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首页> 外文期刊>Development >Unique functions of Sonic hedgehog signaling during external genitalia development.
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Unique functions of Sonic hedgehog signaling during external genitalia development.

机译:声波刺猬信号在外生殖器发育过程中的独特功能。

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摘要

Coordinated growth and differentiation of external genitalia generates a proximodistally elongated structure suitable for copulation and efficient fertilization. The differentiation of external genitalia incorporates a unique process, i.e. the formation of the urethral plate and the urethral tube. Despite significant progress in molecular embryology, few attempts have been made to elucidate the molecular developmental processes for external genitalia. The sonic hedgehog (Shh) gene and its signaling genes have been found to be dynamically expressed during murine external genitalia development. Functional analysis by organ culture revealed that Shh could regulate mesenchymally expressed genes, patched 1 (Ptch1), bone morphogenetic protein 4 (Bmp4), Hoxd13 and fibroblast growth factor 10 (Fgf10), in the anlage: the genital tubercle (GT). Activities of Shh for both GT outgrowth and differentiation were also demonstrated. Shh(-/-) mice displayed complete GT agenesis, which is compatible with such observations. Furthermore, the regulation of apoptosis during GT formation was revealed for the first time. Increased cell death and reduced cell proliferation of the Shh(-/-) mice GT were shown. A search for alterations of Shh downstream gene expression identified a dramatic shift of Bmp4 gene expression from the mesenchyme to the epithelium of the Shh mutant before GT outgrowth. Regulation of mesenchymal Fgf10 gene expression by the epithelial Shh was indicated during late GT development. These results suggest a dual mode of Shh function, first by the regulation of initiating GT outgrowth, and second, by subsequent GT differentiation.
机译:外生殖器的协调生长和分化产生了适合交配和有效受精的近前拉长结构。外生殖器的分化包括独特的过程,即尿道板和尿道管的形成。尽管在分子胚胎学上取得了重大进展,但很少有人试图阐明外生殖器的分子发育过程。已发现声音刺猬(Shh)基因及其信号转导基因在鼠体外生殖器发育过程中动态表达。通过器官培养进行的功能分析表明,Shh可以调节生殖器结节(GT)中的间质表达基因,补丁1(Ptch1),骨形态发生蛋白4(Bmp4),Hoxd13和成纤维细胞生长因子10(Fgf10)。还证明了Shh对于GT的生长和分化的活性。 Shh(-/-)小鼠显示出完全的GT发育不全,与这种观察结果兼容。此外,首次揭示了GT形成过程中凋亡的调控。显示了增加的细胞死亡和减少Shh(-/-)小鼠GT细胞增殖。寻找Shh下游基因表达的改变,发现GT生长之前,Bmp4基因表达从间充质转移到Shh突变体的上皮。在GT晚期发育期间,表明了上皮Shh对间质Fgf10基因表达的调控。这些结果表明Shh功能的双重模式,首先是通过启动GT的生长调控,其次是通过随后的GT分化。

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