MN AND CU/ZN SOD EXPRESSION IN CELLS FROM LPS-SENSITIVE AND LPS-RESISTANT MICE

被引:31
作者
GIBBS, LS
DELVECCHIO, PJ
SHAFFER, JB
机构
[1] NEW YORK STATE DEPT HLTH,WADSWORTH CTR LABS & RES,POB 509,ALBANY,NY 12201
[2] UNION UNIV,DEPT PHYSIOL & CELL BIOL,ALBANY,NY 12208
[3] UNION UNIV,DEPT OPHTHALMOL,ALBANY,NY 12208
关键词
LIPOPOLYSACCHARIDE; ENDOTOXIN; SUPEROXIDE DISMUTASE; LPS-RESISTANCE; MICE; ENDOTHELIUM; MACROPHAGE; FREE RADICALS;
D O I
10.1016/0891-5849(92)90003-Y
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
We examined the effect of lipopolysaccharide (LPS) treatment on the expression of manganese and copper/zinc superoxide dismutase (MnSOD and Cu/ZnSOD) mRNA and protein in resident peritoneal macrophages and lung endothelial cells derived from LPS-sensitive (LPS-s) and LPS-resistant (LPS-r) mice. Macrophages from both LPS-s and LPS-r mice treated with LPS for 24 h produced increased levels of MnSOD mRNA and protein. In contrast, levels of lung endothelial cell MnSOD mRNA and protein from LPS-s mice were increased by LPS treatment, while no increases in these parameters were observed in endothelial cells from LPS-r mice. Tumor necrosis factor-alpha (TNF(alpha)) treatment, however, did increase levels of MnSOD mRNA in both LPS-s and LPS-r endothelial cells to an equal extent. Both macrophage and endothelial cell Cu/ZnSOD mRNA and protein levels were not significantly affected by LPS treatment. These results demonstrate that the mutation that affects susceptibility to LPS in LPS-r mice exerts a differential influence on MnSOD inducibility in a cell specific manner.
引用
收藏
页码:107 / 111
页数:5
相关论文
共 19 条
[11]  
LIBBY P, 1986, AM J PATHOL, V124, P179
[12]  
MEYRICK B, 1991, AM J PATHOL, V138, P93
[13]   THE PRIMARY ROLE OF LYMPHORETICULAR CELLS IN THE MEDIATION OF HOST RESPONSES TO BACTERIAL-ENDOTOXIN [J].
MICHALEK, SM ;
MOORE, RN ;
MCGHEE, JR ;
ROSENSTREICH, DL ;
MERGENHAGEN, SE .
JOURNAL OF INFECTIOUS DISEASES, 1980, 141 (01) :55-63
[14]  
MORRISON DC, 1986, MICROBIOLOGY 1986, P23
[15]   EXPRESSION OF BOVINE AND MOUSE ENDOTHELIAL-CELL ANTIOXIDANT ENZYMES FOLLOWING TNF-ALPHA EXPOSURE [J].
SHAFFER, JB ;
TREANOR, CP ;
DELVECCHIO, PJ .
FREE RADICAL BIOLOGY AND MEDICINE, 1990, 8 (05) :497-502
[16]   ENDOTOXIN INCREASES SUPEROXIDE-DISMUTASE IN CULTURED BOVINE PULMONARY ENDOTHELIAL-CELLS [J].
SHIKI, Y ;
MEYRICK, BO ;
BRIGHAM, KL ;
BURR, IM .
AMERICAN JOURNAL OF PHYSIOLOGY, 1987, 252 (04) :C436-C440
[17]   REGULATION OF TUMOR-NECROSIS-FACTOR (TNF) RELEASE BY MURINE PERITONEAL-MACROPHAGES - ROLE OF CELL STIMULATION AND SPECIFIC PHAGOCYTIC PLASMA-MEMBRANE RECEPTORS [J].
STEIN, M ;
GORDON, S .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1991, 21 (02) :431-437
[18]  
VISNER GA, 1990, J BIOL CHEM, V265, P2856
[19]   IDENTIFICATION AND ISOLATION OF ENDOTHELIAL-CELLS BASED ON THEIR INCREASED UPTAKE OF ACETYLATED-LOW DENSITY LIPOPROTEIN [J].
VOYTA, JC ;
VIA, DP ;
BUTTERFIELD, CE ;
ZETTER, BR .
JOURNAL OF CELL BIOLOGY, 1984, 99 (06) :2034-2040