Suppr超能文献

二甲基苯并(a)蒽预先暴露的气管外植体中特定病变的定位

Localization of specific lesions in dimethylbenz(a)anthracene-preexposed tracheal explants.

作者信息

Marchok A C, Nettesheim P, Johnston W W

出版信息

Am J Pathol. 1982 Dec;109(3):321-9.

Abstract

An experimental model is described for separating out and identifying, by a nondestructive method, lesions induced in rat tracheal implants exposed to 200 micrograms dimethylbenz(a)anthracene (DMBA)-beeswax pellets. The approach was to cut exposed and nonexposed tracheas into 2 x 3-mm explants and place them in organ culture for 24 hours. The medium was collected, and the exfoliated cells in the medium were stained by the Papanicolaou method for cytologic diagnosis. The exfoliated cells were graded according to the degree of atypia by conventional cytologic criteria. To validate the cytologic diagnoses, 60 organ cultures were fixed, sectioned, and stained; and the histopathologic diagnoses were compared. In most cases, the cytologic findings were predictive of the histopathologic results. To test for alterations in growth characteristics of cell populations derived from specific lesions, epithelial cell cultures were established from 35 organ cultures. All primary cultures from explants showing moderate or more severe atypia, and 40% from those showing regular metaplasia or mildly atypical lesions, survived and grew in culture. Cultures from unexposed tracheas did not survive.

摘要

描述了一种实验模型,用于通过无损方法分离和鉴定暴露于200微克二甲基苯并(a)蒽(DMBA)-蜂蜡颗粒的大鼠气管植入物中诱导的病变。方法是将暴露和未暴露的气管切成2×3毫米的外植体,并将它们置于器官培养中24小时。收集培养基,并用巴氏染色法对培养基中的脱落细胞进行染色以进行细胞学诊断。根据传统细胞学标准,根据异型程度对脱落细胞进行分级。为了验证细胞学诊断,对60个器官培养物进行固定、切片和染色,并比较组织病理学诊断。在大多数情况下,细胞学发现可预测组织病理学结果。为了测试源自特定病变的细胞群体生长特性的改变,从35个器官培养物中建立了上皮细胞培养物。来自显示中度或更严重异型性的外植体的所有原代培养物,以及来自显示规则化生或轻度异型性病变的外植体的40%,在培养中存活并生长。来自未暴露气管的培养物未能存活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54cb/1916115/e601d290165c/amjpathol00201-0076-a.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验