CDK5‐dependent activation of dynein in the axon initial segment regulates polarized cargo transport in neurons

  • Eva Klinman
    Neuroscience Graduate Group University of Pennsylvania Philadelphia Pennsylvania
  • Mariko Tokito
    Department of Physiology, Perelman School of Medicine University of Pennsylvania Philadelphia Pennsylvania
  • Erika L. F. Holzbaur
    Neuroscience Graduate Group University of Pennsylvania Philadelphia Pennsylvania

抄録

<jats:p>The unique polarization of neurons depends on selective sorting of axonal and somatodendritic cargos to their correct compartments. Axodendritic sorting and filtering occurs within the axon initial segment (AIS). However, the underlying molecular mechanisms responsible for this filter are not well understood. Here, we show that local activation of the neuronal‐specific kinase cyclin‐dependent kinase 5 (CDK5) is required to maintain AIS integrity, as depletion or inhibition of CDK5 induces disordered microtubule polarity and loss of AIS cytoskeletal structure. Furthermore, CDK5‐dependent phosphorylation of the dynein regulator Ndel1 is required for proper re‐routing of mislocalized somatodendritic cargo out of the AIS; inhibition of this pathway induces profound mis‐sorting defects. While inhibition of the CDK5‐Ndel1‐Lis1‐dynein pathway alters both axonal microtubule polarity and axodendritic sorting, we found that these defects occur on distinct timescales; brief inhibition of dynein disrupts axonal cargo sorting before loss of microtubule polarity becomes evident. Together, these studies identify CDK5 as a master upstream regulator of trafficking in vertebrate neurons, required for both AIS microtubule organization and polarized dynein‐dependent sorting of axodendritic cargos, and support an ongoing and essential role for dynein at the AIS.</jats:p><jats:p><jats:inline-graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="graphic/tra12529-gra-0001.png" xlink:title="image" /></jats:p>

収録刊行物

  • Traffic

    Traffic 18 (12), 808-824, 2017-11-08

    Wiley

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