Tamoxifen-Inducible Podocyte-Specific iCre Recombinase Transgenic Mouse Provides a Simple Approach for Modulation of Podocytes In Vivo

被引:21
|
作者
Wang, Jinrong [1 ]
Wang, Yin [1 ]
Long, Jianyin [1 ]
Chang, Benny H. J. [2 ]
Wilson, Mathew H. [1 ]
Overbeek, Paul [2 ]
Daneshi, Farhad R. [1 ]
机构
[1] Baylor Coll Med, Dept Med, Div Nephrol, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Mol & Cell Biol, Houston, TX 77030 USA
关键词
kidneys; podocin; transgenic mice; Cre-LoxP; ROSA26; CRE RECOMBINASE; ESTROGEN-RECEPTOR; EXPRESSION; GENE; MICE; HEART; GENERATION; SYSTEM; ADULT;
D O I
10.1002/dvg.20635
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
We report the generation and initial characterization of a mouse line expressing tamoxifen-inducible improved Cre (iCre) recombinase (iCre-ERT2) under the regulation of NPHS2 (podocin) gene promoter. The resulting transgenic mouse line was named podociniCreER(T2) mice. The efficiency of iCre activity was confirmed by crossing podocin-iCreER(T2) with the ROSA26 reporter mouse. By using the floxed ROSA reporter mice, we found that tamoxifen specifically induced recombination in the kidneys. In the absence of tamoxifen, recombination was undetectable in podociniCreER(T2);ROSA26 mice. However, following intraperitoneal injection of tamoxifen, selective recombination was observed in the podocytes of adult animals. We further examined the efficiency of recombination by assessing various tamoxifen exposure regimens in adult mice. These results suggest that podocin-iCre-ERT2 mouse provides an excellent genetic tool to examine the function of candidate genes in podocytes in a spatially and temporally-restricted manner. genesis 48:446-451, 2010. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:446 / 451
页数:6
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