Claudin-19 (green) helps form tight junction structures that seal PNS myelin sheaths.
Miyamoto et al. went looking for a claudin family member expressed in the PNS. Claudin-19 fit the bill. Mice lacking functional claudin-19 showed behavioral and morphological abnormalities suggestive of peripheral nerve damage and disruption of the tight junction-like structures. Recordings of compound action potentials showed two currents, one fast and one slow. This change in conductance properties indicated that, without claudin-19, the myelin sheath of Schwann cell appeared to be inadequately sealed from the environment. Thus the mutation may have interfered with normal saltatory travel of neural currents.
The dependence on tight junctions may be greater in thinner myelinated axons than in thicker ones because the thinner axons lack the bulk that would compensate for improperly sealed wrappings. The team is continuing to follow the now two-year-old mice to see if a lack of proper tight junctions induces demyelination later in life.