Aberrant cochlear hair cell attachments caused by Nectin-3 deficiency result in hair bundle abnormalities
Author(s) -
Terunobu Fukuda,
Kanoko Kominami,
Shujie Wang,
Hideru Togashi,
Kenichi Hirata,
Akira Mizoguchi,
Yoshiyuki Rikitake,
Yoshimi Takai
Publication year - 2013
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.15
H-Index - 36
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.094995
Subject(s) - kinocilium , nectin , biology , hair cell , microbiology and biotechnology , tight junction , anatomy , organ of corti , inner ear , epithelium , columnar cell , cell , cell adhesion , genetics
The organ of Corti consists of sensory hair cells (HCs) interdigitated with nonsensory supporting cells (SCs) to form a checkerboard-like cellular pattern. HCs are equipped with hair bundles on their apical surfaces. We previously reported that cell-adhesive nectins regulate the checkerboard-like cellular patterning of HCs and SCs in the mouse auditory epithelium. Nectin-1 and -3 are differentially expressed in normal HCs and SCs, respectively, and in Nectin-3-deficient mice a number of HCs are aberrantly attached to each other. We show here that these aberrantly attached HCs in Nectin-3-deficient mice, but not unattached ones, show disturbances of the orientation and morphology of the hair bundles and the positioning of the kinocilium, with additional abnormal localisation of cadherin-catenin complexes and the apical-basal polarity proteins Pals1 and Par-3. These results indicate that, owing to the loss of Nectin-3, hair cells contact each other inappropriately and form abnormal junctions, ultimately resulting in abnormal hair bundle orientation and morphology.
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