Secretory leukocyte proteinase inhibitor is a major leukocyte elastase inhibitor in human neutrophils

被引:126
作者
Sallenave, JM
Si-Tahar, M
Cox, G
Chignard, M
Gauldie, J
机构
[1] MCMASTER UNIV, ST JOSEPH HOSP, DEPT PATHOL, HAMILTON, ON, CANADA
[2] MCMASTER UNIV, ST JOSEPH HOSP, DEPT MED, HAMILTON, ON, CANADA
[3] INST PASTEUR, UA IP INSERM U285, PARIS, FRANCE
关键词
antiproteinase; cystic fibrosis; lung inflammation;
D O I
10.1002/jlb.61.6.695
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Secretory leukocyte proteinase inhibitor (SLPI) is the main neutrophil elastase (HLE) inhibitor found in the upper airways during pulmonary inflammation, It has been shown to be synthesized and secreted in vitro by epithelial cells and has been localized in tracheal glands and bronchiolar epithelial cells by immunocytochemistry, In this study, using immunodetection and immunopurification techniques with specific anti-SLPI immunoglobulin G (IgG), we show that SLPI is present as a native 14-kDa molecule in neutrophil cytosol. In addition, we demonstrate that SLPI is the major inhibitor of HLE present in neutrophil cytosol because pre-incubation with specific anti-SLPI IgG was able to inhibit completely the anti-HLE activity of the cytosol, SLPI can be secreted (probably in an inactive form) by neutrophils and its secretion is enhanced when the cells are stimulated with phorbol myristate acetate (PMA)). Elafin, an elastase-specific inhibitor, is also present in minute amounts in neutrophil cytosol and its secretion can be up-regulated, The presence of SLPI in the cytosol of neutrophils may serve as a protective screen against proteinases spilling from azurophilic granules, An alternative or supplementary role may be the maintenance of a differentiated phenotype.
引用
收藏
页码:695 / 702
页数:8
相关论文
共 49 条
[1]   EXPRESSION OF THE SECRETORY LEUKOPROTEASE INHIBITOR GENE IN EPITHELIAL-CELLS [J].
ABE, T ;
KOBAYASHI, N ;
YOSHIMURA, K ;
TRAPNELL, BC ;
KIM, H ;
HUBBARD, RC ;
BREWER, MT ;
THOMPSON, RC ;
CRYSTAL, RG .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (06) :2207-2215
[2]   SECRETION OF ANTILEUCOPROTEASE FROM A HUMAN-LUNG TUMOR-CELL LINE [J].
APPELHANS, B ;
ENDER, B ;
SACHSE, G ;
NIKIFOROV, T ;
APPELHANS, H ;
EBERT, W .
FEBS LETTERS, 1987, 224 (01) :14-18
[3]   HUMAN LEUKOCYTE GRANULE ELASTASE - RAPID ISOLATION AND CHARACTERIZATION [J].
BAUGH, RJ ;
TRAVIS, J .
BIOCHEMISTRY, 1976, 15 (04) :836-841
[4]   THE ACUTE-PHASE RESPONSE [J].
BAUMANN, H ;
GAULDIE, J .
IMMUNOLOGY TODAY, 1994, 15 (02) :74-80
[5]  
BIETH JG, 1980, CLIN RES PROC, V16, P183
[6]   THE SERINE-PROTEASE INHIBITOR OF CARTILAGE MATRIX IS NOT A CHONDROCYTIC GENE-PRODUCT [J].
BOHM, B ;
AIGNER, T ;
KINNE, R ;
BURKHARDT, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 207 (02) :773-779
[7]   DOWN-REGULATION OF A SERINE PROTEASE, MYELOBLASTIN, CAUSES GROWTH ARREST AND DIFFERENTIATION OF PROMYELOCYTIC LEUKEMIA-CELLS [J].
BORIES, D ;
RAYNAL, MC ;
SOLOMON, DH ;
DARZYNKIEWICZ, Z ;
CAYRE, YE .
CELL, 1989, 59 (06) :959-968
[8]   MUCUS PROTEINASE-INHIBITOR - A FAST-ACTING INHIBITOR OF LEUKOCYTE ELASTASE [J].
BOUDIER, C ;
BIETH, JG .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 995 (01) :36-41
[9]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[10]   PROTEOLYSIS BY NEUTROPHILS - RELATIVE IMPORTANCE OF CELL-SUBSTRATE CONTACT AND OXIDATIVE INACTIVATION OF PROTEINASE-INHIBITORS INVITRO [J].
CAMPBELL, EJ ;
SENIOR, RM ;
MCDONALD, JA ;
COX, DL .
JOURNAL OF CLINICAL INVESTIGATION, 1982, 70 (04) :845-852