Field M, Karnaky K J, Smith P L, Bolton J E, Kinter W B
J Membr Biol. 1978 Jul 5;41(3):265-93. doi: 10.1007/BF01870433.
The isolated intestinal mucosa of the flounder, Pseudopleuronectes americanus, when bathed in a 20 mM HCO3-Ringer's solution bubbled with 1% CO2 in O2, generated a serosa-negative PD and, when short-circuited, absorbed Cl at almost 3 times the rate of Na. Reducing HCO3 to 5 mM decreased the net Cl flux by more than 60%. The following results suggest that, despite the PD, Na and Cl transport processes are nonelectrically coupled: replacing all Na with choline abolished both the PD and net Cl flux; replacing all Cl with SO4 and mannitol abolished the PD and the net Na flux; and adding ouabain (to 0.5 mM) abolished the PD and the net Cl flux. Nearly all of the unidirectional serosa-to-mucosa Cl flux (JClsm) seemed to be paracellular since it varied with PD and Cl concentration in a manner consistent with simple diffusion. JClsm was only about one-fourth of JNasm, suggesting that the paracellular pathway is highly cation-selective. The data can be explained by the following model: (i) Na and Cl uptake across the brush border are coupled 1 : 1; Na is pumped into the lateral space and Cl follows passively, elevating the salt concentration there; (ii) the tight junction is permeable to Na but relatively impermeable to Cl; and (iii) resistance to Na diffusion is greater in the lateral space (considered in its entirety) than in the tight junction. If these assumptions are correct, the serosa-negative transmural PD is due mainly to a salt diffusion potential across the tight junction and, under short-circuit condition, most of the Na pumped into the lateral space diffuses back into the luminal solution, whereas most of the Cl enters the serosal solution. Morphological features of the epithelium support this interpretation: the cells are unusually long (60 micrometer); there is little distension of the apical 12 micrometer of the lateral space during active fluid absorption; and distension distal to this region is intermittently constricted by desmosomes.
将美洲拟庸鲽的离体肠黏膜置于用含1% CO₂的O₂鼓泡的20 mM HCO₃ - 林格氏液中时,会产生浆膜侧为负的跨膜电位(PD),并且在短路时,其吸收Cl⁻的速率几乎是Na⁺的3倍。将HCO₃⁻浓度降至5 mM会使净Cl⁻通量降低超过60%。以下结果表明,尽管存在跨膜电位,但Na⁺和Cl⁻的转运过程是非电偶联的:用胆碱替代所有Na⁺会使跨膜电位和净Cl⁻通量均消失;用SO₄²⁻和甘露醇替代所有Cl⁻会使跨膜电位和净Na⁺通量消失;加入哇巴因(至0.5 mM)会使跨膜电位和净Cl⁻通量消失。几乎所有从浆膜到黏膜的单向Cl⁻通量(JClsm)似乎都是通过细胞旁途径进行的,因为它随跨膜电位和Cl⁻浓度的变化方式与简单扩散一致。JClsm仅约为JNasm的四分之一,这表明细胞旁途径具有高度的阳离子选择性。这些数据可以用以下模型来解释:(i)Na⁺和Cl⁻通过刷状缘的摄取是1:1偶联的;Na⁺被泵入侧间隙,Cl⁻被动跟随,从而提高那里的盐浓度;(ii)紧密连接对Na⁺可通透,但对Cl⁻相对不通透;(iii)在整个侧间隙中,Na⁺扩散的阻力大于紧密连接中的阻力。如果这些假设正确,浆膜侧为负的跨膜电位主要是由于紧密连接上的盐扩散电位所致,并且在短路条件下,泵入侧间隙的大部分Na⁺会扩散回管腔溶液中,而大部分Cl⁻会进入浆膜侧溶液。上皮细胞的形态学特征支持这一解释:细胞异常长(60微米);在活跃的液体吸收过程中,侧间隙顶端12微米几乎没有扩张;并且该区域远端的扩张会被桥粒间歇性收缩。