Suzuki S, Sakuma T, Koike K, Ono S, Tanita T, Fujimura S
Department of Thoracic Surgery, Institute of Development, Aging and Cancer, Tohoku University.
Nihon Kyobu Shikkan Gakkai Zasshi. 1996 May;34(5):506-10.
To determine the effect of time in culture on epithelial cell function, we evaluated the modulation of Na(+)-K(+)-ATPase activity in rat alveolar type II cells in culture. Ouabain sensitivity testing revealed that the alpha-1 predominance in the enzyme's isoforms was maintained over the 120 hours in culture. Basal Na(+)-K(+)-ATPase activity in the whole cell homogenate did not differ significantly between cells cultured for 48 hours and those cultured for 120 hours. Terbutaline (10 mM) did not activate Na(+)-K(+)-ATPase in the cells cultured for 48 hours, but, it significantly increased the activity of this enzyme in the cells cultured for 120 hours cells cultured for 48 hours, produced intracellular cyclic AMP after exposure to 10 mM of terbutaline. These results indicate that the coupling between Na(+)-K(+)-ATPase and the beta-adrenergic pathway in alveolar type II cells can be influenced by the time in cell culture.
为了确定培养时间对上皮细胞功能的影响,我们评估了培养的大鼠II型肺泡细胞中Na(+)-K(+)-ATP酶活性的调节情况。哇巴因敏感性测试显示,在培养的120小时内,该酶同工型中的α-1优势得以维持。在全细胞匀浆中,培养48小时的细胞与培养120小时的细胞相比,基础Na(+)-K(+)-ATP酶活性无显著差异。特布他林(10 mM)对培养48小时的细胞中的Na(+)-K(+)-ATP酶无激活作用,但在培养120小时的细胞中可显著增加该酶的活性。培养48小时的细胞在暴露于10 mM特布他林后可产生细胞内环磷酸腺苷。这些结果表明,细胞培养时间可影响II型肺泡细胞中Na(+)-K(+)-ATP酶与β-肾上腺素能途径之间的偶联。