Becker S, Wang Z J, Massey H, Arauz A, Labosky P, Hammerschmidt M, St-Jacques B, Bumcrot D, McMahon A, Grabel L
Department of Biology, Wesleyan University, Middletown, Connecticut 06559-0170, USA.
Dev Biol. 1997 Jul 15;187(2):298-310. doi: 10.1006/dbio.1997.8616.
Hedgehog genes in Drosophila and vertebrates control patterning of a number of different structures during embryogenesis. They code for secreted signaling proteins that are cleaved into an active aminopeptide and a carboxypeptide. The aminopeptide can mediate local and long range events and can act as a morphogen, inducing differentiation of distinct cell types in a concentration-dependent manner. We demonstrate here that the expression of Indian hedgehog mRNA and protein is upregulated dramatically as F9 cells differentiate in response to retinoic acid, into either parietal endoderm or embryoid bodies, containing an outer visceral endoderm layer. The ES cell line D3 forms embryoid bodies in suspension culture without addition of retinoic acid and also upregulates Indian hedgehog expression. RT-PCR analysis of blastocyst outgrowth cultures demonstrates that whereas little or no Indian hedgehog message is present in blastocysts, significant levels appear upon subsequent days of culture, coincident with the emergence of parietal endoderm cells. In situ hybridization analysis for Indian hedgehog mRNA expression demonstrates the presence of elevated levels of message in the outer visceral endoderm cells relative to the core cells in mature embryoid bodies and in the visceral endoderm of Day 6.5 embryos. Whole-mount in situ hybridization analysis of Day 7.5 and 8.5 embryos indicates that Indian hedgehog expression is highest in the visceral yolk sac at this stage. F9 cell lines expressing a full length Indian hedgehog cDNA express a number of characteristics of differentiated cells, in the absence of retinoic acid. Taken together, these data suggest that Indian hedgehog is involved in mediating differentiation of extraembryonic endoderm during early mouse embryogenesis.
果蝇和脊椎动物中的刺猬基因在胚胎发育过程中控制着许多不同结构的模式形成。它们编码分泌型信号蛋白,这些蛋白被切割成活性氨基肽和羧基肽。氨基肽可介导局部和远距离事件,并可作为形态发生素,以浓度依赖的方式诱导不同细胞类型的分化。我们在此证明,随着F9细胞在视黄酸的作用下分化为壁内胚层或包含外层脏内胚层的胚状体,印度刺猬蛋白mRNA和蛋白的表达显著上调。ES细胞系D3在不添加视黄酸的悬浮培养中形成胚状体,并且也上调印度刺猬蛋白的表达。对囊胚生长培养物的RT-PCR分析表明,尽管囊胚中几乎没有或没有印度刺猬蛋白的信息,但在随后的培养天数中会出现显著水平,这与壁内胚层细胞的出现一致。对印度刺猬蛋白mRNA表达的原位杂交分析表明,相对于成熟胚状体中的核心细胞和第6.5天胚胎的脏内胚层,外层脏内胚层细胞中信息水平升高。对第7.5天和8.5天胚胎的整体原位杂交分析表明,在此阶段印度刺猬蛋白的表达在内脏卵黄囊中最高。在没有视黄酸的情况下,表达全长印度刺猬蛋白cDNA的F9细胞系表现出一些分化细胞的特征。综上所述,这些数据表明印度刺猬蛋白参与介导小鼠早期胚胎发育过程中外胚层内胚层的分化。