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Recurring BALB/c mouse lung inflammatory responses to episodic allergen exposure

Recurring BALB/c mouse lung inflammatory responses to episodic allergen exposure
Recurring BALB/c mouse lung inflammatory responses to episodic allergen exposure
This study detailed the sequence of recurring inflammatory events associated with episodic allergen exposures of mice resulting in airway hyperreactivity, sustained inflammation, goblet-cell hyperplasia, and fibrogenesis that characterize a lung with chronic asthma. Ovalbumin (OVA)-sensitized female BALB/c mice were exposed to saline-control or OVA aerosols for 1 h per day for episodes of 3 d/wk for up to 8 wk. Lung inflammation was assessed by inflammatory cell recoveries using bronchoalveolar lavages (BAL) and tissue collagenase dispersions. Cell accumulations were observed within airway submucosal and associated perivascular spaces using immunohistochemical and tinctorial staining methods. Airway responsiveness to methacholine aerosols were elevated after 2 wk and further enhanced to a sustained level after wk 4 and 8. Although by wk 8 diminished OVA-induced accumulations of eosinophils, neutrophils, and monocyte-macrophages were observed, suggesting diminished responsiveness, the BAL recovery of lymphocytes remained elevated. Airway but not perivascular lesions persisted with a proliferating cell population, epithelial goblet-cell hyperplasia, and evidence of enhanced collagen deposition. Examination of lung inflammatory cell content before the onset of the first, second, and fourth OVA exposure episodes demonstrated enhancements in residual BAL lymphocyte and BAL and tissue eosinophil recoveries with each exposure episode. Although tissue monocyte-macrophage numbers returned to baseline prior to each exposure episode, the greatest level of accumulation was observed after wk 4. These results provide the basis for establishing the inflammatory and exposure criteria by which episodic environmental exposures to allergen might result in the development of a remodeled lung in asthma.
1528-7394
176-191
Wilson, S.J.
21c6875d-6870-441b-ae7a-603562a646b8
Harmer, M.J.
786bf846-403c-4cc5-9131-acdc3682382c
Lee, R.L.
806f5dee-75e9-404b-a4c5-ed528b56d390
Rigden, H.M.
149cc69f-538b-4bfb-8e5b-a2c97b431b9f
Doyon-Reale, N.M.
60023a21-7cdc-4327-bfa1-afb2dd1d97cb
Forman, K.M.
a528169f-2bfd-46e9-ba76-9c7ce919659e
Gao, X.
afcfd736-e571-4dcc-82bd-10a3be766824
Lieh-Lai, M.W.
036f8904-e242-46d1-86e7-9dfb9f0db879
Bassett, D.J.P.
c5212c58-4457-4cb9-810b-f313a2408a19
Wilson, S.J.
21c6875d-6870-441b-ae7a-603562a646b8
Harmer, M.J.
786bf846-403c-4cc5-9131-acdc3682382c
Lee, R.L.
806f5dee-75e9-404b-a4c5-ed528b56d390
Rigden, H.M.
149cc69f-538b-4bfb-8e5b-a2c97b431b9f
Doyon-Reale, N.M.
60023a21-7cdc-4327-bfa1-afb2dd1d97cb
Forman, K.M.
a528169f-2bfd-46e9-ba76-9c7ce919659e
Gao, X.
afcfd736-e571-4dcc-82bd-10a3be766824
Lieh-Lai, M.W.
036f8904-e242-46d1-86e7-9dfb9f0db879
Bassett, D.J.P.
c5212c58-4457-4cb9-810b-f313a2408a19

Wilson, S.J., Harmer, M.J., Lee, R.L., Rigden, H.M., Doyon-Reale, N.M., Forman, K.M., Gao, X., Lieh-Lai, M.W. and Bassett, D.J.P. (2013) Recurring BALB/c mouse lung inflammatory responses to episodic allergen exposure. Journal of Toxicology and Environmental Health Part A, 76 (3), 176-191. (doi:10.1080/15287394.2013.752323). (PMID:23356647)

Record type: Article

Abstract

This study detailed the sequence of recurring inflammatory events associated with episodic allergen exposures of mice resulting in airway hyperreactivity, sustained inflammation, goblet-cell hyperplasia, and fibrogenesis that characterize a lung with chronic asthma. Ovalbumin (OVA)-sensitized female BALB/c mice were exposed to saline-control or OVA aerosols for 1 h per day for episodes of 3 d/wk for up to 8 wk. Lung inflammation was assessed by inflammatory cell recoveries using bronchoalveolar lavages (BAL) and tissue collagenase dispersions. Cell accumulations were observed within airway submucosal and associated perivascular spaces using immunohistochemical and tinctorial staining methods. Airway responsiveness to methacholine aerosols were elevated after 2 wk and further enhanced to a sustained level after wk 4 and 8. Although by wk 8 diminished OVA-induced accumulations of eosinophils, neutrophils, and monocyte-macrophages were observed, suggesting diminished responsiveness, the BAL recovery of lymphocytes remained elevated. Airway but not perivascular lesions persisted with a proliferating cell population, epithelial goblet-cell hyperplasia, and evidence of enhanced collagen deposition. Examination of lung inflammatory cell content before the onset of the first, second, and fourth OVA exposure episodes demonstrated enhancements in residual BAL lymphocyte and BAL and tissue eosinophil recoveries with each exposure episode. Although tissue monocyte-macrophage numbers returned to baseline prior to each exposure episode, the greatest level of accumulation was observed after wk 4. These results provide the basis for establishing the inflammatory and exposure criteria by which episodic environmental exposures to allergen might result in the development of a remodeled lung in asthma.

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More information

e-pub ahead of print date: 28 January 2013
Published date: 2013
Organisations: Clinical & Experimental Sciences

Identifiers

Local EPrints ID: 352332
URI: http://eprints.soton.ac.uk/id/eprint/352332
ISSN: 1528-7394
PURE UUID: dc52abb9-1a6f-4c3b-a14d-ba104bbe3a90
ORCID for S.J. Wilson: ORCID iD orcid.org/0000-0003-1305-8271

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Date deposited: 09 May 2013 14:16
Last modified: 14 Mar 2024 13:50

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Contributors

Author: S.J. Wilson ORCID iD
Author: M.J. Harmer
Author: R.L. Lee
Author: H.M. Rigden
Author: N.M. Doyon-Reale
Author: K.M. Forman
Author: X. Gao
Author: M.W. Lieh-Lai
Author: D.J.P. Bassett

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