Borok Z, Danto S I, Dimen L L, Zhang X L, Lubman R L
Will Rogers Institute Pulmonary Research Center, Division of Pulmonary and Critical Care Medicine, University of Southern California, Los Angeles 90033, USA.
Am J Physiol. 1998 Jan;274(1):L149-58. doi: 10.1152/ajplung.1998.274.1.L149.
We evaluated the effects of keratinocyte growth factor (KGF) on alveolar epithelial cell (AEC) active ion transport and on rat epithelial Na channel (rENaC) subunit and Na(+)-K(+)-adenosinetriphosphatase (ATPase) subunit isoform expression using monolayers of AEC grown in primary culture. Rat alveolar type II cells were plated on polycarbonate filters in serum-free medium, and KGF (10 ng/ml) was added to confluent AEC monolayers on day 4 in culture. Exposure of AEC monolayers to KGF on day 4 resulted in dose-dependent increases in short-circuit current (Isc) compared with controls by day 5, with further increases occurring through day 8. Relative Na(+)-K(+)-ATPase alpha 1-subunit mRNA abundance was increased by 41% on days 6 and 8 after exposure to KGF, whereas alpha 2-subunit mRNA remained only marginally detectable in both the absence and presence of KGF. Levels of mRNA for the beta 1-subunit of Na(+)-K(+)-ATPase did not increase, whereas cellular alpha 1- and beta 1-subunit protein increased 70 and 31%, respectively, on day 6. mRNA for alpha-, beta-, and gamma-rENaC all decreased in abundance after treatment with KGF. These results indicate that KGF upregulates active ion transport across AEC monolayers via a KGF-induced increase in Na pumps, primarily due to increased Na(+)-K(+)-ATPase alpha 1-subunit mRNA expression. We conclude that KGF may enhance alveolar fluid clearance after acute lung injury by upregulating Na pump expression and transepithelial Na transport across the alveolar epithelium.
我们使用原代培养的肺泡上皮细胞(AEC)单层,评估了角质形成细胞生长因子(KGF)对肺泡上皮细胞主动离子转运、大鼠上皮钠通道(rENaC)亚基以及钠钾腺苷三磷酸酶(ATPase)亚基异构体表达的影响。将大鼠II型肺泡细胞接种于无血清培养基中的聚碳酸酯滤膜上,在培养第4天向汇合的AEC单层中加入KGF(10 ng/ml)。在培养第4天将AEC单层暴露于KGF,与对照组相比,到第5天短路电流(Isc)呈剂量依赖性增加,至第8天进一步增加。暴露于KGF后第6天和第8天,相对钠钾ATP酶α1亚基mRNA丰度增加了41%,而在有无KGF的情况下,α2亚基mRNA仅勉强可检测到。钠钾ATP酶β1亚基的mRNA水平未增加,而在第6天,细胞α1和β1亚基蛋白分别增加了70%和31%。用KGF处理后,α-、β-和γ-rENaC的mRNA丰度均下降。这些结果表明,KGF通过KGF诱导的钠泵增加来上调跨AEC单层的主动离子转运,主要是由于钠钾ATP酶α1亚基mRNA表达增加。我们得出结论,KGF可能通过上调钠泵表达和跨肺泡上皮的上皮钠转运来增强急性肺损伤后的肺泡液体清除。