Little is known about whether the properties of respiratory mucins are altered as a result of airway irritation, but histochemical studies of respiratory tract secretory cells show a more ‘acidic’ staining pattern after exposure to tobacco smoke. Furthermore it has been suggested that proteoglycans are the major glycoconjugates in ‘normal’ respiratory secretions, whereas mucins predominate in sputum. To investigate these observations further, mucins from secretions collected from the tracheal surface of healthy non-smoking ‘normal’ subjects and sputum from patients with chronic bronchitis were compared. All samples contained one major mucin population after density-gradient centrifugation, and a small amount of ‘denser’ mucin was present in some chronic bronchitic and one of the ‘normal’ samples. Proteoglycans were not a major component of ‘normal’ secretions. The major mucin population from chronic bronchitic samples had molecular masses between 10 and 30 MDa and behaved as random coils in solution. Whole mucins from ‘normal’ individuals and chronic bronchitic patients were excluded from Sepharose CL-2B, whereas reduced subunits were included. Proteolysis of subunits yielded two populations of high-molecular-mass glycopeptides differing in size, suggesting the presence of two different tandem repeat regions in the mucins. Finally, mucins from patients with chronic bronchitis are less, rather than more, acidic than those from ‘normal’ individuals. Mucins from bronchitic sputum and ‘normal’ secretions are thus similar in their macromolecular properties, but differ slightly in charge density.
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January 1996
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Research Article|
January 15 1996
Mucins in airway secretions from healthy and chronic bronchitic subjects Available to Purchase
Julia R. DAVIES;
Julia R. DAVIES
¶
*Department of Cell and Molecular Biology, Section for Molecular Pathogenesis, Lund University, Box 94, S-221 00, Lund, Sweden
¶To whom correspondence should be addressed.
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Hans W. HOVENBERG;
Hans W. HOVENBERG
*Department of Cell and Molecular Biology, Section for Molecular Pathogenesis, Lund University, Box 94, S-221 00, Lund, Sweden
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Carl-Johan LINDÉN;
Carl-Johan LINDÉN
†Department of Lung Medicine, University Hospital of Lund, S-221 85, Lund, Sweden
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Richard HOWARD;
Richard HOWARD
‡Department of Anaesthetics, St George's Hospital, London SW17 0RE, U.K.
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Paul S. RICHARDSON;
Paul S. RICHARDSON
§Department of Physiology, St George's Hospital Medical School, London SW17 0RE, U.K.
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John K. SHEEHAN;
John K. SHEEHAN
ǁDepartment of Biochemistry and Molecular Biology, University of Manchester, Manchester M13 9PT, U.K.
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Ingemar CARLSTEDT
Ingemar CARLSTEDT
*Department of Cell and Molecular Biology, Section for Molecular Pathogenesis, Lund University, Box 94, S-221 00, Lund, Sweden
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Publisher: Portland Press Ltd
Received:
May 30 1995
Revision Received:
August 11 1995
Accepted:
August 29 1995
Online ISSN: 1470-8728
Print ISSN: 0264-6021
The Biochemical Society, London © 1996
1996
Biochem J (1996) 313 (2): 431–439.
Article history
Received:
May 30 1995
Revision Received:
August 11 1995
Accepted:
August 29 1995
Citation
Julia R. DAVIES, Hans W. HOVENBERG, Carl-Johan LINDÉN, Richard HOWARD, Paul S. RICHARDSON, John K. SHEEHAN, Ingemar CARLSTEDT; Mucins in airway secretions from healthy and chronic bronchitic subjects. Biochem J 15 January 1996; 313 (2): 431–439. doi: https://doi.org/10.1042/bj3130431
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