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实验性致癌过程中肥大细胞的顺序性浸润和脱颗粒

Sequential mast cell infiltration and degranulation during experimental carcinogenesis.

作者信息

Flynn E A, Schwartz J L, Shklar G

机构信息

Harvard School of Dental Medicine, Department of Oral Medicine and Oral Pathology, Boston, MA 02115.

出版信息

J Cancer Res Clin Oncol. 1991;117(2):115-22. doi: 10.1007/BF01613134.

Abstract

Mast cell density, distribution, and ultrastructure were studied by light and electron microscopy in hamster buccal pouches undergoing chemically induced carcinogenesis. Epidermoid carcinomas in the pouches were induced by three topical applications per week of 0.5% 7,12-dimethylbenz[a]anthracene (DMBA) in oil using a brush. Four experimental, DMBA-treated and two normal, untreated hamsters were sacrificed after 8, 10, 12, 14, and 16 weeks. After 8 weeks of DMBA treatment, the epithelium showed the pathological signs of dysplasia and hyperkeratosis. In the dermis an increased number of mast cells were evident, some of which showed degranulation. A few mast cells had started to migrate upwards towards the dysplastic epithelium after 10 weeks of DMBA treatment. Rapid degranulation was also apparent in some mast cells. These processes of upward migration and degranulation continued progressively during the 12- and 14-week periods of DMBA application in correlation with the progression of the tumor. By 16 weeks of treatment with the carcinogen, more mast cells had migrated closer to the invasive carcinoma, and many had degranulated. In the connective tissue mast cells were fully packed with many granules, and some mast cells were in proximity to macrophages and eosinophils. Our observations demonstrate that there is a positive correlation between developing carcinomas and mast cell density. Mast cell migration towards the carcinoma and degranulation were also evident.

摘要

通过光学显微镜和电子显微镜研究了化学诱导致癌过程中仓鼠颊囊内肥大细胞的密度、分布和超微结构。每周用刷子在颊囊局部涂抹三次0.5%溶于油中的7,12-二甲基苯并[a]蒽(DMBA),诱导颊囊发生表皮样癌。在第8、10、12、14和16周后,处死4只经DMBA处理的实验仓鼠和2只未经处理的正常仓鼠。DMBA处理8周后,上皮细胞出现发育异常和角化过度的病理迹象。真皮内肥大细胞数量明显增加,其中一些出现脱颗粒现象。DMBA处理10周后,一些肥大细胞开始向上迁移至发育异常的上皮细胞。在12周和14周的DMBA涂抹期间,随着肿瘤进展,向上迁移和脱颗粒过程也逐渐持续。到致癌物处理16周时,更多肥大细胞迁移至浸润性癌附近,且许多已经脱颗粒。在结缔组织中,肥大细胞充满许多颗粒,一些肥大细胞靠近巨噬细胞和嗜酸性粒细胞。我们的观察表明,正在发生的癌与肥大细胞密度之间存在正相关。肥大细胞向癌的迁移和脱颗粒也很明显。

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