II-V spectrin bridges the plasma membrane and cortical lattice in the lateral wall of the auditory outer hair cells

The sensitivity and frequency selectivity of the mammalian cochlea involves a mechanical amplification process called electromotility, which requires prestin-dependent length changes of the outer hair cell (OHC) lateral wall in response to changes in membrane electric potential. The cortical lattice, the highly organized cytoskeleton underlying the OHC lateral plasma membrane, is made up of F-actin and spectrin. Here, we show that II and two of the five -spectrin subunits, II and V, are present in OHCs. II spectrin is restricted to the cuticular plate, a dense apical network of actin filaments, whereas V spectrin is concentrated at the cortical lattice. Moreover, we show that II-V spectrin directly interacts with F-actin and band 4.1, two components of the OHC cortical lattice. V spectrin is progressively recruited into the cortical lattice between postnatal day 2 (P2) and P10 in the mouse, in parallel with prestin membrane insertion, which itself parallels the maturation of cell electromotility. Although V spectrin does not directly interact with prestin, we found that addition of lysates derived from mature auditory organs, but not from the brain or liver, enables V spectrin-prestin interaction. Using this assay, V spectrin, via its PH domain, indirectly interacts with the C-terminal cytodomain of prestin. We conclude that the cortical network involved in the sound-induced electromotility of OHCs contains II-V spectrin, and not the conventional II-II spectrin.