Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1

Author:

Poliak Sebastian1,Salomon Daniela1,Elhanany Hadas1,Sabanay Helena1,Kiernan Brent2,Pevny Larysa2,Stewart Colin L.3,Xu Xiaorong4,Chiu Shing-Yan5,Shrager Peter4,Furley Andrew J.W.2,Peles Elior1

Affiliation:

1. Department of Molecular Cell Biology, The Weizmann Institute of Science, Rehovot 76100, Israel

2. Centre for Developmental Genetics, School of Medicine and Biomedical Science, University of Sheffield, Sheffield S10 2TN, UK

3. Cancer and Developmental Biology Laboratory, National Cancer Institute at Frederick, Frederick, MD 21702

4. Department of Neurobiology and Anatomy, University of Rochester Medical Center, Rochester, NY 14642

5. Department of Physiology, University of Wisconsin School of Medicine, Madison, WI 53706

Abstract

In myelinated axons, K+ channels are concealed under the myelin sheath in the juxtaparanodal region, where they are associated with Caspr2, a member of the neurexin superfamily. Deletion of Caspr2 in mice by gene targeting revealed that it is required to maintain K+ channels at this location. Furthermore, we show that the localization of Caspr2 and clustering of K+ channels at the juxtaparanodal region depends on the presence of TAG-1, an immunoglobulin-like cell adhesion molecule that binds Caspr2. These results demonstrate that Caspr2 and TAG-1 form a scaffold that is necessary to maintain K+ channels at the juxtaparanodal region, suggesting that axon–glia interactions mediated by these proteins allow myelinating glial cells to organize ion channels in the underlying axonal membrane.

Publisher

Rockefeller University Press

Subject

Cell Biology

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