Loss of immunoreactivity for RT140, a type I cell-specific protein in the alveolar epithelium of rat lungs with bleomycin-induced fibrosis

被引:25
作者
Koslowski, R
Dobbs, LG
Wenzel, KW
Schuh, D
Müller, M
Kasper, M
机构
[1] Dresden Univ Technol, Med Fac Carl Gustav Carus, Inst Physiol Chem, D-01109 Dresden, Germany
[2] Dresden Univ Technol, Inst Pathol, D-01109 Dresden, Germany
[3] Dresden Univ Technol, Inst Anat, D-01109 Dresden, Germany
[4] Univ Calif San Francisco, Inst Cardiovasc Res, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
关键词
bleomycin; epithelium; fibrosis; lung; type I cell;
D O I
10.1183/09031936.98.12061397
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
After lung injury, the epithelial cells lining the alveolar surface in rat lung show an altered distribution of several membrane proteins, Pulmonary fibrosis was induced by intratracheal administration of bleomycin into the lung of rats and the distribution of RTI40, a recently detected alveolar epithelial type I cell antigen, was examined, as well as the relationship between RTI40 and a type I cell-specific antigen recognized by the monoclonal antibody MEP-1 and the type I cell-binding lectin Bauhinia purpurea in serial sections and double stainings, Loss of RTI40 protein was observed in fibrotic lungs, particularly in areas with obliteration of alveoli. Pre-embedding immunoelectron microscopy confirmed this observation by detection of RTI40 protein in the alveolar lumen, Western blot analysis revealed elevated levels of RTI40 in the bronchoalveolar fluid of bleomycin-treated rats with a maximum at day 7 after treatment. Twenty-eight days after bleomycin application, the bronchoalveolar fluid contained three times the amount of RTI40 mg protein(-1) of control lungs, as determined by semiquantitative dot blot. These results suggest RTI40 as a tool for the evaluation of alveolar epithelial type I cell behaviour during re-epithelialization processes.
引用
收藏
页码:1397 / 1403
页数:7
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