results suggest a putative miRNA regulatory mechanism controlling the LDIR-induced stress response, and illustrate that LDIR exposure, and the cell's microenvironment, can affect specific gene expression, both directly and indirectly, resulting in altered protein expression.