Differential Contribution of Cadm1-Cadm3 Cell Adhesion Molecules to Peripheral Myelinated Axons

Cell adhesion proteins of the Cadm (SynCAM/Necl) family regulate myelination and the organization of myelinated axons. In the peripheral nervous system (PNS), intercellular contact between Schwann cells and their underlying axons is believed to be mediated by binding of glial Cadm4 to axonal Cadm3 or Cadm2. Nevertheless, given that distinct neurons express different combinations of the Cadm proteins, the identity of the functional axonal ligand for Cadm4 remains to be determined. Here, we took a genetic approach to compare the phenotype of Cadm4 null mice, which exhibit abnormal distribution of Caspr and Kv1 potassium channels, with mice lacking different combinations of Cadm1-Cadm3 genes. We show that in con trast to mice lacking the single Cadm1, Cadm2, or Cadm3 genes, genetic ablation of all three phenocopies the abnormalities detected in the absence of Cadm4. Similar defects were observed in double mutant mice lacking Cadm3 and Cadm2 (i.e., Cadm3(-/-)/Cadm2(-/-)) or Cadm3 and Cadm1 (i.e., Cadm3(-/-)/Cadm1(-/-)), but not in mice lacking Cadm1 and Cadm2 (i.e., Cadm1(-/-)/Cadm2(-/-)). Furthermore, axonal organization abnormalities were also detected in Cadm3 null mice that were heterozygous for the two other axonal Cadms. Our results identify Cadm3 as the main axonal ligand for glial Cadm4, and reveal that its absence could be compensated by the combined action of Cadm2 and Cadm1.

Automated summary

Cell adhesion proteins of the Cadm family play a crucial role in myelination and axonal organization. The study reveals that Cadm3 is the main axonal ligand for glial Cadm4, and the combined action of Cadm2 and Cadm1 can compensate for its absence. Genetic ablation of all three Cadm genes phenocopies the abnormalities detected in the absence of Cadm4, indicating their interplay in regulating myelination and axonal organization.