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Lgr4控制小鼠雌性性腺的特化。

Lgr4 controls specialization of female gonads in mice.

作者信息

Koizumi Masae, Oyama Kazunori, Yamakami Yukiko, Kida Tomoyo, Satoh Ryo, Kato Shigeki, Hidema Shizu, Oe Tomoyuki, Goto Takaaki, Clevers Hans, Nawa Akihiro, Nishimori Katsuhiko

机构信息

Laboratory of Molecular Biology, Graduate School of Agricultural Science, Tohoku University, Sendai, Japan Department of Obstetrics and Gynecology, Ehime University School of Medicine, Toon, Japan.

Laboratory of Molecular Biology, Graduate School of Agricultural Science, Tohoku University, Sendai, Japan.

出版信息

Biol Reprod. 2015 Oct;93(4):90. doi: 10.1095/biolreprod.114.123638. Epub 2015 Sep 2.

Abstract

Leucine-rich repeat-containing G protein-coupled receptor 4 (Lgr4) is a type of membrane receptor with a seven-transmembrane structure. LGR4 is homologous to gonadotropin receptors, such as follicle-stimulating hormone receptor (Fshr) and luteinizing hormone/choriogonadotropin receptor (Lhcgr). Recently, it has been reported that Lgr4 is a membrane receptor for R-spondin ligands, which mediate Wnt/beta-catenin signaling. Defects of R-spondin homolog (Rspo1) and wingless-type MMTV integration site family, member 4 (Wnt4) cause masculinization of female gonads. We observed that Lgr4(-/-) female mice show abnormal development of the Wolffian ducts and somatic cells similar to that in the male gonads. Lgr4(-/-) female mice exhibited masculinization similar to that observed in Rspo1-deficient mice. In Lgr4(-/-) ovarian somatic cells, the expression levels of lymphoid enhancer-binding factor 1 (Lefl) and Axin2 (Axin2), which are target genes of Wnt/beta-catenin signaling, were lower than they were in wild-type mice. This study suggests that Lgr4 is critical for ovarian somatic cell specialization via the cooperative signaling of Rspo1 and Wnt/beta-catenin.

摘要

富含亮氨酸重复序列的G蛋白偶联受体4(Lgr4)是一种具有七跨膜结构的膜受体。LGR4与促性腺激素受体同源,如促卵泡激素受体(Fshr)和促黄体生成素/绒毛膜促性腺激素受体(Lhcgr)。最近,有报道称Lgr4是R-spondin配体的膜受体,其介导Wnt/β-连环蛋白信号传导。R-spondin同源物(Rspo1)和无翅型MMTV整合位点家族成员4(Wnt4)的缺陷会导致雌性性腺雄性化。我们观察到Lgr4基因敲除(Lgr4-/-)的雌性小鼠显示出与雄性性腺中类似的中肾管和体细胞异常发育。Lgr4-/-雌性小鼠表现出与Rspo1缺陷小鼠中观察到的类似的雄性化。在Lgr4-/-卵巢体细胞中,作为Wnt/β-连环蛋白信号传导靶基因的淋巴样增强子结合因子1(Lefl)和Axin2的表达水平低于野生型小鼠。这项研究表明,Lgr4通过Rspo1和Wnt/β-连环蛋白的协同信号传导对卵巢体细胞特化至关重要。

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