Surfactant protein C expression in urethane-induced murine pulmonary tumors

被引:101
作者
Mason, RJ
Kalina, M
Nielsen, LD
Malkinson, AM
Shannon, JM
机构
[1] Natl Jewish Med & Res Ctr, Dept Med, Denver, CO 80206 USA
[2] Tel Aviv Univ, Sackler Sch Med, Dept Histol & Cell Biol, IL-69978 Tel Aviv, Israel
[3] Univ Colorado, Sch Pharm, Dept Pharmaceut Sci, Denver, CO 80202 USA
关键词
D O I
10.1016/S0002-9440(10)64717-7
中图分类号
R36 [病理学];
学科分类号
100104 [病理学与病理生理学];
摘要
Mice injected with urethane develop tumors with distinct histological patterns, which are classified as solid, papillary, or a mixture of these two patterns within the same tumor. Most investigators agree that solid tumors arise from alveolar type II cells, but the cellular origin of papillary tumors is less certain, being attributed to either type II cells or nonciliated bronchiolar epithelial (Clara) cells. To characterize the state of differentiation of these tumors more precisely and to provide additional information on gene expression, we used immunocytochemistry and/or in situ hybridization to determine the cellular localization of surfactant-associated proteins A (SP-A), SP-B, SP-C, and SP-D; Clara cell-associated protein CC-10; and thyroid transcription factor-1. In normal mouse lung, the messenger RNAs (mRNAs) for SP-A, SP-B, and SP-D were expressed in both type II cells and Clara cells. SP-C mRNA, however, was expressed only in type II cells, and CC-10 expression of mRNA was restricted to Clara cells. All tumors examined, both solid and papillary, expressed SP-A, SP-B, SP-C, SP-D, and thyroid transcription factor-1, but not CC-10, However, SP-C expression was slightly diminished in larger (older) papillary tumors. These results demonstrate that urethane-induced murine lung tumors express the type II cell phenotype.
引用
收藏
页码:175 / 182
页数:8
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