Meyer M M, Verkman A S
J Membr Biol. 1987;96(2):107-19. doi: 10.1007/BF01869237.
Water transport mechanisms in rabbit proximal convoluted cell membranes were examined by measurement of: osmotic (Pf) and diffusional (Pd) water permeabilities, inhibition of Pf by mercurials, and activation energies (Ea) for Pf. Pf was measured in PCT brush border (BBMV) and basolateral membrane (BLMV) vesicles, and in viable PCT cells by stopped-flow light scattering; Pd was measured in PCT cells by proton NMR T1 relaxation times using Mn as a paramagnetic quencher. In BLMV, Pf (0.019 cm/sec, 23 degrees C) was inhibited 65% by 5 mM pCMBS and 75% by 300 microM HgCl2 (KI = 42 microM); Ea increased from 3.6 to 7.6 kcal/mole (15-40 degrees C) with 300 microM HgCl2. In BBMV, Pf (0.073 cm/sec, 23 degrees C, Ea = 2.8 kcal/mole, less than 33 degrees C and 13.7 kcal/mole, greater than 33 degrees C) was inhibited 65% with HgCl2 with Ea = 9.4 kcal/mole (15-45 degrees C). Mercurial inhibition in BLMV and BBMV was reversed with 10 microM mercaptoethanol. Viable PCT cells were isolated from renal cortex by Dounce homogenization and differential seiving. Impedence sizing studies show that PCT cells are perfect osmometers (100-1000 mOsm). Assuming a cell surface-to-volume ratio of 25,000 cm-1, Pf was 0.010 +/- 0.002 cm/sec (37 degrees C) and Pd was 0.0032 cm/sec. Pf was independent of osmotic gradient size (25-1000 mOsm) with Ea 2.5 kcal/mole (less than 27 degrees C) and 12.7 kcal/mole (greater than 27 degrees C). Cell Pf was inhibited 53% by 300 microM HgCl2 (23 degrees C) with Ea 6.2 kcal/mole. These findings indicate that cell Pf is not restricted by extracellular or cytoplasmic unstirred layers and that cell Pf is not flow-dependent. The high BLMV and BBMV Pf, inhibition by HgCl2, low Ea which increases with inhibition, and the measured Pf/Pd greater than 1 in cells in the absence of unstirred layers provide strong evidence for the existence of water channels in proximal tubule brush border and basolateral membranes. These channels are similar to those found in erythrocytes and are likely required for rapid PCT transcellular water flow.
渗透水通透性(Pf)和扩散水通透性(Pd)、汞剂对Pf的抑制作用以及Pf的活化能(Ea)。通过停流光散射在近端曲管刷状缘(BBMV)和基底外侧膜(BLMV)囊泡以及活的近端曲管细胞中测量Pf;通过使用锰作为顺磁猝灭剂的质子核磁共振T1弛豫时间在近端曲管细胞中测量Pd。在BLMV中,5 mM对氯汞苯甲酸(pCMBS)使Pf(0.019 cm/秒,23℃)降低65%,300 μM HgCl2使其降低75%(抑制常数KI = 42 μM);300 μM HgCl2使Ea(15 - 40℃)从3.6千卡/摩尔增加到7.6千卡/摩尔。在BBMV中,HgCl2使Pf(0.073 cm/秒,23℃,Ea = 2.8千卡/摩尔,低于33℃时;13.7千卡/摩尔,高于33℃时)降低65%,此时Ea = 9.4千卡/摩尔(15 - 45℃)。BLMV和BBMV中的汞剂抑制作用可被10 μM巯基乙醇逆转。通过杜恩斯匀浆法和差速筛分从肾皮质中分离出活的近端曲管细胞。阻抗大小研究表明近端曲管细胞是完美的渗透压计(100 - 1000毫渗量)。假设细胞表面积与体积之比为25,000 cm-1,Pf为0.010±0.002 cm/秒(37℃),Pd为0.0032 cm/秒。Pf与渗透梯度大小(25 - 1000毫渗量)无关,Ea在低于27℃时为2.5千卡/摩尔,高于27℃时为12.7千卡/摩尔。300 μM HgCl2(23℃)使细胞Pf降低53%,此时Ea为6.2千卡/摩尔。这些发现表明细胞Pf不受细胞外或细胞质静止层的限制,且细胞Pf不依赖于流量。BLMV和BBMV中较高的Pf、HgCl2的抑制作用、抑制时升高的低Ea以及在不存在静止层的细胞中测得的Pf/Pd大于1,为近端小管刷状缘和基底外侧膜中存在水通道提供了有力证据。这些通道与红细胞中的通道相似,可能是近端曲管快速跨细胞水流所必需的。