Rodriguez H J, Edelman I S
J Membr Biol. 1979 Apr 9;45(3-4):185-214. doi: 10.1007/BF01869285.
The present report describes high yield enzymatic radio-iodination of the apical and basal-lateral plasma membranes of toad bladder epithelium, by a procedure that does not breach the functional integrity of the epithelium, as assessed by the basal and vasopressin-sensitive short-circuit current (SCC). Restriction of the label to the membrane surface, was ascertained by light and electron-microscopic autoradiographs. On the apical surface, the grains were over the glycocalyx and the plasma membrane. Analysis of the labeled glycocalyx by agarose gel filtration, sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), as well as enzymatic and pH-dependent hydrolysis indicated that the glycocalyx is a trichloro-acetic acid-soluble macromolecular complex of high molecular weight composed of a peptide moiety attached to large prosthetic groups (presumably carbohydrates) by O-glycosidic bonds. Analysis of the labeled apical plasma membrane components by agarose gel filtration and SDS-PAGE disclosed the presence of six major species of apparent molecular weights: 23,000, 28,000, 37,000, 44,000, 68,000, and 95,000. More than half of the membrane-associated radio-iodine was in two bands of molecular weights 37,000 and 44,000. Concentrations of vasopressin and cyclic AMP sufficient to increase the SCC significantly did not modify the extent of membrane labeling or the distribution of the label among the apical membrane components (presumably proteins) as assessed by SDS-PAGE. Iodination in the presence of amiloride inhibited incorporation but did not change the pattern of the distribution of the label among the components resolved by SDS-PAGE. Iodination of basal-lateral plasma membranes, at a yield comparable to that obtained with apical labeling, was attained after about 30 min of exposure of the intact bladder to the labeling solutions. Approximately 25% of the basal-lateral labeling was lost when the epithelial cells were harvested after collagenase treatment, implying that some iodination of the basement membrane had taken place. Less than 10% of iodination of the apical or basal-lateral surfaces was accounted for by lipid-labeling. Analysis of the labeled apical and basal-lateral species by enzymatic digestion and thin layer chromatography disclosed that virtually all the radioactivity was present as mono-iodotyrosine (MIT).
本报告描述了蟾蜍膀胱上皮细胞顶端和基底外侧质膜的高产率酶促放射性碘化过程,该过程不会破坏上皮细胞的功能完整性,这一点通过基底和对血管加压素敏感的短路电流(SCC)来评估。通过光镜和电镜放射自显影片确定标记物仅限于膜表面。在顶端表面,颗粒位于糖萼和质膜上。通过琼脂糖凝胶过滤、十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)以及酶促和pH依赖性水解对标记的糖萼进行分析表明,糖萼是一种可溶于三氯乙酸的高分子量大分子复合物,由通过O-糖苷键连接到大型辅基(可能是碳水化合物)的肽部分组成。通过琼脂糖凝胶过滤和SDS-PAGE对标记的顶端质膜成分进行分析,发现存在六种主要的表观分子量物种:23,000、28,000、37,000、44,000、68,000和95,000。超过一半的与膜相关的放射性碘存在于分子量为37,000和44,000的两条带中。足以显著增加SCC的血管加压素和环磷酸腺苷浓度并未改变膜标记的程度或标记物在顶端膜成分(可能是蛋白质)之间的分布,这一点通过SDS-PAGE评估。在存在氨氯吡咪的情况下进行碘化抑制了掺入,但没有改变标记物在SDS-PAGE分离的成分之间的分布模式。将完整膀胱暴露于标记溶液约30分钟后,获得了与顶端标记相当产率的基底外侧质膜碘化。胶原酶处理后收获上皮细胞时,约25%的基底外侧标记丢失,这意味着基底膜发生了一些碘化。顶端或基底外侧表面碘化的不到10%是由脂质标记引起的。通过酶促消化和薄层色谱对标记的顶端和基底外侧物种进行分析表明,几乎所有的放射性都以单碘酪氨酸(MIT)的形式存在。