Leucine-rich repeat-containing g protein-coupled receptor-4 (LGR4, Gpr48) is essential for renal development in mice

被引:66
作者
Kato, Shigeki
Matsubara, Mitsunobu
Matsuo, Tsuyoshi
Mohri, Yasuaki
Kazama, Itsuro
Hatano, Ryo
Umezawa, Akihiro
Nishimori, Katsuhiko
机构
[1] Tohoku Univ, Grad Sch Agr Sci, Mol Biol Lab, Aoba Ku, Sendai, Miyagi 9818555, Japan
[2] Tohoku Univ, Sch Med, Ctr Translat & Adv Anim Res, Div Mol Med, Sendai, Miyagi 9818555, Japan
[3] Natl Res Inst Child Hlth & Dev, Tokyo, Japan
来源
NEPHRON EXPERIMENTAL NEPHROLOGY | 2006年 / 104卷 / 02期
关键词
G protein-coupled receptor; leucine-rich; repeat-containing; glycoprotein hormone receptor homology; leucine-rich repeats; renal hypoplasia;
D O I
10.1159/000093999
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Leucine-rich repeat-containing G protein-coupled receptor (LGR)-4 is a G protein-coupled receptor (GPCR) with a seven-transmembrane domain structure. ILGRs are evolutionally and structurally phylogenetic, classified into three subgroups and are members of the so-called orphan receptors whose ligands have yet to be identified. We generated knockout mice lacking Lgr4 (Gpr48) by targeted deletion of part of exon 18, which codes for the transmembrane and signal-transducing domains of the receptor. Lgr4 null mice were born at much less than the 25% expected frequency from crosses of Lgr4 heterozygous mice (Lgr4(+/-)). Lgr4 null mice that survived in utero died shortly after birth in almost all cases. We observed striking renal hypoplasia in the null mice, accompanied by elevated concentration of plasma creatinine. Histological analysis of the PO null mouse kidney showed a notable decrease in the total number and density of the glomerulus. Thus, the function of Lgr4 is essential to regulate renal development in the mouse. This study suggests that the Lgr4 gene is a new and important member of LGRs involved in a group of genes responsible for hereditary disease in the kidney. Copyright (c) 2006 S. Karger AG, Basel.
引用
收藏
页码:E63 / E75
页数:13
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