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Induction of mitochondrial manganese superoxide dismutase by interleukin 1
Author(s) -
Masuda Akinori,
Longo Dan L.,
Kobayashi Yoshiro,
Appella Ettore,
Oppenheim Joost J.,
Matsushima Kouji
Publication year - 1988
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.2.15.3263930
Subject(s) - superoxide dismutase , amino acid , chemistry , biochemistry , peptide sequence , microbiology and biotechnology , peripheral blood mononuclear cell , mitochondrion , superoxide , interleukin , moiety , enzyme , biology , cytokine , stereochemistry , immunology , in vitro , gene
Interleukin 1 (IL 1) inhibits the growth of human melanoma A375 cells (1). To identify the subcellular events preceding inhibition of growth by IL 1, we have examined the effect of IL 1 on protein synthesis caused by A375 cells. IL 1 selectively and predominantly induced a 25‐kDa polypeptide (p25) in A375 cells after 12 h. On subcellular fractionation, p25 was exclusively located in the 10,000 x g ‐pelleted (mitochondria‐enriched) fraction. To identify the p25 moiety, it was purified to homogeneity by sequential chromatography on DEAE‐Sephacel and reverse‐phase, high‐pressure liquid chromatography and its amino‐terminal amino acid sequence was determined. The sequence of the 35 amino‐terminal amino acids of the p25 moiety was identical to that of human manganese superoxide dismutase (Mn SOD) (2). The enzymatic activities of SOD were induced only in the mitochondria‐enriched fraction of IL 1‐treated A375 cells. However, IL 1 also induced Mn SOD in normal human skin fibroblasts and peripheral blood mononuclear cells, whose growth was stimulated by IL 1. The results show that induction of Mn SOD by IL 1 is a common biochemical event in IL 1‐responsive cells.—M asuda , A.; L ongo , D. L.; K obayashi , Y.; A ppella , E.; O ppenheim , J. J.; M atsushima , K. Induction of mitochondrial manganese superoxide dismutase by interleukin 1. FASEB J. 2: 3087‐3091; 1988.