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Transglutaminase activity during the differentiation of macrophages
Authors:R Kannagi  K Teshigawara  N Noro  T Masuda
Affiliation:1. Department of Biochemistry, Saitama Cancer Center Research Institute, Ina-machi, Kitaadachi-gun, Saitama 362, Japan;2. Biophysics Division, National Cancer Center Research Institute Tsukiji, Chuo-ku, Tokyo 104, Japan
Abstract:For the examination of the participation of the microsomal electron transport system in mutagenic activation by 4-dimethylaminoazobenzene (DAB), 4-methylaminoazobenzene (MAB) and their 3′-methyl-derivatives (3′-methyl-DAB and 3′-methyl-MAB), monospecific antibodies to NADPH-cytochrome P-450 reductase, 3-methylcholanthrene-inducible major P-450 (MC-P-448) and phenobarbital-inducible major P-450 (PB-P-450) were used. In Ames' assay system, the antibody to NADPH-cytochrome P-450 reductase inhibited the mutagenicities of DAB, MAB, 3′-methyl-DAB and 3′-methyl-MAB by 94, 94, 90 and 87%, respectively. The antibody to MC-P-448 inhibited their mutagenicities by more than 90%, while the antibody to PB-P-450 inhibited the mutagenicities less than 20%. These results indicate that the microsomal electron transport system, especially MC-P-448, is involved in activation of these dyes.
Keywords:MC-P-448  3-methylcholanthrene-inducible major cytochrome P-450  PB-P-450  phenobarbital-inducible major cytochrome P-450  PCB  polychlorinated biphenyls  Ig  immunoglobulin  DAB  4-dimethylaminoazobenzene  MAB  4-methyl-aminoazobenzene  AB  4-aminoazobenzene
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