Ullrich K J, Frömter E, Murer H
Klin Wochenschr. 1979 Oct 1;57(19):977-91. doi: 10.1007/BF01479983.
Epithelia of kidney and small intestine consist of one layer of cells which, at their luminal edge, are linked together by terminal bars. Solute transport proceeds either across the cells, which is true of all active transports, or it proceeds paracellularly through the basolateral spaces and terminal bars and is then passive. The driving force for the active transport of a substance is derived either directly from metabolism (primary active transport), or from the gradient of another solute, usually Na+, which in turn is created by primary active transport. In the latter case the transport is referred to as secondary active. The driving forces of passive transport are the electrochemical gradient of the respective substance and solvent drag. The proximal parts of the kidney as well as of the intestine are leaky so that a considerable part of net reabsorption proceeds passively. Their distal parts, however, where the transport is regulated, are tight so that large concentration differences can be created and maintained. Transcellular active transport is only possible if the cells are polar, i.e., the transport characteristics of the luminal cell membrane differ from those of the contraluminal cell membrane. By measuring the cellular electrical potential difference or by measuring transport into isolated plasma membrane vesicles from either cell side the driving forces for the two transport steps, the luminal and contraluminal, have been elucidated. Schemes for the transport steps in the proximal tubule and in the small intestine are given. They show the principal similarity of the transport of many substances in both epithelia.
肾脏和小肠的上皮由一层细胞组成,这些细胞在其管腔边缘通过终末杆连接在一起。溶质转运要么跨细胞进行,所有主动转运都是如此,要么通过基底外侧间隙和终末杆进行细胞旁转运,然后是被动转运。物质主动转运的驱动力要么直接来自新陈代谢(原发性主动转运),要么来自另一种溶质(通常是Na+)的梯度,而这种梯度又是由原发性主动转运产生的。在后一种情况下,转运被称为继发性主动转运。被动转运的驱动力是各自物质的电化学梯度和溶剂拖曳。肾脏和小肠近端部分是渗漏的,因此相当一部分的净重吸收是被动进行的。然而,它们的远端部分,即转运受到调节的部分,是紧密的,因此可以产生并维持较大的浓度差异。只有当细胞具有极性时,即管腔细胞膜的转运特性与对侧细胞膜的转运特性不同时,跨细胞主动转运才有可能。通过测量细胞电位差或通过测量从细胞两侧进入分离的质膜囊泡的转运,已经阐明了管腔和对侧这两个转运步骤的驱动力。给出了近端小管和小肠中转运步骤的示意图。它们显示了两种上皮中许多物质转运的主要相似性。