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1 Mount Sinai Hospital, Toronto, Canada M5G 1X5; 2 University of Nebraska Medical Center, Omaha, Nebraska 68198; 3 Pulmonary Medicine, Tokyo Medical and Dental University, Tokyo 113-8519; 4 Department of Respiratory Medicine, University of Tokyo, Tokyo 113-8655, Japan; 5 Department of Respiratory Diseases, Jincheng Hospital, Lanzhou 730050, China; and 6 Department of Internal Medicine, Seoul Adventist Hospital, Seoul 130-650, Korea
Cigarette smoke exposure has been
associated with a variety of diseases, including emphysema. The current
study evaluated the interaction of cell density and cigarette smoke
extract (CSE) on fibroblast contraction of collagen gels. Protein
levels of transforming growth factor (TGF)-
1, fibronectin,
PGE2, and TGF-
1 mRNA were quantified. Although both 5 and 10% CSE inhibited contraction by low-density fibroblasts (1 × 105 cell/ml), only 5% CSE augmented contraction in
higher-density cultures (3-5 × 105 cells/ml).
CSE also inhibited fibronectin and TGF-
1 production in low-density
cultures but stimulated fibronectin production in high-density
cultures. Active TGF-
1 was readily detectable only in higher-density
cultures and was markedly augmented by 5% CSE. In contrast, although
TGF-
1 mRNA expression was inhibited in high-density cultures by 10%
CSE, expression was increased in the presence of 5% CSE. These results
suggest that CSE-induced inhibition of low-density fibroblast
contraction is due to inhibition of fibronectin production, whereas
CSE's stimulatory effect on high-density cells is the result of
increased release of TGF-
1. These effects may help explain the
varied pathologies associated with exposure to cigarette smoke.
cigarette smoke extract; collagen gels; transforming growth
factor-
; lung
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