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Langerhans cell migration patterns from sheep skin following topical application of carcinogens.

机译:局部应用致癌物后朗格汉斯细胞从羊皮中迁移的模式。

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摘要

Application of tumour promoters or complete chemical carcinogens to skin alters the density and/or morphology of epidermal Langerhans cells (LC). To examine the hypothesis that these chemical carcinogens alter LC migration kinetics from the epidermis, pseudoafferent lymphatic vessels draining defined areas of carcinogen treated sheep skin were cannulated and the number of LC migrating enumerated using indirect immunofluorescence and flow cytometry. The complete carcinogen benzo[a]pyrene (BP) and the tumour promoter 12-O-tetradecanoylphorbol-13-acetate (TPA) caused an immediate two to four-fold increase in the rate of LC migration, while the tumour initiator urethane did not alter LC migration. The antigenicity of the carcinogens utilized was assessed in contact hypersensitivity experiments in mice. BP and TPA were mildly antigenic whereas urethane failed to initiate a contact hypersensitivity response in sensitized mice. It is concluded that the initial increase in LC migration from skin following the application of the tumour promoter TPA and the complete carcinogen BP is partly due to LC recognizing these carcinogens as antigens.
机译:将肿瘤促进剂或完全化学致癌物应用于皮肤会改变表皮朗格汉斯细胞(LC)的密度和/或形态。为了检验这些化学致癌物改变表皮的LC迁移动力学的假说,将引流经过致癌剂处理的绵羊皮肤的指定区域的拟affe性淋巴管插管,并使用间接免疫荧光和流式细胞术计数LC迁移的数量。完全的致癌物苯并[a] py(BP)和肿瘤促进剂12-O-十四烷酰phorbol-13-乙酸盐(TPA)导致LC迁移速率立即增加了2到4倍,而肿瘤引发剂氨基甲酸酯却没有更改LC迁移。在小鼠接触性超敏反应实验中评估了所用致癌物的抗原性。 BP和TPA具有轻度抗原性,而尿烷未能在致敏小鼠中引发接触超敏反应。结论是,在应用肿瘤促进剂TPA和完整的致癌物BP后,LC从皮肤的迁移最初增加,部分原因是LC将这些致癌物识别为抗原。

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