Literature DB >> 1581047

Carbohydrates in the cell surface of hair cells from the guinea pig cochlea.

P K Plinkert1, B Plinkert, H P Zenner.   

Abstract

The presence of cell surface carbohydrates was investigated in intact, non-fixed outer hair cells (OHCs) of guinea pigs using fluorescein isothiocyanate (FITC) and rhodamine (TRITC) lectins. By means of wheat germ agglutinin (WGA) N-acetyl-D-glucosamine was shown in the entire OHC membrane, including the stereocilia. Binding of WGA in OHCs to neuraminic acid was excluded by preincubation with neuraminidase. Moreover, FITC-Limulus polyphemus, a specific lectin for neuraminic acid, showed no fluorescence on OHCs. Neutral saccharides, like alpha-D-mannose and/or alpha-D-glucose, were mainly observed at the cuticular plate and at the basal cell pole with FITC-concanavalin A. A weaker fluorescence was seen at the lateral cell wall. Two branched oligosaccharides, composed of beta-galactose, N-acetyl-D-glucosamine and mannose, were demonstrated by TRITC-Phaseolus vulgaris (PHA-E/L) in the entire OHC membrane. A spot-like binding of soybean agglutinin to N-acetyl-D-galactosamine could be demonstrated in the region of the cuticular plate. However, using Helix pomatia, the subtype N-acetyl-alpha-D-galactosamine was not detectable. Moreover, there was no binding of Ulex europaeus or of Arachis hypogea (PNA) to OHCs, suggesting the absence of considerable amounts of L-fucose and of galactose-beta-3-N-acetylgalactosamine. The results indicate that N-acetyl-D-glucosamine, alpha-D-mannose and alpha-D-glucose can be considered the major components of the OHC glycocalix. We suggest that they have a function as an anchoring structure in interstereociliary links as well as in hair bundle connections to the tectorial membrane.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1992        PMID: 1581047     DOI: 10.1007/bf00186449

Source DB:  PubMed          Journal:  Eur Arch Otorhinolaryngol        ISSN: 0937-4477            Impact factor:   2.503


  45 in total

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2.  Wheat germ agglutinin and Helix pomatia agglutinin lectin binding on cochlear hair cells.

Authors:  P Gil-Loyzaga; W E Brownell
Journal:  Hear Res       Date:  1988-07-15       Impact factor: 3.208

3.  Electrokinetic shape changes of cochlear outer hair cells.

Authors:  B Kachar; W E Brownell; R Altschuler; J Fex
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Authors:  G L Nicolson
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5.  A nicotinic acetylcholine receptor-like alpha-bungarotoxin-binding site on outer hair cells.

Authors:  P K Plinkert; H P Zenner; E Heilbronn
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6.  Visualization and functional testing of acetylcholine receptor-like molecules in cochlear outer hair cells.

Authors:  P K Plinkert; A H Gitter; U Zimmermann; T Kirchner; S Tzartos; H P Zenner
Journal:  Hear Res       Date:  1990-02       Impact factor: 3.208

7.  Interaction of sulfated glycosaminoglycans with lectins.

Authors:  N Toda; A Doi; A Jimbo; I Matsumoto; N Seno
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Authors:  J Vergara; R Y Tsien; M Delay
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  1 in total

Review 1.  Molecular Composition of Vestibular Hair Bundles.

Authors:  Jocelyn F Krey; Peter G Barr-Gillespie
Journal:  Cold Spring Harb Perspect Med       Date:  2019-01-02       Impact factor: 6.915

  1 in total

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