Grichtchenko I I, Romero M F, Boron W F
Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
J Gen Physiol. 2000 May;115(5):533-46. doi: 10.1085/jgp.115.5.533.
We studied the extracellular [HCOabstract (3) (-)] dependence of two renal clones of the electrogenic Na/HCO(3) cotransporter (NBC) heterologously expressed in Xenopus oocytes. We used microelectrodes to measure the change in membrane potential (DeltaV(m)) elicited by the NBC cloned from the kidney of the salamander Ambystoma tigrinum (akNBC) and by the NBC cloned from the kidney of rat (rkNBC). We used a two-electrode voltage clamp to measure the change in current (DeltaI) elicited by rkNBC. Briefly exposing an NBC-expressing oocyte to HCOabstract (3 )(-)/CO(2) (0.33-99 mM HCOabstract (3)(-), pH(o) 7.5) elicited an immediate, DIDS (4, 4-diisothiocyanatostilbene-2,2-disulfonic acid)-sensitive and Na(+)-dependent hyperpolarization (or outward current). In DeltaV(m) experiments, the apparent K(m ) for HCOabstract (3)(-) of akNBC (10. 6 mM) and rkNBC (10.8 mM) were similar. However, under voltage-clamp conditions, the apparent K(m) for HCOabstract (3)(-) of rkNBC was less (6.5 mM). Because it has been reported that SOabstract (3)(=)/HSO abstract (3)(-) stimulates Na/HCO(3 ) cotransport in renal membrane vesicles (a result that supports the existence of a COabstract (3)(=) binding site with which SOabstract (3)(=) interacts), we examined the effect of SOabstract (3)(=)/HSO abstract (3)(-) on rkNBC. In voltage-clamp studies, we found that neither 33 mM SOabstract (4)(=) nor 33 mM SOabstract (3) (=)/HSOabstract (3)(-) substantially affects the apparent K(m) for HCO abstract (3)(-). We also used microelectrodes to monitor intracellular pH (pH(i)) while exposing rkNBC-expressing oocytes to 3.3 mM HCOabstract (3 )(-)/0.5% CO(2). We found that SO abstract (3)(=)/HSOabstract (3 )(-) did not significantly affect the DIDS-sensitive component of the pH(i) recovery from the initial CO(2 )-induced acidification. We also monitored the rkNBC current while simultaneously varying CO(2), pH(o), and COabstract (3)(=) at a fixed HCOabstract (3)(-) of 33 mM. A Michaelis-Menten equation poorly fitted the data expressed as current versus COabstract (3)(=). However, a pH titration curve nicely fitted the data expressed as current versus pH(o). Thus, rkNBC expressed in Xenopus oocytes does not appear to interact with SOabstract (3 )(=), HSOabstract (3)(-), or COabstract (3)(=).
我们研究了在非洲爪蟾卵母细胞中异源表达的两种肾源性电中性钠/碳酸氢根共转运体(NBC)克隆体对细胞外[HCO₃⁻]的依赖性。我们使用微电极测量了从虎纹钝口螈肾脏克隆的NBC(akNBC)和从大鼠肾脏克隆的NBC(rkNBC)引起的膜电位变化(ΔVₘ)。我们使用双电极电压钳测量rkNBC引起的电流变化(ΔI)。将表达NBC的卵母细胞短暂暴露于HCO₃⁻/CO₂(0.33 - 99 mM HCO₃⁻,pHₒ 7.5)会引起立即的、对4,4 - 二异硫氰酸根合芪 - 2,2 - 二磺酸(DIDS)敏感且依赖于Na⁺的超极化(或外向电流)。在ΔVₘ实验中,akNBC(10.6 mM)和rkNBC(10.8 mM)对HCO₃⁻的表观米氏常数(Kₘ)相似。然而,在电压钳条件下,rkNBC对HCO₃⁻的表观Kₘ较小(6.5 mM)。因为有报道称SO₃²⁻/HSO₃⁻刺激肾膜囊泡中的钠/碳酸氢根共转运(这一结果支持存在一个SO₃²⁻与之相互作用的CO₃²⁻结合位点),所以我们研究了SO₃²⁻/HSO₃⁻对rkNBC的影响。在电压钳研究中,我们发现33 mM SO₄²⁻和33 mM SO₃²⁻/HSO₃⁻均未显著影响HCO₃⁻的表观Kₘ。我们还使用微电极监测表达rkNBC的卵母细胞暴露于3.3 mM HCO₃⁻/0.5% CO₂时的细胞内pH(pHᵢ)。我们发现SO₃²⁻/HSO₃⁻对pHᵢ从初始CO₂诱导的酸化中恢复的DIDS敏感成分没有显著影响。我们还在固定的[HCO₃⁻]ₒ为33 mM的情况下,同时改变[CO₂]ₒ、pHₒ和[CO₃²⁻]ₒ时监测rkNBC电流。米氏方程对以电流与[CO₃²⁻]ₒ表示的数据拟合不佳。然而,pH滴定曲线对以电流与pHₒ表示的数据拟合良好。因此,在非洲爪蟾卵母细胞中表达的rkNBC似乎不与SO₃²⁻、HSO₃⁻或CO₃²⁻相互作用。