Protective effects of an aptamer inhibitor of neutrophil elastase in lung inflammatory injury

被引:49
作者
Bless, NM
Smith, D
Charlton, J
Czermak, BJ
Schmal, H
Friedl, HP
Ward, PA
机构
[1] NEXSTAR PHARMACEUT INC, BOULDER, CO 80301 USA
[2] UNIV ZURICH, DEPT SURG, CH-8091 ZURICH, SWITZERLAND
[3] UNIV MICHIGAN, SCH MED, DEPT PATHOL, ANN ARBOR, MI 48109 USA
关键词
D O I
10.1016/S0960-9822(06)00376-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neutrophils play an important part in the development of acute inflammatory injury. Human neutrophils contain high levels of the serine protease elastase, which is stored in azurophilic granules and is secreted in response to inflammatory stimuli, Elastase is capable of degrading many components of extracellular matrix [1-4] and has cytotoxic effects on endothelial cells [5-7] and airway epithelial cells, Three types of endogenous protease inhibitors control the activity of neutrophil elastase, including alpha-1 protease inhibitor (alpha-1PI), alpha-2 macroglobulin and secreted leukoproteinase inhibitor (SLPI) [8-10], A disturbed balance between neutrophil elastase and these inhibitors has been found in various acute clinical conditions (such as adult respiratory syndrome and ischemia-reperfusion injury) and in chronic diseases, We investigated the effect of NX21909, a selected oligonucleotide (aptamer) inhibitor of elastase, in an animal model of acute lung inflammatory disease [11-14], This inhibitor was previously selected from a hybrid library of randomized DNA and a small-molecule irreversible inhibitor of elastase (a valine diphenyl ester phosphonate, Figure 1), by the blended SELEX process [15]. We show that NX21909 inhibits lung injury and neutrophil influx in a dose dependent manner, the first demonstration of efficacy by an aptamer in an animal disease model.
引用
收藏
页码:877 / 880
页数:4
相关论文
共 23 条
[1]   Highly potent irreversible inhibitors of neutrophil elastase generated by selection from a randomized DNA-valine phosphonate library [J].
Charlton, J ;
Kirschenheuter, GP ;
Smith, D .
BIOCHEMISTRY, 1997, 36 (10) :3018-3026
[2]  
DORING G, 1994, AM J RESP CRIT CARE, V150, pS114
[3]   ADVERSE-EFFECTS OF NEUTROPHILS ON THE LUNG [J].
GADEK, JE .
AMERICAN JOURNAL OF MEDICINE, 1992, 92 :S27-S31
[4]   OLIGONUCLEOTIDES AS RESEARCH, DIAGNOSTIC, AND THERAPEUTIC AGENTS [J].
GOLD, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (23) :13581-13584
[5]   DIVERSITY OF OLIGONUCLEOTIDE FUNCTIONS [J].
GOLD, L ;
POLISKY, B ;
UHLENBECK, O ;
YARUS, M .
ANNUAL REVIEW OF BIOCHEMISTRY, 1995, 64 :763-797
[6]  
HENSON P, 1998, INFLAMMATION BASIC P, P363
[7]  
HUBBARD RC, 1991, LUNG SCI F, V2, P1775
[8]  
JANOFF A, 1985, ANNU REV MED, V36, P207
[9]   ACUTE IMMUNOLOGICAL PULMONARY ALVEOLITIS [J].
JOHNSON, KJ ;
WARD, PA .
JOURNAL OF CLINICAL INVESTIGATION, 1974, 54 (02) :349-357
[10]   ROLE OF ANTILEUKOPROTEASE IN THE HUMAN LUNG [J].
KRAMPS, JA ;
RUDOLPHUS, A ;
STOLK, J ;
WILLEMS, LNA ;
DIJKMAN, JH .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1991, 624 :97-108