共 40 条
A New Mouse Model for Temporal- and Tissue-Specific Control of Extracellular Superoxide Dismutase
被引:9
作者:
Zou, Yani
[1
]
Chen, Chih-Hsin
[1
]
Fike, John R.
[2
]
Huang, Ting-Ting
[1
,3
]
机构:
[1] Stanford Univ, Dept Neurol & Neurol Sci, Stanford, CA 94305 USA
[2] Univ Calif San Francisco, Dept Neurol Surg & Radiat Oncol, San Francisco, CA 94143 USA
[3] VA Palo Alto Hlth Care Syst, GRECC, Palo Alto, CA USA
来源:
基金:
美国国家卫生研究院;
关键词:
EC-SOD;
TRE promoter;
CamKII-tTA;
LAP-tTA;
transgenic mouse model;
INDUCED LUNG INJURY;
TRANSGENIC MICE;
GENE-EXPRESSION;
ANTIOXIDATIVE PROTECTION;
REGULATED EXPRESSION;
INCREASED RESISTANCE;
CEREBRAL-ISCHEMIA;
INDUCIBLE SYSTEM;
SMOOTH-MUSCLE;
NITRIC-OXIDE;
D O I:
10.1002/dvg.20470
中图分类号:
Q [生物科学];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
The extracellular isoform of superoxide dismutase (EC-SOD, Sod3) plays a protective role against various diseases and injuries mediated by oxidative stress. To investigate the pathophysiological roles of EC-SOD, we generated tetracycline-inducible Sod3 transgenic mice and directed the tissue-specific expression of transgenes by crossing Sod3 transgenic mice with tissue-specific transactivator transgenics. Double transgenic mice with liver-specific expression of Sod3 showed increased EC-SOD levels predominantly in the plasma as the circulating form, whereas double transgenic mice with neuronal-specific expression expressed higher levels of EC-SOD in hippocampus and cortex with intact EC-SOD as the dominant form. EC-SOD protein levels also correlated well with increased SOD activities in double transgenic mice. In addition to enabling tissue-specific expression, the transgene expression can be quickly turned on and off by doxycycline supplementation in the mouse chow. This mouse model, thus, provides the flexibility for on-off control of transgene expression in multiple target tissues. genesis 47:142-154, 2009. (c) 2009 Wiley-Liss, Inc.
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页码:142 / 154
页数:13
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