The sorting receptor Rer1 controls Purkinje cell function via voltage gated sodium channels.

Rer1 is a sorting receptor in the early secretory pathway that controls the assembly and the cell surface transport of selected multimeric membrane protein complexes. Mice with a Purkinje cell (PC) specific deletion of Rer1 showed normal polarization and differentiation of PCs and normal development of the cerebellum. However, PC-specific loss of Rer1 led to age-dependent motor deficits in beam walk, ladder climbing and gait. Analysis of brain sections revealed a specific degeneration of PCs in the anterior cerebellar lobe in old animals. Electrophysiological recordings demonstrated severe deficits in spontaneous action potential generation. Measurements of resurgent currents indicated decreased surface densities of voltage-gated sodium channels (Na_v), but not changes in individual channels. Analysis of mice with a whole brain Rer1-deletion demonstrated a strong down-regulation of Na_v1.6 and 1.1 in the absence of Rer1, whereas protein levels of the related Ca_v2.1 and of K_v3.3 and 7.2 channels were not affected. The data suggest that Rer1 controls the assembly and transport of Na_v1.1 and 1.6, the principal sodium channels responsible for recurrent firing, in PCs.

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