Publication | Open Access
Neural crest stem cell maintenance by combinatorial Wnt and BMP signaling
186
Citations
40
References
2005
Year
SclerostinAdult Stem CellCombinatorial WntSynaptic SignalingSensory NeurogenesisSocial SciencesTissue DevelopmentBone BiologyBone Morphogenic ProteinSignaling PathwayCraniofacial DevelopmentStem CellsWnt ActivityMolecular SignalingNeural CrestMolecular NeuroscienceMorphogenesisCell BiologyMesenchymal Stem CellCanonical WntDevelopmental BiologyStem Cell ResearchNeuroscienceCochlear DevelopmentMedicineNeural Stem Cell
Canonical Wnt signaling instructively promotes sensory neurogenesis in early neural crest stem cells (eNCSCs) (Lee, H.Y., M. Kleber, L. Hari, V. Brault, U. Suter, M.M. Taketo, R. Kemler, and L. Sommer. 2004. Science. 303:1020-1023). However, during normal development Wnt signaling induces a sensory fate only in a subpopulation of eNCSCs while other cells maintain their stem cell features, despite the presence of Wnt activity. Hence, factors counteracting Wnt signaling must exist. Here, we show that bone morphogenic protein (BMP) signaling antagonizes the sensory fate-inducing activity of Wnt/beta-catenin. Intriguingly, Wnt and BMP act synergistically to suppress differentiation and to maintain NCSC marker expression and multipotency. Similar to NCSCs in vivo, NCSCs maintained in culture alter their responsiveness to instructive growth factors with time. Thus, stem cell development is regulated by combinatorial growth factor activities that interact with changing cell-intrinsic cues.
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