Moore-Scott Billie A, Manley Nancy R
Institute for Molecular Medicine and Genetics, Medical College of Georgia, Augusta, GA 30912, USA.
Dev Biol. 2005 Feb 15;278(2):323-35. doi: 10.1016/j.ydbio.2004.10.027.
Previous studies have implicated Sonic hedgehog (Shh) as an important regulator of pharyngeal region development. Here we show that Shh is differentially expressed within the pharyngeal endoderm along the anterior-posterior axis. In Shh-/- mutants, the pharyngeal pouches and arches formed by E9.5 and marker expression showed that initial patterning was normal. However, by E10.5-E11.0, the first arch had atrophied and the first pouch was missing. Although small, the second, third, and fourth arches and pouches were present. The expression patterns of Fgf8, Pax1, and Bmp4 suggested that pouch identity was abnormal at E10.5 and that Shh is a negative regulator of these genes in the pouches. Despite the loss of pouch identity and an increase in mesenchymal cell death, arch identity markers were expressed normally. Our data show that a Shh-dependent patterning mechanism is required to maintain pouch patterning, independent or downstream of arch identity. Changes in the distribution of Bmp4 and Gcm2 in the third pouch endoderm and subsequent organ phenotypes in Shh-/- mutants suggested that exclusion of Shh from the third pouch is required for dorsal-ventral patterning and for parathyroid specification and organogenesis. Furthermore, this function for Shh may be opposed by Bmp4. Our data suggest that, as in the posterior gut endoderm, exclusion of Shh expression from developing primordia is required for the proper development of pharyngeal-derived organs.
先前的研究表明,音猬因子(Shh)是咽区发育的重要调节因子。在此我们发现,Shh沿前后轴在咽内胚层中呈差异表达。在Shh基因敲除(Shh-/-)突变体中,E9.5时形成的咽囊和咽弓以及标记物表达显示初始模式正常。然而,到E10.5 - E11.0时,第一咽弓萎缩,第一咽囊缺失。虽然第二、第三和第四咽弓及咽囊较小,但仍然存在。Fgf8、Pax1和Bmp4的表达模式表明,在E10.5时咽囊特征异常,且Shh是这些基因在咽囊中的负调节因子。尽管咽囊特征丧失且间充质细胞死亡增加,但咽弓特征标记物仍正常表达。我们的数据表明,维持咽囊模式需要一种依赖Shh的模式形成机制,该机制独立于或位于咽弓特征的下游。Shh基因敲除突变体中第三咽囊内胚层中Bmp4和Gcm2分布的变化以及随后的器官表型表明,第三咽囊中排除Shh对于背腹模式形成以及甲状旁腺的特化和器官发生是必需的。此外,Shh的这种功能可能受到Bmp4的拮抗。我们的数据表明,与后肠内胚层一样,发育中的原基排除Shh表达对于咽衍生器官的正常发育是必需的。