Comparative loss of activity of recombinant secretory leukoprotease inhibitor and alpha(1)-protease inhibitor caused by different forms of oxidative stress

被引:24
作者
Vogelmeier, C
Biedermann, T
Maier, K
Behr, J
Krombach, F
Buhl, R
机构
[1] GSF FORSCHUNGSZENTRUM UMWELT & GESUNDHEIT GMBH,INST INHALAT BIOL,NEUHERBERG,GERMANY
[2] UNIV MUNICH,INST CHIRURG FORSCH,D-81366 MUNICH,GERMANY
[3] UNIV FRANKFURT,ZENTRUM INNERE MED,ABT PNEUMOL,D-6000 FRANKFURT,GERMANY
关键词
alpha(1)-protease inhibitor; inactivation; reactive oxygen metabolites; secretory leukoprotease inhibitor; therapy;
D O I
10.1183/09031936.97.10092114
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Secretory leukoprotease inhibitor (SLPI) and alpha(1)-protease inhibitor (alpha(1)-PI) are powerful antiproteases currently under investigation for their potential to protect the lung from neutrophil elastase (NE). The aim of this study was to determine whether the recombinant form of SLPI (rSLPI) and alpha(1)-PI show different grades of loss of inhibitory activity when exposed to reactive oxygen metabolites. We incubated rSLPI and alpha(1)-PI with N-chlorosuccinimide (NCS), chloramines, activated polymorphonuclear leucocytes (PMNs) and activated alveolar macrophages (AMs). Under all conditions evaluated, both antiproteases were partially inactivated, The resulting anti-NE activity of rSLPI was not significantly different from that of alpha(1)-PI after exposure to NCS (p>0.5), chloramines (p>0.6), activated PMNs (p> 0.07) and activated AMs (p>0.9). In conclusion, recombinant secretory leukoprotease inhibitor and alpha(1)-protease inhibitor lose antineutrophil elastase activity to a similar extent when expressed to conditions that may be present in inflammatory lung disorders.
引用
收藏
页码:2114 / 2119
页数:6
相关论文
共 44 条
[21]   DIFFERENT SELECTIVITIES OF OXIDANTS DURING OXIDATION OF METHIONINE RESIDUES IN THE ALPHA-1-PROTEINASE INHIBITOR [J].
MAIER, KL ;
MATEJKOVA, E ;
HINZE, H ;
LEUSCHEL, L ;
WEBER, H ;
BECKSPEIER, I .
FEBS LETTERS, 1989, 250 (02) :221-226
[22]   PHARMACOKINETICS OF RECOMBINANT SECRETORY LEUKOPROTEASE INHIBITOR AEROSOLIZED TO NORMALS AND INDIVIDUALS WITH CYSTIC-FIBROSIS [J].
MCELVANEY, NG ;
DOUJAIJI, B ;
MOAN, MJ ;
BURNHAM, MR ;
WU, MC ;
CRYSTAL, RG .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1993, 148 (04) :1056-1060
[23]   MODULATION OF AIRWAY INFLAMMATION IN CYSTIC-FIBROSIS - INVIVO SUPPRESSION OF INTERLEUKIN-8 LEVELS ON THE RESPIRATORY EPITHELIAL SURFACE BY AEROSOLIZATION OF RECOMBINANT SECRETORY LEUKOPROTEASE INHIBITOR [J].
MCELVANEY, NG ;
NAKAMURA, H ;
BIRRER, P ;
HEBERT, CA ;
WONG, WL ;
ALPHONSO, M ;
BAKER, JB ;
CATALANO, MA ;
CRYSTAL, RG .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (04) :1296-1301
[24]   AEROSOL ALPHA-1-ANTITRYPSIN TREATMENT FOR CYSTIC-FIBROSIS [J].
MCELVANEY, NG ;
HUBBARD, RC ;
BIRRER, P ;
CHERNICK, MS ;
CAPLAN, DB ;
FRANK, MM ;
CRYSTAL, RG .
LANCET, 1991, 337 (8738) :392-394
[25]   SECRETORY LEUKOCYTE PROTEASE INHIBITOR BINDING TO MESSENGER-RNA AND DNA AS A POSSIBLE CAUSE OF TOXICITY TO ESCHERICHIA-COLI [J].
MILLER, KW ;
EVANS, RJ ;
EISENBERG, SP ;
THOMPSON, RC .
JOURNAL OF BACTERIOLOGY, 1989, 171 (04) :2166-2172
[26]   INACTIVATION OF ALPHA-1-PROTEINASE INHIBITOR BY PEROXYNITRITE [J].
MORENO, JJ ;
PRYOR, WA .
CHEMICAL RESEARCH IN TOXICOLOGY, 1992, 5 (03) :425-431
[27]   CONTRIBUTION OF SECRETORY LEUKOCYTE PROTEINASE-INHIBITOR TO THE ANTIPROTEASE DEFENSE SYSTEM OF THE PERIPHERAL LUNG - EFFECT OF OZONE-INDUCED ACUTE-INFLAMMATION [J].
NADZIEJKO, C ;
FINKELSTEIN, I ;
BALMES, JR .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1995, 152 (05) :1592-1598
[28]   Z-TYPE ALPHA1-ANTITRYPSIN IS LESS COMPETENT THAN M1-TYPE ALPHA1-ANTITRYPSIN AS AN INHIBITOR OF NEUTROPHIL ELASTASE [J].
OGUSHI, F ;
FELLS, GA ;
HUBBARD, RC ;
STRAUS, SD ;
CRYSTAL, RG .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 80 (05) :1366-1374
[29]   RISK-FACTORS FOR EMPHYSEMA - CIGARETTE-SMOKING IS ASSOCIATED WITH A REDUCTION IN THE ASSOCIATION RATE-CONSTANT OF LUNG ALPHA-1-ANTITRYPSIN FOR NEUTROPHIL ELASTASE [J].
OGUSHI, F ;
HUBBARD, RC ;
VOGELMEIER, C ;
FELLS, GA ;
CRYSTAL, RG .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (03) :1060-1065
[30]   ISOLATION AND PROPERTIES OF HUMAN PLASMA ALPHA-1-PROTEINASE INHIBITOR [J].
PANNELL, R ;
JOHNSON, D ;
TRAVIS, J .
BIOCHEMISTRY, 1974, 13 (26) :5439-5445