Increased expression of p21waf cyclin-dependent kinase inhibitor in asthmatic bronchial epithelium
Increased expression of p21waf cyclin-dependent kinase inhibitor in asthmatic bronchial epithelium
Because the asthmatic bronchial epithelium is characterized by widespread damage, we postulated that this is associated with expression of cell cycle inhibitors that control proliferation. Using bronchial biopsies, the epithelium was the major site of expression of the cyclin-dependent kinase inhibitor, p21waf. Immunostaining usually occurred in the cytoplasm of columnar cells; however, in severe asthma, nuclear staining was also evident in the proliferative, basal cell compartment. p21waf expression was significantly higher in asthmatic versus nonasthmatic epithelium and was unaffected by corticosteroid treatment; proliferating cell nuclear antigen was not significantly different in any group. p21waf, but not p27kip1, mRNA and protein were induced by treatment of bronchial epithelial cells in vitro with transforming growth factor (TGF)-ß or H2O2, but not by dexamethasone, which induced p57kip2. TGF-ß and dexamethasone inhibited epidermal growth factor (EGF)-induced DNA synthesis, whereas low concentrations of H2O2 synergized with EGF; at higher doses, growth inhibition and induction of apoptosis occurred. TGF-ß caused p21waf to become nuclear, suggesting interaction with the replicative machinery; however, in oxidant-stressed cells, p21waf was predominantly cytoplasmic, where it has been linked to cell survival. We conclude that p21waf overexpression in asthma influences cell proliferation and survival. This may cause abnormal repair responses that contribute to airway inflammation and remodeling.
61-68
Puddicombe, Sarah M.
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Torres-Lozano, Carlos
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Richter, Audrey
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Bucchieri, Fabio
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Lordan, James L.
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Howarth, Peter H.
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Vrugt, Bart
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Albers, Rene
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Djukanovic, Ratko
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Holgate, Stephen T.
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Wilson, Susan J.
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Davies, Donna E.
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1 January 2003
Puddicombe, Sarah M.
fd8d76d1-203d-4f06-a7c2-678c946fb931
Torres-Lozano, Carlos
e355e442-e415-49be-b1e5-fa3f4de11b6e
Richter, Audrey
5b4fb888-b3a7-4b81-a8a7-ffd2c046a196
Bucchieri, Fabio
3f85c9c8-2bc0-4fd0-b481-a03935fe3cb0
Lordan, James L.
15a9bdfb-bf61-4aea-a0f4-d83868eb39d0
Howarth, Peter H.
ff19c8c4-86b0-4a88-8f76-b3d87f142a21
Vrugt, Bart
417ac3a6-ba83-47ea-84b4-e4fd1278337b
Albers, Rene
3084cf21-9a9f-4148-9763-a76650510837
Djukanovic, Ratko
d9a45ee7-6a80-4d84-a0ed-10962660a98d
Holgate, Stephen T.
2e7c17a9-6796-436e-8772-1fe6d2ac5edc
Wilson, Susan J.
21c6875d-6870-441b-ae7a-603562a646b8
Davies, Donna E.
7de8fdc7-3640-4e3a-aa91-d0e03f990c38
Puddicombe, Sarah M., Torres-Lozano, Carlos, Richter, Audrey, Bucchieri, Fabio, Lordan, James L., Howarth, Peter H., Vrugt, Bart, Albers, Rene, Djukanovic, Ratko, Holgate, Stephen T., Wilson, Susan J. and Davies, Donna E.
(2003)
Increased expression of p21waf cyclin-dependent kinase inhibitor in asthmatic bronchial epithelium.
American Journal of Respiratory Cell and Molecular Biology, 28 (1), .
(doi:10.1165/rcmb.4715).
Abstract
Because the asthmatic bronchial epithelium is characterized by widespread damage, we postulated that this is associated with expression of cell cycle inhibitors that control proliferation. Using bronchial biopsies, the epithelium was the major site of expression of the cyclin-dependent kinase inhibitor, p21waf. Immunostaining usually occurred in the cytoplasm of columnar cells; however, in severe asthma, nuclear staining was also evident in the proliferative, basal cell compartment. p21waf expression was significantly higher in asthmatic versus nonasthmatic epithelium and was unaffected by corticosteroid treatment; proliferating cell nuclear antigen was not significantly different in any group. p21waf, but not p27kip1, mRNA and protein were induced by treatment of bronchial epithelial cells in vitro with transforming growth factor (TGF)-ß or H2O2, but not by dexamethasone, which induced p57kip2. TGF-ß and dexamethasone inhibited epidermal growth factor (EGF)-induced DNA synthesis, whereas low concentrations of H2O2 synergized with EGF; at higher doses, growth inhibition and induction of apoptosis occurred. TGF-ß caused p21waf to become nuclear, suggesting interaction with the replicative machinery; however, in oxidant-stressed cells, p21waf was predominantly cytoplasmic, where it has been linked to cell survival. We conclude that p21waf overexpression in asthma influences cell proliferation and survival. This may cause abnormal repair responses that contribute to airway inflammation and remodeling.
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Published date: 1 January 2003
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Local EPrints ID: 27346
URI: http://eprints.soton.ac.uk/id/eprint/27346
ISSN: 1044-1549
PURE UUID: 60317661-4c48-47ca-9c94-41fd7fcd15d6
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Date deposited: 27 Apr 2006
Last modified: 16 Mar 2024 02:36
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Author:
Sarah M. Puddicombe
Author:
Carlos Torres-Lozano
Author:
Audrey Richter
Author:
Fabio Bucchieri
Author:
James L. Lordan
Author:
Bart Vrugt
Author:
Rene Albers
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