共 31 条
IMMUNOCHEMICAL DETECTION OF INDUCIBLE NO SYNTHASE IN HUMAN LUNG
被引:89
作者:
TRACEY, WR
[1
]
XUE, C
[1
]
KLINGHOFER, V
[1
]
BARLOW, J
[1
]
POLLOCK, JS
[1
]
FORSTERMANN, U
[1
]
JOHNS, RA
[1
]
机构:
[1] UNIV VIRGINIA,HLTH SCI CTR,DEPT ANESTHESIOL,CHARLOTTESVILLE,VA 22908
来源:
AMERICAN JOURNAL OF PHYSIOLOGY
|
1994年
/
266卷
/
06期
关键词:
NITRIC OXIDE SYNTHASE;
MACROPHAGE;
CYTOKINE;
PULMONARY;
BRONCHIECTASIS;
PNEUMONIA;
CHRONIC OBSTRUCTIVE PULMONARY DISEASE;
ADULT RESPIRATORY DISTRESS SYNDROME;
INFLAMMATION;
LIVER;
D O I:
10.1152/ajplung.1994.266.6.L722
中图分类号:
Q4 [生理学];
学科分类号:
071003 ;
摘要:
Type II (inducible) nitric oxide synthase (NOS) may play an important role in pulmonary pathophysiology, yet it remains controversial whether human tissues are capable of expressing this protein. Therefore, a polyclonal antibody (8196) was raised against type II NOS from induced RAW 264.7 macrophages and used to investigate the expression of this enzyme in human lung tissue. Anti-type II NOS antibody did not cross-react with either neuronal (type I) or endothelial (type III) constitutive NOS, whereas a 130-kDa protein was detected in cytosol from induced macrophages or liver removed from lipopolysaccharide (25 mg/kg)-treated rats. Cells or tissues that lacked NOS activity did not express immunoreactive proteins. Similarly, in grossly normal human lung tissue, no immunoreactivity was detected with the anti-type II NOS antibody. In contrast, strong immunoreactivity was detected in alveolar macrophages present in lung tissue from a patient with bronchiectasis and acute bronchopneumonia. These data demonstrate that human alveolar macrophages are able to express type II NOS and support a role for this enzyme in pulmonary inflammatory pathophysiology.
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页码:L722 / L727
页数:6
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