TY - JOUR T1 - Interactions of Wnt/β-Catenin Signaling and Sonic Hedgehog Regulate the Neurogenesis of Ventral Midbrain Dopamine Neurons JF - The Journal of Neuroscience JO - J. Neurosci. SP - 9280 LP - 9291 DO - 10.1523/JNEUROSCI.0860-10.2010 VL - 30 IS - 27 AU - Mianzhi Tang AU - J. Carlos Villaescusa AU - Sarah X. Luo AU - Camilla Guitarte AU - Simonia Lei AU - Yasunori Miyamoto AU - Makoto M. Taketo AU - Ernest Arenas AU - Eric J. Huang Y1 - 2010/07/07 UR - http://www.jneurosci.org/content/30/27/9280.abstract N2 - Signaling mechanisms involving Wnt/β-catenin and sonic hedgehog (Shh) are known to regulate the development of ventral midbrain (vMB) dopamine neurons. However, the interactions between these two mechanisms and how such interactions can be targeted to promote a maximal production of dopamine neurons are not fully understood. Here we show that conditional mouse mutants with region-specific activation of β-catenin signaling in vMB using the Shh–Cre mice show a marked expansion of Sox2-, Ngn2-, and Otx2-positive progenitors but perturbs their cell cycle exit and reduces the generation of dopamine neurons. Furthermore, activation of β-catenin in vMB also results in a progressive loss of Shh expression and Shh target genes. Such antagonistic effects between the activation of Wnt/β-catenin and Shh can be recapitulated in vMB progenitors and in mouse embryonic stem cell cultures. Notwithstanding these antagonistic interactions, cell-type-specific activation of β-catenin in the midline progenitors using the tyrosine hydroxylase–internal ribosomal entry site–Cre (Th-IRES-Cre) mice leads to increased dopaminergic neurogenesis. Together, these results indicate the presence of a delicate balance between Wnt/β-catenin and Shh signaling mechanisms in the progression from progenitors to dopamine neurons. Persistent activation of β-catenin in early progenitors perturbs their cell cycle progression and antagonizes Shh expression, whereas activation of β-catenin in midline progenitors promotes the generation of dopamine neurons. ER -