Bleomycin induces cellular senescence in alveolar epithelial cells

被引:135
作者
Aoshiba, K [1 ]
Tsuji, T [1 ]
Nagai, A [1 ]
机构
[1] Tokyo Womens Med Univ, Dept Med 1, Shinjuku Ku, Tokyo 1628666, Japan
关键词
cell aging; interstitial lung diseases; pulmonary fibrosis;
D O I
10.1183/09031936.03.00011903
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Cellular senescence is a state of irreversible growth arrest. In this paper the authors examined whether bleomycin, an agent that causes pulmonary fibrosis, induces the senescence of alveolar epithelial cells. Type II-like alveolar epithelial (A549) cells or rat primary type II cells were exposed to bleomycin and then evaluated for markers of cellular senescence. Bleomycin was also administered intratracheally in C57BL/6 mice. The authors found that exposure to bleomycin induced cellular senescence in A549 cells and rat primary type II cells. The senescence was characterised by a dose- and time-dependent increase in senescence-associated beta-galactosidase activity, senescence-associated changes in cell morphology, an increase in cell size and lysosomal mass, the overexpression of p21 protein, and irreversible growth arrest. The intratracheal injection of bleomycin in mice induced an increase in senescence-associated beta-galactosidase activity in type If epithelial cells, reaching a maximum at day 7. These results suggest that bleomycin induces a phenotype that is indistinguishable from that of senescence in alveolar epithelial cells. The induction of epithelial senescence by bleomycin may contribute to the pathway of impaired re-epithelialisation leading to pulmonary fibrosis.
引用
收藏
页码:436 / 443
页数:8
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