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首页> 外文期刊>American Journal of Physiology >KGF prevents hyperoxia-induced reduction of active ion transport in alveolar epithelial cells.
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KGF prevents hyperoxia-induced reduction of active ion transport in alveolar epithelial cells.

机译:KGF可防止高氧诱导的肺泡上皮细胞中活性离子转运的减少。

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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.
机译:我们评估了急性高氧暴露对肺泡上皮细胞(AEC)活性离子转运以及对Na +泵(Na + -K + -ATPase)和大鼠上皮Na +通道亚基表达的影响。大鼠AEC在聚碳酸酯过滤器上的最低限度无血清培养基(MDSF)中培养。从第5天开始,将汇合的单分子层暴露于95%空气-5%CO2(常氧)或95%O2-5%CO2(高氧症)中48小时。在曝光前后确定跨上皮电阻(Rt)和短路电流(Isc)。 Na +通道的α,β和γ亚基以及Na + -K + -ATPaseα1和β1亚基mRNA水平通过Northern分析进行定量。 Na +泵α1和β1亚基蛋白的丰度通过蛋白质印迹法定量。高氧暴露后,相对于常氧条件下维持的单层,在48 h时,AEC单层的Isc降低了约60%。 Na +通道β-亚基mRNA表达因高氧而降低,而α-和γ-亚基mRNA表达未改变。 Na +泵的α1亚基mRNA不变,而高氧血症使β1亚基mRNA降低约80%,同时β1亚基蛋白减少。由于最近已证明在常氧条件下,角质形成细胞生长因子(KGF)会上调AEC活性离子运输和Na + -K + -ATPase的表达,因此我们通过补充KGF培养基来评估KGF防止高氧诱导的活性离子运输变化的能力从第2天起(10 ng / ml)。相对于常氧对照组,KGF的存在阻止了高氧血症对离子转运的影响(通过Isc测量)。与仅在MDSF中培养的那些相比,在MDSF和KGF中维持的单层中β1mRNA和蛋白的水平相对保持不变。这些结果表明,高氧血症48小时后,AEC净活性离子迁移减少,这可能是由于每个细胞中功能性Na +泵的数量减少所致。 KGF通过保留Na +泵的表达,至少部分地防止了活性离子迁移的这种降低,至少部分地。

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