Bonanno J A, Giasson C
Morton D. Sarver Center for Cornea and Contact Lens Research, University of California, School of Optometry, Berkeley 94720.
Invest Ophthalmol Vis Sci. 1992 Oct;33(11):3058-67.
A detailed comparison of intracellular pH (pHi) regulatory mechanisms was made between fresh (FBCE) and cultured (CBCE) bovine corneal endothelium to: (1) identify the ion transport mechanisms that could directly or indirectly affect transendothelial HCO3- transport; and (2) determine if cultured cells could serve as a model for studying transendothelial bicarbonate transport. We used the pH-sensitive fluorescent probe BCECF-AM to measure pHi. FBCE and CBCE readily incorporated the dye and showed pHi calibration curves that were not significantly different with respect to pK (7.39 for FBCE and 7.35 for CBCE). Resting pHi in bicarbonate free Ringer's (pH 7.5) was significantly lower in cultured cells (7.17 +/- .02, n = 50) than in fresh cells (7.30 +/- .02, n = 54). Steady-state pHi was reduced by addition of 0.5 mmol/l amiloride, a Na+/H+ exchange blocker (-.16 pH U for FBCE, -.18 for CBCE) or removal of Na+ (-.47 pH U for FBCE, -.51 for CBCE). Recovery from an (NH4)2SO4-induced acid load was blocked by Na+ removal, and the rate of recovery was inhibited 74% and 79% in the presence of amiloride for FBCE and CBCE, respectively. The dependence of proton efflux on Na+0 showed simple saturating kinetics (apparent Km = 30 and 31 mmol/l for FBCE and CBCE, respectively), consistent with the presence of Na+/H+ exchange in FBCE and CBCE. Na+/H+ exchange activity, as measured by amiloride-sensitive acid recovery, was inversely proportional to pHi. The activity in FBCE was about twice that in CBCE. Furthermore, the zero flux point for Na+/H+ exchange was at least 0.1 pH U higher in FBCE. Changing from bicarbonate-free Ringer's to bicarbonate Ringer's (5% CO2/28 mmol/l HCO3-, pH 7.5) induced a rapid and short acidification followed by an alkalinization .09 and .18 pH U above the starting pHi for FBCE (final pHi 7.37) and CBCE (final pHi 7.33), respectively. This transition was unaffected by amiloride. Similarly, amiloride had no effect on resting pHi in bicarbonate Ringer's for FBCE or CBCE, indicating that Na+/H+ exchange does not contribute to the maintenance of the steady-state resting pHi in bicarbonate Ringer's. Although most of the characteristics of Na+/H+ exchange for FBCE and CBCE were similar, the differences in overall activity and the low levels of activity in resting cells must be considered when using CBCE to model ion coupled fluid transport in BCE.
对新鲜牛角膜内皮细胞(FBCE)和培养的牛角膜内皮细胞(CBCE)的细胞内pH(pHi)调节机制进行了详细比较,目的是:(1)确定可能直接或间接影响跨内皮HCO3-转运的离子转运机制;(2)确定培养的细胞是否可作为研究跨内皮碳酸氢盐转运的模型。我们使用对pH敏感的荧光探针BCECF-AM来测量pHi。FBCE和CBCE很容易摄取该染料,并且显示出的pHi校准曲线在pK方面没有显著差异(FBCE为7.39,CBCE为7.35)。在无碳酸氢盐的林格氏液(pH 7.5)中,培养细胞的静息pHi(7.17±0.02,n = 50)显著低于新鲜细胞(7.30±0.02,n = 54)。添加0.5 mmol/l氨氯吡咪(一种Na+/H+交换阻滞剂,FBCE降低0.16 pH单位,CBCE降低0.18 pH单位)或去除Na+(FBCE降低0.47 pH单位,CBCE降低0.51 pH单位)可使稳态pHi降低。Na+去除可阻断由(NH4)2SO4诱导的酸负荷后的恢复,并且在氨氯吡咪存在下,FBCE和CBCE的恢复速率分别被抑制74%和79%。质子外流对Na+0的依赖性表现出简单的饱和动力学(FBCE和CBCE的表观Km分别为30和31 mmol/l),这与FBCE和CBCE中存在Na+/H+交换一致。通过氨氯吡咪敏感的酸恢复测量的Na+/H+交换活性与pHi成反比。FBCE中的活性约为CBCE中的两倍。此外,FBCE中Na+/H+交换的零通量点至少比CBCE高0.1 pH单位。从无碳酸氢盐的林格氏液改为含碳酸氢盐的林格氏液(5% CO2/28 mmol/l HCO3-,pH 7.5)会引起快速且短暂的酸化,随后碱化,FBCE(最终pHi 7.37)和CBCE(最终pHi 7.33)分别比起始pHi高0.09和0.18 pH单位。这种转变不受氨氯吡咪影响。同样,氨氯吡咪对FBCE或CBCE在含碳酸氢盐林格氏液中的静息pHi没有影响,这表明Na+/H+交换对维持含碳酸氢盐林格氏液中的稳态静息pHi没有贡献。尽管FBCE和CBCE的Na+/H+交换的大多数特征相似,但在使用CBCE模拟BCE中的离子偶联流体转运时,必须考虑总体活性的差异以及静息细胞中活性水平较低的情况。