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(Chest. 1996;109:780-786.)
© 1996 American College of Chest Physicians

Increased Expression of Platelet-Derived Growth Factor A and Insulin-Like Growth Factor-I in BAL Cells During the Development of Bleomycin-lnduced Pulmonary Fibrosis in Mice

Akihiro Maeda MD1; Keiko Hiyama MD1; Hideto Yamakido MD1; Shinichi Ishioka MD1; and Michio Yamakido MD, FCCP1

1 From the Second Department of Internal Medicine, Hiroshima (Japan) University School of Medicine

Current concepts suggest that macrophages may play a central role in pulmonary fibrosis by virtue of their ability to release a variety of cytokines. In this study, the expression of interleukin (IL)-1agr and β, platelet-derived growth factor (PDGF) A and B, and insulinlike growth factor (IGF) I in BAL cells, which may be involved in fibroblast proliferation, was investigated in murine bleomycin (BLM)-induced pulmonary fibrosis. BAL cells were obtained at 1, 15, and 29 days from Institute for Cancer Research mice after 10 days of intraperitoneal administration of BLM. The relative amounts of cytokine messenger RNA (mRNA) were evaluated by the reverse transcription-polymerase chain reaction method, which simultaneously amplified complementary DNA for cytokines and β-actin as an internal control. The level of IL-1β mRNA in BLM-treated mice was increased 4.5-fold compared with that in saline solution-treated (control) mice 1 day after treatment, while no significant differences were observed between the two groups at 15 and 29 days. The mRNAs of PDGF-A and IGF-I in BLM-treated mice were sustained at levels eightfold and threefold to fourfold, respectively, those of controls over 4 weeks. No significant differences were noted in IL-1agr and PDGF-B expression between the two groups. We conclude that IL-1β released from macrophages may be important in the early phase of inflammatory responses and that PDGF-A and IGF-I may play important roles in the development of BLM-induced pulmonary fibrosis.

Key Words: bleomycin • bronchoalveolar lavage (BAL) • insulin-like growth factor (IGF)-I • mouse • platelet-derived growth factor (PDGF) • pulmonary fibrosis • reverse transcription-polymerase chain reaction (RT-PCR)

Submitted on July 11, 1995
Accepted on September 11, 2007




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