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Local translation of TC10 is required for membrane expansion during axon outgrowth

Author

Listed:
  • Neilia G. Gracias

    (The Taub Institute for Research on Alzheimer’s Disease and the Aging Brain, Columbia University Medical Center)

  • Nicole J. Shirkey-Son

    (The Taub Institute for Research on Alzheimer’s Disease and the Aging Brain, Columbia University Medical Center
    Present address: Department of Neuroscience, University of Minnesota, Minneapolis, Minnesota 55455, USA)

  • Ulrich Hengst

    (The Taub Institute for Research on Alzheimer’s Disease and the Aging Brain, Columbia University Medical Center
    Columbia University Medical Center)

Abstract

The surface of developing axons expands in a process mediated by the exocyst complex. The spatio-temporal regulation of the exocyst is only partially understood. Here we report that stimulated membrane enlargement in dorsal root ganglion (DRG) axons is triggered by intra-axonal synthesis of TC10, a small GTPase required for exocyst function. Induced membrane expansion and axon outgrowth are inhibited after axon-specific knockdown of TC10 mRNA. To determine the relationship of intra-axonal TC10 synthesis with the previously described stimulus-induced translation of the cytoskeletal regulator Par3, we investigate the signalling pathways controlling their local translation in response to NGF. Phosphoinositide 3-kinase (PI3K)-dependent activation of the Rheb-mTOR pathway triggers the simultaneous local synthesis of TC10 and Par3. These results reveal the importance of local translation in the control of membrane dynamics and demonstrate that localized, mTOR-dependent protein synthesis triggers the simultaneous activation of parallel pathways.

Suggested Citation

  • Neilia G. Gracias & Nicole J. Shirkey-Son & Ulrich Hengst, 2014. "Local translation of TC10 is required for membrane expansion during axon outgrowth," Nature Communications, Nature, vol. 5(1), pages 1-13, May.
  • Handle: RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms4506
    DOI: 10.1038/ncomms4506
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