Lgr4-Deficient Mice Showed Premature Differentiation of Ureteric Bud With Reduced Expression of Wnt Effector Lef1 and Gata3

被引:27
作者
Mohri, Yasuaki [1 ]
Oyama, Kazunori [1 ]
Akamatsu, Atsushi [1 ]
Kato, Shigeki [1 ]
Nishimori, Katsuhiko [1 ]
机构
[1] Tohoku Univ, Mol Biol Lab, Grad Sch Agr Sci, Aoba Ku, Sendai, Miyagi 9818555, Japan
基金
日本学术振兴会;
关键词
Lgr4; knockout mice; kidney morphogenesis; ureteric bud; Wnt canonical pathway; COUPLED RECEPTOR 48; MOUSE KIDNEY DEVELOPMENT; MALE REPRODUCTIVE-TRACT; ENTERIC NERVOUS-SYSTEM; TYROSINE KINASE; LACKING GDNF; BRANCHING MORPHOGENESIS; POSTNATAL-DEVELOPMENT; SIGNALING PATHWAY; RENAL DEVELOPMENT;
D O I
10.1002/dvdy.22651
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
We previously reported that Lgr4 has a critical role in the morphogenesis of kidney, but the detailed functions of Lgr4 in kidney development have not been elucidated. In contrast to Lgr4 null mice with 129Ola 3 C57BL/6J mixed background, C57BL/6J-backcrossed Lgr4 null mice (Lgr4(-/-)) showed the severe phenotype of embryonic lethality and also had dilated tubules in kidneys at E16.5. Based on quantitative RT-PCR and in situ hybridization, branching morphogenesis at E15.5 in the Lgr4(-/-) was arrested earlier, and both DBA-lectin staining and immunohistochemical analysis using Aqp3 antibodies showed that the ureteric bud (UB) of Lgr4(-/-) kidneys underwent premature differentiation. Furthermore, quantitative RT-PCR and histological analysis suggested that the impaired UB differentiation was caused by down-regulation of the Wnt pathway and Gata3 in the Lgr4(-/-) kidneys. We demonstrate here that Lgr4 has a novel function for maintaining the UB in an undifferentiated state. Developmental Dynamics 240:1626-1634, 2011. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:1626 / 1634
页数:9
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