Open AccessModulation of reactive oxygen species by Rac1 or catalase prevents asbestos-induced pulmonary fibrosis
Author(s) -
Shubha Murthy,
Andrea AdamcakovaDodd,
Sarah S. Perry,
Linda A. Tephly,
Richard M. Keller,
Nervana Metwali,
David K. Meyerholz,
Yongqiang Wang,
Michael Glogauer,
Peter S. Thorne,
A. Brent Carter
Publication year - 2009
Publication title -
american journal of physiology. lung cellular and molecular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.892
H-Index - 163
eISSN - 1522-1504
pISSN - 1040-0605
DOI - 10.1152/ajplung.90590.2008
Subject(s) - pulmonary fibrosis , reactive oxygen species , fibrosis , catalase , rac1 , asbestos , in vivo , chemistry , pathology , cancer research , immunology , biology , medicine , oxidative stress , microbiology and biotechnology , signal transduction , biochemistry , materials science , metallurgy
The release of reactive oxygen species (ROS) and cytokines by alveolar macrophages has been demonstrated in asbestos-induced pulmonary fibrosis, but the mechanism linking alveolar macrophages to the pathogenesis is not known. The GTPase Rac1 is a second messenger that plays an important role in host defense. In this study, we demonstrate that Rac1 null mice are protected from asbestos-induced pulmonary fibrosis, as determined by histological and biochemical analysis. We hypothesized that Rac1 induced pulmonary fibrosis via generation of ROS. Asbestos increased TNF-alpha and ROS in a Rac1-dependent manner. TNF-alpha was elevated only 1 day after exposure, whereas ROS generation progressively increased in bronchoalveolar lavage cells obtained from wild-type (WT) mice. To determine whether ROS generation contributed to pulmonary fibrosis, we overexpressed catalase in WT monocytes and observed a decrease in ROS generation in vitro. More importantly, administration of catalase to WT mice attenuated the development of fibrosis in vivo. For the first time, these results demonstrate that Rac1 plays a crucial role in asbestos-induced pulmonary fibrosis. Moreover, it suggests that a simple intervention may be useful to prevent progression of the disease.