Thor G, Probstmeier R, Schachner M
Department of Neurobiology, University of Heidelberg, FRG.
EMBO J. 1987 Sep;6(9):2581-6. doi: 10.1002/j.1460-2075.1987.tb02548.x.
To gain insight into the cellular and molecular mechanisms underlying epithelial cell surface interactions in the adult mouse intestine, we have characterized the cell adhesion molecules L1, N-CAM and J1 by immunocytological, biochemical and cell biological methods. Whereas N-CAM and J1 expression was found to be confined to the mesenchymal and neuroectodermally-derived parts of the intestine, L1 was localized in the proliferating epithelial progenitor cells of crypts, but not in the more differentiated epithelial cells of villi. L1 was detected in crypt cells by Western blot analysis in the molecular forms characteristic of peripheral neural cells, with apparent mol. wts of 230, 180 and 150 kd. Aggregation of single, enriched crypt, but not villus cells, was strongly inhibited in the presence of Fab fragments of polyclonal L1 antibodies. These observations show that L1 is not confined to the nervous system and that it may play a functional role in the histogenesis of the intestine in the adult animal.
为深入了解成年小鼠肠道上皮细胞表面相互作用的细胞和分子机制,我们通过免疫细胞化学、生物化学和细胞生物学方法对细胞粘附分子L1、N-CAM和J1进行了表征。结果发现,N-CAM和J1的表达局限于肠道间充质和神经外胚层来源的部分,而L1则定位于隐窝中增殖的上皮祖细胞,而非绒毛中分化程度更高的上皮细胞。通过蛋白质印迹分析在隐窝细胞中检测到L1,其分子形式为外周神经细胞特有的,表观分子量为230、180和150kd。在存在多克隆L1抗体的Fab片段的情况下,单个富集的隐窝细胞(而非绒毛细胞)的聚集受到强烈抑制。这些观察结果表明,L1不仅局限于神经系统,而且可能在成年动物肠道的组织发生中发挥功能作用。