Wnt antagonism of Shh facilitates midbrain floor plate neurogenesis

The floor plate is not usually a neurogenic structure, but in the embryonic midbrain, dopaminergic neurons do develop from floor plate. This study shows that the high levels of Shh that are present in the floor plate generally suppress neurogenesis and that for neurons to be generated, Shh must be d...

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Veröffentlicht in:Nature neuroscience 2009-02, Vol.12 (2), p.125-131
Hauptverfasser: Joksimovic, Milan, Yun, Beth A, Kittappa, Raja, Anderegg, Angela M, Chang, Wendy W, Taketo, Makoto M, McKay, Ronald D G, Awatramani, Rajeshwar B
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Sprache:eng
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Zusammenfassung:The floor plate is not usually a neurogenic structure, but in the embryonic midbrain, dopaminergic neurons do develop from floor plate. This study shows that the high levels of Shh that are present in the floor plate generally suppress neurogenesis and that for neurons to be generated, Shh must be downregulated by Wnt signaling in the midbrain. The floor plate, an essential ventral midline organizing center that produces the morphogen Shh, has distinct properties along the neuraxis. The neurogenic potential of the floor plate and its underlying mechanisms remain unknown. Using Shh as a driver for lineage analysis, we found that the mouse midbrain, but not the hindbrain, floor plate is neurogenic, giving rise to dopamine (DA) neurons. Distinct spatiotemporal Shh and Wnt expression may distinguish the neurogenetic potential of these structures. We discovered an inhibitory role for Shh: removal of Shh resulted in neurogenesis from the hindbrain midline and, conversely, high doses of Shh inhibited proliferation and DA neuron production in midbrain cultures. We found that Wnt/beta-catenin signaling is necessary and sufficient for antagonizing Shh , DA progenitor marker induction and promotion of dopaminergic neurogenesis. These findings demonstrate how the dynamic interplay of canonical Wnt/beta-catenin signaling and Shh may orchestrate floor plate neurogenesis or a lack thereof.
ISSN:1097-6256
1546-1726
DOI:10.1038/nn.2243