Increased expression of gelatinases and collagenase in rat lungs exposed to 100% oxygen

被引:66
作者
Pardo, A
Selman, M
Ridge, K
Barrios, R
Sznajder, JI
机构
[1] INST NACL ENFERMEDADES RESP, TLALPAN, DF, MEXICO
[2] BAYLOR COLL MED, DEPT PATHOL, HOUSTON, TX 77030 USA
[3] UNIV ILLINOIS, MICHAEL REESE HOSP, CHICAGO, IL USA
关键词
D O I
10.1164/ajrccm.154.4.8887609
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Exposure of adult rats to 100% O-2 produces a lethal injury by 72 h. We reasoned that matrix metalloproteinases participate in the pathogenesis of hyperoxic lung injury. To that end we studied the expression and activity of gelatinases A and B and interstitial collagenase in lung tissues and bronchoalveolar ravage fluids (BALF) of rats exposed to 100% oxygen for 60 h. Gelatin zymography of BALF samples revealed a similar to 72 kDa molecular species both in controls and oxygen-exposed animals. In addition, BALF from hyperoxic rats exhibited a 95-kDa gelatinase. Likewise, BALF total gelatinolytic and collagenolytic activities were significantly increased in oxygen-exposed rats. In situ hybridization revealed an increase in type IV collagenases as well as interstitial collagenase mRNAs in the oxygen-exposed lungs. The three enzymes were expressed by alveolar macrophages, and in variable degrees by interstitial and alveolar epithelial cells. Immunoreactive gelatinase B and collagenase paralleled the cell localization of the mRNAs but were also detected in the alveolar walls and interstitium. In situ zymography showed gelatinolytic activity in frozen sections of oxygen-exposed lungs but not in normal lungs. The upregulation of these metalloproteinases during acute exposure to 100% O-2 suggests that they might contribute to hyperoxic lung damage through the degradation of extracellular matrix components.
引用
收藏
页码:1067 / 1075
页数:9
相关论文
共 35 条
[1]   RESPONSE OF ALVEOLAR MACROPHAGE-DEPLETED RATS TO HYPEROXIA [J].
BERG, JT ;
WHITE, JE ;
TSAN, MF .
EXPERIMENTAL LUNG RESEARCH, 1995, 21 (01) :175-185
[2]  
CLARK JM, 1971, PHARMACOL REV, V23, P37
[3]  
COLLIER IE, 1988, J BIOL CHEM, V263, P6579
[4]  
CRAPO JD, 1986, ANNU REV PHYSIOL, V48, P721
[5]  
CRAPO JD, 1980, AM REV RESPIR DIS, V122, P123
[6]   MATRIX METALLOPROTEINASE AND ELASTASE ACTIVITIES IN LPS-INDUCED ACUTE LUNG INJURY IN GUINEA-PIGS [J].
DORTHO, MP ;
JARREAU, PH ;
DELACOURT, C ;
MACQUINMAVIER, I ;
LEVAME, M ;
PEZET, S ;
HARF, A ;
LAFUMA, C .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (03) :L209-L216
[7]   OXYGEN-TOXICITY IN NEONATAL AND ADULT ANIMALS OF VARIOUS SPECIES [J].
FRANK, L ;
BUCHER, JR ;
ROBERTS, RJ .
JOURNAL OF APPLIED PHYSIOLOGY, 1978, 45 (05) :699-704
[8]  
FREIJE JMP, 1994, J BIOL CHEM, V269, P16766
[9]   INCREASED EXPRESSION OF MATRIX METALLOPROTEINASES AND MATRIX-DEGRADING ACTIVITY IN VULNERABLE REGIONS OF HUMAN ATHEROSCLEROTIC PLAQUES [J].
GALIS, ZS ;
SUKHOVA, GK ;
LARK, MW ;
LIBBY, P .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (06) :2493-2503
[10]  
GOLDBERG GI, 1986, J BIOL CHEM, V261, P6600