Hatou Shin, Yamada Masakazu, Mochizuki Hiroshi, Shiraishi Atsushi, Joko Takeshi, Nishida Teruo
Division for Vision Research, National Institute of Sensory Organs, National Tokyo Medical Center, Tokyo, Japan.
Curr Eye Res. 2009 May;34(5):347-54. doi: 10.1080/02713680902829624.
The Na(+)- and K(+)-dependent ATPase (Na,K-ATPase) expressed in the basolateral membrane of corneal endothelial cells plays an important role in the pump function of the corneal endothelium. We investigated the possible role of dexamethasone in the regulation of Na,K-ATPase activity and pump function in corneal endothelial cells.
Confluent monolayers of mouse corneal endothelial cells were exposed to dexamethasone. ATPase activity of the cells was evaluated by spectrophotometric measurement of phosphate released from ATP with the use of ammonium molybdate, with Na,K-ATPase activity being defined as the portion of total ATPase activity sensitive to ouabain. Pump function of the cells was measured with the use of an Ussing chamber, with the pump function attributable to Na,K-ATPase activity being defined as the portion of the total short-circuit current sensitive to ouabain. Western blot analysis was examined to measure the expression of the Na,K-ATPase alpha(1)-subunit.
Dexamethasone (1 or 10 microM) increased the Na,K-ATPase activity and pump function of the cultured cells. These effects of dexamethasone were blocked by cycloheximide, a protein synthesis inhibitor. Western blot analysis also indicated that dexamethasone increased the expression of the Na,K-ATPase alpha(1)-subunit, whereas it decreased the expression of the phospho-Na,K-ATPase alpha(1)-subunit.
Our results suggest that dexamethasone stimulates Na,K-ATPase activity in mouse corneal endothelial cells. The effect of dexamethasone activation in these cells is mediated by Na,K-ATPase synthesis and increase in an enzymatic activity by dephosphorylation of Na,K-ATPase alpha(1)-subunits.
角膜内皮细胞基底外侧膜中表达的钠钾依赖型ATP酶(Na,K - ATP酶)在角膜内皮的泵功能中起重要作用。我们研究了地塞米松在调节角膜内皮细胞中Na,K - ATP酶活性和泵功能方面的可能作用。
将汇合的小鼠角膜内皮细胞单层暴露于地塞米松。通过使用钼酸铵分光光度法测量从ATP释放的磷酸盐来评估细胞的ATP酶活性,其中Na,K - ATP酶活性定义为对哇巴因敏感的总ATP酶活性的一部分。使用尤斯灌流小室测量细胞的泵功能,将归因于Na,K - ATP酶活性的泵功能定义为对哇巴因敏感的总短路电流的一部分。进行蛋白质印迹分析以测量Na,K - ATP酶α(1)亚基的表达。
地塞米松(1或10 microM)增加了培养细胞的Na,K - ATP酶活性和泵功能。地塞米松的这些作用被蛋白质合成抑制剂环己酰亚胺阻断。蛋白质印迹分析还表明,地塞米松增加了Na,K - ATP酶α(1)亚基的表达,而降低了磷酸化的Na,K - ATP酶α(1)亚基的表达。
我们的结果表明,地塞米松刺激小鼠角膜内皮细胞中的Na,K - ATP酶活性。地塞米松在这些细胞中的激活作用是通过Na,K - ATP酶的合成以及通过Na,K - ATP酶α(1)亚基的去磷酸化增加酶活性来介导的。