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Radixin is a constituent of stereocilia in hair cells.

ABSTRACT: Proteins of the ezrin-radixin-moesin family are ubiquitous constituents of the submembrane cortex, especially in epithelial cells. Earlier biochemical results suggested that a protein of this family occurs in the hair bundle, the cluster of actin-filled stereocilia that serves as the mechanoreceptive organelle of each hair cell in the inner ear. We prepared antipeptide antisera directed against chicken radixin and ezrin and demonstrated their specificity and absence of crossreactivity. When used in immunocytochemical studies of isolated hair cells, anti-radixin produced an intense band of labeling at the bases of hair bundles from the chicken, frog, mouse, and zebrafish. Electron microscopic immunocytochemistry disclosed that radixin labeling commenced in the stereociliary taper, peaked in the lower stereociliary shaft, and declined progressively toward the hair bundle's top. Labeling with anti-ezrin produced no signal in hair bundles. Radixin is thus a prominent constituent of stereocilia, where it may participate in anchoring the "pointed" ends of actin filaments to the membrane.

SUBMITTER: Pataky F

PROVIDER: S-EPMC356996 | biostudies-literature | 2004 Feb

REPOSITORIES: biostudies-literature

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Radixin is a constituent of stereocilia in hair cells.

Pataky F F Pironkova R R Hudspeth A J AJ

Proceedings of the National Academy of Sciences of the United States of America 20040201 8

Proteins of the ezrin-radixin-moesin family are ubiquitous constituents of the submembrane cortex, especially in epithelial cells. Earlier biochemical results suggested that a protein of this family occurs in the hair bundle, the cluster of actin-filled stereocilia that serves as the mechanoreceptive organelle of each hair cell in the inner ear. We prepared antipeptide antisera directed against chicken radixin and ezrin and demonstrated their specificity and absence of crossreactivity. When used ...[more]

PMID: 14983055

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Project description:Assembly of the hair bundle, the sensory organelle of the inner ear, depends on differential growth of actin-based stereocilia. Separate rows of stereocilia, labeled 1 through 3 from tallest to shortest, lengthen or shorten during discrete time intervals during development. We used lattice structured illumination microscopy and surface rendering to measure dimensions of stereocilia from mouse apical inner hair cells during early postnatal development; these measurements revealed a sharp transition at postnatal day 8 between stage III (row 1 and 2 widening; row 2 shortening) and stage IV (final row 1 lengthening and widening). Tip proteins that determine row 1 lengthening did not accumulate simultaneously during stages III and IV; while the actin-bundling protein EPS8 peaked at the end of stage III, GNAI3 peaked several days later-in early stage IV-and GPSM2 peaked near the end of stage IV. To establish the contributions of key macromolecular assemblies to bundle structure, we examined mouse mutants that eliminated tip links (Cdh23v2J or Pcdh15av3J), transduction channels (TmieKO), or the row 1 tip complex (Myo15ash2). Cdh23v2J/v2J and Pcdh15av3J/av3J bundles had adjacent stereocilia in the same row that were not matched in length, revealing that a major role of these cadherins is to synchronize lengths of side-by-side stereocilia. Use of the tip-link mutants also allowed us to distinguish the role of transduction from effects of transduction proteins themselves. While levels of GNAI3 and GPSM2, which stimulate stereocilia elongation, were greatly attenuated at the tips of TmieKO/KO row 1 stereocilia, they accumulated normally in Cdh23v2J/v2J and Pcdh15av3J/av3J stereocilia. These results reinforced the suggestion that the transduction proteins themselves facilitate localization of proteins in the row 1 complex. By contrast, EPS8 concentrates at tips of all TmieKO/KO, Cdh23v2J/v2J, and Pcdh15av3J/av3J stereocilia, correlating with the less polarized distribution of stereocilia lengths in these bundles. These latter results indicated that in wild-type hair cells, the transduction complex prevents accumulation of EPS8 at the tips of shorter stereocilia, causing them to shrink (rows 2 and 3) or disappear (row 4 and microvilli). Reduced rhodamine-actin labeling at row 2 stereocilia tips of tip-link and transduction mutants suggests that transduction's role is to destabilize actin filaments there. These results suggest that regulation of stereocilia length occurs through EPS8 and that CDH23 and PCDH15 regulate stereocilia lengthening beyond their role in gating mechanotransduction channels.

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Radixin is a constituent of stereocilia in hair cells.

Publications

Radixin is a constituent of stereocilia in hair cells.

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