Harvey B, Lacoste I, Ehrenfeld J
Laboratoire Jean Maetz, Départment de Biologie, Commissariat à l'Energie Atomique, Villefranche-sur-mer, France.
J Gen Physiol. 1991 Apr;97(4):749-76. doi: 10.1085/jgp.97.4.749.
We have compared the response of proton and water transport to oxytocin treatment in isolated frog skin and urinary bladder epithelia to provide further insights into the nature of water flow and H+ flux across individual apical and basolateral cell membranes. In isolated spontaneous sodium-transporting frog skin epithelia, lowering the pH of the apical solution from 7.4 to 6.4, 5.5, or 4.5 produced a fall in pHi in principal cells which was completely blocked by amiloride (50 microM), indicating that apical Na+ channels are permeable to protons. When sodium transport was blocked by amiloride, the H+ permeability of the apical membranes of principal cells was negligible but increased dramatically after treatment with antidiuretic hormone (ADH). In the latter condition, lowering the pH of the apical solution caused a voltage-dependent intracellular acidification, accompanied by membrane depolarization, and an increase in membrane conductance and transepithelial current. These effects were inhibited by adding Hg2+ (100 microM) or dicyclohexylcarbodiimide (DCCD, 10(-5) M) to the apical bath. Net titratable H+ flux across frog skin was increased from 30 +/- 8 to 115 +/- 18 neq.h-1.cm-2 (n = 8) after oxytocin treatment (at apical pH 5.5 and serosal pH 7.4) and was completely inhibited by DCCD (10(-5) M). The basolateral membranes of the principal cells in frog skin epithelium were found to be spontaneously permeable to H+ and passive electrogenic H+ transport across this membrane was not affected by oxytocin. Lowering the pH of the basolateral bathing solution (pHb) produced an intracellular acidification and membrane depolarization (and an increase in conductance when the normal dominant K+ conductance of this membrane was abolished by Ba2+ 1 mM). These effects of low pHb were blocked by micromolar concentrations of heavy metals (Zn2+, Ni2+, Co2+, Cd2+, and Hg2+). Lowering pHb in the presence of oxytocin (50 mU/ml) produced a transepithelial current (3 microA.cm-2 at pHb 5.5) which was blocked by 100 microM of Hg2+, Zn2+, or Ni2+ at the basolateral side, and by DCCD (10(-5) M) or Hg2+ (100 microM) from the apical side. The net hydroosmotic water flux (JH2O) induced by oxytocin in frog bladder sacs was blocked by inhibitors of H(+)-adenosine triphosphatase (ATPase). Diethylstilbestrol (DES 10(-5) M), oligomycin (10(-8) M), and DCCD (10(-5) M) prevented JH2O when present in the lumen. These effects cannot be attributed to inhibition of metabolism since cyanide (10(-4) M), or 2-deoxyglucose (10(-3) M) had no effect on JH2O.(ABSTRACT TRUNCATED AT 400 WORDS)
我们比较了质子和水运输对催产素处理的反应,实验对象为分离出的蛙皮和膀胱上皮,目的是进一步深入了解水流量和氢离子通量在单个顶端和基底外侧细胞膜上的特性。在分离出的具有自发钠转运功能的蛙皮上皮中,将顶端溶液的pH从7.4降至6.4、5.5或4.5,会使主细胞内的pH值下降,而这一现象被amiloride(50微摩尔)完全阻断,这表明顶端钠通道对质子具有通透性。当钠转运被amiloride阻断时,主细胞顶端膜的氢离子通透性可忽略不计,但在抗利尿激素(ADH)处理后会显著增加。在后一种情况下,降低顶端溶液的pH会导致电压依赖性细胞内酸化,伴有膜去极化,以及膜电导和跨上皮电流增加。通过向顶端浴槽中添加Hg2 +(100微摩尔)或二环己基碳二亚胺(DCCD,10^(-5) M),这些效应会受到抑制。催产素处理后(顶端pH 5.5,浆膜pH 7.4),蛙皮上可滴定氢离子的净通量从30±8增加到115±18纳eq·h^(-1)·cm^(-2)(n = 8),并被DCCD(10^(-5) M)完全抑制。发现蛙皮上皮主细胞的基底外侧膜对氢离子具有自发通透性,且跨该膜的被动生电氢离子运输不受催产素影响。降低基底外侧浴液(pHb)的pH会导致细胞内酸化和膜去极化(当该膜正常占主导的钾电导被1 mM Ba2 +消除时,电导增加)。低pHb的这些效应被微摩尔浓度的重金属(Zn2 +、Ni2 +、Co2 +、Cd2 +和Hg2 +)阻断。在催产素(50 mU/ml)存在的情况下降低pHb会产生跨上皮电流(pHb 5.5时为3微安/cm2),在基底外侧加入100微摩尔的Hg2 +、Zn2 +或Ni2 +,以及从顶端加入DCCD(10^(-5) M)或Hg2 +(100微摩尔)可阻断该电流。催产素在蛙膀胱囊中诱导的净渗透水通量(JH2O)被氢离子 - 三磷酸腺苷酶(ATPase)抑制剂阻断。己烯雌酚(DES 10^(-5) M)、寡霉素(10^(-8) M)和DCCD(10^(-5) M)存在于管腔中时可阻止JH2O。这些效应不能归因于代谢抑制,因为氰化物(10^(-4) M)或2 - 脱氧葡萄糖(10^(-3) M)对JH2O没有影响。(摘要截断于400字)