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实验性皮肤致癌作用和促癌作用过程中扫描电子显微镜下观察到的表皮-真皮交界处

Epidermal-dermal junction during experimental skin carcinogenesis and cocarcinogenesis as revealed by scanning electron microscopy.

作者信息

Komitowski D

出版信息

J Invest Dermatol. 1982 May;78(5):395-401. doi: 10.1111/1523-1747.ep12507548.

Abstract

During epidermal carcinogenesis important changes in the epidermal-dermal junction take place. Because of methodological difficulties may be these changes, especially those concerned with three-dimensional organization of the junction, remain unsatisfactorily investigated. To obtain new information, we studied with scanning electron microscopy (SEM) the development of carcinogenic changes in the epidermis of mice induced by DMBA-TPA, DMBA alone, and by the cocarcinogen TPA alone. We correlated the results with those from transmission electron microscopy and light microscopy. Although the epidermal changes morphologically showed similarities, biologically they differed. With them, distinct changes in the epidermal-dermal junction developed, that could be followed through early, hyperplastic and neoplastic phases. With the SEM the first changes were seen in the basal layer of the epidermis and concerned the cell arrangement. SEM provided information about the localization and development of incipient epidermal carcinomas induced by DMBA-TPA and DMBA treatment, as well as about the changes in the basal lamina. These can be classified by their surface, their extent and their frequency throughout large regions. Our studies indicate that these changes vary greatly, depending upon the treatment used and the time of their development. Only the progressive disintegration of the basal lamina is characteristic of carcinogenesis.

摘要

在表皮癌发生过程中,表皮 - 真皮交界处会发生重要变化。由于方法学上的困难,这些变化,尤其是那些与交界处三维组织结构有关的变化,仍未得到充分研究。为了获取新信息,我们用扫描电子显微镜(SEM)研究了由二甲基苯并蒽 - 十四酰佛波醇乙酯(DMBA - TPA)、单独的DMBA以及单独的促癌剂TPA诱导的小鼠表皮致癌变化的发展过程。我们将结果与透射电子显微镜和光学显微镜的结果进行了关联。尽管表皮变化在形态学上显示出相似性,但在生物学上它们有所不同。伴随这些变化,表皮 - 真皮交界处出现了明显的变化,这些变化可以贯穿早期、增生期和肿瘤期进行追踪。通过扫描电子显微镜观察到的最初变化出现在表皮的基底层,涉及细胞排列。扫描电子显微镜提供了有关由DMBA - TPA和DMBA处理诱导的早期表皮癌的定位和发展信息,以及有关基膜变化的信息。这些变化可以根据其表面、范围以及在大区域内的频率进行分类。我们的研究表明,这些变化差异很大,取决于所使用的处理方法及其发展时间。只有基膜的逐渐崩解是致癌作用的特征。

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