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Wnt4,一种多效信号,可在女性卵泡的卵母细胞成熟过程中控制细胞极性、基底膜完整性和抗苗勒管激素表达。

Wnt4, a pleiotropic signal for controlling cell polarity, basement membrane integrity, and antimüllerian hormone expression during oocyte maturation in the female follicle.

机构信息

1Laboratory of Developmental Biology, Department of Medical Biochemistry and Molecular Biology, University of Oulu and Biocenter Oulu, Aapistie 5, P. O. Box 5000, FIN-90220, Oulu, Finland.

出版信息

FASEB J. 2014 Apr;28(4):1568-81. doi: 10.1096/fj.13-233247. Epub 2013 Dec 26.

DOI:10.1096/fj.13-233247
PMID:24371124
Abstract

Wnt4 is a key signal that channels the developmental fate of the indifferent mammalian gonad toward the ovary, but whether Wnt4 has later roles during ovary development remains unknown. To investigate this, we inactivated the Wnt4 gene by crossing Amhr2Cre and doxycycline-inducible Rosa(rtTA)-knock-in Cre mice with mice carrying a floxed Wnt4 allele and used a novel Wnt4(mCherry)-knock-in mouse. In these models, ovarian folliculogenesis was compromised, and female fertility was severely reduced, and Wnt4 deficiency eventually led to premature ovarian failure. These anomalies were associated with cell polarity defects in the follicle. Within the follicle, laminin and type IV collagen assembled ectopic basement membrane-like structures, the cell adherens junction components N-cadherin and β-catenin lost their polarized expression pattern, and expression of the gap junction protein connexin 43 was reduced by ~30% when compared with that of the controls. Besides these changes, expression of antimüllerian hormone (Amh) was inhibited in the absence of Wnt4 signaling in vivo. Consistent with this, Wnt4 signaling up-regulated Amh gene expression in KK1 cells in vitro. Thus, Wnt4 signaling is necessary during maturation of the ovarian follicles, where it coordinates expression of Amh, cell survival, and polarized organization of the follicular cells.

摘要

Wnt4 是一种关键信号,它将哺乳动物未分化性腺的发育命运引导到卵巢,但 Wnt4 在卵巢发育过程中是否具有后期作用尚不清楚。为了研究这一点,我们通过将 Amhr2Cre 和强力霉素诱导的 Rosa(rtTA)-knock-in Cre 小鼠与携带 floxed Wnt4 等位基因的小鼠以及新型 Wnt4(mCherry)-knock-in 小鼠进行杂交,使 Wnt4 基因失活。在这些模型中,卵泡发生受损,雌性生育力严重降低,Wnt4 缺乏最终导致卵巢早衰。这些异常与卵泡中的细胞极性缺陷有关。在卵泡内,层粘连蛋白和 IV 型胶原组装异位基底膜样结构,细胞黏着连接成分 N-钙黏蛋白和 β-连环蛋白失去其极化表达模式,与对照组相比,间隙连接蛋白 43 的表达减少了约 30%。除了这些变化,体内缺乏 Wnt4 信号时,抗缪勒管激素 (Amh) 的表达受到抑制。与此一致的是,Wnt4 信号在体外上调 KK1 细胞中 Amh 基因的表达。因此,Wnt4 信号在卵巢卵泡的成熟过程中是必要的,它协调 Amh 的表达、细胞存活和卵泡细胞的极化组织。

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