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上皮细胞膜组织过程中作为极化标记的钠-糖共转运系统

Na+-sugar cotransport system as a polarization marker during organization of epithelial membrane.

作者信息

Lasheras C, Scott J A, Rabito C A

机构信息

Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston 02114.

出版信息

Am J Physiol. 1988 Dec;255(6 Pt 1):C745-53. doi: 10.1152/ajpcell.1988.255.6.C745.

Abstract

The present study analyzed the changes in Na+-dependent sugar transport and transepithelial electrical resistance as LLC-PK1 cells reorganize into epithelial membranes. Sugar influx increased to reach a maximum 9 h after plating. The increase in the transepithelial electrical resistance, however, showed a significant delay, reaching steady state 15 h after plating. No changes in the electrochemical Na+ gradient were observed during the reorganization of the epithelial membranes. Kinetic analysis and [3H]phlorizin-binding studies showed that the increase in sugar influx resulted from an increase in the number of carriers. Unidirectional sugar influx measurements indicated that the sugar transporters were primarily located at the apical surface of the epithelial cells. These observations are consistent with the hypothesis that the sorting of native proteins occurs intracellularly before their insertion in the apical membrane, or as an alternative that they are randomly inserted, but then immediately sorted such as any carrier could be detected in the basolateral side during the reorganization process. In addition, the results suggest that the functional development of the apical membrane may occur before the complete sealing of the intercellular space during the development of the occluding junctions. Furthermore, development of the sugar transport system and occluding junctions was inhibited by cycloheximide and puromycin but not by actinomycin D, suggesting that the expression of epithelial cell polarization is probably a posttranslational event in the protein synthesis.

摘要

本研究分析了LLC-PK1细胞重组成上皮膜过程中钠依赖性糖转运和跨上皮电阻的变化。接种后9小时,糖流入量增加至最大值。然而,跨上皮电阻的增加出现了显著延迟,接种后15小时达到稳态。在上皮膜重组过程中,未观察到电化学钠梯度的变化。动力学分析和[3H]根皮素结合研究表明,糖流入量的增加是由于载体数量的增加。单向糖流入测量表明,糖转运蛋白主要位于上皮细胞的顶端表面。这些观察结果与以下假设一致:天然蛋白质在插入顶端膜之前在细胞内进行分选,或者另一种情况是它们被随机插入,但随后立即进行分选,例如在重组过程中可以在基底外侧检测到任何载体。此外,结果表明,在紧密连接形成过程中,顶端膜的功能发育可能在细胞间空间完全封闭之前就已发生。此外,环己酰亚胺和嘌呤霉素可抑制糖转运系统和紧密连接的发育,但放线菌素D则无此作用,这表明上皮细胞极化的表达可能是蛋白质合成中的一个翻译后事件。

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