Role of EPAC in axon determination

Pablo Andrés Munoz Llancao

    Research output: ThesisThesis fully internal (DIV)

    1952 Downloads (Pure)

    Abstract

    The acquisition and maintenance of spatial differences in structure of the neuron, a phenomenon referred to as neuronal polarity, is a crucial event that may be key in understanding neuronal wiring fundamental to our brain function. The aim of this thesis was to investigate how EPAC, a protein activated by the second messenger cyclic AMP (cAMP), controls neuronal polarity, using freshly isolated hippocampal neurons from mouse brain. We observed that pharmacological inhibition of EPAC and genetic activation can induce opposite changes in terms of neuronal morphology. Inhibition creates neurons with multiple axons, whereas activation reduces the length of the axon and the number of neurons that are polarized, a phenomenon shared by several other regulators of polarity. Mechanistically, we determined that an important target of EPAC in the regulation of neuronal polarity is Rap1B, a small GTPase that historically has also been observed to drive polarization processes. The solidity of this signalling event becomes evident by the fact that also in neuroblastoma cells EPAC activation can lead to the development of axon-like structures, a phenomenon that was previously only attributed to PKA, which is also activated by cAMP. The work presented here provides a better understanding of the mechanisms underlying neuronal polarity and the development of the axon, expanding on the functions of cyclic AMP in this system and highlighting EPAC as a crucial and novel mediator of cAMP-driven polarity.
    Original languageEnglish
    QualificationDoctor of Philosophy
    Awarding Institution
    • University of Groningen
    Supervisors/Advisors
    • Boddeke, Erik, Supervisor
    • Schmidt, Martina, Supervisor
    • Gonzalez-Billault, Christian, Supervisor, External person
    Award date23-Nov-2015
    Place of Publication[Groningen]
    Publisher
    Print ISBNs978-90-367-8396-5
    Publication statusPublished - 2015

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