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Characterization of mucins from cultured normal human tracheobronchial epithelial cells.

Characterization of mucins from cultured normal human tracheobronchial epithelial cells. Research Abstract Details 

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  • Characterization of mucins from cultured normal human tracheobronchial epithelial cells. Abstract Text:

    d j thorntonD J Thornton,t grayT Gray,p nettesheimP Nettesheim,m howardM Howard,j s kooJ S Koo,j k sheehanJ K Sheehan,

    Early-passage normal human tracheobronchial epithelial (NHTBE) cells grown in air-liquid interface cultures in medium containing retinoids differentiate into a mucociliary epithelium over a 2- to 3-wk period and express increasing mRNA levels of the airway mucin genes MUC5AC and MUC5B as the cultures age; the levels of MUC2 mRNA were very low throughout the study. Using specific antibodies to MUC5AC and MUC5B mucins, we noted a gradual increase in these two mucins in the intracellular and apically secreted pools as a function of time. A low level of MUC2 mucin was detected, which did not change with time. The intracellular and apically secreted mucins isolated from day 14 and day 21 cultures by density gradient centrifugation were similar in density to those previously isolated from human respiratory mucus secretions. The sedimentation rate of the apically secreted mucins indicated that they were highly oligomerized, polydisperse macromolecules similar to those previously documented from in vivo secretions. In contrast, the cell-associated mucins from the cultured NHTBE cells were much smaller, possibly only monomers and dimers. Anion-exchange chromatography detected no differences in charge density between the reduced and carboxymethylated cell-associated and secreted forms of the MUC5AC and MUC5B mucins. The MUC5AC mucin was of similar charge density to its in vivo counterpart; however, MUC5B was more homogeneous than that found in vivo. Finally, evidence is presented for an intracellular NH(2)-terminal cleavage of the MUC5B mucins. These studies indicate that the mucins produced by cultured NHTBE cells are similar to those found in human airways, suggesting that this cell culture model is suited for studies of respiratory mucin biosynthesis, processing, and assembly.

    Characterization of mucins from cultured normal human tracheobronchial epithelial cells. Publishing Authors By Initials

    dj thorntonDJ Thornton,t grayT Gray,p nettesheimP Nettesheim,m howardM Howard,js kooJS Koo,jk sheehanJK Sheehan,

    For similar respiratory system: trachea research abstracts see: respiratory system: trachea research

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    Characterization of mucins from cultured normal human tracheobronchial epithelial cells. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: American journal of physiology. Lung cellular and

    VOLUME: 278

    Page Numbers: L1118-28

    Journal Abbreviation: Am. J. Physiol. Lung Cell Mol.

    ISSN: 1040-0605

    DAY: 29

    MONTH: Jun

    YEAR: 2000

    Characterization of mucins from cultured normal human tracheobronchial epithelial cells. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 100901229

    Characterization of mucins from cultured normal human tracheobronchial epithelial cells. Keywords Mesh Terms:

    KEYWORDS: Trachea

    MESH TERMS: secretion

    Chemical & Substance for Abstract: Characterization of mucins from cultured normal human tracheobronchial epithelial cells. Information

    Substance Name: mucin 5AC

    Registry Number: 0

    Grant and Affiliation Information for Characterization of mucins from cultured normal human tracheobronchial epithelial cells.

    AFFILIATION: The Wellcome Trust Centre for Cell-Matrix Research, Division of Biochemistry, School of Biological Sciences, University of Manchester, United Kingdom. Dave.Thorton@man.ac.uk

    Country: UNITED STATES

    UNITED STATES Research PublicationUNITED STATES Research Publication

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    MEDLINETA: Am J Physiol Lung Cell Mol Phy

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