Proceedings of the National Academy of Sciences · 2010 · 185 citations · 29 references
Sensory Cell DevelopmentNeurotologyCellular PhysiologyInner Ear MorphogenesisSignaling PathwayProsensory SpecificationNotch ActivityAuditory ScienceIntercellular CommunicationCell SignalingNeural CrestMammalian Inner EarHealth SciencesVestibular SystemMorphogenesisSpecifies Prosensory DomainsAuditory ResearchHuman HearingNervous SystemCell BiologyAuditory Hair CellsCell LineageDevelopmental BiologySignal TransductionNeuroanatomyLateral InductionAuditory PhysiologyNeuroscienceCochlear DevelopmentCell Fate DeterminationMedicineAuditory System
Prosensory specification defines the six inner ear organs, and evidence indicates that Notch signaling—particularly Jagged1—is essential, as its inhibition disrupts and its activation induces ectopic sensory patches. The study tests whether Notch activity alone can drive prosensory specification in the mouse inner ear by conditionally activating the pathway in nonsensory regions. Using a Cre/loxP system, the authors conditionally activated Notch signaling in nonsensory otic epithelium at various developmental stages to assess its sufficiency for prosensory induction. Early ectopic Notch activation induced prosensory markers throughout the epithelium, while later activation produced ectopic sensory patches that differentiated fully, and isolated activation triggered Jag1 lateral induction spreading prosensory specification to neighboring cells, supporting a lateral induction model.
During inner ear morphogenesis, the process of prosensory specification defines the specific regions of the otic epithelium that will give rise to the six separate inner ear organs essential for hearing and balance. The mechanism of prosensory specification is not fully understood, but there is evidence that the Notch intercellular signaling pathway plays a critical role. The Notch ligand Jagged1 (Jag1) is expressed in the prosensory domains, and mutation of Jag1 impairs sensory formation. Furthermore, pharmacological inhibition of Notch in vitro during prosensory specification disrupts the prosensory process. Additionally, activation of Notch by cDNA electroporation in chick otocysts results in formation of ectopic sensory patches. Here we test whether Notch activity is sufficient for prosensory specification in the mouse, using a Cre-/loxP approach to conditionally activate the Notch pathway in nonsensory regions of the inner ear epithelia during different stages of otic vesicle morphogenesis. We find that broad ectopic activation of Notch at very early developmental stages causes induction of prosensory markers throughout the entire otic epithelium. At later stages of development, activation of Notch in nonsensory regions leads to induction of sensory patches that later differentiate to form complete ectopic sensory structures. Activation of Notch in isolated nonsensory cells results in lateral induction of Jag1 expression in neighboring cells and spreading of prosensory specification to the adjacent cells through an intercellular mechanism. These results support a model where activation of Notch and propagation through lateral induction promote prosensory character in specific regions of the developing otocyst.
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