AI Article Synopsis

  • Phosphoinositide 3-kinases (PI3Ks) promote axon growth and branching by regulating the accumulation of PI(3,4,5)P, but the presence of PTEN, which counteracts this process, complicates understanding how sufficient levels of PI(3,4,5)P are maintained.* -
  • Research shows that proper axon development relies on balancing elongation and branching, with PRG2 playing a key role by inhibiting PTEN to stabilize PI(3,4,5)P at the axon membrane.* -
  • PRG2 is essential for the formation of axon filopodia and branches by enabling local PTEN inhibition, indicating it is

Article Abstract

In developing neurons, phosphoinositide 3-kinases (PI3Ks) control axon growth and branching by positively regulating PI3K/PI(3,4,5)P, but how neurons are able to generate sufficient PI(3,4,5)P in the presence of high levels of the antagonizing phosphatase PTEN is difficult to reconcile. We find that normal axon morphogenesis involves homeostasis of elongation and branch growth controlled by accumulation of PI(3,4,5)P through PTEN inhibition. We identify a plasma membrane-localized protein-protein interaction of PTEN with plasticity-related gene 2 (PRG2). PRG2 stabilizes membrane PI(3,4,5)P by inhibiting PTEN and localizes in nanoclusters along axon membranes when neurons initiate their complex branching behavior. We demonstrate that PRG2 is both sufficient and necessary to account for the ability of neurons to generate axon filopodia and branches in dependence on PI3K/PI(3,4,5)P and PTEN. Our data indicate that PRG2 is part of a neuronal growth program that induces collateral branch growth in axons by conferring local inhibition of PTEN.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856728PMC
http://dx.doi.org/10.1016/j.celrep.2019.10.039DOI Listing

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