Beyenbach K W
Division of Biological Sciences, Cornell University, Ithaca, N.Y.
Magnes Trace Elem. 1990;9(5):233-54.
The movement of Mg across biological membranes is reviewed from the perspectives of (1) passive transport, (2) primary active transport and (3) secondary active transport. Since all cells maintain intracellular Mg2+ at a lower electrochemical potential than extracellular Mg2+, active transport pumps bringing Mg2+ into the cell have neither been postulated nor been confirmed. Most evidence points to influx leaks, presumably via membrane channels and carriers which do not perfectly exclude Mg2+. However, Mg2+ currents have been measured in prokaryotic and eukaryotic cells suggesting the presence of Mg2+ channels. Mg2+ influx through channels is largely driven by the membrane voltage because transmembrane Mg2+ concentration differences are not very large. Efflux mechanisms have attracted most of the investigative focus. Secondary active transport by way of Na/Mg exchange appears to be widely distributed in eukaryotic cells. The early investigations of Na/Mg exchange had Mg2+ efflux driven solely by the Na+ influx (secondary active transport). However, recent studies have revealed an ATP dependence of Na/Mg exchange which may reflect the operation of an Mg2+ pump (primary active transport). Similar mechanisms of Mg2+ influx and efflux appear to operate in epithelial tissues which may net absorb or secrete Mg2+. In recent years, the intact red blood cell has emerged as the model of choice for studies of Mg2+ membrane transport. However, further probing of the details of individual transport mechanisms may be complicated by the presence of multiple parallel Mg2+ influx and efflux systems in intact cells. Accordingly, it would appear that the next round of advances in membrane transport of Mg2+ will come from studies at subcellular levels, which aim at the isolation of transporters and their reconstitution. These studies should now be possible at least for Na/Mg exchange given our fair understanding of this system in intact red blood cells.
(1)被动转运;(2)原发性主动转运;(3)继发性主动转运。由于所有细胞内的镁离子电化学势均低于细胞外,因此尚未推测或证实存在将镁离子转运至细胞内的主动转运泵。多数证据表明镁离子是通过流入渗漏进入细胞的,推测其可能通过不能完全阻止镁离子通过的膜通道和载体进入细胞。然而,在原核细胞和真核细胞中均检测到了镁离子电流,这表明存在镁离子通道。由于跨膜镁离子浓度差异不大,因此通过通道的镁离子内流主要受膜电位驱动。镁离子外流机制一直是研究的重点。通过钠/镁离子交换进行的继发性主动转运似乎在真核细胞中广泛存在。早期对钠/镁离子交换的研究表明,镁离子外流仅由钠离子内流驱动(继发性主动转运)。然而,最近的研究发现钠/镁离子交换依赖于ATP,这可能反映了镁离子泵的作用(原发性主动转运)。在可能净吸收或分泌镁离子的上皮组织中,似乎存在类似的镁离子流入和流出机制。近年来,完整红细胞已成为研究镁离子膜转运的首选模型。然而,完整细胞中存在多个平行的镁离子流入和流出系统,这可能会使对单个转运机制细节的进一步探究变得复杂。因此,镁离子膜转运的下一轮进展可能来自亚细胞水平的研究,其目的是分离转运体并进行重组。鉴于我们对完整红细胞中该系统有了较为充分的了解,目前至少对于钠/镁离子交换而言,这些研究应该是可行的。