Role of Metallothionein in Antigen-Related Airway Inflammation

Author:

Inoue Ken-Ichiro1,Takano Hirohisa12,Yanagisawa Rie1,Sakurai Miho1,Ichinose Takamichi3,Sadakane Kaori3,Hiyoshi Kyoko1,Sato Masahiko4,Shimada Akinori5,Inoue Mamoru2,Yoshikawa Toshikazu2

Affiliation:

1. National Institute for Environmental Studies, Tsukuba, Japan

2. Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan

3. Department of Health Science, Oita University of Nursing and Health Science, Oita, Japan

4. Department of Hygienics, Gifu Pharmaceutical University, Gifu, Japan

5. Department of Veterinary Pathology, Faculty of Agriculture, Tottori University, Tottori, Japan

Abstract

Metallothionein (MT) is a protein that can be induced by inflammatory mediators and participates in cytoprotection. However, its role in antigen-related inflammation remains to be established. We determined whether intrinsic MT protects against antigen-related airway inflammation induced by ovalbumin (OVA) in MT-I/II null (MT [–/–]) mice and in corresponding wild-type (WT) mice. MT (–/–) mice and WT mice were intratracheally challenged with OVA (1 µg per body) biweekly four times. Twenty-four hours after the last OVA challenge, significant increases were shown in the numbers of total cells, eosinophils, and neutrophils in bronchoalveolar lavage fluid from MT (–/–) mice than in those from WT mice. The protein level of interleukin-1β (IL-1β) was significantly greater in MT (–/–) mice than in WT mice after OVA challenge. Immunohistochemical analysis showed that the formations of 8-oxy-deoxyguanosine and nitrotyrosine in the lung were more intense in MT (–/–) mice than in WT mice after OVA challenge. These results indicate that endogenous MT is a protective molecule against antigen-related airway inflammation induced by OVA, at least partly, via the suppression of enhanced lung expression of IL-1β and via the antioxidative properties. Our findings suggest that MT may be a therapeutic target for the treatment of antigen-related airway inflammatory diseases such as bronchial asthma.

Publisher

SAGE Publications

Subject

General Biochemistry, Genetics and Molecular Biology

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