Benkoel Liliane, Dodero Frank, Hardwigsen Jean, Mas Eric, Benoliel Anne-Marie, Botta-Fridlund Danielle, Le Treut Yves Patrice, Chamlian Albert, Lombardo Dominique
INSERM U 559, Faculté de Médecine, 27 boulevard Jean Moulin, 13385 Marseille Cedex 05, France.
Dig Dis Sci. 2004 Sep;49(9):1387-93. doi: 10.1023/b:ddas.0000042235.72622.16.
We have analyzed the effect of ischemia-reperfusion on expression of hepatic Na+,K+-ATPase on bile canalicular (BCM) and basolateral membranes (BLM) in human liver allografts using confocal laser scanning microscopy imaging. Na+, K+-ATPase, an integral membrane enzyme, plays a key role in the physiology and structure of hepatocytes, where it maintains the electrochemical gradients for Na+ and K+ across the cell membrane. The concentrations of these ions as well as their gradients regulate the active transport across the plasma membrane for bile acid and water from sinusoidal to canalicular membranes. In addition, Na+,K+-ATPase is also involved in cellular structure because of its close relationship with submembrane microfilaments and its implication in tight junction assembly. Therefore, Na+,K+-ATPase appears as an indicator of tissue viability and hepatic functionality during liver transplantation. Its localization and its function in BCM are still controversial. As in previous studies, we found an enzyme expression in both BLM and BCM. We show that ischemia induced a decrease in Na+,K+-ATPase expression only in BCM. This result could be explained by the differences in biochemical membrane environment between basolateral and bile canalicular Na+,K+-ATPase. Membrane lipid fluidity, which is more elevated in BLM than in BCM, could protect the enzyme during ischemia. After reperfusion, Na+,K+-ATPase expression was strongly decreased in both BCM and BLM. This alteration following reperfusion is probably due to multiple factors: direct alteration of the enzyme catalytic subunit and modification of its environment and membrane lipid fluidity by free radicals and changes in ATP levels and ionic distribution. This important decrease in Na+,K+-ATPase expression of both BLM and BCM could disturb not only hepatic secretory function but also cellular volume and structure during the postoperative period.
我们使用共聚焦激光扫描显微镜成像技术,分析了缺血再灌注对人肝移植中肝毛细胆管膜(BCM)和基底外侧膜(BLM)上肝钠钾ATP酶表达的影响。钠钾ATP酶是一种整合膜酶,在肝细胞的生理和结构中起关键作用,它维持细胞膜两侧钠和钾的电化学梯度。这些离子的浓度及其梯度调节胆汁酸和水从肝血窦膜到毛细胆管膜的跨质膜主动转运。此外,由于钠钾ATP酶与膜下微丝密切相关且参与紧密连接组装,它也与细胞结构有关。因此,钠钾ATP酶似乎是肝移植期间组织活力和肝功能的一个指标。其在BCM中的定位和功能仍存在争议。与之前的研究一样,我们在BLM和BCM中都发现了该酶的表达。我们发现缺血仅导致BCM中钠钾ATP酶表达下降。这一结果可以通过基底外侧和毛细胆管钠钾ATP酶生化膜环境的差异来解释。BLM中的膜脂流动性高于BCM,可能在缺血期间保护了该酶。再灌注后,BCM和BLM中的钠钾ATP酶表达均大幅下降。再灌注后的这种改变可能是多种因素导致的:酶催化亚基的直接改变、自由基对其环境和膜脂流动性的修饰、ATP水平和离子分布的变化。BLM和BCM中钠钾ATP酶表达的这种显著下降不仅会干扰术后肝脏的分泌功能,还会影响细胞体积和结构。