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Sfrp1 and Sfrp2 are not involved in Wnt/β-catenin signal silencing during lens induction but are required for maintenance of Wnt/β-catenin signaling in lens epithelial cells

机译:Sfrp1和Sfrp2在晶状体诱导过程中不参与Wnt /β-catenin信号沉默但在晶状体上皮细胞中维持Wnt /β-catenin信号传导是必需的

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摘要

During eye lens development, regulation of Wnt/β-catenin signaling is critical for two major processes: initially it must be silent in the lens placode for lens development to proceed, but subsequently it is required for maintenance of the lens epithelium. It is not known how these different phases of Wnt/β-catenin activity/inactivity are regulated. Secreted frizzled related protein-2 (Sfrp2), a putative Wnt-Fz antagonist, is expressed in lens placode and in lens epithelial cells and has been put forward as a candidate for regional Wnt/β-catenin pathway regulation. Here we show its closely-related isoform, Sfrp1, has a complimentary pattern of expression in the lens, being absent from the placode and epithelium but expressed in the fibers. As mice with single knockouts of Sfrp1 or Sfrp2 had no defects in lens formation, we examined lenses of Sfrp1;Sfrp2 double knockout (DKO) mice and showed that they formed lens placode and subsequent lens structures. Consistent with this we did not observe ectopic TCF/Lef activity in lens placode of DKOs. This indicates that Sfrp1 and Sfrp2 individually, or together, do not constitute the putative negative regulator that blocks Wnt/β-catenin signaling during lens induction. In contrast, Sfrp1 and Sfrp2 appear to have a positive regulatory function because Wnt/β-catenin signaling in lens epithelial cells was reduced in Sfrp1;Sfrp2 DKO mice. Lenses that formed in DKO mice were smaller than controls and exhibited a deficient epithelium. Thus Sfrps play a role in lens development, at least in part, by regulating aspects of Wnt/β-catenin signaling in lens epithelial cells.
机译:在眼晶状体发育过程中,Wnt /β-catenin信号的调节对于两个主要过程至关重要:起初,晶状体必须保持沉默才能继续进行晶状体发育,但随后需要维持晶状体上皮。尚不知道如何调节Wnt /β-catenin活性/无活性的这些不同阶段。分泌的卷曲相关蛋白2(Sfrp2),一种假定的Wnt-Fz拮抗剂,在晶状体斑块和晶状体上皮细胞中表达,并已被提议作为区域性Wnt /β-catenin途径调控的候选者。在这里,我们显示了其密切相关的同种型Sfrp1,在晶状体中具有互补的表达模式,不在斑节和上皮中,​​但在纤维中表达。由于单次敲除Sfrp1或Sfrp2的小鼠在晶状体形成方面没有缺陷,因此我们检查了Sfrp1; Sfrp2双敲除(DKO)小鼠的晶状体,发现它们形成晶状体和随后的晶状体结构。与此相一致,我们在DKO的晶状体中未观察到异位TCF / Lef活性。这表明Sfrp1和Sfrp2单独或一起不构成假定的负调节剂,该负调节剂在晶状体诱导过程中阻断Wnt /β-catenin信号传导。相反,Sfrp1和Sfrp2似乎具有正调节功能,因为Sfrp1; Sfrp2 DKO小鼠的晶状体上皮细胞中的Wnt /β-catenin信号传导减少。在DKO小鼠中形成的晶状体比对照组小,并且上皮缺乏。因此,Sfrps至少部分地通过调节晶状体上皮细胞中Wnt /β-连环蛋白信号传导的方面在晶状体发育中起作用。

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