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Figure 6 | BMC Cell Biology

Figure 6

From: All-trans retinoic acid promotes neural lineage entry by pluripotent embryonic stem cells via multiple pathways

Figure 6

A. Interaction between RA and the ERK pathway during promoted neural specification. FGF receptor tyrosine kinase inhibitor SU5402 and MEK1/2 inhibitors PD184352 and PD0325901, respectively suppresses neural differentiation of ESCs. In RA-treated cultures, PD184352, PD0325901 and RARα-selective antagonist Ro 415253 could inhibit the neural specification of ESCs, while SU5402 shows weak neural inhibition effect. RA probably enhances ERK phosphorylation via MEK1/2 or its upstream but not in a manner that is dependent on FGF signaling, and activated ERK1/2 mediates phosphorylation of the MAPK sites of Smad1 (pSmad1MAPK), which inhibits the inhibitory function of the bone morphogenetic proteins (BMPs)-Smad1 pathway on neural differentiation. Blockade of RA signaling might affect the activation of the upstream of ERK1/2, which leads to failure of neural specification of ESCs even with the stimulation of FGF signaling. B. Possible roles of Wnt signaling in RA-promoted neural differentiation. RA promotes neural specification probably by up-regulating Sfrp2, which inhibits the Wnt-β-catenin anti-neural pathway. Upon adding LiCl or CHIR99021, which stimulates the β-catenin signaling and/or BMP signaling through inhibition of GSK3, the suppression effects on neural specification of β-catenin pathway can be passed down even with the stimuli of RA. RA also may promote neural differentiation by up-regulating RAR, which may decrease β-catenin/LEF/TCF mediated transactivation. There exists a possibility that RA may suppress the inhibition effects on neural differentiation of Wnt-β-catenin pathway by sequestration of β-catenin. pSmad1GSK3 indicates phosphorylation of the GSK3 sites of Smad1.

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