Motohiro Takeya
Department Kumamoto Health Science University Department of Medical Technology, Faculty of Health Science Position Professor |
|
Research Period | 2005~2007 |
Research Topic | Oxidative stress regulation through NO-induced nucleic acid nitration in pulmonary diseases |
Research Type | KAKENHI Research |
Consignor | Ministry of Education, Culture, Sports, Science and Technology |
Research Program Type | Grants-in-Aid for Scientific Research(基盤研究(C)),基盤研究(C) |
KAKENHI Grant No. | 17590797 |
Representative Person | 寺崎 泰弘, Kiyoshi TAKAHASHI |
Collaborative Researcher | 高橋 潔, Motohiro TAKEYA, Takaaki AKAIKE |
Details | 8-nitroguanosine, a modified base, draws people's attention as a marker for nucleic acid damage during carcinogenesis or other gene modification. Since we have succeeded in producing a specific antibody against 8-nitroguanosine, we studied the generation and localization of 8-nitroguanosine in various pulmonary diseases using the antibody.In pulmonary fibrosis, strong immunostaining for 8-nitroguanosine was observed in metaplastic epithelial cells as well as macrophages and alveolar epithelia. Colocalization of 8-nitroguanosine with iNOS, eNOS, hemoxygenase-1, 8-nitotyrosine, and p53 was detected in confocal laser scanning microscopy. In lung cancer, 8-nitroguanosine is observed both in cytoplasm and nuclei of cancer cells. These results suggest that 8-nitroguanosin is involved in injury of air-space epithelia and also in pulmonary carcinogenesis. In lung injury mouse models induced by hyperoxia-exposure or bleomycin showed that 8-nitorguanosine is generated in air-space epitheial cells as well as in macrophages accumulated in injured tissue indicating that 8-nitroguanosine is involved in such disease processes.We have previously shown that 8-nitro-cyclic GMP, a nitroguanosine deri |
Permalink URL | https://kaken.nii.ac.jp/d/p/17590797.ja.html |