Neuronal activity disrupts myelinated axon integrity in the absence of NKCC1b
Katy LH Marshall-Phelps, Linde Kegel, Marion Baraban, Torben Ruhwedel, Rafael Almeida, Maria Rubio-Brotons, Anna Klingseisen, Silvia Benito-Kwiecinski, Jason J. Early, Jenea M. Bin, Daumante Šuminaite, Matthew R. Livesey, Wiebke Möbius, Richard J. Poole, David A. Lyons
Abstract
Through a genetic screen in zebrafish, we identified a mutant with disruption to myelin in both the CNS and PNS caused by a mutation in a previously uncharacterized gene, slc12a2b, predicted to encode a Na+, K+, and Cl- (NKCC) cotransporter, NKCC1b. slc12a2b/NKCC1b mutants exhibited a severe and progressive pathology in the PNS, characterized by dysmyelination and swelling of the periaxonal space at the axon-myelin interface. Cell-type-specific loss of slc12a2b/NKCC1b in either neurons or myelinating Schwann cells recapitulated these pathologies. Given that NKCC1 is critical for ion homeostasis, we asked whether the disruption to myelinated axons in slc12a2b/NKCC1b mutants is affected by neuronal activity. Strikingly, we found that blocking neuronal activity completely prevented and could even rescue the pathology in slc12a2b/NKCC1b mutants. Together, our data indicate that NKCC1b is required to maintain neuronal activity-related solute homeostasis at the axon-myelin interface, and the integrity of myelinated axons.