Borok Z, Mihyu S, Fernandes V F, Zhang X L, Kim K J, Lubman R L
Will Rogers Institute Pulmonary Research Center, Division of Pulmonary and Critical Care Medicine, University of Southern California, Los Angeles, California 90033, USA.
Am J Physiol. 1999 Jun;276(6):C1352-60. doi: 10.1152/ajpcell.1999.276.6.C1352.
We evaluated the effects of acute hyperoxic exposure on alveolar epithelial cell (AEC) active ion transport and on expression of Na+ pump (Na+-K+-ATPase) and rat epithelial Na+ channel subunits. Rat AEC were cultivated in minimal defined serum-free medium (MDSF) on polycarbonate filters. Beginning on day 5, confluent monolayers were exposed to either 95% air-5% CO2 (normoxia) or 95% O2-5% CO2 (hyperoxia) for 48 h. Transepithelial resistance (Rt) and short-circuit current (Isc) were determined before and after exposure. Na+ channel alpha-, beta-, and gamma-subunit and Na+-K+-ATPase alpha1- and beta1-subunit mRNA levels were quantified by Northern analysis. Na+ pump alpha1- and beta1-subunit protein abundance was quantified by Western blotting. After hyperoxic exposure, Isc across AEC monolayers decreased by approximately 60% at 48 h relative to monolayers maintained under normoxic conditions. Na+ channel beta-subunit mRNA expression was reduced by hyperoxia, whereas alpha- and gamma-subunit mRNA expression was unchanged. Na+ pump alpha1-subunit mRNA was unchanged, whereas beta1-subunit mRNA was decreased approximately 80% by hyperoxia in parallel with a reduction in beta1-subunit protein. Because keratinocyte growth factor (KGF) has recently been shown to upregulate AEC active ion transport and expression of Na+-K+-ATPase under normoxic conditions, we assessed the ability of KGF to prevent hyperoxia-induced changes in active ion transport by supplementing medium with KGF (10 ng/ml) from day 2. The presence of KGF prevented the effects of hyperoxia on ion transport (as measured by Isc) relative to normoxic controls. Levels of beta1 mRNA and protein were relatively preserved in monolayers maintained in MDSF and KGF compared with those cultivated in MDSF alone. These results indicate that AEC net active ion transport is decreased after 48 h of hyperoxia, likely as a result of a decrease in the number of functional Na+ pumps per cell. KGF largely prevents this decrease in active ion transport, at least in part, by preserving Na+ pump expression.
我们评估了急性高氧暴露对肺泡上皮细胞(AEC)主动离子转运以及对钠泵(Na⁺-K⁺-ATP酶)和大鼠上皮钠通道亚基表达的影响。大鼠AEC在聚碳酸酯滤膜上的最低限度限定无血清培养基(MDSF)中培养。从第5天开始,将汇合的单层细胞暴露于95%空气-5%二氧化碳(常氧)或95%氧气-5%二氧化碳(高氧)环境中48小时。在暴露前后测定跨上皮电阻(Rt)和短路电流(Isc)。通过Northern分析对钠通道α、β和γ亚基以及Na⁺-K⁺-ATP酶α1和β1亚基的mRNA水平进行定量。通过蛋白质印迹法对钠泵α1和β1亚基的蛋白质丰度进行定量。高氧暴露后,相对于在常氧条件下维持的单层细胞,48小时时AEC单层细胞的Isc降低了约60%。高氧使钠通道β亚基的mRNA表达降低,而α和γ亚基的mRNA表达未改变。钠泵α1亚基的mRNA未改变,而β1亚基的mRNA在高氧条件下降低了约80%,同时β1亚基蛋白也减少。由于最近已证明角质形成细胞生长因子(KGF)在常氧条件下可上调AEC主动离子转运和Na⁺-K⁺-ATP酶的表达,我们从第2天开始在培养基中添加KGF(10 ng/ml),评估KGF预防高氧诱导的主动离子转运变化的能力。与常氧对照相比,KGF的存在预防了高氧对离子转运(通过Isc测量)的影响。与仅在MDSF中培养的单层细胞相比,在MDSF和KGF中维持的单层细胞中β1 mRNA和蛋白质水平相对保持。这些结果表明,高氧暴露48小时后AEC的净主动离子转运降低,这可能是由于每个细胞中功能性钠泵数量减少所致。KGF至少部分地通过保留钠泵表达来很大程度上预防主动离子转运的这种降低。