Conditional Knockout of Lgr4 Leads to Impaired Ductal Elongation and Branching Morphogenesis in Mouse Mammary Glands

被引:30
作者
Oyama, K.
Mohri, Y.
Sone, M.
Nawa, A. [2 ]
Nishimori, K. [1 ]
机构
[1] Tohoku Univ, Mol Biol Lab, Grad Sch Agr Sci, Aoba Ku, Sendai, Miyagi 9818555, Japan
[2] Nagoya Univ, Grad Sch Med, Dept Obstet & Gynecol, Nagoya, Aichi 4648601, Japan
基金
日本学术振兴会;
关键词
Knockout mouse; Lgr4; Mammary gland; Morphogenesis; ESTROGEN-RECEPTOR-ALPHA; MALE REPRODUCTIVE-TRACT; POSTNATAL-DEVELOPMENT; REDUCED EXPRESSION; SIGNALING PATHWAY; DOWN-REGULATION; MICE; TISSUE; ADULT; REVEALS;
D O I
10.1159/000329476
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
We have analyzed the function of LGR4 in the development of various mouse epithelial tissues. Here we first report the retarded invasion of mammary ducts into the fat pad observed in Lgr4(K5) (KO) mice at 4 weeks, compared with that of age-matched Lgr4(K5) (ctrl). Furthermore, we demonstrate a significant decrease in mammary ductal branching in Lgr4(K5) (KO) at several stages (4, 6 and 8 weeks). On the other hand, immunohistochemical analysis of the mammary gland of Lgr4(K5) (KO) using anti-alpha SMA, anti-K18 and anti-laminin antibodies showed structures similar to those of Lgr4(K5) (ctrl) mammary glands. In addition, we did not detect significant differences in the expression of ER alpha, which was suggested to be a downstream molecule of LGR4, and Lgr4(K5) (KO) showed no retarded invasion in the response to 17 beta-estradiol administration. Furthermore, the phosphorylated form of Smad1/5/8 was normally detected in the mammary gland of Lgr4(K5) (KO). Copyright (C) 2011 S. Karger AG, Basel
引用
收藏
页码:205 / 212
页数:8
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