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Expression of MUC5AC and MUC5B mucins in normal and cystic fibrosis lung.

Expression of MUC5AC and MUC5B mucins in normal and cystic fibrosis lung. Research Abstract Details 

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  • Expression of MUC5AC and MUC5B mucins in normal and cystic fibrosis lung. Abstract Text:

    d a gronebergD A Groneberg,p r eynottP R Eynott,t oatesT Oates,s limS Lim,r wuR Wu,i carlstedtI Carlstedt,a g nicholsonA G Nicholson,k f chungK F Chung,

    Hypersecretion of airway mucus is a characteristic feature of chronic airway diseases like cystic fibrosis (CF) and leads via impairment of the muco-ciliary clearance and bacterial superinfection to respiratory failure. The major components of the mucus matrix forming family of mucins in the airways are MUC5AC and MUC5B. To investigate the expression of these glycoproteins in CF, immunohistochemistry was carried out on trachea, bronchi and peripheral lung obtained from CF patients and compared to normal lung tissues. MUC5AC immunohistochemistry demonstrated signals in goblet cells of the epithelial lining. Also, goblet cells inside glandular secretory ducts revealed MUC5AC-positive staining. In comparison to those from normal subjects, CF sections were characterized by inflammatory changes and goblet cell hyperplasia, resulting in increased numbers of MUC5AC-positive cells. Immunohistochemical staining for MUC5B showed abundant staining of submucosal glands and epithelial goblet cells. Inside the glands, the immunoreactivity was restricted to glandular mucous cells. MUC5AC and MUC5B are expressed in the same histological pattern in CF compared to normal tissues with an increase of MUC5AC-positive cells due to goblet cell hyper- and metaplasia.

    Expression of MUC5AC and MUC5B mucins in normal and cystic fibrosis lung. Publishing Authors By Initials

    da gronebergDA Groneberg,pr eynottPR Eynott,t oatesT Oates,s limS Lim,r wuR Wu,i carlstedtI Carlstedt,ag nicholsonAG Nicholson,kf chungKF Chung,

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

    PUBMED ID PMID:

    MEDLINE DATE:

    Expression of MUC5AC and MUC5B mucins in normal and cystic fibrosis lung. Journal Published:

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

    Journal: Respiratory medicine

    VOLUME: 96

    Page Numbers: 81-6

    Journal Abbreviation:

    ISSN: 0954-6111

    DAY: 29

    MONTH: Feb

    YEAR: 2002

    Expression of MUC5AC and MUC5B mucins in normal and cystic fibrosis lung. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 8908438

    Expression of MUC5AC and MUC5B mucins in normal and cystic fibrosis lung. Keywords Mesh Terms:

    KEYWORDS: Trachea

    MESH TERMS: chemistry

    Chemical & Substance for Abstract: Expression of MUC5AC and MUC5B mucins in normal and cystic fibrosis lung. Information

    Substance Name: mucin 5AC

    Registry Number: 0

    Grant and Affiliation Information for Expression of MUC5AC and MUC5B mucins in normal and cystic fibrosis lung.

    AFFILIATION: Thoracic Medicine, National Heart and Lung Institute, Imperial College of Science Technology and Medicine, London, UK.

    Country: England

    England Research PublicationEngland Research Publication

    AGENCY:

    GRANT:

    ACRONYM:

    MEDLINETA: Respir Med

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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