Expression of c-erbB receptors and ligands in the bronchial epithelium of asthmatic subjects
Expression of c-erbB receptors and ligands in the bronchial epithelium of asthmatic subjects
Background: The c-erbB family of receptor tyrosine kinases act in a combinatorial fashion to regulate cell behavior. Disturbances in this system have been associated with neoplastic and inflammatory diseases.
Objectives: Although expression of the epidermal growth factor receptor (EGFR; c-erbB1) is increased in the bronchial epithelium in asthma, there is no information on expression of other members of the c-erbB receptor and ligand family that can modulate EGFR function.
Methods: Immunohistochemistry was used to compare expression of EGFR, c-erbB2, c-erbB3, epidermal growth factor, heparin-binding epidermal growth factor–like growth factor, and transforming growth factor ? in bronchial biopsy specimens from normal and asthmatic subjects. Scrape-wounded monolayers of 16HBE 14o– cells were used as an in vitro model of damage and repair. Changes in EGFR, c-erbB2, and c-erbB3 distribution were measured by means of immunocytochemistry, whereas tyrosine phosphorylation was measured by means of immunoprecipitation and Western blotting.
Results: Although epithelial staining for the EGFR was significantly increased in asthmatic epithelium (P < .001), there was no difference in staining for the other receptors and ligands studied. In scrape-wounded epithelial monolayers, tyrosine phosphorylation of EGFR, c-erbB2, and c-erbB3 occurred immediately after damage; however, only EGFR showed a change in expression in response to damage.
Conclusions: Even though EGFR levels are increased in asthma, this is not linked to changes in expression of its activating ligands or other c-erbB receptors. Because bronchial epithelial cells respond to physical damage through activation of several c-erbB family members, the shift in favor of increased EGFR levels in asthma may lead to altered epithelial function by influencing the number and type of heterodimeric signaling complexes, assuming sufficient ligand availability.
asthma, bronchial epithelium, erbB receptor, epidermal growth factor, transforming growth factor ?, phosphorylation, wound repair
75-81
Polosa, Riccardo
8eaf4eb4-d2fc-4e22-b6c7-e9a2e28d95ec
Puddicombe, Sarah M.
fd8d76d1-203d-4f06-a7c2-678c946fb931
Krishna, M. Thirumala
224cbfd8-4073-4fe1-8400-6f67e20cc642
Tuck, Angela B.
3e99e3e2-4661-4aff-a107-e952073abeca
Howarth, Peter H.
ff19c8c4-86b0-4a88-8f76-b3d87f142a21
Holgate, Stephen T.
2e7c17a9-6796-436e-8772-1fe6d2ac5edc
Davies, Donna E.
7de8fdc7-3640-4e3a-aa91-d0e03f990c38
2002
Polosa, Riccardo
8eaf4eb4-d2fc-4e22-b6c7-e9a2e28d95ec
Puddicombe, Sarah M.
fd8d76d1-203d-4f06-a7c2-678c946fb931
Krishna, M. Thirumala
224cbfd8-4073-4fe1-8400-6f67e20cc642
Tuck, Angela B.
3e99e3e2-4661-4aff-a107-e952073abeca
Howarth, Peter H.
ff19c8c4-86b0-4a88-8f76-b3d87f142a21
Holgate, Stephen T.
2e7c17a9-6796-436e-8772-1fe6d2ac5edc
Davies, Donna E.
7de8fdc7-3640-4e3a-aa91-d0e03f990c38
Polosa, Riccardo, Puddicombe, Sarah M., Krishna, M. Thirumala, Tuck, Angela B., Howarth, Peter H., Holgate, Stephen T. and Davies, Donna E.
(2002)
Expression of c-erbB receptors and ligands in the bronchial epithelium of asthmatic subjects.
Journal of Allergy and Clinical Immunology, 109 (1), .
(doi:10.1067/mai.2002.120274).
Abstract
Background: The c-erbB family of receptor tyrosine kinases act in a combinatorial fashion to regulate cell behavior. Disturbances in this system have been associated with neoplastic and inflammatory diseases.
Objectives: Although expression of the epidermal growth factor receptor (EGFR; c-erbB1) is increased in the bronchial epithelium in asthma, there is no information on expression of other members of the c-erbB receptor and ligand family that can modulate EGFR function.
Methods: Immunohistochemistry was used to compare expression of EGFR, c-erbB2, c-erbB3, epidermal growth factor, heparin-binding epidermal growth factor–like growth factor, and transforming growth factor ? in bronchial biopsy specimens from normal and asthmatic subjects. Scrape-wounded monolayers of 16HBE 14o– cells were used as an in vitro model of damage and repair. Changes in EGFR, c-erbB2, and c-erbB3 distribution were measured by means of immunocytochemistry, whereas tyrosine phosphorylation was measured by means of immunoprecipitation and Western blotting.
Results: Although epithelial staining for the EGFR was significantly increased in asthmatic epithelium (P < .001), there was no difference in staining for the other receptors and ligands studied. In scrape-wounded epithelial monolayers, tyrosine phosphorylation of EGFR, c-erbB2, and c-erbB3 occurred immediately after damage; however, only EGFR showed a change in expression in response to damage.
Conclusions: Even though EGFR levels are increased in asthma, this is not linked to changes in expression of its activating ligands or other c-erbB receptors. Because bronchial epithelial cells respond to physical damage through activation of several c-erbB family members, the shift in favor of increased EGFR levels in asthma may lead to altered epithelial function by influencing the number and type of heterodimeric signaling complexes, assuming sufficient ligand availability.
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Published date: 2002
Keywords:
asthma, bronchial epithelium, erbB receptor, epidermal growth factor, transforming growth factor ?, phosphorylation, wound repair
Identifiers
Local EPrints ID: 27332
URI: http://eprints.soton.ac.uk/id/eprint/27332
ISSN: 0091-6749
PURE UUID: 513a5890-ba6f-48de-9bde-a99510fae7a6
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Date deposited: 27 Apr 2006
Last modified: 16 Mar 2024 02:34
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Contributors
Author:
Riccardo Polosa
Author:
Sarah M. Puddicombe
Author:
M. Thirumala Krishna
Author:
Angela B. Tuck
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