Jentsch T J, Keller S K, Koch M, Wiederholt M
J Membr Biol. 1984;81(3):189-204. doi: 10.1007/BF01868713.
Using intracellular microelectrode technique, the response of the voltage V across the plasma membrane of cultured bovine corneal endothelial cells to changes in sodium and bicarbonate concentrations was investigated. (1) The electrical response to changes in [HCO3-]o (depolarization upon lowering and hyperpolarization upon raising [HCO3-]o) was dependent on sodium. Lithium could fairly well be substituted for sodium, whereas potassium or choline were much less effective. (2) Removal of external sodium caused a depolarization, while a readdition led to a hyperpolarization, which increased with time of preincubation in the sodium-depleted medium. (3) The response to changes in [Na+]o was dependent on bicarbonate. In a nominally bicarbonate-free medium, its amplitude was decreased or even reversed in sign. (4) Application of SITS or DIDS (10(-3) M) had a similar effect on the response to sodium as bicarbonate-depleted medium. (5) At [Na+]o = 151 mM and [HCO3-]o = 46 mM, the transients of V depended, with 39.0 +/- 9.0 (SD) mV/decade, on bicarbonate and, with 15.3 +/- 5.8 (SD) mV/decade, on sodium. (6) After the preincubation of cells with lithium, replacement of Li by choline led to similar effects as the replacement of sodium by choline, though the response of V was smaller with Li. This response could be reduced or reversed by the removal of bicarbonate or by the application of SITS. (7) Amiloride (10(-3) M) caused a reversible hyperpolarization of the steady-state potential by 8.5 +/- 2.6 mV (SD). It did not affect the immediate response to changes in [Na+]o or [HCO3-]o, but reduced the speed of regaining the steady-state potential after a change in [HCO3-]o. (8) Ouabain (10(-4) M) caused a fast depolarization of -6.8 +/- 1.1 (SD) mV, which was followed by a continuing slower depolarization. The effect was almost identical at 10(-5) M. (9) It is suggested, that corneal endothelial cells possess a cotransport for sodium and bicarbonate, which transports net negative charge with these ions. It is inhibitable by stilbenes, but not directly affected by amiloride or ouabain. Lithium is a good substitute for sodium with respect to bicarbonate transport and is transported itself. In addition, the effect of amiloride provides indirect evidence for the existence of a Na+/H+-antiport. A model for the transepithelial transport of bicarbonate across the corneal endothelium is proposed.
运用细胞内微电极技术,研究了培养的牛角膜内皮细胞质膜两侧电压V对钠和碳酸氢盐浓度变化的反应。(1) 对[HCO₃⁻]ₒ变化的电反应(降低[HCO₃⁻]ₒ时去极化,升高[HCO₃⁻]ₒ时超极化)依赖于钠。锂能较好地替代钠,而钾或胆碱的效果则差得多。(2) 去除细胞外钠会导致去极化,重新加入钠则会导致超极化,且超极化程度会随着在无钠培养基中预孵育时间的延长而增加。(3) 对[Na⁺]ₒ变化的反应依赖于碳酸氢盐。在名义上无碳酸氢盐的培养基中,其幅度会减小甚至符号反转。(4) 应用SITS或DIDS(10⁻³ M)对钠反应的影响与碳酸氢盐缺乏的培养基类似。(5) 在[Na⁺]ₒ = 151 mM和[HCO₃⁻]ₒ = 46 mM时,V的瞬变以39.0 ± 9.0(标准差)mV/十倍变化率依赖于碳酸氢盐,以15.3 ± 5.8(标准差)mV/十倍变化率依赖于钠。(6) 用锂预孵育细胞后,用胆碱替代锂产生的效果与用胆碱替代钠类似,不过V的反应在锂的情况下较小。去除碳酸氢盐或应用SITS可降低或反转这种反应。(7) 氨氯吡脒(10⁻³ M)使稳态电位可逆性超极化8.5 ± 2.6 mV(标准差)。它不影响对[Na⁺]ₒ或[HCO₃⁻]ₒ变化的即时反应,但会降低[HCO₃⁻]ₒ变化后恢复稳态电位的速度。(8) 哇巴因(10⁻⁴ M)导致快速去极化 - 6.8 ± 1.1(标准差)mV,随后是持续较慢的去极化。在10⁻⁵ M时效果几乎相同。(9) 提示角膜内皮细胞具有钠和碳酸氢盐的协同转运体,该转运体与这些离子一起转运净负电荷。它可被芪类化合物抑制,但不受氨氯吡脒或哇巴因直接影响。就碳酸氢盐转运而言,锂是钠的良好替代物且自身可被转运。此外,氨氯吡脒效应为Na⁺/H⁺逆向转运体的存在提供了间接证据。提出了碳酸氢盐跨角膜内皮细胞上皮转运的模型。