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Extracellular catalase activity protects cysteine cathepsins from inactivation by hydrogen peroxide
Authors:Hervé-Grépinet Virginie  Veillard Florian  Godat Emmanuel  Heuzé-Vourc'h Nathalie  Lecaille Fabien  Lalmanach Gilles
Affiliation:INSERM U 618, Protéases et Vectorisation Pulmonaires, Equipe Protéases et Pathologies Pulmonaires, Tours F-37000, France.
Abstract:The resistance of secreted cysteine cathepsins to peroxide inactivation was evaluated using as model THP-1 cells. Differentiated cells released mostly cathepsin B, but also cathepsins H, K, and L, with a maximum of endopeptidase activity at day 6. Addition of non-cytotoxic concentrations of H(2)O(2) did not affect mRNA expression levels and activity of cathepsins, while the catalase activity remained also unchanged, consistently with RT-PCR analysis. Conversely inhibition of extracellular catalase led to a striking inactivation of secreted cysteine cathepsins by H(2)O(2). This report suggests that catalase may participate in the protection of extracellular cysteine proteases against peroxidation.
Keywords:AMC, 7-amino-4-methyl coumarin   3-AT, 3-amino-l, 2, 4-triazole   BALF, bronchoalveolar lavage fluid   BCA, bicinchoninic acid   CA-074, N-(  smallcaps"  >l-3-trans-propylcarbamoyl oxirane-2-carbonyl)-  smallcaps"  >l-isoleucyl-  smallcaps"  >l-proline   CP, cysteine protease   DTT,   smallcaps"  >dl-dithiothreitol   E-64,   smallcaps"  >l-3-carboxy-trans-2.3-epoxypropionyl-leucylamido-(4-guanidino) butane   ECM, extra cellular matrix   FBS, fetal bovine serum   GM-CSF, granulocyte-macrophage colony-stimulating factor   MDM, monocyte-derived macrophage   MMTS, methylmethanethiosulfonate   PMA, phorbol myristate acetate   PMSF, phenylmethylsulfonyl fluoride   ROS, reactive oxygen species   Z, benzyloxycarbonyl
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