Published 2003 | Version v1
Book

A leukocyte antigen, Leu-13, is involved in induction of resistance of human cells to x-ray cell killing by interferon-α

  • 1. Chiba Univ., Graduate School of Medicine, Chiba (Japan)

Description

We previously reported on human interferon (HuIFN)-induced resistance of human cells to X-ray and UV cell killing. In this study, we searched for the genes whose expression is responsible for the resistance, using a PCR-based mRNA differential display method and Northern blotting analysis. RSa cells were used for this analysis, because they show increased resistance to X-ray- and UV-caused cell killing by HuIFN-α treatment prior to irradiation. Messenger RNA expression levels for Leu-13, a leukocyte antigen, were markedly up-regulated in RSa cells after HuIFN-α treatment. Furthermore, pretreatment of RSa cells with antisense oligonucleotides for Leu-13 mRNA resulted in the suppression of the HuIFN-α-induced resistance of the cells to X-ray cell killing, but did not modulate HuIFN-α-induced resistance to UV cell killing. These results suggest that Leu-13 is involved in HuIFN-α-induced resistance of human cells to X-ray cell killing, but not to UV cell killing. (author)

Part of:
Molecular mechanisms for radiation-induced cellular response and cancer development. Proceedings of the international symposium on biological effects of low dose radiation

Additional details

Publishing Information

Publisher
Inst. for Environmental Sciences
Imprint Place
Rokkasho, Aomori (Japan)
ISBN
4-9980604-5-7
Imprint Title
Molecular mechanisms for radiation-induced cellular response and cancer development. Proceedings of the international symposium on biological effects of low dose radiation
Imprint Pagination
367 p.
Journal Page Range
p. 323-327

Conference

Title
Molecular mechanisms for radiation-induced cellular response and cancer development
Acronym
International symposium on biological effects of low dose radiation
Dates
9-11 Oct 2002
Place
Rokkasho, Aomori (Japan)

Optional Information

Notes
12 refs., 2 figs.