Ura H, Nowak P, Litwin S, Watts P, Bonfil R D, Klein-Szanto A J
Department of Pathology, Fox Chase Cancer Center, Philadelphia, PA 19111.
Am J Pathol. 1989 Jan;134(1):99-106.
Epithelial cells obtained from autopsies of full-term fetuses or infants less than 1 year old were isolated, amplified in primary cultures and inoculated in deepithelialized rat tracheas. These tracheas were then sealed and transplanted subcutaneously into irradiated athymic nude mice. Four weeks after transplantation the tracheal lumen was completely covered by epithelium, most of which was of mucociliary respiratory type. At this stage, tracheal transplants containing tracheobronchial epithelium from 20 different donors were exposed to silastic devices containing 0, 0.5, 1 and 2 mg paraformaldehyde. The tracheal transplants were examined histologically at 2, 4, 8, and 16 weeks after transplantation. Before sacrifice, all animals were injected with a single pulse of tritiated thymidine. Important epithelial alterations could be seen in the formaldehyde treated transplants with a maximum effect visible at 2 weeks after exposure. The highest dose of 2 mg produced, in most cases, numerous areas of epithelial erosion and inflammation whereas this effect was not as evident with the lower doses. All doses produced areas of hyperplastic epithelium alternating with areas of pleomorphic-atrophic epithelium. Although the differences in predominance of different types of epithelium was not clearly dose-dependent, the labeling index (LI) showed dose dependence between 2 and 4 weeks after initiation of exposure. The maximum mean LI was three to four times higher than normal, although in some focal hyperplastic-metaplastic lesions the LI was increased up to 20 times. These studies show that formaldehyde, although toxic at higher doses, is able to elicit at lower doses a proliferative response of the human respiratory epithelium that is not preceded by a massive toxic effect. This response is similar, although less intense than that of the rat respiratory epithelium in which formaldehyde proved to be a carcinogen.
从足月胎儿或1岁以下婴儿的尸检中获取上皮细胞,进行原代培养扩增后接种到去上皮化的大鼠气管中。然后将这些气管密封并皮下移植到经照射的无胸腺裸鼠体内。移植4周后,气管腔完全被上皮覆盖,其中大部分为黏液纤毛呼吸型上皮。在此阶段,将来自20个不同供体的含有气管支气管上皮的气管移植暴露于含有0、0.5、1和2毫克多聚甲醛的硅橡胶装置中。在移植后2、4、8和16周对气管移植进行组织学检查。在处死前,所有动物均注射一次氚标记胸腺嘧啶核苷。在甲醛处理的移植组织中可观察到重要的上皮改变,暴露后2周可见最大效应。在大多数情况下,最高剂量2毫克会导致大量上皮糜烂和炎症区域,而较低剂量时这种效应不明显。所有剂量均产生增生性上皮区域与多形性萎缩上皮区域交替出现的情况。虽然不同类型上皮优势的差异并非明显呈剂量依赖性,但标记指数(LI)在暴露开始后2至4周显示出剂量依赖性。最大平均LI比正常情况高3至4倍,尽管在一些局灶性增生性化生病变中LI增加高达20倍。这些研究表明,甲醛虽然在高剂量时有毒,但在低剂量时能够引发人呼吸道上皮的增殖反应,且在此之前没有大规模的毒性作用。这种反应与大鼠呼吸道上皮的反应相似,尽管强度较小,在大鼠呼吸道上皮中甲醛被证明是一种致癌物。