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As electromotility may arise from a conformational change of the molecules' 'protein motors', which might be distributed along the outer hair cell (OHC) lateral wall, the force generated by the OHC electromotility would be related not only to the conformational change of the protein motors but also to the mechanical properties of the lateral wall. Therefore, a detailed understanding of the mechanical properties of the OHC lateral wall is important. In our previous reports, to understand the difference in the stiffness along the cell axis, the local deformation of the OHC in response to hypotonic stimulation was analyzed by measuring the displacement of microspheres attached randomly to the cell lateral wall, and the distribution of Young's modulus along the cell axis was obtained using the contact mode of an atomic force microscope (AFM). These investigations revealed that the stiffness of the cell in the apical region was greater than that in other regions where the stiffness is constant. In this study, the ultrastructure of the OHC lateral wall was investigated with the oscillation imaging mode of the AFM (Tapping Mode), and the relationship between the stiffness along the cell axis and the ultrastructure that was observed by the AFM imaging was analyzed. From the analysis, it was concluded that the circumferential filaments observed in the tapping mode AFM are actins which are part of the cortical lattice, and that the difference between the intervals of the circumferential filaments in the apical region and those in other regions is one factor that causes the high stiffness in the apical region.

The outer hair cell (OHC) plays an important role in the normal functioning of the cochlea, and cochlear amplification is believed to be based on OHC electromotility. This electromotility putatively arises from a conformational change of molecules, i.e., 'protein motors', which would be distributed along the plasma membrane. Although it has been assumed that protein motors are distributed in a restricted area of the plasma membrane, details of such distribution remain unclarified. In this study, first, in order to understand the difference in the stiffness along the cell axis, the local deformation of the OHC in response to hypotonic stimulation is analyzed by measuring the displacement of microspheres attached randomly to the lateral wall of the cell. As a result, the stiffness is expected to be constant throughout the region except in the apical part of the cell, and the stiffness of the apical part is expected to be higher than that of the other regions. Then, the local elongation and contraction of the OHC in response to sinusoidal voltage stimulation are analyzed by measuring the displacement of the microspheres in the same way as in the case of the hypotonic stimulation. From the two measurements mentioned above, it is concluded that there are no motors in the apical and basal parts of the cell, and that the motors are equally distributed along the cell lateral wall in the middle part of the cell.