Cellular distribution of c-Jun and c-Fos in rat lung before and after bleomycin induced injury

被引:24
作者
Haase, M
Koslowski, R
Lengnick, A
Hahn, R
Wenzel, KW
Schuh, D
Kasper, M
Muller, M
机构
[1] Tech Univ Dresden, Fac Med, Inst Pathol, D-01307 Dresden, Germany
[2] Tech Univ Dresden, Fac Med, Inst Physiol Chem, D-8027 Dresden, Germany
来源
VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY | 1997年 / 431卷 / 06期
关键词
transcription factor AP-1; pulmonary fibrosis; bleomycin; mitochondria; proliferation;
D O I
10.1007/s004280050121
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
C-Jun and c-Fos transcription factors have been associated with enhanced cellular proliferation. We studied their cellular distribution in normal and fibrotic rat lung. Pulmonary fibrosis was induced by intratracheal administration of bleomycin. In normal rat lung, c-dun and c-Fos are present in alveolar macrophages and type II pneumocytes, in the bronchiolar epithelium and in smooth muscle cells of bronchioli and blood vessels. Subcellular fractionation of proteins revealed a predominant presence of both c-dun and c-Fos in the heavy membrane fraction containing mitochondria and secretory granules. This was confirmed by immunoelectron microscopy. which also revealed a different localization of c-Jun and c-Fos in different cell types. Whereas in type LI pneumocytes and in macrophages cytoplasmic c-Jun and c-Fos is associated with mitochondria, in Clara cells of the bronchial epithelium only secretory granules contain c-Jun and c-Fos. In addition, c-Jun is strongly present in the nuclear fraction. In the fibrotic rat lung c-Jun and c-Fos are located in the same cell types as in control lungs. In addition, fibroblasts contain c-dun and c-Fos in areas of proliferation whereas in areas of complete fibrosis then is only a very weak expression of c-Jun and c-Fos.
引用
收藏
页码:441 / 448
页数:8
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