Srinivas S P, Guan Y, Bonanno J A
Morton D. Sarver Center for Cornea and Contact Lens Research, University of California, School of Optometry, Berkeley, CA, 94720, USA.
Exp Eye Res. 1999 Feb;68(2):165-77. doi: 10.1006/exer.1998.0595.
Swelling induced enhancement of anion permeability was investigated using the halide-sensitive fluorescent dye SPQ in cultured bovine corneal endothelial cells (BCEC). Rates of anion influx were quantified in terms of the rate of change of SPQ fluorescence during exposure to short duration pulses of Cl-, I-or NO3-while the cells were being perfused with I-, NO3-or Cl-Ringer, respectively. Since SPQ fluorescence is quenched to different extents by these anions, their influx or efflux causes significant changes in fluorescence. The ratio of the maximum rate of change of fluorescence during the pulse period under hyposmotic conditions to that under isosmotic conditions, referred to as the enhancement ratio (ER), was calculated as a measure of the increase in anion permeability. When cells were perfused with NO3-Ringer, exposure to I-pulses yielded an ER=9.0+/-2.6 for 110+/-5 mosmhyposmotic shock. This was higher than with Cl-/I-(6.4+/-0.7) or NO3-/Cl-(3.2+/-0.8) anion-pairs for the same level of shocks. In all cases, the enhancement occurred within approximately 100 seconds after swelling but decreased with continued progress of regulatory volume decrease (RVD). ER returned to approximately 1 within 4 minutes after returning to isosmotic conditions. The membrane potential (Em) depolarized immediately after hyposmotic shock. When cells were depolarized prior to the shocks by high [K+], changes in Emwere relatively small. ER, for the NO3-/I-anion-pair, was significantly reduced by DIDS (100% at 500 microm), NPPB ( approximately 80% at 100 microm) and tamoxifen (approximately 85% at 12 microm). Tamoxifen and NPPB also inhibited swelling induced depolarization. Increasing cationic conductance with Gramicidin D at approximately 2 minutes following hyposmotic shock induced NPPB-inhibitable secondary swelling or accelerated RVD under normal or low Na+conditions, respectively. These results demonstrate that BCEC express swelling activated Cl-channels, which facilitate RVD by enhancing anionic permeability and also by providing a favorable electrical gradient for K+efflux.
利用卤化物敏感荧光染料SPQ在培养的牛角膜内皮细胞(BCEC)中研究肿胀诱导的阴离子通透性增强。在细胞分别用碘离子、硝酸根离子或氯离子林格液灌注时,通过短时间脉冲施加氯离子、碘离子或硝酸根离子期间SPQ荧光的变化率来量化阴离子内流速率。由于这些阴离子对SPQ荧光的猝灭程度不同,它们的内流或外流会导致荧光发生显著变化。将低渗条件下脉冲期荧光最大变化率与等渗条件下的荧光最大变化率之比,称为增强率(ER),作为阴离子通透性增加的一种度量来计算。当细胞用硝酸根离子林格液灌注时,对于110±5 mosm的低渗休克,暴露于碘离子脉冲产生的ER = 9.0±2.6。对于相同程度的休克,这高于氯离子/碘离子(6.4±0.7)或硝酸根离子/氯离子(3.2±0.8)阴离子对。在所有情况下,增强在肿胀后约100秒内发生,但随着调节性容积减小(RVD)的持续进行而降低。回到等渗条件后4分钟内,ER恢复到约1。低渗休克后膜电位(Em)立即去极化。当细胞在休克前通过高钾离子浓度去极化时,Em的变化相对较小。对于硝酸根离子/碘离子阴离子对,ER被二氮嗪(DIDS,500 μM时为100%)、5-硝基-2-(3-苯丙氨基)苯甲酸(NPPB,100 μM时约为80%)和他莫昔芬(12 μM时约为85%)显著降低。他莫昔芬和NPPB也抑制肿胀诱导的去极化。在低渗休克后约2分钟用短杆菌肽D增加阳离子电导,分别在正常或低钠离子条件下诱导NPPB可抑制的继发性肿胀或加速RVD。这些结果表明,BCEC表达肿胀激活的氯离子通道,其通过增强阴离子通透性以及为钾离子外流提供有利的电梯度来促进RVD。