Eveloff J, Karnaky K J, Silva P, Epstein F H, Kinter W B
J Cell Biol. 1979 Oct;83(1):16-32. doi: 10.1083/jcb.83.1.16.
Specific binding of radiolabeled inhibitor was employed to localize the Na-pump sites (Na,K-ATPase) in rectal gland epithelium, a NaCl-secreting osmoregulatory tissue which is particularly rich in pump sites. Slices of gland tissue from spiny dogfish were incubated in suitable [3H]ouabain-containing media and then prepared for Na,K-ATPase assay, measurement of radiolabel binding, or quantitative freeze-dry autoradiography at the light microscope level. Gross freezing or drying artifacts were excluded by comparison with additional aldehyde-fixed slices. Characterization experiments demonstrated high-affinity binding which correlated with Na,K-ATPase inhibition and half-saturated at approximately 5 microM [3H]ouabain. At this concentration, the normal half-loading time was approximately 1 h and low-affinity binding to nonspecific sites was negligible. Autoradiographs from both 1- and 4-h incubated slices showed approximately 85% of the bound [3H]ouabain to be localized within a 1-micrometer wide boundary region where the highly infolded basal-lateral cell membrane are closest to the mitochondria. These results establish that most of the enormous Na,K-ATPase activity associated with rectal gland epithelium is in the basal-lateral cell membrane facing interstitial fluid and not in the luminal membrane facing secreted fluid. Moreover, distribution along the basal-lateral membrane appears to be nonuniform with a higher density of enzyme sites close to mitochondria.
利用放射性标记抑制剂的特异性结合来定位直肠腺上皮中的钠泵位点(钠钾 - ATP酶),直肠腺上皮是一种分泌氯化钠的渗透调节组织,富含泵位点。将棘鲨的腺组织切片在含有合适的[³H]哇巴因的培养基中孵育,然后制备用于钠钾 - ATP酶测定、放射性标记结合测量或光镜水平的定量冷冻干燥放射自显影。通过与额外的醛固定切片比较,排除了严重的冷冻或干燥假象。表征实验表明存在高亲和力结合,其与钠钾 - ATP酶抑制相关,在约5微摩尔[³H]哇巴因时达到半饱和。在此浓度下,正常的半加载时间约为1小时,与非特异性位点的低亲和力结合可忽略不计。孵育1小时和4小时的切片的放射自显影片显示,约85%结合的[³H]哇巴因位于一个1微米宽的边界区域内,在此区域高度内褶的基底外侧细胞膜最靠近线粒体。这些结果表明,与直肠腺上皮相关的大量钠钾 - ATP酶活性大部分位于面向间质液的基底外侧细胞膜,而非面向分泌液的腔面膜。此外,沿基底外侧膜的分布似乎不均匀,靠近线粒体的酶位点密度更高。