Am. J. Respir. Cell Mol. Biol., Vol 16, No. 4, 04 1997, 388-397.
Hepatocyte growth factor in bronchoalveolar lavage fluids and cells in patients with inflammatory chest diseases of the lower respiratory tract: detection by RIA and in situ hybridization
T Sakai, K Satoh, K Matsushima, S Shindo, S Abe, T Abe, M Motomiya, T Kawamoto, Y Kawabata, T Nakamura and T Nukiwa
Department of Respiratory Oncology and Molecular Medicine, Tohoku University, Aobaku, Sendai, Japan.
Pulmonary fibrosis is a chronic inflammatory disorder characterized by
diffuse fibrous remodeling of alveolar spaces. Although much interest is
focused on mechanisms of the inflammatory process in pulmonary fibrosis,
little is known about the repair and regenerative process. Hepatocyte
growth factor (HGF), originally discovered as a mitogen for hepatocyte
regeneration, is now recognized as a multifunctional mesenchymal factor for
epithelial regeneration, including the regeneration of alveolar type II
epithelial cells. Involvement of HGF and its receptor (c-met) is evident in
animal models of acute lung injury produced by hydrochloride inhalation. We
studied the role of HGF in patients with idiopathic pulmonary fibrosis
(IPF) (25 cases), lung fibrosis associated with rheumatoid arthritis (22
cases), and sarcoidosis (39 cases). Immunohistochemical evaluation
demonstrated that hyperplastic alveolar type II epithelial cells, as well
as alveolar macrophages, were strongly stained with anti-HGF antibody in
tissues of patients with IPF. The concentration of HGF in bronchoalveolar
lavage fluid (BALF) was significantly higher than in normal controls (0.23
+/- 0.09 pg/microg) in patients with IPF (0.77 +/- 0.88 pg of HGF/microg of
albumin, P < 0.001), lung fibrosis associated with rheumatoid arthritis
(0.50 +/- 0.64 pg/microg, P < 0.01), and sarcoidosis (0.41 +/- 0.61
pg/microg, P < 0.05). In situ hybridization revealed mRNA for HGF in
alveolar macrophages (especially small monocytelike macrophages). These
results indicate that the increase in HGF concentration in patients'
peripheral air spaces is due to augmented HGF production by alveolar
epithelial cells and alveolar macrophages. HGF, through a paracrine
mechanism, may play an important role in the repair and healing of the
inflammatory lung damage in pulmonary fibrosis.
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Copyright © 1997 American Thoracic Society.
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