The Rockefeller University, 1230 York Avenue, New York, NY 10021-6339, USA, , , , , , US.
Dev Genes Evol. 1997 May;207(1):19-28. doi: 10.1007/s004270050088.
In Xenopus embryos, a truncated type II activin receptor (Delta1XAR1), capable of blocking signals by several transforming growth factor (TGF)-beta family members, can induce neural tissue suggesting neural fate is under inhibitory control. Activin and bone morphogenetic protein 4 (BMP4) can act as neural inhibitors but only BMP4 can induce epidermis in Xenopus ectodermal cells. We have used the pluripotent mouse embryonal carcinoma cell line P19 to examine whether the mechanisms of ectodermal cell fate decisions are conserved among vertebrates. We show that a P19 cell line expressing Delta1XAR1 will differentiate into neurons. In addition, BMP4 inhibits retinoic acid (RA)-induced neural differentiation of P19 cells and induces keratin expression. These results suggest that in mammals as in amphibians neural fate is under inhibitory control and BMP4 can alter ectodermal differentiation.
在非洲爪蟾胚胎中,一种截断的 II 型激活素受体(Delta1XAR1)能够阻断几种转化生长因子(TGF)-β家族成员的信号,可诱导神经组织,表明神经命运受到抑制控制。激活素和骨形态发生蛋白 4(BMP4)可以作为神经抑制剂,但只有 BMP4 可以诱导非洲爪蟾外胚层细胞的表皮。我们使用多能性小鼠胚胎癌细胞系 P19 来研究脊椎动物中表皮细胞命运决定的机制是否保守。我们表明,表达 Delta1XAR1 的 P19 细胞系将分化为神经元。此外,BMP4 抑制视黄酸(RA)诱导的 P19 细胞的神经分化,并诱导角蛋白表达。这些结果表明,在哺乳动物中,与两栖动物一样,神经命运受到抑制控制,BMP4 可以改变外胚层分化。