Kim A S, Anderson S A, Rubenstein J L, Lowenstein D H, Pleasure S J
Neurodevelopmental Disorders Laboratory, Department of Neurology, University of California, San Francisco, California 94143, USA.
J Neurosci. 2001 Mar 1;21(5):RC132. doi: 10.1523/JNEUROSCI.21-05-j0002.2001.
Wnt signaling regulates a wide range of developmental processes such as proliferation, cell migration, axon guidance, and cell fate determination. In this report, we studied the expression of secreted frizzled related protein-2 (SFRP-2), which codes for a putative Wnt inhibitor, in the developing nervous system. SFRP-2 is expressed in several discrete neuroepithelial domains, including the diencephalon, the insertion of the eminentia thalami into the caudal telencephalon, and the pallial-subpallial boundary (PSB). We also noted that Wnt-7b expression was similar to SFRP-2 expression. Because many of these structures are disrupted in Pax-6 mutant mice, we examined SFRP-2 and Wnt-7b expression in the forebrains of Pax-6 Sey/Sey mice. We found that Pax-6 mutants lack SFRP-2 expression in the PSB and diencephalon. Interestingly, Pax-6 mutants also lack Wnt-7b expression in the PSB, but Wnt-7b expression in the diencephalon is preserved. Furthermore, in the spinal cord of Pax-6 mutants, SFRP-2 and Wnt-7b expression was greatly reduced. Our results suggest that by virtue of its apposition to Wnt-7b expression, SFRP-2 may modulate its function, particularly at boundaries such as the PSB, and that changes in Wnt signaling contribute to the phenotype of Pax-6 mutants.
Wnt信号通路调控着广泛的发育过程,如细胞增殖、细胞迁移、轴突导向和细胞命运决定。在本报告中,我们研究了分泌型卷曲相关蛋白2(SFRP-2)在发育中的神经系统中的表达,该蛋白编码一种假定的Wnt抑制剂。SFRP-2在几个离散的神经上皮区域表达,包括间脑、丘脑隆起插入尾侧端脑的部位以及皮质-皮质下边界(PSB)。我们还注意到Wnt-7b的表达与SFRP-2的表达相似。由于在Pax-6突变小鼠中许多这些结构被破坏,我们检查了Pax-6 Sey/Sey小鼠前脑中SFRP-2和Wnt-7b的表达。我们发现Pax-6突变体在PSB和间脑中缺乏SFRP-2表达。有趣的是,Pax-6突变体在PSB中也缺乏Wnt-7b表达,但间脑中的Wnt-7b表达得以保留。此外,在Pax-6突变体的脊髓中,SFRP-2和Wnt-7b的表达大幅降低。我们的结果表明,由于SFRP-2与Wnt-7b表达相邻,它可能调节其功能,特别是在PSB等边界处,并且Wnt信号通路的变化导致了Pax-6突变体的表型。