炎症・再生
Online ISSN : 1880-5795
Print ISSN : 1346-8022
ISSN-L : 1346-8022
Original Article
慢性肉芽腫症におけるNADPHオキシダーゼ構成成分p67phoxの細胞内不安定性と分解酵素について
長谷部 武染谷 明正岩渕 和久藤田 宏夫布井 博幸長岡 功
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ジャーナル フリー

2004 年 24 巻 1 号 p. 47-54

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抄録
Chronic granulomatous disease (CGD) is characterized by the failure of phagocytes to kill certain bacteria and fungi. This is caused by deficiencies in one of the components of NADPH oxidase, a superoxide-producing enzyme in phagocytic leukocytes. In some cases with missense mutations in the p67phox gene, mRNA for p67phox is present in normal amounts; however, p67phox protein is missing, suggesting that the missense p67phox protein is labile in the cytosol of phagocytic cells in CGD. In this study, we evaluated the degradation of missense mutants of p67phox using p67phox G78E (78Gly → Glu) and A128Val (128Ala → Val) as target molecules. By incubation with the cytosol factions of human peripheral blood neutrophils and promyelocytic HL-60 cells, G78E and A128V were time-dependently degraded, whereas wild-type p67phox was not degraded. Importantly, the degradation of missense mutant G78E was completely abolished by inhibitors for serine proteases such as DFP, PMSF and soybean trypsin inhibitor, but was not affected by proteasome inhibitor MG-132 and calpain inhibitor ALLN. These observations suggest that missense mutants of p67phox are labile and likely to be degraded in CGD by cytosolic serine protease(s) in phagocytic cells, and proteasome and calpain are unlikely to be involved in the degradation.
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© 2004 日本炎症・再生医学会
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