Brasitus T A, Goldfarb J P, Hsu K C, Tannenbaum M
Histochemistry. 1982;76(2):197-209. doi: 10.1007/BF00501922.
Cryostat and paraffin embedded sections from cecum, proximal and distal colonic segments of male Sherman rats were examined by fluorescence microscopy after labeling with six fluorescein-conjugated lectins. These FITC-conjugated lectins were used as specific probes to define the labeling pattern of carbohydrate containing components of the lumenal and basolateral surfaces of epithelial cells, goblet cell mucin and lumenal mucin at all three sites. Marked regional differences in labeling were detected, indicating that the various carbohydrate components of these cells differ significantly along the length of the colon. Furthermore, the patterns of labeling components with each lectin appeared to vary depending on the fixation technique employed. Cryostat preparations generally resulted in a broader distribution of label and more intense staining with these lectins than fixed paraffin sections. While the reason(s) for these variations remain unclear at this time and will require further studies, the present data emphasize the importance of the fixation method when interpreting results obtained utilizing FITC-conjugated lectins.
用六种异硫氰酸荧光素偶联凝集素标记后,通过荧光显微镜检查雄性谢尔曼大鼠盲肠、近端和远端结肠段的冰冻切片和石蜡包埋切片。这些异硫氰酸荧光素偶联凝集素用作特异性探针,以确定上皮细胞腔面和基底外侧表面、杯状细胞粘蛋白以及所有三个部位的腔内粘蛋白中含碳水化合物成分的标记模式。检测到明显的区域差异,表明这些细胞的各种碳水化合物成分在结肠长度上有显著差异。此外,每种凝集素标记成分的模式似乎因所采用的固定技术而异。与固定石蜡切片相比,冰冻切片通常导致这些凝集素的标记分布更广泛、染色更强。虽然目前尚不清楚这些差异的原因,需要进一步研究,但目前的数据强调了在解释利用异硫氰酸荧光素偶联凝集素获得的结果时固定方法的重要性。