Overexpression of manganese superoxide dismutase protects lung epithelial cells against oxidant injury

被引:57
作者
Ilizarov, AM
Koo, HC
Kazzaz, JA
Mantell, LL
Li, YC
Bhapat, R
Pollack, S
Horowitz, S
Davis, JM
机构
[1] SUNY Stony Brook, Winthrop Univ Hosp, Sch Med, Cardiopulm Res Inst, Mineola, NY 11501 USA
[2] SUNY Stony Brook, Winthrop Univ Hosp, Sch Med, Dept Pediat, Mineola, NY 11501 USA
[3] SUNY Stony Brook, Winthrop Univ Hosp, Sch Med, Dept Med Pulm & Crit Care Med, Mineola, NY 11501 USA
[4] SUNY Stony Brook, Winthrop Univ Hosp, Sch Med, Dept Cardiovasc Thorac Surg, Mineola, NY 11501 USA
[5] SUNY Stony Brook, Winthrop Univ Hosp, Sch Med, Dept Biostat, Mineola, NY 11501 USA
[6] St Johns Univ, Dept Comp Informat Syst & Decis Sci, Jamaica, NY 11439 USA
[7] Jewish Hosp, Heart & Lung Inst, Lexington, KY USA
关键词
D O I
10.1165/ajrcmb.24.4.4240
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
To determine whether overexpression of antioxidant enzymes in lung epithelial cells prevents damage from oxidant injury, stable cell lines were generated with complementary DNAs encoding manganese superoxide dismutase (MnSOD) and/or catalase (CAT). Cell lines overexpressing MnSOD, CAT, or MnSOD + CAT were assessed for tolerance to hyperoxia or paraquat. After exposure to 95% O-2 for 10 d, 44 to 57% of cells overexpressing both MnSOD and CAT and 37 to 47% of cells overexpressing MnSOD alone were viable compared with 7 to 12% of empty vector or parental cells (P < 0.05). To assess if viable cells were capable of cell division after hyperoxic exposures (up to 5 d), a clonogenicity assay was performed. The clonogenic potential of cells overexpressing MnSOD + CAT and MnSOD alone were significantly better than those expressing CAT alone or empty vector controls. In addition, 54 to 72% of cells overexpressing both MnSOD and CAT survived in 1 mM paraquat compared with 58 to 73% with MnSOD alone and 27% with control cells. Overexpression of CAT alone did not improve survival in hyperoxia or paraquat. The combination of MnSOD + CAT did not provide additional protection from paraquat. Data demonstrate that overexpression of MnSOD protects cells from oxidant injury and CAT offers additional protection from hyperoxic injury when co-expressed with MnSOD.
引用
收藏
页码:436 / 441
页数:6
相关论文
共 29 条
[1]  
AEBI H, 1984, METHOD ENZYMOL, V105, P121
[2]   MICE LACKING EXTRACELLULAR-SUPEROXIDE DISMUTASE ARE MORE SENSITIVE TO HYPEROXIA [J].
CARLSSON, LM ;
JONSSON, J ;
EDLUND, T ;
MARKLUND, SL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (14) :6264-6268
[3]   INHIBITION OF LUNG EPITHELIAL-CELL PROLIFERATION BY HYPEROXIA - POSTTRANSCRIPTIONAL REGULATION OF PROLIFERATION-RELATED GENES [J].
CLEMENT, A ;
EDEAS, M ;
CHADELAT, K ;
BRODY, JS .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (05) :1812-1818
[4]   Simultaneous expression of multi-subunit proteins in mammalian cells using a convenient set of mammalian cell expression vectors [J].
Cockett, MI ;
Ochalski, R ;
Benwell, K ;
Franco, R ;
WardwellSwanson, J .
BIOTECHNIQUES, 1997, 23 (03) :402-+
[5]  
Crapo J D, 1978, Methods Enzymol, V53, P382
[6]   Safety and pharmacokinetics of multiple doses of recombinant human CuZn superoxide dismutase administered intratracheally to premature neonates with respiratory distress syndrome [J].
Davis, JM ;
Rosenfeld, WN ;
Richter, SE ;
Parad, R ;
Gewolb, IH ;
Spitzer, AR ;
Carlo, WA ;
Couser, RJ ;
Price, A ;
Flaster, E ;
Kassem, N ;
Edwards, L ;
Tierney, J ;
Horowitz, S .
PEDIATRICS, 1997, 100 (01) :24-30
[7]   PROPHYLACTIC EFFECTS OF RECOMBINANT HUMAN SUPEROXIDE-DISMUTASE IN NEONATAL LUNG INJURY [J].
DAVIS, JM ;
ROSENFELD, WN ;
SANDERS, RJ ;
GONENNE, A .
JOURNAL OF APPLIED PHYSIOLOGY, 1993, 74 (05) :2234-2241
[8]  
Davis JM, 1999, NEONATOLOGY, P509
[9]   NORMOBARIC OXYGEN-TOXICITY OF THE LUNG [J].
DENEKE, SM ;
FANBURG, BL .
NEW ENGLAND JOURNAL OF MEDICINE, 1980, 303 (02) :76-86
[10]  
FRACICA P, 1992, LUNG INJURY, P333