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
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.
引用
收藏
页码:142 / 154
页数:13
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