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培养的牛角膜内皮细胞中顶端和基底外侧的二氧化碳-碳酸氢根通透性

Apical and basolateral CO2-HCO3- permeability in cultured bovine corneal endothelial cells.

作者信息

Bonanno J A, Guan Y, Jelamskii S, Kang X J

机构信息

School of Optometry, Indiana University, Bloomington, Indiana 47401, USA.

出版信息

Am J Physiol. 1999 Sep;277(3):C545-53. doi: 10.1152/ajpcell.1999.277.3.C545.

Abstract

Corneal endothelial function is dependent on HCO3- transport. However, the relative HCO3- permeabilities of the apical and basolateral membranes are unknown. Using changes in intracellular pH secondary to removing CO2-HCO3- (at constant pH) or removing HCO3- alone (at constant CO2) from apical or basolateral compartments, we determined the relative apical and basolateral HCO3- permeabilities and their dependencies on Na+ and Cl-. Removal of CO2-HCO3- from the apical side caused a steady-state alkalinization (+0.08 pH units), and removal from the basolateral side caused an acidification (-0.05 pH units). Removal of HCO3- at constant CO(2) indicated that the basolateral HCO3- fluxes were about three to four times the apical fluxes. Reducing perfusate Na+ concentration to 10 mM had no effect on apical flux but slowed basolateral HCO3- flux by one-half. In the absence of Cl-, there was an apparent increase in apical HCO3- flux under constant-pH conditions; however, no net change could be measured under constant-CO2 conditions. Basolateral flux was slowed approximately 30% in the absence of Cl-, but the net flux was unchanged. The steady-state alkalinization after removal of CO2-HCO3- apically suggests that CO2 diffusion may contribute to apical HCO3- flux through the action of a membrane-associated carbonic anhydrase. Indeed, apical CO2 fluxes were inhibited by the extracellular carbonic anhydrase inhibitor benzolamide and partially restored by exogenous carbonic anhydrase. The presence of membrane-bound carbonic anhydrase (CAIV) was confirmed by immunoblotting. We conclude that the Na+-dependent basolateral HCO3- permeability is consistent with Na+-nHCO3- cotransport. Changes in HCO3- flux in the absence of Cl- are most likely due to Na+-nHCO3- cotransport-induced membrane potential changes that cannot be dissipated. Apical HCO3- permeability is relatively low, but may be augmented by CO2 diffusion in conjunction with a CAIV.

摘要

角膜内皮功能依赖于HCO3-转运。然而,顶端膜和基底外侧膜的相对HCO3-通透性尚不清楚。通过从顶端或基底外侧隔室去除CO2-HCO3-(在恒定pH下)或单独去除HCO3-(在恒定CO2下)继发的细胞内pH变化,我们确定了顶端和基底外侧的相对HCO3-通透性及其对Na+和Cl-的依赖性。从顶端侧去除CO2-HCO3-导致稳态碱化(+0.08 pH单位),从基底外侧侧去除导致酸化(-0.05 pH单位)。在恒定CO(2)下去除HCO3-表明基底外侧HCO3-通量约为顶端通量的三到四倍。将灌注液Na+浓度降低到10 mM对顶端通量没有影响,但使基底外侧HCO3-通量减慢一半。在没有Cl-的情况下,在恒定pH条件下顶端HCO3-通量明显增加;然而,在恒定CO2条件下无法测量到净变化。在没有Cl-的情况下,基底外侧通量减慢约30%,但净通量不变。顶端去除CO2-HCO3-后的稳态碱化表明,CO2扩散可能通过膜相关碳酸酐酶的作用促进顶端HCO3-通量。事实上,顶端CO2通量受到细胞外碳酸酐酶抑制剂苯甲酰胺的抑制,并通过外源性碳酸酐酶部分恢复。通过免疫印迹证实了膜结合碳酸酐酶(CAIV)的存在。我们得出结论,Na+依赖的基底外侧HCO3-通透性与Na+-nHCO3-共转运一致。在没有Cl-的情况下HCO3-通量的变化很可能是由于Na+-nHCO3-共转运诱导的膜电位变化无法消散。顶端HCO3-通透性相对较低,但可能通过与CAIV结合的CO2扩散而增强。

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