These cultures did, however, proceed normally to become gliogenic after the phase of neurogenesis had ended. In contrast, upper-layer neurons seemed comparatively well represented (roughly half, by our qualitative assessment

of the data) among differentiated mESCs after being cultured by the SFEBq method without Luminespib price any growth factors (Eiraku et al., 2008). These observations suggest that some features of aggregate culture are more permissive for upper-layer neuron production, whereas low-density culture is somewhat prohibitive. The removal of neural stem cells from their neuroepithelial environment probably results in less efficient Notch and β-catenin signaling, which are facilitated through apically

localized proteins in radial http://www.selleckchem.com/products/JNJ-26481585.html glial cells (Bultje et al., 2009 and Zhang et al., 2010). Ectopic FGF2 can compensate for both of these deficiencies (Shimizu et al., 2008 and Yoon et al., 2004), but not without tradeoffs. FGF2 can act as a caudalizing agent for cells whose telencephalic identities are not yet fixed (Cox and Hemmati-Brivanlou, 1995), and a ventralizing agent for those whose identities are (Abematsu et al., 2006 and Bithell et al., 2008). The effects of FGF2 on patterning can take place over multiple cell cycles (Koch et al., 2009), possibly explaining why early-born neurons were correctly specified but later-born subtypes were poorly represented in the experiments of Gaspard et al. (2008) and Shen et al. (2006). It may be possible to use other combinations of mitogens and morphogens, including Notch and Wnt ligands, to maintain cortical progenitor identity in low-density cultures through the duration of the neurogenic sequence.

SFEBq aggregates below appear to autonomously produce the right factors in the right combinations and levels to mimic the developing cortical neuroepithelium. Although mouse SFEBq aggregates successfully produced upper layer neurons, human SFEBq aggregates apparently did not (Eiraku et al., 2008). If human SFEBq aggregates follow a natural developmental time course, when might we expect upper layer neurons to be produced? By immunostaining fixed sections from human fetal cortex, we have observed the emergence of Satb2+ neurons in the proliferative zone by gestational week 14 (GW14), and their arrival in the cortical plate begins by GW15 (unpublished data). The clinical term “gestational week” is defined by the female patient’s last menses, so GW14 actually refers to roughly the 12th week of fetal development. Thus, going from the blastocyst embryo (the stage at which hESCs are harvested) to upper-layer neuron production in the cortex requires ∼75 days of differentiation. The data shown by Eiraku et al. (2008) were obtained after 45–60 days of SFEBq culture, which could explain why they did not report upper-layer neurogenesis.