Fisher E R, Paulson J D, McCoy M M
Arch Pathol Lab Med. 1981 Jan;105(1):29-37.
Rats treated with 1,2-dimethylhydrazine (DMH) exhibited colonic mucosal dysplastic foci prior to the development of tumors. Ultrastructurally, these, as well as the cancers that subsequently developed, were characterized by alterations in plasma membranes and an increase in cytoplasmic ribosomal particles, principally in stem cells and their absorptive derivatives. Rare Kulchitsky cells appeared preserved, but the mucin-producing or goblet-cell elements were compressed and atrophic. In addition, nuclear aberrations were more pronounced in the cancer than in the dysplastic foci. The principal ultrastructural difference between the so-called well-differentiated and mucinous forms of DMH-induced cancers was the presence of frequent intracytoplasmic lumens in the mucinous form. Such structures represented the analogues of signet ring cells observed by light microscopy. This experimental model of human colonic cancer shows that the mucosal stem-cell and dysplastic lesions represent their cytogenetic and histogenetic progenitors.
用1,2 - 二甲基肼(DMH)处理的大鼠在肿瘤发生之前出现结肠黏膜发育异常病灶。在超微结构上,这些病灶以及随后发生的癌症的特征是质膜改变和细胞质核糖体颗粒增加,主要发生在干细胞及其吸收性衍生物中。罕见的库尔契茨基细胞似乎保持完好,但产生黏液的细胞或杯状细胞成分被压缩且萎缩。此外,癌症中的核畸变比发育异常病灶中更明显。DMH诱导的癌症所谓的高分化型和黏液型之间的主要超微结构差异是黏液型中频繁出现胞质内腔。这种结构相当于光镜下观察到的印戒细胞。这种人类结肠癌实验模型表明,黏膜干细胞和发育异常病变代表了它们的细胞遗传学和组织遗传学祖细胞。