N-cadherin directs the collective Schwann cell migration required for nerve regeneration through Slit2/3-mediated contact inhibition of locomotion

• DOI: 10.7554/elife.88872
• Publication Date: 2024-04-09T09:55:10Z
• Authors: Julian JA Hoving; Elizabeth Harford...; Patrick Wingfield...; Anne-Laure Cattin; Mariana Campana; Alex Power; Toby Morgan; Erica Torchiaro; Victor Quereda; Alison C Lloyd
• Keywords: 0301 basic medicine; contact inhibition of locomotion; cell–cell interactions; QH301-705.5; Science; Nerve Tissue Proteins; Mice; 03 medical and health sciences; Cell Movement; Cell Adhesion; Animals; Schwann cells; nerve regneration; Biology (General); N-cadherin; Cancer Biology; collective cell migration; Contact Inhibition; Q; R; Membrane Proteins; Cadherins; Nerve Regeneration; Medicine; Intercellular Signaling Peptides and Proteins; Schwann Cells; Locomotion; Signal Transduction

Collective cell migration is fundamental for the development of organisms and in the adult for tissue regeneration and in pathological conditions such as cancer. Migration as a coherent group requires the maintenance of cell–cell interactions, while contact inhibition of locomotion (CIL), a local repulsive force, can propel the group forward. Here we show that the cell–cell interaction molecule, N-cadherin, regulates both adhesion and repulsion processes during Schwann cell (SC) collective migration, which is required for peripheral nerve regeneration. However, distinct from its role in cell–cell adhesion, the repulsion process is independent of N-cadherin trans-homodimerisation and the associated adherens junction complex. Rather, the extracellular domain of N-cadherin is required to present the repulsive Slit2/Slit3 signal at the cell surface. Inhibiting Slit2/Slit3 signalling inhibits CIL and subsequently collective SC migration, resulting in adherent, nonmigratory cell clusters. Moreover, analysis of ex vivo explants from mice following sciatic nerve injury showed that inhibition of Slit2 decreased SC collective migration and increased clustering of SCs within the nerve bridge. These findings provide insight into how opposing signals can mediate collective cell migration and how CIL pathways are promising targets for inhibiting pathological cell migration.