Hattori T, Fujita S
Pathol Res Pract. 1979 Jan;164(3):224-37. doi: 10.1016/S0344-0338(79)80045-X.
The non-diseased portions of the antral mucosa of patients suffering from gastric cancer or ulcer were biopsied. The biopsy specimens were then labelled with 3H-thymidine in vitro, and distribution of the labelled epithelial cells in the normal pyloric and in the intestinalized mucosa was studied with autoradiography, and modes of histogenesis and spreading of the intestinal metaplasia were studied, and kinetic characteristics of the intestinalized mucosa were discussed. In the normal pyloric mucosa, the labelled cells were confined to the isthmus region (the middle one-third level of the mucosa), indicating that the surface epithelial and the pyloric glandular cells are normally replaced from the isthmus region. On the other hand, a zone of the labelled cells was found at the lower one-third level in the intestinalized mucosa. The absorptive and the goblet cells in the intestinalized mucosa appear to be renewed by about 70 hours in a fashion similar to that of the small intestine. Microscopic and autoradiographic analysis of the antral mucosa in the course of intestinalization indicates that the intestinal metaplasia begins in the isthmus region of the pyloric glandular tubules of an intact mucosa unaffected by gross injury through transformation of the generative cells from a pyloric to an intestinal pattern. This permits the pyloric lining cells to be replaced with intestinal villous cells and also permits the generative cell zone of the intestinal tubules to shift from the isthmus to the base of the gland until the process is complete. The downward shift of the intestinal tubules occurs in a framework of one of the branched pyloric glands and other glands disappear, resulting in a change of mucosal architectures of the antrum from a branched to a simple tubular gland. The intestinal metaplasia spreads in the mucosa through multi-focal (and sporadical) transformation of the neck generative cells in individual glandular tubules.
对患有胃癌或溃疡患者的胃窦黏膜非病变部分进行活检。然后将活检标本在体外用³H-胸腺嘧啶核苷标记,用放射自显影术研究标记上皮细胞在正常幽门黏膜和肠化生黏膜中的分布,研究肠化生的组织发生方式和扩散情况,并讨论肠化生黏膜的动力学特征。在正常幽门黏膜中,标记细胞局限于峡部区域(黏膜的中三分之一水平),这表明表面上皮细胞和幽门腺细胞通常由峡部区域更新。另一方面,在肠化生黏膜的下三分之一水平发现了一个标记细胞区。肠化生黏膜中的吸收细胞和杯状细胞似乎以类似于小肠的方式在约70小时内更新。对肠化生过程中胃窦黏膜的显微镜和放射自显影分析表明,肠化生始于未受严重损伤的完整黏膜的幽门腺管峡部区域,通过生殖细胞从幽门型向肠型的转变。这使得幽门内衬细胞被肠绒毛细胞取代,也使得肠管的生殖细胞区从峡部转移到腺底部,直到过程完成。肠管的向下转移发生在一个分支幽门腺的框架内,其他腺体消失,导致胃窦黏膜结构从分支状变为简单管状腺。肠化生通过单个腺管颈部生殖细胞的多灶性(和散发性)转变在黏膜中扩散。