BAC-Dkk3-EGFP Transgenic Mouse: An In Vivo Analytical Tool for Dkk3 Expression

被引:4
|
作者
Muranishi, Yuki [1 ,2 ]
Furukawa, Takahisa [1 ,2 ,3 ]
机构
[1] JST, CREST, Suita, Osaka 5650871, Japan
[2] Osaka Biosci Inst, Dept Dev Biol, Suita, Osaka 5650874, Japan
[3] Osaka Univ, Inst Prot Res, Lab Mol & Dev Biol, Suita, Osaka 5650871, Japan
来源
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY | 2012年
基金
日本科学技术振兴机构;
关键词
MULLER GLIA; NEURAL REGENERATION; DICKKOPF GENES; CHICKEN RETINA; BETA-CATENIN; WNT; PATHWAY; CANCER; CELLS; PROLIFERATE;
D O I
10.1155/2012/973140
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Dickkopf (DKK) family proteins are secreted modulators of the Wnt signaling pathway and are capable of regulating the development of many organs and tissues. We previously identified Dkk3 to be a molecule predominantly expressed in the mouse embryonic retina. However, which cell expresses Dkk3 in the developing and mature mouse retina remains to be elucidated. To examine the precise expression of the Dkk3 protein, we generated BAC-Dkk3-EGFP transgenic mice that express EGFP integrated into the Dkk3 gene in a BAC plasmid. Expression analysis using the BAC-Dkk3-EGFP transgenic mice revealed that Dkk3 is expressed in retinal progenitor cells (RPCs) at embryonic stages and in Muller glial cells in the adult retina. Since Muller glial cells may play a potential role in retinal regeneration, BAC-Dkk3-EGFP mice could be useful for retinal regeneration studies.
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页数:8
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