Maye Peter, Becker Sandy, Siemen Henrike, Thorne Jeffrey, Byrd Noah, Carpentino Joseph, Grabel Laura
Biology Department, Wesleyan University, Middletown, CT 06459-0170, USA.
Dev Biol. 2004 Jan 1;265(1):276-90. doi: 10.1016/j.ydbio.2003.09.027.
Mouse embryonic stem cells can differentiate in vitro into cells of the nervous system, neurons and glia. This differentiation mimics stages observed in vivo, including the generation of primitive ectoderm and neurectoderm in embryoid body culture. We demonstrate here that embryonic stem cell lines mutant for components of the Hedgehog signaling cascade are deficient at generating neurectoderm-containing embryoid bodies. The embryoid bodies derived from mutant cells are also unable to respond to retinoic acid treatment by producing nestin-positive neural stem cells, a response observed in cultures of heterozygous cells, and contain cores apparently arrested at the primitive ectoderm stage. The mutant cultures are also deficient in their capacity to differentiate into mature neurons and glia. These data are consistent with a role for Hedgehog signaling in generating neurectoderm capable of producing the appropriate neuronal and glial progenitors in ES cell culture.
小鼠胚胎干细胞在体外可分化为神经系统细胞、神经元和神经胶质细胞。这种分化模拟了体内观察到的阶段,包括在胚状体培养中原始外胚层和神经外胚层的生成。我们在此证明,刺猬信号级联反应成分发生突变的胚胎干细胞系在生成含神经外胚层的胚状体方面存在缺陷。源自突变细胞的胚状体也无法通过产生巢蛋白阳性神经干细胞来响应视黄酸处理,杂合细胞培养中可观察到这种反应,并且其核心显然停滞在原始外胚层阶段。突变培养物在分化为成熟神经元和神经胶质细胞的能力方面也存在缺陷。这些数据与刺猬信号在生成能够在胚胎干细胞培养中产生适当神经元和神经胶质祖细胞的神经外胚层中的作用一致。