A midline switch of receptor processing regulates commissural axon guidance in vertebrates

  1. Homaira Nawabi1,4,
  2. Anne Briançon-Marjollet1,4,
  3. Christopher Clark1,
  4. Isabelle Sanyas1,
  5. Hyota Takamatsu2,
  6. Tatsusada Okuno2,
  7. Atsushi Kumanogoh2,
  8. Muriel Bozon1,
  9. Kaori Takeshima3,
  10. Yutaka Yoshida3,
  11. Frédéric Moret1,
  12. Karima Abouzid1 and
  13. Valérie Castellani1,5
  1. 1University of Lyon, University of Lyon 1, Claude Bernard Lyon1, CGMC, UMR, CNRS 5534, F-69000 Lyon, France;
  2. 2Department of Immunology, Research Institute for Microbial Diseases, Osaka University, Osaka, 565-0871, Japan;
  3. 3Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio 45229, USA
    1. 4 These authors contributed equally to this work.

    Abstract

    Commissural axon guidance requires complex modulations of growth cone sensitivity to midline-derived cues, but underlying mechanisms in vertebrates remain largely unknown. By using combinations of ex vivo and in vivo approaches, we uncovered a molecular pathway controlling the gain of response to a midline repellent, Semaphorin3B (Sema3B). First, we provide evidence that Semaphorin3B/Plexin-A1 signaling participates in the guidance of commissural projections at the vertebrate ventral midline. Second, we show that, at the precrossing stage, commissural neurons synthesize the Neuropilin-2 and Plexin-A1 Semaphorin3B receptor subunits, but Plexin-A1 expression is prevented by a calpain1-mediated processing, resulting in silencing commissural responsiveness. Third, we report that, during floor plate (FP) in-growth, calpain1 activity is suppressed by local signals, allowing Plexin-A1 accumulation in the growth cone and sensitization to Sema3B. Finally, we show that the FP cue NrCAM mediates the switch of Plexin-A1 processing underlying growth cone sensitization to Sema3B. This reveals pathway-dependent modulation of guidance receptor processing as a novel mechanism for regulating guidance decisions at intermediate targets.

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    Keywords

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