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Vol. 124, No. 1-3, 2001
Issue release date: January–March 2001
Section title: Asthma
Int Arch Allergy Immunol 2001;124:259–261
(DOI:10.1159/000053727)

In vivo Effects of Apoptosis in Asthma Examined by a Murine Model

Ohta K. · Yamashita N. · Tajima M. · Miyasaka T. · Kawashima R. · Nakano J. · Arioka H. · Ishii A. · Horiuchi T. · Miyamoto T.
aDepartment of Medicine, Teikyo University School of Medicine, bUniversity of Tokyo School of Medicine, cKanto Chuo Hospital, and dJapanese Institute of Clinical Allergy, Tokyo, Japan

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Article / Publication Details

First-Page Preview
Abstract of Asthma

Published online: 1/24/2012

Number of Print Pages: 3
Number of Figures: 0
Number of Tables: 0

ISSN: 1018-2438 (Print)
eISSN: 1423-0097 (Online)

For additional information: http://www.karger.com/IAA

Abstract

Background: One of the characteristic features of bronchial asthma is the accumulation of various inflammatory cells, predominantly eosinophils, at the subepithelial region beneath the basement membrane of the airway. Apoptosis is a form of physiological cell death, through which the cellular contents including biologically active substances are kept in the cell membrane and are removed without their harmful effects. So, attempts were made to clarify whether the induction of apoptosis is beneficial in asthma by using a murine model with ovalbumin (OA) as responsible allergen. Methods: A/J mice, which are genetically predisposed to be hyperresponsive to acetylcholine, were immunized with OA and alum, accompanied by OA inhalation for 2 weeks, during which some of the mice were also treated with either anti-Fas monoclonal antibody or sham control hamster IgG intranasally. Airway responsiveness to acetylcholine was then analyzed by measuring airway resistance with a body plethysmograph box. Apoptosis was assessed by propidium iodide and TUNEL staining. Results: Inhalation of OA increased both airway responsiveness to acetylcholine and the number of cells, mostly eosinophils, infiltrated into the airway. Administration of anti-Fas antibody induced apoptosis in the infiltrated eosinophils and abolished augmentation of airway hyperresponsiveness caused by OA inhalation. Conclusion: Induction of apoptosis in proinflammatory cells including eosinophils at the airway may have a beneficial effect on suppressing airway hyperresponsiveness.


  

Author Contacts

Correspondence to: Dr. Ken Ohta
Department of Medicine, Teikyo University School of Medicine
2-11-1 Kaga, Itabashi-ku
Tokyo 173-8605 (Japan)
Tel. +81 3 3964 1211, ext. 1583, Fax +81 3 3964 5436, E-mail kenohta@med.teikyo-u.ac.jp

  

Article Information

Number of Print Pages : 3
Number of Figures : 0, Number of Tables : 0, Number of References : 11

  

Publication Details

International Archives of Allergy and Immunology
Founded 1950

Vol. 124, No. 1-3, Year 2001 (Cover Date: January-March 2001)

Journal Editor: D. Kraft, Vienna
ISSN: 1018–2438 (print), 1423–0097 (Online)

For additional information:http://www.karger.com/journals/iaa


Article / Publication Details

First-Page Preview
Abstract of Asthma

Published online: 1/24/2012

Number of Print Pages: 3
Number of Figures: 0
Number of Tables: 0

ISSN: 1018-2438 (Print)
eISSN: 1423-0097 (Online)

For additional information: http://www.karger.com/IAA


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