MICE LACKING EXTRACELLULAR-SUPEROXIDE DISMUTASE ARE MORE SENSITIVE TO HYPEROXIA

被引:388
作者
CARLSSON, LM
JONSSON, J
EDLUND, T
MARKLUND, SL
机构
[1] UMEA UNIV HOSP, DEPT CLIN CHEM, S-90187 UMEA, SWEDEN
[2] UMEA UNIV, DEPT MICROBIOL, S-90187 UMEA, SWEDEN
关键词
OXYGEN RADICALS; GENE TARGETING; LUNG;
D O I
10.1073/pnas.92.14.6264
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Extracellular superoxide dismutase (EC-SOD; superoxide:superoxide oxidoreductase, EC 1.15.1.1) is a secreted Cu- and Zn-containing tetrameric glycoprotein, the bulk of which is bound to heparan sulfate proteoglycans in the interstitium of tissues, To test the function of EC-SOD in vivo, mite carrying a targeted disruption of the EC-SOD gene were generated. The EC-SOD null mutant mice develop normally and remain healthy until at least 14 months of age. No compensatory induction of other SOD isoenzymes or other antioxidant enzymes was observed, When stressed by exposure to >99% oxygen, the EC-SOD null mutant mice display a considerable reduction in survival time compared to wild-type mice and an earlier onset of severe lung edema, These findings suggest that while under normal physiological conditions other antioxidant systems may substitute for the loss of EC-SOD; when the animal is stressed these systems are unable to provide adequate protection.
引用
收藏
页码:6264 / 6268
页数:5
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