Duan H, Gao F, Li S, Nagata T
Department of Anatomy and Cell Biology, Shinshu University School of Medicine, Matsumoto, Japan.
Cell Mol Biol (Noisy-le-grand). 1993 May;39(3):309-16.
DNA synthesis and fine structure of the esophageal epithelium of ddY mouse in different age groups, from neonatal to senescent, were investigated by light and electron microscopic radioautography after 3H-thymidine labeling in vitro. At 1-3 days after birth, the esophagus was lined with two cell types, ciliated and nonciliated cells. From 1 week on, ciliated cells could not be found. At 2 weeks, the superficial cells still possessed nuclei and short microvilli on the apical plasma membranes. From 1 month, the superficial cells became keratinized and the microvilli on the apical plasma membrane disappeared. With aging of the mice, the epithelia became markedly thick. These results show that disappearance of ciliated cells, keratinization of superficial cells and increase of the thickness are the main changes in structure of mouse esophageal epithelium from neonatal to senescent ages. By light microscopic radioautography, labelled cells were almost confined in the basal layer, regardless of the aging stages. The highest labeling index was recorded at 1 day after birth, then decreased with age. By electron microscopic radioautography, silver grains indicating DNA synthesis were observed in nuclei. As compared with those of unlabelled cells in the basal layer, the nuclei and nucleoli of labelled cells were larger, with fewer cell organelles. The present study provides, for the first time, the basic quantitative data regarding cell proliferation of mouse esophageal epithelium from neonatal to senescent stage.
