Effects of Hyperoxia on Cytoplasmic Thioredoxin System in Alveolar Type Epithelial Cells of Premature Rats

• Published in: Journal of Huazhong University of Science and Technology. Medical sciences Vol. 31; no. 2; pp. 258 - 263
• Main Author: 单瑞艳 常立文 李文斌 刘伟 容志惠 陈燕 曾凌空
• Format: Journal Article
• Language: English
• Published: Heidelberg Huazhong University of Science and Technology 01.04.2011; Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China%Department of Pediatrics, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China
• Subjects: Animals; Cell Hypoxia; Cells, Cultured; Cytoplasm - metabolism; Endothelial Cells - cytology; Endothelial Cells - metabolism; Female; Fetus; Lung - cytology; Lung Injury - physiopathology; Medicine; Medicine & Public Health; Pregnancy; Pulmonary Alveoli - cytology; Pulmonary Alveoli - metabolism; Rats; Rats, Sprague-Dawley; Thioredoxin Reductase 1 - metabolism; Thioredoxins - metabolism; 上皮细胞; 大鼠; 早产; 硫氧还蛋白还原酶; 系统; 细胞质; 肺泡; 高氧; hyperoxia; lung injury; thioredoxin reductase-1; apoptosis; thioredoxin-1; premature rats; alveolar type II epithelial cell; alveolar type Ⅱ epithelial cell
• ISSN: 1672-0733; 1993-1352
• DOI: 10.1007/s11596-011-0263-0

This study investigated the effects of hyperoxia on dynamic changes of thioredoxin-1 （Trx1） and thioredoxin reductase-1 （TrxR1） in alveolar type Ⅱ epithelial cells （AECⅡ） of premature rats. Pregnant Sprague-Dawley rats were sacrificed on day 19 of gestation. AECⅡ were isolated and purified from the lungs of premature rats. When cultured to 80% confluence, in vitro cells were randomly divided into air group and hyperoxia group. Cells in the hyperoxia group were continuously exposed to 95% O2/5% CO2 and those in the air group to 95% air/5% CO2. After 12, 24 and 48 h, cells in the two groups were harvested to detect their reactive oxygen species （ROS）, apoptosis, TrxR1 activity and the expressions of Trx1 and TrxR1 by corresponding protocols, respectively. The results showed that AECⅡ exposed to hyperoxia generated excessive ROS and the apoptosis percentage in the hyperoxia group was increased significantly at each time points as compared with that in the air group （P0.001）. Moreover, TrxR1 activity was found to be markedly depressed in the hyperoxia group in comparison to that in the air group （P0.001）. RT-PCR showed the expressions of both Trx1 and TrxR1 mRNA were significantly increased in AECⅡ exposed to hyperoxia for 12 and 24 h （P0.01）, respectively. At 48 h, the level of Trx1 mRNA as well as that of TrxR1 mRNA in the hyperoxia group was reduced and showed no significant difference from that in the air group （P0.05）. Western blotting showed the changes of Trx1 protein expressions in the hyperoxia group paralleled those of Trx1 mRNA expressions revealed by RT-PCR. It was concluded that hyperoxia can up-regulate the protective Trx1/TrxR1 expressed by AECⅡ in a certain period, however, also cause dysfunction of the cytoplasmic thioredoxin system by decreasing TrxR1 activity, which may contribute to the progression of oxidative stress and cell apoptosis and finally result in lung injury.