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水通道蛋白1在视网膜新生血管形成中的表达:小鼠实验

[Expression of aquaporin 1 in retinal neovascularization: experiment with mice].

作者信息

Wang Xun, Xu Xun, Gu Qing

机构信息

Department of Ophthalmology, Shanghai Jiaotong University Afiliated First People's Hospital, Shanghai 200080, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2008 Jun 10;88(22):1569-71.

Abstract

OBJECTIVE

To investigate the expression of aquaporin (AQP) 1 in retina during neovascularization.

METHODS

Sixty C57BL/6J 7-day-old mice were randomly divided into 2 equal groups. The 30 mice of the model group were raised in 75% +/- 2% oxygen for 5 days and then returned to condition with normal oxygen (room air) for 3-5 days. 12, 15, and 17 days after birth (on the postnatal day 12, 15, and 17) 10 mice from each group were killed respectively. Immunohistochemistry was used on 6 eyes and RT-PCR and Western blotting were used to detect the mRNA and protein expression of AQP1 in 7 eyes respectively. Thirty mice were raised in normal oxygen as controls.

RESULTS

The retinal neovascularization rate on P17 in the model group was 100%. AQP1 expression in retina was seen in 1 eye from the model and control groups each on P12, and in all mice of both groups on P15 and P17, especially in the lateral retina. AQP1 expression in retinal endothelial cells was seen in the model mice and not in the control mice. There were not significant differences in the AQP1 mRNA expression level on P12 and P15 between the 2 groups, however, the AQP1 mRNA expression level on P17 was significantly higher in the model group than in the control group (1.81 +/- 1.02 vs 1.15 +/- 0.01, P = 0.000). AQP1 protein expression was seen on P12, P15, and P17 in both groups, and the AQP1 protein expression level at P17 of the model group was significantly higher than that of the control group (1.82 +/- 0.05 vs 1.57 +/- 0.04, P = 0.000).

CONCLUSION

AQP1 protein may play an important role in retinal neovascularization.

摘要

目的

研究水通道蛋白(AQP)1在视网膜新生血管形成过程中的表达情况。

方法

将60只7日龄C57BL/6J小鼠随机分为两组,每组30只。模型组的30只小鼠在75%±2%的氧气环境中饲养5天,然后放回正常氧气环境(室内空气)中3 - 5天。分别在出生后12天、15天和17天(即生后第12天、15天和17天),每组各处死10只小鼠。6只眼睛用于免疫组织化学检测,7只眼睛分别用于逆转录-聚合酶链反应(RT-PCR)和蛋白质印迹法检测AQP1的mRNA和蛋白表达。30只小鼠在正常氧气环境中饲养作为对照。

结果

模型组在P17时视网膜新生血管形成率为100%。在P12时,模型组和对照组各有1只眼睛可见视网膜中AQP1表达;在P15和P17时,两组所有小鼠均可见AQP1表达,尤其是在视网膜外侧。模型组小鼠视网膜内皮细胞可见AQP1表达,而对照组小鼠未见。两组在P12和P15时AQP1 mRNA表达水平无显著差异,但模型组在P17时AQP1 mRNA表达水平显著高于对照组(1.81±1.02 vs 1.15±0.01,P = 0.000)。两组在P12、P15和P17时均可见AQP1蛋白表达,模型组在P17时AQP1蛋白表达水平显著高于对照组(1.82±0.05 vs 1.57±0.04,P = 从0.000)。

结论

AQP1蛋白可能在视网膜新生血管形成中起重要作用。

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